PubMed:20431083
Annnotations
LitCoin-sentences
{"project":"LitCoin-sentences","denotations":[{"id":"T1","span":{"begin":0,"end":134},"obj":"Sentence"},{"id":"T2","span":{"begin":135,"end":158},"obj":"Sentence"},{"id":"T3","span":{"begin":159,"end":327},"obj":"Sentence"},{"id":"T4","span":{"begin":328,"end":495},"obj":"Sentence"},{"id":"T5","span":{"begin":496,"end":504},"obj":"Sentence"},{"id":"T6","span":{"begin":505,"end":814},"obj":"Sentence"},{"id":"T7","span":{"begin":815,"end":934},"obj":"Sentence"},{"id":"T8","span":{"begin":935,"end":943},"obj":"Sentence"},{"id":"T9","span":{"begin":944,"end":1258},"obj":"Sentence"},{"id":"T10","span":{"begin":1259,"end":1458},"obj":"Sentence"},{"id":"T11","span":{"begin":1459,"end":1688},"obj":"Sentence"},{"id":"T12","span":{"begin":1689,"end":1878},"obj":"Sentence"},{"id":"T13","span":{"begin":1879,"end":1891},"obj":"Sentence"},{"id":"T14","span":{"begin":1892,"end":2023},"obj":"Sentence"},{"id":"T15","span":{"begin":2024,"end":2130},"obj":"Sentence"}],"text":"Antithrombotic drug use, cerebral microbleeds, and intracerebral hemorrhage: a systematic review of published and unpublished studies.\nBACKGROUND AND PURPOSE: Cerebral microbleeds (MB) are potential risk factors for intracerebral hemorrhage (ICH), but it is unclear if they are a contraindication to using antithrombotic drugs. Insights could be gained by pooling data on MB frequency stratified by antithrombotic use in cohorts with ICH and ischemic stroke (IS)/transient ischemic attack (TIA).\nMETHODS: We performed a systematic review of published and unpublished data from cohorts with stroke or TIA to compare the presence of MB in: (1) antithrombotic users vs nonantithrombotic users with ICH; (2) antithrombotic users vs nonusers with IS/TIA; and (3) ICH vs ischemic events stratified by antithrombotic use. We also analyzed published and unpublished follow-up data to determine the risk of ICH in antithrombotic users with MB.\nRESULTS: In a pooled analysis of 1460 ICH and 3817 IS/TIA, MB were more frequent in ICH vs IS/TIA in all treatment groups, but the excess increased from 2.8 (odds ratio; range, 2.3-3.5) in nonantithrombotic users to 5.7 (range, 3.4-9.7) in antiplatelet users and 8.0 (range, 3.5-17.8) in warfarin users (P difference=0.01). There was also an excess of MB in warfarin users vs nonusers with ICH (OR, 2.7; 95% CI, 1.6-4.4; P\u003c0.001) but none in warfarin users with IS/TIA (OR, 1.3; 95% CI, 0.9-1.7; P=0.33; P difference=0.01). There was a smaller excess of MB in antiplatelet users vs nonusers with ICH (OR, 1.7; 95% CI, 1.3-2.3; P\u003c0.001), but findings were similar for antiplatelet users with IS/TIA (OR, 1.4; 95% CI, 1.2-1.7; P\u003c0.001; P difference=0.25). In pooled follow-up data for 768 antithrombotic users, presence of MB at baseline was associated with a substantially increased risk of subsequent ICH (OR, 12.1; 95% CI, 3.4-42.5; P\u003c0.001).\nCONCLUSIONS: The excess of MB in warfarin users with ICH compared to other groups suggests that MB increase the risk of warfarin-associated ICH. Limited prospective data corroborate these findings, but larger prospective studies are urgently required."}
LitCoin-entities
{"project":"LitCoin-entities","denotations":[{"id":"7294","span":{"begin":0,"end":19},"obj":"ChemicalEntity"},{"id":"7295","span":{"begin":25,"end":45},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7296","span":{"begin":51,"end":75},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7297","span":{"begin":159,"end":179},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7298","span":{"begin":181,"end":183},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7299","span":{"begin":216,"end":240},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7300","span":{"begin":242,"end":245},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7301","span":{"begin":306,"end":326},"obj":"ChemicalEntity"},{"id":"7302","span":{"begin":372,"end":374},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7303","span":{"begin":434,"end":437},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7304","span":{"begin":442,"end":457},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7305","span":{"begin":459,"end":461},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7306","span":{"begin":463,"end":488},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7307","span":{"begin":490,"end":493},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7308","span":{"begin":590,"end":596},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7309","span":{"begin":600,"end":603},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7310","span":{"begin":631,"end":633},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7311","span":{"begin":695,"end":698},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7312","span":{"begin":742,"end":744},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7313","span":{"begin":745,"end":748},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7314","span":{"begin":758,"end":761},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7315","span":{"begin":765,"end":773},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7316","span":{"begin":898,"end":901},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7317","span":{"begin":931,"end":933},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7318","span":{"begin":973,"end":976},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7319","span":{"begin":986,"end":988},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7320","span":{"begin":989,"end":992},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7321","span":{"begin":994,"end":996},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7322","span":{"begin":1019,"end":1022},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7323","span":{"begin":1026,"end":1028},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7324","span":{"begin":1029,"end":1032},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7325","span":{"begin":1223,"end":1231},"obj":"ChemicalEntity"},{"id":"7326","span":{"begin":1287,"end":1289},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7327","span":{"begin":1293,"end":1301},"obj":"ChemicalEntity"},{"id":"7328","span":{"begin":1325,"end":1328},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7329","span":{"begin":1377,"end":1385},"obj":"ChemicalEntity"},{"id":"7330","span":{"begin":1397,"end":1399},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7331","span":{"begin":1400,"end":1403},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7332","span":{"begin":1489,"end":1491},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7333","span":{"begin":1531,"end":1534},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7334","span":{"begin":1626,"end":1628},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7335","span":{"begin":1629,"end":1632},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7336","span":{"begin":1756,"end":1758},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7337","span":{"begin":1836,"end":1839},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7338","span":{"begin":1906,"end":1908},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7339","span":{"begin":1912,"end":1920},"obj":"ChemicalEntity"},{"id":"7340","span":{"begin":1932,"end":1935},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7341","span":{"begin":1975,"end":1977},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7342","span":{"begin":1999,"end":2007},"obj":"ChemicalEntity"},{"id":"7343","span":{"begin":2019,"end":2022},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A34","pred":"db_id","subj":"7327","obj":"MESH:D014859"},{"id":"A9","pred":"db_id","subj":"7302","obj":"MESH:D002543"},{"id":"A18","pred":"db_id","subj":"7311","obj":"MESH:D002543"},{"id":"A27","pred":"db_id","subj":"7320","obj":"MESH:D002546"},{"id":"A50","pred":"db_id","subj":"7343","obj":"MESH:D002543"},{"id":"A37","pred":"db_id","subj":"7330","obj":"MESH:D002544"},{"id":"A2","pred":"db_id","subj":"7295","obj":"MESH:D002543"},{"id":"A30","pred":"db_id","subj":"7323","obj":"MESH:D002544"},{"id":"A22","pred":"db_id","subj":"7315","obj":"MESH:D007511"},{"id":"A47","pred":"db_id","subj":"7340","obj":"MESH:D002543"},{"id":"A10","pred":"db_id","subj":"7303","obj":"MESH:D002543"},{"id":"A39","pred":"db_id","subj":"7332","obj":"MESH:D002543"},{"id":"A3","pred":"db_id","subj":"7296","obj":"MESH:D002543"},{"id":"A13","pred":"db_id","subj":"7306","obj":"MESH:D002546"},{"id":"A15","pred":"db_id","subj":"7308","obj":"MESH:D020521"},{"id":"A4","pred":"db_id","subj":"7297","obj":"MESH:D002543"},{"id":"A1","pred":"db_id","subj":"7294","obj":"MESH:D005343"},{"id":"A17","pred":"db_id","subj":"7310","obj":"MESH:D002543"},{"id":"A42","pred":"db_id","subj":"7335","obj":"MESH:D002546"},{"id":"A49","pred":"db_id","subj":"7342","obj":"MESH:D014859"},{"id":"A31","pred":"db_id","subj":"7324","obj":"MESH:D002546"},{"id":"A32","pred":"db_id","subj":"7325","obj":"MESH:D014859"},{"id":"A20","pred":"db_id","subj":"7313","obj":"MESH:D002546"},{"id":"A33","pred":"db_id","subj":"7326","obj":"MESH:D002543"},{"id":"A11","pred":"db_id","subj":"7304","obj":"MESH:D002544"},{"id":"A29","pred":"db_id","subj":"7322","obj":"MESH:D002543"},{"id":"A46","pred":"db_id","subj":"7339","obj":"MESH:D014859"},{"id":"A36","pred":"db_id","subj":"7329","obj":"MESH:D014859"},{"id":"A21","pred":"db_id","subj":"7314","obj":"MESH:D002543"},{"id":"A38","pred":"db_id","subj":"7331","obj":"MESH:D002546"},{"id":"A45","pred":"db_id","subj":"7338","obj":"MESH:D002543"},{"id":"A8","pred":"db_id","subj":"7301","obj":"MESH:D005343"},{"id":"A14","pred":"db_id","subj":"7307","obj":"MESH:D002546"},{"id":"A12","pred":"db_id","subj":"7305","obj":"MESH:D002544"},{"id":"A25","pred":"db_id","subj":"7318","obj":"MESH:D002543"},{"id":"A44","pred":"db_id","subj":"7337","obj":"MESH:D002543"},{"id":"A24","pred":"db_id","subj":"7317","obj":"MESH:D002543"},{"id":"A43","pred":"db_id","subj":"7336","obj":"MESH:D002543"},{"id":"A7","pred":"db_id","subj":"7300","obj":"MESH:D002543"},{"id":"A19","pred":"db_id","subj":"7312","obj":"MESH:D002544"},{"id":"A35","pred":"db_id","subj":"7328","obj":"MESH:D002543"},{"id":"A5","pred":"db_id","subj":"7298","obj":"MESH:D002543"},{"id":"A6","pred":"db_id","subj":"7299","obj":"MESH:D002543"},{"id":"A16","pred":"db_id","subj":"7309","obj":"MESH:D002546"},{"id":"A41","pred":"db_id","subj":"7334","obj":"MESH:D002544"},{"id":"A26","pred":"db_id","subj":"7319","obj":"MESH:D002544"},{"id":"A23","pred":"db_id","subj":"7316","obj":"MESH:D002543"},{"id":"A40","pred":"db_id","subj":"7333","obj":"MESH:D002543"},{"id":"A48","pred":"db_id","subj":"7341","obj":"MESH:D002543"},{"id":"A28","pred":"db_id","subj":"7321","obj":"MESH:D002543"}],"namespaces":[{"prefix":"_base","uri":"https://w3id.org/biolink/vocab/"},{"prefix":"MESH","uri":"http://id.nlm.nih.gov/mesh/"},{"prefix":"NCBITaxon","uri":"https://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?id="},{"prefix":"NCBIGene","uri":"https://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"OMIM","uri":"https://www.omim.org/entry/"},{"prefix":"DBSNP","uri":"https://www.ncbi.nlm.nih.gov/snp/"}],"text":"Antithrombotic drug use, cerebral microbleeds, and intracerebral hemorrhage: a systematic review of published and unpublished studies.\nBACKGROUND AND PURPOSE: Cerebral microbleeds (MB) are potential risk factors for intracerebral hemorrhage (ICH), but it is unclear if they are a contraindication to using antithrombotic drugs. Insights could be gained by pooling data on MB frequency stratified by antithrombotic use in cohorts with ICH and ischemic stroke (IS)/transient ischemic attack (TIA).\nMETHODS: We performed a systematic review of published and unpublished data from cohorts with stroke or TIA to compare the presence of MB in: (1) antithrombotic users vs nonantithrombotic users with ICH; (2) antithrombotic users vs nonusers with IS/TIA; and (3) ICH vs ischemic events stratified by antithrombotic use. We also analyzed published and unpublished follow-up data to determine the risk of ICH in antithrombotic users with MB.\nRESULTS: In a pooled analysis of 1460 ICH and 3817 IS/TIA, MB were more frequent in ICH vs IS/TIA in all treatment groups, but the excess increased from 2.8 (odds ratio; range, 2.3-3.5) in nonantithrombotic users to 5.7 (range, 3.4-9.7) in antiplatelet users and 8.0 (range, 3.5-17.8) in warfarin users (P difference=0.01). There was also an excess of MB in warfarin users vs nonusers with ICH (OR, 2.7; 95% CI, 1.6-4.4; P\u003c0.001) but none in warfarin users with IS/TIA (OR, 1.3; 95% CI, 0.9-1.7; P=0.33; P difference=0.01). There was a smaller excess of MB in antiplatelet users vs nonusers with ICH (OR, 1.7; 95% CI, 1.3-2.3; P\u003c0.001), but findings were similar for antiplatelet users with IS/TIA (OR, 1.4; 95% CI, 1.2-1.7; P\u003c0.001; P difference=0.25). In pooled follow-up data for 768 antithrombotic users, presence of MB at baseline was associated with a substantially increased risk of subsequent ICH (OR, 12.1; 95% CI, 3.4-42.5; P\u003c0.001).\nCONCLUSIONS: The excess of MB in warfarin users with ICH compared to other groups suggests that MB increase the risk of warfarin-associated ICH. Limited prospective data corroborate these findings, but larger prospective studies are urgently required."}
LitCoin_Mondo
{"project":"LitCoin_Mondo","denotations":[{"id":"T1","span":{"begin":25,"end":33},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":51,"end":75},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":159,"end":167},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":216,"end":240},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T5","span":{"begin":463,"end":488},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"0002645"},{"id":"A2","pred":"mondo_id","subj":"T2","obj":"0013792"},{"id":"A3","pred":"mondo_id","subj":"T3","obj":"0002645"},{"id":"A4","pred":"mondo_id","subj":"T4","obj":"0013792"},{"id":"A5","pred":"mondo_id","subj":"T5","obj":"0005264"}],"text":"Antithrombotic drug use, cerebral microbleeds, and intracerebral hemorrhage: a systematic review of published and unpublished studies.\nBACKGROUND AND PURPOSE: Cerebral microbleeds (MB) are potential risk factors for intracerebral hemorrhage (ICH), but it is unclear if they are a contraindication to using antithrombotic drugs. Insights could be gained by pooling data on MB frequency stratified by antithrombotic use in cohorts with ICH and ischemic stroke (IS)/transient ischemic attack (TIA).\nMETHODS: We performed a systematic review of published and unpublished data from cohorts with stroke or TIA to compare the presence of MB in: (1) antithrombotic users vs nonantithrombotic users with ICH; (2) antithrombotic users vs nonusers with IS/TIA; and (3) ICH vs ischemic events stratified by antithrombotic use. We also analyzed published and unpublished follow-up data to determine the risk of ICH in antithrombotic users with MB.\nRESULTS: In a pooled analysis of 1460 ICH and 3817 IS/TIA, MB were more frequent in ICH vs IS/TIA in all treatment groups, but the excess increased from 2.8 (odds ratio; range, 2.3-3.5) in nonantithrombotic users to 5.7 (range, 3.4-9.7) in antiplatelet users and 8.0 (range, 3.5-17.8) in warfarin users (P difference=0.01). There was also an excess of MB in warfarin users vs nonusers with ICH (OR, 2.7; 95% CI, 1.6-4.4; P\u003c0.001) but none in warfarin users with IS/TIA (OR, 1.3; 95% CI, 0.9-1.7; P=0.33; P difference=0.01). There was a smaller excess of MB in antiplatelet users vs nonusers with ICH (OR, 1.7; 95% CI, 1.3-2.3; P\u003c0.001), but findings were similar for antiplatelet users with IS/TIA (OR, 1.4; 95% CI, 1.2-1.7; P\u003c0.001; P difference=0.25). In pooled follow-up data for 768 antithrombotic users, presence of MB at baseline was associated with a substantially increased risk of subsequent ICH (OR, 12.1; 95% CI, 3.4-42.5; P\u003c0.001).\nCONCLUSIONS: The excess of MB in warfarin users with ICH compared to other groups suggests that MB increase the risk of warfarin-associated ICH. Limited prospective data corroborate these findings, but larger prospective studies are urgently required."}
LitCoin-GeneOrGeneProduct-v0
{"project":"LitCoin-GeneOrGeneProduct-v0","denotations":[{"id":"T1","span":{"begin":181,"end":183},"obj":"GeneOrGeneProduct"},{"id":"T2","span":{"begin":204,"end":215},"obj":"GeneOrGeneProduct"},{"id":"T3","span":{"begin":258,"end":265},"obj":"GeneOrGeneProduct"},{"id":"T4","span":{"begin":372,"end":374},"obj":"GeneOrGeneProduct"},{"id":"T5","span":{"begin":375,"end":384},"obj":"GeneOrGeneProduct"},{"id":"T6","span":{"begin":490,"end":493},"obj":"GeneOrGeneProduct"},{"id":"T7","span":{"begin":496,"end":503},"obj":"GeneOrGeneProduct"},{"id":"T8","span":{"begin":600,"end":603},"obj":"GeneOrGeneProduct"},{"id":"T9","span":{"begin":631,"end":633},"obj":"GeneOrGeneProduct"},{"id":"T10","span":{"begin":695,"end":703},"obj":"GeneOrGeneProduct"},{"id":"T11","span":{"begin":745,"end":748},"obj":"GeneOrGeneProduct"},{"id":"T12","span":{"begin":750,"end":757},"obj":"GeneOrGeneProduct"},{"id":"T13","span":{"begin":876,"end":885},"obj":"GeneOrGeneProduct"},{"id":"T14","span":{"begin":931,"end":933},"obj":"GeneOrGeneProduct"},{"id":"T15","span":{"begin":947,"end":955},"obj":"GeneOrGeneProduct"},{"id":"T16","span":{"begin":989,"end":992},"obj":"GeneOrGeneProduct"},{"id":"T17","span":{"begin":994,"end":996},"obj":"GeneOrGeneProduct"},{"id":"T18","span":{"begin":1029,"end":1032},"obj":"GeneOrGeneProduct"},{"id":"T19","span":{"begin":1036,"end":1039},"obj":"GeneOrGeneProduct"},{"id":"T20","span":{"begin":1066,"end":1072},"obj":"GeneOrGeneProduct"},{"id":"T21","span":{"begin":1105,"end":1110},"obj":"GeneOrGeneProduct"},{"id":"T22","span":{"begin":1112,"end":1115},"obj":"GeneOrGeneProduct"},{"id":"T23","span":{"begin":1156,"end":1161},"obj":"GeneOrGeneProduct"},{"id":"T24","span":{"begin":1203,"end":1208},"obj":"GeneOrGeneProduct"},{"id":"T25","span":{"begin":1277,"end":1283},"obj":"GeneOrGeneProduct"},{"id":"T26","span":{"begin":1287,"end":1289},"obj":"GeneOrGeneProduct"},{"id":"T27","span":{"begin":1330,"end":1337},"obj":"GeneOrGeneProduct"},{"id":"T28","span":{"begin":1369,"end":1373},"obj":"GeneOrGeneProduct"},{"id":"T29","span":{"begin":1400,"end":1403},"obj":"GeneOrGeneProduct"},{"id":"T30","span":{"begin":1471,"end":1478},"obj":"GeneOrGeneProduct"},{"id":"T31","span":{"begin":1479,"end":1485},"obj":"GeneOrGeneProduct"},{"id":"T32","span":{"begin":1489,"end":1491},"obj":"GeneOrGeneProduct"},{"id":"T33","span":{"begin":1557,"end":1560},"obj":"GeneOrGeneProduct"},{"id":"T34","span":{"begin":1576,"end":1584},"obj":"GeneOrGeneProduct"},{"id":"T35","span":{"begin":1590,"end":1597},"obj":"GeneOrGeneProduct"},{"id":"T36","span":{"begin":1629,"end":1632},"obj":"GeneOrGeneProduct"},{"id":"T37","span":{"begin":1756,"end":1758},"obj":"GeneOrGeneProduct"},{"id":"T38","span":{"begin":1896,"end":1902},"obj":"GeneOrGeneProduct"},{"id":"T39","span":{"begin":1906,"end":1908},"obj":"GeneOrGeneProduct"},{"id":"T40","span":{"begin":1948,"end":1953},"obj":"GeneOrGeneProduct"},{"id":"T41","span":{"begin":1975,"end":1977},"obj":"GeneOrGeneProduct"},{"id":"T42","span":{"begin":2024,"end":2031},"obj":"GeneOrGeneProduct"},{"id":"T43","span":{"begin":2067,"end":2075},"obj":"GeneOrGeneProduct"}],"text":"Antithrombotic drug use, cerebral microbleeds, and intracerebral hemorrhage: a systematic review of published and unpublished studies.\nBACKGROUND AND PURPOSE: Cerebral microbleeds (MB) are potential risk factors for intracerebral hemorrhage (ICH), but it is unclear if they are a contraindication to using antithrombotic drugs. Insights could be gained by pooling data on MB frequency stratified by antithrombotic use in cohorts with ICH and ischemic stroke (IS)/transient ischemic attack (TIA).\nMETHODS: We performed a systematic review of published and unpublished data from cohorts with stroke or TIA to compare the presence of MB in: (1) antithrombotic users vs nonantithrombotic users with ICH; (2) antithrombotic users vs nonusers with IS/TIA; and (3) ICH vs ischemic events stratified by antithrombotic use. We also analyzed published and unpublished follow-up data to determine the risk of ICH in antithrombotic users with MB.\nRESULTS: In a pooled analysis of 1460 ICH and 3817 IS/TIA, MB were more frequent in ICH vs IS/TIA in all treatment groups, but the excess increased from 2.8 (odds ratio; range, 2.3-3.5) in nonantithrombotic users to 5.7 (range, 3.4-9.7) in antiplatelet users and 8.0 (range, 3.5-17.8) in warfarin users (P difference=0.01). There was also an excess of MB in warfarin users vs nonusers with ICH (OR, 2.7; 95% CI, 1.6-4.4; P\u003c0.001) but none in warfarin users with IS/TIA (OR, 1.3; 95% CI, 0.9-1.7; P=0.33; P difference=0.01). There was a smaller excess of MB in antiplatelet users vs nonusers with ICH (OR, 1.7; 95% CI, 1.3-2.3; P\u003c0.001), but findings were similar for antiplatelet users with IS/TIA (OR, 1.4; 95% CI, 1.2-1.7; P\u003c0.001; P difference=0.25). In pooled follow-up data for 768 antithrombotic users, presence of MB at baseline was associated with a substantially increased risk of subsequent ICH (OR, 12.1; 95% CI, 3.4-42.5; P\u003c0.001).\nCONCLUSIONS: The excess of MB in warfarin users with ICH compared to other groups suggests that MB increase the risk of warfarin-associated ICH. Limited prospective data corroborate these findings, but larger prospective studies are urgently required."}
LitCoin-GeneOrGeneProduct-v2
{"project":"LitCoin-GeneOrGeneProduct-v2","denotations":[{"id":"T1","span":{"begin":258,"end":265},"obj":"GeneOrGeneProduct"},{"id":"T2","span":{"begin":375,"end":384},"obj":"GeneOrGeneProduct"},{"id":"T3","span":{"begin":1330,"end":1337},"obj":"GeneOrGeneProduct"},{"id":"T4","span":{"begin":1369,"end":1373},"obj":"GeneOrGeneProduct"},{"id":"T5","span":{"begin":1471,"end":1478},"obj":"GeneOrGeneProduct"},{"id":"T6","span":{"begin":1590,"end":1597},"obj":"GeneOrGeneProduct"},{"id":"T7","span":{"begin":1948,"end":1953},"obj":"GeneOrGeneProduct"},{"id":"T8","span":{"begin":2024,"end":2031},"obj":"GeneOrGeneProduct"}],"text":"Antithrombotic drug use, cerebral microbleeds, and intracerebral hemorrhage: a systematic review of published and unpublished studies.\nBACKGROUND AND PURPOSE: Cerebral microbleeds (MB) are potential risk factors for intracerebral hemorrhage (ICH), but it is unclear if they are a contraindication to using antithrombotic drugs. Insights could be gained by pooling data on MB frequency stratified by antithrombotic use in cohorts with ICH and ischemic stroke (IS)/transient ischemic attack (TIA).\nMETHODS: We performed a systematic review of published and unpublished data from cohorts with stroke or TIA to compare the presence of MB in: (1) antithrombotic users vs nonantithrombotic users with ICH; (2) antithrombotic users vs nonusers with IS/TIA; and (3) ICH vs ischemic events stratified by antithrombotic use. We also analyzed published and unpublished follow-up data to determine the risk of ICH in antithrombotic users with MB.\nRESULTS: In a pooled analysis of 1460 ICH and 3817 IS/TIA, MB were more frequent in ICH vs IS/TIA in all treatment groups, but the excess increased from 2.8 (odds ratio; range, 2.3-3.5) in nonantithrombotic users to 5.7 (range, 3.4-9.7) in antiplatelet users and 8.0 (range, 3.5-17.8) in warfarin users (P difference=0.01). There was also an excess of MB in warfarin users vs nonusers with ICH (OR, 2.7; 95% CI, 1.6-4.4; P\u003c0.001) but none in warfarin users with IS/TIA (OR, 1.3; 95% CI, 0.9-1.7; P=0.33; P difference=0.01). There was a smaller excess of MB in antiplatelet users vs nonusers with ICH (OR, 1.7; 95% CI, 1.3-2.3; P\u003c0.001), but findings were similar for antiplatelet users with IS/TIA (OR, 1.4; 95% CI, 1.2-1.7; P\u003c0.001; P difference=0.25). In pooled follow-up data for 768 antithrombotic users, presence of MB at baseline was associated with a substantially increased risk of subsequent ICH (OR, 12.1; 95% CI, 3.4-42.5; P\u003c0.001).\nCONCLUSIONS: The excess of MB in warfarin users with ICH compared to other groups suggests that MB increase the risk of warfarin-associated ICH. Limited prospective data corroborate these findings, but larger prospective studies are urgently required."}
LitCoin-Disease-MeSH
{"project":"LitCoin-Disease-MeSH","denotations":[{"id":"T1","span":{"begin":51,"end":75},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":216,"end":240},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":242,"end":245},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":434,"end":437},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T5","span":{"begin":442,"end":457},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T6","span":{"begin":463,"end":488},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T7","span":{"begin":590,"end":596},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T8","span":{"begin":695,"end":698},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T9","span":{"begin":758,"end":761},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T10","span":{"begin":765,"end":773},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T11","span":{"begin":898,"end":901},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T12","span":{"begin":973,"end":976},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T13","span":{"begin":1019,"end":1022},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T14","span":{"begin":1325,"end":1328},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T15","span":{"begin":1531,"end":1534},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T16","span":{"begin":1836,"end":1839},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T17","span":{"begin":1932,"end":1935},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T18","span":{"begin":2019,"end":2022},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A4","pred":"originalLabel","subj":"T4","obj":"D002543"},{"id":"A9","pred":"originalLabel","subj":"T9","obj":"D002543"},{"id":"A13","pred":"originalLabel","subj":"T13","obj":"D002543"},{"id":"A1","pred":"originalLabel","subj":"T1","obj":"D002543"},{"id":"A11","pred":"originalLabel","subj":"T11","obj":"D002543"},{"id":"A6","pred":"originalLabel","subj":"T6","obj":"D002546"},{"id":"A14","pred":"originalLabel","subj":"T14","obj":"D002543"},{"id":"A5","pred":"originalLabel","subj":"T5","obj":"D000083242"},{"id":"A7","pred":"originalLabel","subj":"T7","obj":"D020521"},{"id":"A18","pred":"originalLabel","subj":"T18","obj":"D002543"},{"id":"A17","pred":"originalLabel","subj":"T17","obj":"D002543"},{"id":"A12","pred":"originalLabel","subj":"T12","obj":"D002543"},{"id":"A15","pred":"originalLabel","subj":"T15","obj":"D002543"},{"id":"A16","pred":"originalLabel","subj":"T16","obj":"D002543"},{"id":"A10","pred":"originalLabel","subj":"T10","obj":"DISEASE"},{"id":"A3","pred":"originalLabel","subj":"T3","obj":"D002543"},{"id":"A8","pred":"originalLabel","subj":"T8","obj":"D002543"},{"id":"A2","pred":"originalLabel","subj":"T2","obj":"D002543"}],"text":"Antithrombotic drug use, cerebral microbleeds, and intracerebral hemorrhage: a systematic review of published and unpublished studies.\nBACKGROUND AND PURPOSE: Cerebral microbleeds (MB) are potential risk factors for intracerebral hemorrhage (ICH), but it is unclear if they are a contraindication to using antithrombotic drugs. Insights could be gained by pooling data on MB frequency stratified by antithrombotic use in cohorts with ICH and ischemic stroke (IS)/transient ischemic attack (TIA).\nMETHODS: We performed a systematic review of published and unpublished data from cohorts with stroke or TIA to compare the presence of MB in: (1) antithrombotic users vs nonantithrombotic users with ICH; (2) antithrombotic users vs nonusers with IS/TIA; and (3) ICH vs ischemic events stratified by antithrombotic use. We also analyzed published and unpublished follow-up data to determine the risk of ICH in antithrombotic users with MB.\nRESULTS: In a pooled analysis of 1460 ICH and 3817 IS/TIA, MB were more frequent in ICH vs IS/TIA in all treatment groups, but the excess increased from 2.8 (odds ratio; range, 2.3-3.5) in nonantithrombotic users to 5.7 (range, 3.4-9.7) in antiplatelet users and 8.0 (range, 3.5-17.8) in warfarin users (P difference=0.01). There was also an excess of MB in warfarin users vs nonusers with ICH (OR, 2.7; 95% CI, 1.6-4.4; P\u003c0.001) but none in warfarin users with IS/TIA (OR, 1.3; 95% CI, 0.9-1.7; P=0.33; P difference=0.01). There was a smaller excess of MB in antiplatelet users vs nonusers with ICH (OR, 1.7; 95% CI, 1.3-2.3; P\u003c0.001), but findings were similar for antiplatelet users with IS/TIA (OR, 1.4; 95% CI, 1.2-1.7; P\u003c0.001; P difference=0.25). In pooled follow-up data for 768 antithrombotic users, presence of MB at baseline was associated with a substantially increased risk of subsequent ICH (OR, 12.1; 95% CI, 3.4-42.5; P\u003c0.001).\nCONCLUSIONS: The excess of MB in warfarin users with ICH compared to other groups suggests that MB increase the risk of warfarin-associated ICH. Limited prospective data corroborate these findings, but larger prospective studies are urgently required."}
LitCoin_Mondo_095
{"project":"LitCoin_Mondo_095","denotations":[{"id":"T1","span":{"begin":51,"end":75},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":216,"end":240},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":242,"end":245},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":434,"end":437},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T5","span":{"begin":451,"end":457},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T6","span":{"begin":463,"end":488},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T7","span":{"begin":490,"end":493},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T9","span":{"begin":590,"end":596},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T10","span":{"begin":600,"end":603},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T12","span":{"begin":695,"end":698},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T13","span":{"begin":745,"end":748},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T15","span":{"begin":758,"end":761},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T16","span":{"begin":898,"end":901},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T17","span":{"begin":973,"end":976},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T18","span":{"begin":989,"end":992},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T20","span":{"begin":1019,"end":1022},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T21","span":{"begin":1029,"end":1032},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T23","span":{"begin":1325,"end":1328},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T24","span":{"begin":1400,"end":1403},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T26","span":{"begin":1531,"end":1534},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T27","span":{"begin":1629,"end":1632},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T29","span":{"begin":1836,"end":1839},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T30","span":{"begin":1932,"end":1935},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T31","span":{"begin":2019,"end":2022},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A5","pred":"mondo_id","subj":"T5","obj":"0005098"},{"id":"A16","pred":"mondo_id","subj":"T16","obj":"0013792"},{"id":"A30","pred":"mondo_id","subj":"T30","obj":"0013792"},{"id":"A29","pred":"mondo_id","subj":"T29","obj":"0013792"},{"id":"A3","pred":"mondo_id","subj":"T3","obj":"0013792"},{"id":"A17","pred":"mondo_id","subj":"T17","obj":"0013792"},{"id":"A23","pred":"mondo_id","subj":"T23","obj":"0013792"},{"id":"A31","pred":"mondo_id","subj":"T31","obj":"0013792"},{"id":"A12","pred":"mondo_id","subj":"T12","obj":"0013792"},{"id":"A26","pred":"mondo_id","subj":"T26","obj":"0013792"},{"id":"A9","pred":"mondo_id","subj":"T9","obj":"0005098"},{"id":"A20","pred":"mondo_id","subj":"T20","obj":"0013792"},{"id":"A10","pred":"mondo_id","subj":"T10","obj":"0007047"},{"id":"A11","pred":"mondo_id","subj":"T10","obj":"0005264"},{"id":"A18","pred":"mondo_id","subj":"T18","obj":"0007047"},{"id":"A19","pred":"mondo_id","subj":"T18","obj":"0005264"},{"id":"A7","pred":"mondo_id","subj":"T7","obj":"0007047"},{"id":"A8","pred":"mondo_id","subj":"T7","obj":"0005264"},{"id":"A21","pred":"mondo_id","subj":"T21","obj":"0007047"},{"id":"A22","pred":"mondo_id","subj":"T21","obj":"0005264"},{"id":"A2","pred":"mondo_id","subj":"T2","obj":"0013792"},{"id":"A4","pred":"mondo_id","subj":"T4","obj":"0013792"},{"id":"A24","pred":"mondo_id","subj":"T24","obj":"0007047"},{"id":"A25","pred":"mondo_id","subj":"T24","obj":"0005264"},{"id":"A15","pred":"mondo_id","subj":"T15","obj":"0013792"},{"id":"A13","pred":"mondo_id","subj":"T13","obj":"0007047"},{"id":"A14","pred":"mondo_id","subj":"T13","obj":"0005264"},{"id":"A27","pred":"mondo_id","subj":"T27","obj":"0007047"},{"id":"A28","pred":"mondo_id","subj":"T27","obj":"0005264"},{"id":"A6","pred":"mondo_id","subj":"T6","obj":"0005264"},{"id":"A1","pred":"mondo_id","subj":"T1","obj":"0013792"}],"text":"Antithrombotic drug use, cerebral microbleeds, and intracerebral hemorrhage: a systematic review of published and unpublished studies.\nBACKGROUND AND PURPOSE: Cerebral microbleeds (MB) are potential risk factors for intracerebral hemorrhage (ICH), but it is unclear if they are a contraindication to using antithrombotic drugs. Insights could be gained by pooling data on MB frequency stratified by antithrombotic use in cohorts with ICH and ischemic stroke (IS)/transient ischemic attack (TIA).\nMETHODS: We performed a systematic review of published and unpublished data from cohorts with stroke or TIA to compare the presence of MB in: (1) antithrombotic users vs nonantithrombotic users with ICH; (2) antithrombotic users vs nonusers with IS/TIA; and (3) ICH vs ischemic events stratified by antithrombotic use. We also analyzed published and unpublished follow-up data to determine the risk of ICH in antithrombotic users with MB.\nRESULTS: In a pooled analysis of 1460 ICH and 3817 IS/TIA, MB were more frequent in ICH vs IS/TIA in all treatment groups, but the excess increased from 2.8 (odds ratio; range, 2.3-3.5) in nonantithrombotic users to 5.7 (range, 3.4-9.7) in antiplatelet users and 8.0 (range, 3.5-17.8) in warfarin users (P difference=0.01). There was also an excess of MB in warfarin users vs nonusers with ICH (OR, 2.7; 95% CI, 1.6-4.4; P\u003c0.001) but none in warfarin users with IS/TIA (OR, 1.3; 95% CI, 0.9-1.7; P=0.33; P difference=0.01). There was a smaller excess of MB in antiplatelet users vs nonusers with ICH (OR, 1.7; 95% CI, 1.3-2.3; P\u003c0.001), but findings were similar for antiplatelet users with IS/TIA (OR, 1.4; 95% CI, 1.2-1.7; P\u003c0.001; P difference=0.25). In pooled follow-up data for 768 antithrombotic users, presence of MB at baseline was associated with a substantially increased risk of subsequent ICH (OR, 12.1; 95% CI, 3.4-42.5; P\u003c0.001).\nCONCLUSIONS: The excess of MB in warfarin users with ICH compared to other groups suggests that MB increase the risk of warfarin-associated ICH. Limited prospective data corroborate these findings, but larger prospective studies are urgently required."}
LitCoin-GeneOrGeneProduct-v3
{"project":"LitCoin-GeneOrGeneProduct-v3","denotations":[{"id":"T1","span":{"begin":1330,"end":1337},"obj":"GeneOrGeneProduct"}],"text":"Antithrombotic drug use, cerebral microbleeds, and intracerebral hemorrhage: a systematic review of published and unpublished studies.\nBACKGROUND AND PURPOSE: Cerebral microbleeds (MB) are potential risk factors for intracerebral hemorrhage (ICH), but it is unclear if they are a contraindication to using antithrombotic drugs. Insights could be gained by pooling data on MB frequency stratified by antithrombotic use in cohorts with ICH and ischemic stroke (IS)/transient ischemic attack (TIA).\nMETHODS: We performed a systematic review of published and unpublished data from cohorts with stroke or TIA to compare the presence of MB in: (1) antithrombotic users vs nonantithrombotic users with ICH; (2) antithrombotic users vs nonusers with IS/TIA; and (3) ICH vs ischemic events stratified by antithrombotic use. We also analyzed published and unpublished follow-up data to determine the risk of ICH in antithrombotic users with MB.\nRESULTS: In a pooled analysis of 1460 ICH and 3817 IS/TIA, MB were more frequent in ICH vs IS/TIA in all treatment groups, but the excess increased from 2.8 (odds ratio; range, 2.3-3.5) in nonantithrombotic users to 5.7 (range, 3.4-9.7) in antiplatelet users and 8.0 (range, 3.5-17.8) in warfarin users (P difference=0.01). There was also an excess of MB in warfarin users vs nonusers with ICH (OR, 2.7; 95% CI, 1.6-4.4; P\u003c0.001) but none in warfarin users with IS/TIA (OR, 1.3; 95% CI, 0.9-1.7; P=0.33; P difference=0.01). There was a smaller excess of MB in antiplatelet users vs nonusers with ICH (OR, 1.7; 95% CI, 1.3-2.3; P\u003c0.001), but findings were similar for antiplatelet users with IS/TIA (OR, 1.4; 95% CI, 1.2-1.7; P\u003c0.001; P difference=0.25). In pooled follow-up data for 768 antithrombotic users, presence of MB at baseline was associated with a substantially increased risk of subsequent ICH (OR, 12.1; 95% CI, 3.4-42.5; P\u003c0.001).\nCONCLUSIONS: The excess of MB in warfarin users with ICH compared to other groups suggests that MB increase the risk of warfarin-associated ICH. Limited prospective data corroborate these findings, but larger prospective studies are urgently required."}
LitCoin-MeSH-Disease-2
{"project":"LitCoin-MeSH-Disease-2","denotations":[{"id":"T1","span":{"begin":25,"end":45},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":51,"end":75},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":159,"end":179},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":181,"end":183},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T5","span":{"begin":216,"end":240},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T6","span":{"begin":242,"end":245},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T8","span":{"begin":372,"end":374},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T9","span":{"begin":434,"end":437},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T11","span":{"begin":442,"end":457},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T12","span":{"begin":463,"end":488},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T13","span":{"begin":590,"end":596},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T15","span":{"begin":631,"end":633},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T16","span":{"begin":695,"end":698},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T18","span":{"begin":758,"end":761},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T20","span":{"begin":765,"end":773},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T21","span":{"begin":898,"end":901},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T23","span":{"begin":931,"end":933},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T24","span":{"begin":973,"end":976},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T26","span":{"begin":994,"end":996},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T27","span":{"begin":1019,"end":1022},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T29","span":{"begin":1287,"end":1289},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T30","span":{"begin":1325,"end":1328},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T32","span":{"begin":1489,"end":1491},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T33","span":{"begin":1531,"end":1534},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T35","span":{"begin":1756,"end":1758},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T36","span":{"begin":1836,"end":1839},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T38","span":{"begin":1906,"end":1908},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T39","span":{"begin":1932,"end":1935},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T41","span":{"begin":1975,"end":1977},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T42","span":{"begin":2019,"end":2022},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A12","pred":"ID:","subj":"T12","obj":"D002546"},{"id":"A4","pred":"ID:","subj":"T4","obj":"DISEASE"},{"id":"A41","pred":"ID:","subj":"T41","obj":"DISEASE"},{"id":"A11","pred":"ID:","subj":"T11","obj":"D000083242"},{"id":"A33","pred":"ID:","subj":"T33","obj":"DISEASE"},{"id":"A34","pred":"ID:","subj":"T33","obj":"D002543"},{"id":"A29","pred":"ID:","subj":"T29","obj":"DISEASE"},{"id":"A9","pred":"ID:","subj":"T9","obj":"DISEASE"},{"id":"A10","pred":"ID:","subj":"T9","obj":"D002543"},{"id":"A5","pred":"ID:","subj":"T5","obj":"D002543"},{"id":"A21","pred":"ID:","subj":"T21","obj":"DISEASE"},{"id":"A22","pred":"ID:","subj":"T21","obj":"D002543"},{"id":"A27","pred":"ID:","subj":"T27","obj":"DISEASE"},{"id":"A28","pred":"ID:","subj":"T27","obj":"D002543"},{"id":"A35","pred":"ID:","subj":"T35","obj":"DISEASE"},{"id":"A16","pred":"ID:","subj":"T16","obj":"DISEASE"},{"id":"A17","pred":"ID:","subj":"T16","obj":"D002543"},{"id":"A36","pred":"ID:","subj":"T36","obj":"DISEASE"},{"id":"A37","pred":"ID:","subj":"T36","obj":"D002543"},{"id":"A42","pred":"ID:","subj":"T42","obj":"DISEASE"},{"id":"A43","pred":"ID:","subj":"T42","obj":"D002543"},{"id":"A20","pred":"ID:","subj":"T20","obj":"DISEASE"},{"id":"A18","pred":"ID:","subj":"T18","obj":"DISEASE"},{"id":"A19","pred":"ID:","subj":"T18","obj":"D002543"},{"id":"A2","pred":"ID:","subj":"T2","obj":"D002543"},{"id":"A8","pred":"ID:","subj":"T8","obj":"DISEASE"},{"id":"A23","pred":"ID:","subj":"T23","obj":"DISEASE"},{"id":"A30","pred":"ID:","subj":"T30","obj":"DISEASE"},{"id":"A31","pred":"ID:","subj":"T30","obj":"D002543"},{"id":"A1","pred":"ID:","subj":"T1","obj":"DISEASE"},{"id":"A15","pred":"ID:","subj":"T15","obj":"DISEASE"},{"id":"A13","pred":"ID:","subj":"T13","obj":"DISEASE"},{"id":"A14","pred":"ID:","subj":"T13","obj":"D020521"},{"id":"A24","pred":"ID:","subj":"T24","obj":"DISEASE"},{"id":"A25","pred":"ID:","subj":"T24","obj":"D002543"},{"id":"A32","pred":"ID:","subj":"T32","obj":"DISEASE"},{"id":"A6","pred":"ID:","subj":"T6","obj":"DISEASE"},{"id":"A7","pred":"ID:","subj":"T6","obj":"D002543"},{"id":"A39","pred":"ID:","subj":"T39","obj":"DISEASE"},{"id":"A40","pred":"ID:","subj":"T39","obj":"D002543"},{"id":"A26","pred":"ID:","subj":"T26","obj":"DISEASE"},{"id":"A38","pred":"ID:","subj":"T38","obj":"DISEASE"},{"id":"A3","pred":"ID:","subj":"T3","obj":"DISEASE"}],"text":"Antithrombotic drug use, cerebral microbleeds, and intracerebral hemorrhage: a systematic review of published and unpublished studies.\nBACKGROUND AND PURPOSE: Cerebral microbleeds (MB) are potential risk factors for intracerebral hemorrhage (ICH), but it is unclear if they are a contraindication to using antithrombotic drugs. Insights could be gained by pooling data on MB frequency stratified by antithrombotic use in cohorts with ICH and ischemic stroke (IS)/transient ischemic attack (TIA).\nMETHODS: We performed a systematic review of published and unpublished data from cohorts with stroke or TIA to compare the presence of MB in: (1) antithrombotic users vs nonantithrombotic users with ICH; (2) antithrombotic users vs nonusers with IS/TIA; and (3) ICH vs ischemic events stratified by antithrombotic use. We also analyzed published and unpublished follow-up data to determine the risk of ICH in antithrombotic users with MB.\nRESULTS: In a pooled analysis of 1460 ICH and 3817 IS/TIA, MB were more frequent in ICH vs IS/TIA in all treatment groups, but the excess increased from 2.8 (odds ratio; range, 2.3-3.5) in nonantithrombotic users to 5.7 (range, 3.4-9.7) in antiplatelet users and 8.0 (range, 3.5-17.8) in warfarin users (P difference=0.01). There was also an excess of MB in warfarin users vs nonusers with ICH (OR, 2.7; 95% CI, 1.6-4.4; P\u003c0.001) but none in warfarin users with IS/TIA (OR, 1.3; 95% CI, 0.9-1.7; P=0.33; P difference=0.01). There was a smaller excess of MB in antiplatelet users vs nonusers with ICH (OR, 1.7; 95% CI, 1.3-2.3; P\u003c0.001), but findings were similar for antiplatelet users with IS/TIA (OR, 1.4; 95% CI, 1.2-1.7; P\u003c0.001; P difference=0.25). In pooled follow-up data for 768 antithrombotic users, presence of MB at baseline was associated with a substantially increased risk of subsequent ICH (OR, 12.1; 95% CI, 3.4-42.5; P\u003c0.001).\nCONCLUSIONS: The excess of MB in warfarin users with ICH compared to other groups suggests that MB increase the risk of warfarin-associated ICH. Limited prospective data corroborate these findings, but larger prospective studies are urgently required."}
LitCoin-MONDO_bioort2019
{"project":"LitCoin-MONDO_bioort2019","denotations":[{"id":"T1","span":{"begin":25,"end":45},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":51,"end":75},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":159,"end":179},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":181,"end":183},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T5","span":{"begin":216,"end":240},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T6","span":{"begin":242,"end":245},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T8","span":{"begin":372,"end":374},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T9","span":{"begin":434,"end":437},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T11","span":{"begin":442,"end":457},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T12","span":{"begin":463,"end":488},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T13","span":{"begin":590,"end":596},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T14","span":{"begin":631,"end":633},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T15","span":{"begin":695,"end":698},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T17","span":{"begin":758,"end":761},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T19","span":{"begin":765,"end":773},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T20","span":{"begin":898,"end":901},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T22","span":{"begin":931,"end":933},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T23","span":{"begin":973,"end":976},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T25","span":{"begin":994,"end":996},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T26","span":{"begin":1019,"end":1022},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T28","span":{"begin":1287,"end":1289},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T29","span":{"begin":1325,"end":1328},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T31","span":{"begin":1489,"end":1491},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T32","span":{"begin":1531,"end":1534},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T34","span":{"begin":1756,"end":1758},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T35","span":{"begin":1836,"end":1839},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T37","span":{"begin":1906,"end":1908},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T38","span":{"begin":1932,"end":1935},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T40","span":{"begin":1975,"end":1977},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T41","span":{"begin":2019,"end":2022},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A31","pred":"#label","subj":"T31","obj":"DISEASE"},{"id":"A1","pred":"#label","subj":"T1","obj":"DISEASE"},{"id":"A26","pred":"#label","subj":"T26","obj":"DISEASE"},{"id":"A27","pred":"#label","subj":"T26","obj":"D002543"},{"id":"A19","pred":"#label","subj":"T19","obj":"DISEASE"},{"id":"A40","pred":"#label","subj":"T40","obj":"DISEASE"},{"id":"A2","pred":"#label","subj":"T2","obj":"D002543"},{"id":"A37","pred":"#label","subj":"T37","obj":"DISEASE"},{"id":"A9","pred":"#label","subj":"T9","obj":"DISEASE"},{"id":"A10","pred":"#label","subj":"T9","obj":"D002543"},{"id":"A6","pred":"#label","subj":"T6","obj":"DISEASE"},{"id":"A7","pred":"#label","subj":"T6","obj":"D002543"},{"id":"A32","pred":"#label","subj":"T32","obj":"DISEASE"},{"id":"A33","pred":"#label","subj":"T32","obj":"D002543"},{"id":"A20","pred":"#label","subj":"T20","obj":"DISEASE"},{"id":"A21","pred":"#label","subj":"T20","obj":"D002543"},{"id":"A23","pred":"#label","subj":"T23","obj":"DISEASE"},{"id":"A24","pred":"#label","subj":"T23","obj":"D002543"},{"id":"A4","pred":"#label","subj":"T4","obj":"DISEASE"},{"id":"A11","pred":"#label","subj":"T11","obj":"D000083242"},{"id":"A22","pred":"#label","subj":"T22","obj":"DISEASE"},{"id":"A29","pred":"#label","subj":"T29","obj":"DISEASE"},{"id":"A30","pred":"#label","subj":"T29","obj":"D002543"},{"id":"A13","pred":"#label","subj":"T13","obj":"D020521"},{"id":"A15","pred":"#label","subj":"T15","obj":"DISEASE"},{"id":"A16","pred":"#label","subj":"T15","obj":"D002543"},{"id":"A8","pred":"#label","subj":"T8","obj":"DISEASE"},{"id":"A12","pred":"#label","subj":"T12","obj":"D002546"},{"id":"A35","pred":"#label","subj":"T35","obj":"DISEASE"},{"id":"A36","pred":"#label","subj":"T35","obj":"D002543"},{"id":"A3","pred":"#label","subj":"T3","obj":"DISEASE"},{"id":"A17","pred":"#label","subj":"T17","obj":"DISEASE"},{"id":"A18","pred":"#label","subj":"T17","obj":"D002543"},{"id":"A28","pred":"#label","subj":"T28","obj":"DISEASE"},{"id":"A38","pred":"#label","subj":"T38","obj":"DISEASE"},{"id":"A39","pred":"#label","subj":"T38","obj":"D002543"},{"id":"A5","pred":"#label","subj":"T5","obj":"D002543"},{"id":"A14","pred":"#label","subj":"T14","obj":"DISEASE"},{"id":"A34","pred":"#label","subj":"T34","obj":"DISEASE"},{"id":"A41","pred":"#label","subj":"T41","obj":"DISEASE"},{"id":"A42","pred":"#label","subj":"T41","obj":"D002543"},{"id":"A25","pred":"#label","subj":"T25","obj":"DISEASE"}],"text":"Antithrombotic drug use, cerebral microbleeds, and intracerebral hemorrhage: a systematic review of published and unpublished studies.\nBACKGROUND AND PURPOSE: Cerebral microbleeds (MB) are potential risk factors for intracerebral hemorrhage (ICH), but it is unclear if they are a contraindication to using antithrombotic drugs. Insights could be gained by pooling data on MB frequency stratified by antithrombotic use in cohorts with ICH and ischemic stroke (IS)/transient ischemic attack (TIA).\nMETHODS: We performed a systematic review of published and unpublished data from cohorts with stroke or TIA to compare the presence of MB in: (1) antithrombotic users vs nonantithrombotic users with ICH; (2) antithrombotic users vs nonusers with IS/TIA; and (3) ICH vs ischemic events stratified by antithrombotic use. We also analyzed published and unpublished follow-up data to determine the risk of ICH in antithrombotic users with MB.\nRESULTS: In a pooled analysis of 1460 ICH and 3817 IS/TIA, MB were more frequent in ICH vs IS/TIA in all treatment groups, but the excess increased from 2.8 (odds ratio; range, 2.3-3.5) in nonantithrombotic users to 5.7 (range, 3.4-9.7) in antiplatelet users and 8.0 (range, 3.5-17.8) in warfarin users (P difference=0.01). There was also an excess of MB in warfarin users vs nonusers with ICH (OR, 2.7; 95% CI, 1.6-4.4; P\u003c0.001) but none in warfarin users with IS/TIA (OR, 1.3; 95% CI, 0.9-1.7; P=0.33; P difference=0.01). There was a smaller excess of MB in antiplatelet users vs nonusers with ICH (OR, 1.7; 95% CI, 1.3-2.3; P\u003c0.001), but findings were similar for antiplatelet users with IS/TIA (OR, 1.4; 95% CI, 1.2-1.7; P\u003c0.001; P difference=0.25). In pooled follow-up data for 768 antithrombotic users, presence of MB at baseline was associated with a substantially increased risk of subsequent ICH (OR, 12.1; 95% CI, 3.4-42.5; P\u003c0.001).\nCONCLUSIONS: The excess of MB in warfarin users with ICH compared to other groups suggests that MB increase the risk of warfarin-associated ICH. Limited prospective data corroborate these findings, but larger prospective studies are urgently required."}
LitCoin-NCBITaxon-2
{"project":"LitCoin-NCBITaxon-2","denotations":[{"id":"T1","span":{"begin":490,"end":493},"obj":"OrganismTaxon"},{"id":"T2","span":{"begin":600,"end":603},"obj":"OrganismTaxon"},{"id":"T3","span":{"begin":745,"end":748},"obj":"OrganismTaxon"},{"id":"T4","span":{"begin":989,"end":992},"obj":"OrganismTaxon"},{"id":"T5","span":{"begin":1029,"end":1032},"obj":"OrganismTaxon"},{"id":"T6","span":{"begin":1400,"end":1403},"obj":"OrganismTaxon"},{"id":"T7","span":{"begin":1629,"end":1632},"obj":"OrganismTaxon"}],"text":"Antithrombotic drug use, cerebral microbleeds, and intracerebral hemorrhage: a systematic review of published and unpublished studies.\nBACKGROUND AND PURPOSE: Cerebral microbleeds (MB) are potential risk factors for intracerebral hemorrhage (ICH), but it is unclear if they are a contraindication to using antithrombotic drugs. Insights could be gained by pooling data on MB frequency stratified by antithrombotic use in cohorts with ICH and ischemic stroke (IS)/transient ischemic attack (TIA).\nMETHODS: We performed a systematic review of published and unpublished data from cohorts with stroke or TIA to compare the presence of MB in: (1) antithrombotic users vs nonantithrombotic users with ICH; (2) antithrombotic users vs nonusers with IS/TIA; and (3) ICH vs ischemic events stratified by antithrombotic use. We also analyzed published and unpublished follow-up data to determine the risk of ICH in antithrombotic users with MB.\nRESULTS: In a pooled analysis of 1460 ICH and 3817 IS/TIA, MB were more frequent in ICH vs IS/TIA in all treatment groups, but the excess increased from 2.8 (odds ratio; range, 2.3-3.5) in nonantithrombotic users to 5.7 (range, 3.4-9.7) in antiplatelet users and 8.0 (range, 3.5-17.8) in warfarin users (P difference=0.01). There was also an excess of MB in warfarin users vs nonusers with ICH (OR, 2.7; 95% CI, 1.6-4.4; P\u003c0.001) but none in warfarin users with IS/TIA (OR, 1.3; 95% CI, 0.9-1.7; P=0.33; P difference=0.01). There was a smaller excess of MB in antiplatelet users vs nonusers with ICH (OR, 1.7; 95% CI, 1.3-2.3; P\u003c0.001), but findings were similar for antiplatelet users with IS/TIA (OR, 1.4; 95% CI, 1.2-1.7; P\u003c0.001; P difference=0.25). In pooled follow-up data for 768 antithrombotic users, presence of MB at baseline was associated with a substantially increased risk of subsequent ICH (OR, 12.1; 95% CI, 3.4-42.5; P\u003c0.001).\nCONCLUSIONS: The excess of MB in warfarin users with ICH compared to other groups suggests that MB increase the risk of warfarin-associated ICH. Limited prospective data corroborate these findings, but larger prospective studies are urgently required."}
LitCoin-Chemical-MeSH-CHEBI
{"project":"LitCoin-Chemical-MeSH-CHEBI","denotations":[{"id":"T1","span":{"begin":0,"end":19},"obj":"ChemicalEntity"},{"id":"T2","span":{"begin":306,"end":326},"obj":"ChemicalEntity"},{"id":"T3","span":{"begin":1223,"end":1231},"obj":"ChemicalEntity"},{"id":"T5","span":{"begin":1293,"end":1301},"obj":"ChemicalEntity"},{"id":"T7","span":{"begin":1377,"end":1385},"obj":"ChemicalEntity"},{"id":"T9","span":{"begin":1912,"end":1920},"obj":"ChemicalEntity"},{"id":"T11","span":{"begin":1999,"end":2007},"obj":"ChemicalEntity"}],"attributes":[{"id":"A11","pred":"ID:","subj":"T11","obj":"D014859"},{"id":"A12","pred":"ID:","subj":"T11","obj":"http://purl.obolibrary.org/obo/CHEBI_10033"},{"id":"A3","pred":"ID:","subj":"T3","obj":"D014859"},{"id":"A4","pred":"ID:","subj":"T3","obj":"http://purl.obolibrary.org/obo/CHEBI_10033"},{"id":"A7","pred":"ID:","subj":"T7","obj":"D014859"},{"id":"A8","pred":"ID:","subj":"T7","obj":"http://purl.obolibrary.org/obo/CHEBI_10033"},{"id":"A2","pred":"ID:","subj":"T2","obj":"ChemicalEntity"},{"id":"A5","pred":"ID:","subj":"T5","obj":"D014859"},{"id":"A6","pred":"ID:","subj":"T5","obj":"http://purl.obolibrary.org/obo/CHEBI_10033"},{"id":"A1","pred":"ID:","subj":"T1","obj":"ChemicalEntity"},{"id":"A9","pred":"ID:","subj":"T9","obj":"D014859"},{"id":"A10","pred":"ID:","subj":"T9","obj":"http://purl.obolibrary.org/obo/CHEBI_10033"}],"text":"Antithrombotic drug use, cerebral microbleeds, and intracerebral hemorrhage: a systematic review of published and unpublished studies.\nBACKGROUND AND PURPOSE: Cerebral microbleeds (MB) are potential risk factors for intracerebral hemorrhage (ICH), but it is unclear if they are a contraindication to using antithrombotic drugs. Insights could be gained by pooling data on MB frequency stratified by antithrombotic use in cohorts with ICH and ischemic stroke (IS)/transient ischemic attack (TIA).\nMETHODS: We performed a systematic review of published and unpublished data from cohorts with stroke or TIA to compare the presence of MB in: (1) antithrombotic users vs nonantithrombotic users with ICH; (2) antithrombotic users vs nonusers with IS/TIA; and (3) ICH vs ischemic events stratified by antithrombotic use. We also analyzed published and unpublished follow-up data to determine the risk of ICH in antithrombotic users with MB.\nRESULTS: In a pooled analysis of 1460 ICH and 3817 IS/TIA, MB were more frequent in ICH vs IS/TIA in all treatment groups, but the excess increased from 2.8 (odds ratio; range, 2.3-3.5) in nonantithrombotic users to 5.7 (range, 3.4-9.7) in antiplatelet users and 8.0 (range, 3.5-17.8) in warfarin users (P difference=0.01). There was also an excess of MB in warfarin users vs nonusers with ICH (OR, 2.7; 95% CI, 1.6-4.4; P\u003c0.001) but none in warfarin users with IS/TIA (OR, 1.3; 95% CI, 0.9-1.7; P=0.33; P difference=0.01). There was a smaller excess of MB in antiplatelet users vs nonusers with ICH (OR, 1.7; 95% CI, 1.3-2.3; P\u003c0.001), but findings were similar for antiplatelet users with IS/TIA (OR, 1.4; 95% CI, 1.2-1.7; P\u003c0.001; P difference=0.25). In pooled follow-up data for 768 antithrombotic users, presence of MB at baseline was associated with a substantially increased risk of subsequent ICH (OR, 12.1; 95% CI, 3.4-42.5; P\u003c0.001).\nCONCLUSIONS: The excess of MB in warfarin users with ICH compared to other groups suggests that MB increase the risk of warfarin-associated ICH. Limited prospective data corroborate these findings, but larger prospective studies are urgently required."}
LitCoin-training-merged
{"project":"LitCoin-training-merged","denotations":[{"id":"T11","span":{"begin":1999,"end":2007},"obj":"ChemicalEntity"},{"id":"T9","span":{"begin":1912,"end":1920},"obj":"ChemicalEntity"},{"id":"T7","span":{"begin":1377,"end":1385},"obj":"ChemicalEntity"},{"id":"T5","span":{"begin":1293,"end":1301},"obj":"ChemicalEntity"},{"id":"T3","span":{"begin":1223,"end":1231},"obj":"ChemicalEntity"},{"id":"T2","span":{"begin":306,"end":326},"obj":"ChemicalEntity"},{"id":"T1","span":{"begin":0,"end":19},"obj":"ChemicalEntity"},{"id":"T92456","span":{"begin":1330,"end":1337},"obj":"GeneOrGeneProduct"},{"id":"T41","span":{"begin":2019,"end":2022},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T40","span":{"begin":1975,"end":1977},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T38","span":{"begin":1932,"end":1935},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T37","span":{"begin":1906,"end":1908},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T35","span":{"begin":1836,"end":1839},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T34","span":{"begin":1756,"end":1758},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T32","span":{"begin":1531,"end":1534},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T31","span":{"begin":1489,"end":1491},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T29","span":{"begin":1325,"end":1328},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T28","span":{"begin":1287,"end":1289},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T26","span":{"begin":1019,"end":1022},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T25","span":{"begin":994,"end":996},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T23","span":{"begin":973,"end":976},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T22","span":{"begin":931,"end":933},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T20","span":{"begin":898,"end":901},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T19","span":{"begin":765,"end":773},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T17","span":{"begin":758,"end":761},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T15","span":{"begin":695,"end":698},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T14","span":{"begin":631,"end":633},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T13","span":{"begin":590,"end":596},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T12","span":{"begin":463,"end":488},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T12296","span":{"begin":442,"end":457},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T28187","span":{"begin":434,"end":437},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T8","span":{"begin":372,"end":374},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T6","span":{"begin":242,"end":245},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T76907","span":{"begin":216,"end":240},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":181,"end":183},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T64999","span":{"begin":159,"end":179},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T98896","span":{"begin":51,"end":75},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T41183","span":{"begin":25,"end":45},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T8978","span":{"begin":1629,"end":1632},"obj":"OrganismTaxon"},{"id":"T84037","span":{"begin":1400,"end":1403},"obj":"OrganismTaxon"},{"id":"T66981","span":{"begin":1029,"end":1032},"obj":"OrganismTaxon"},{"id":"T84687","span":{"begin":989,"end":992},"obj":"OrganismTaxon"},{"id":"T80332","span":{"begin":745,"end":748},"obj":"OrganismTaxon"},{"id":"T26050","span":{"begin":600,"end":603},"obj":"OrganismTaxon"},{"id":"T88122","span":{"begin":490,"end":493},"obj":"OrganismTaxon"}],"attributes":[{"id":"A25","pred":"#label","subj":"T25","obj":"DISEASE"},{"id":"A36","pred":"#label","subj":"T35","obj":"D002543"},{"id":"A35","pred":"#label","subj":"T35","obj":"DISEASE"},{"id":"A31","pred":"#label","subj":"T31","obj":"DISEASE"},{"id":"A4","pred":"ID:","subj":"T3","obj":"http://purl.obolibrary.org/obo/CHEBI_10033"},{"id":"A3","pred":"ID:","subj":"T3","obj":"D014859"},{"id":"A22","pred":"#label","subj":"T22","obj":"DISEASE"},{"id":"A27","pred":"#label","subj":"T26","obj":"D002543"},{"id":"A26","pred":"#label","subj":"T26","obj":"DISEASE"},{"id":"A13","pred":"#label","subj":"T13","obj":"D020521"},{"id":"A12","pred":"ID:","subj":"T11","obj":"http://purl.obolibrary.org/obo/CHEBI_10033"},{"id":"A11","pred":"ID:","subj":"T11","obj":"D014859"},{"id":"A16","pred":"#label","subj":"T15","obj":"D002543"},{"id":"A15","pred":"#label","subj":"T15","obj":"DISEASE"},{"id":"A10","pred":"ID:","subj":"T9","obj":"http://purl.obolibrary.org/obo/CHEBI_10033"},{"id":"A9","pred":"ID:","subj":"T9","obj":"D014859"},{"id":"A52471","pred":"#label","subj":"T98896","obj":"D002543"},{"id":"A21","pred":"#label","subj":"T20","obj":"D002543"},{"id":"A20","pred":"#label","subj":"T20","obj":"DISEASE"},{"id":"A39","pred":"#label","subj":"T38","obj":"D002543"},{"id":"A38","pred":"#label","subj":"T38","obj":"DISEASE"},{"id":"A1","pred":"ID:","subj":"T1","obj":"ChemicalEntity"},{"id":"A28","pred":"#label","subj":"T28","obj":"DISEASE"},{"id":"A30","pred":"#label","subj":"T29","obj":"D002543"},{"id":"A29","pred":"#label","subj":"T29","obj":"DISEASE"},{"id":"A74364","pred":"#label","subj":"T12","obj":"D002546"},{"id":"A37","pred":"#label","subj":"T37","obj":"DISEASE"},{"id":"A6","pred":"ID:","subj":"T5","obj":"http://purl.obolibrary.org/obo/CHEBI_10033"},{"id":"A5","pred":"ID:","subj":"T5","obj":"D014859"},{"id":"A19","pred":"#label","subj":"T19","obj":"DISEASE"},{"id":"A14","pred":"#label","subj":"T14","obj":"DISEASE"},{"id":"A51066","pred":"#label","subj":"T6","obj":"D002543"},{"id":"A21787","pred":"#label","subj":"T6","obj":"DISEASE"},{"id":"A33","pred":"#label","subj":"T32","obj":"D002543"},{"id":"A32","pred":"#label","subj":"T32","obj":"DISEASE"},{"id":"A22538","pred":"#label","subj":"T28187","obj":"D002543"},{"id":"A64589","pred":"#label","subj":"T28187","obj":"DISEASE"},{"id":"A62817","pred":"#label","subj":"T4","obj":"DISEASE"},{"id":"A34","pred":"#label","subj":"T34","obj":"DISEASE"},{"id":"A2","pred":"ID:","subj":"T2","obj":"ChemicalEntity"},{"id":"A49502","pred":"#label","subj":"T12296","obj":"D000083242"},{"id":"A10144","pred":"#label","subj":"T41183","obj":"DISEASE"},{"id":"A93957","pred":"#label","subj":"T8","obj":"DISEASE"},{"id":"A24","pred":"#label","subj":"T23","obj":"D002543"},{"id":"A23","pred":"#label","subj":"T23","obj":"DISEASE"},{"id":"A18","pred":"#label","subj":"T17","obj":"D002543"},{"id":"A17","pred":"#label","subj":"T17","obj":"DISEASE"},{"id":"A8","pred":"ID:","subj":"T7","obj":"http://purl.obolibrary.org/obo/CHEBI_10033"},{"id":"A7","pred":"ID:","subj":"T7","obj":"D014859"},{"id":"A40","pred":"#label","subj":"T40","obj":"DISEASE"},{"id":"A41515","pred":"#label","subj":"T64999","obj":"DISEASE"},{"id":"A98383","pred":"#label","subj":"T76907","obj":"D002543"},{"id":"A42","pred":"#label","subj":"T41","obj":"D002543"},{"id":"A41","pred":"#label","subj":"T41","obj":"DISEASE"}],"text":"Antithrombotic drug use, cerebral microbleeds, and intracerebral hemorrhage: a systematic review of published and unpublished studies.\nBACKGROUND AND PURPOSE: Cerebral microbleeds (MB) are potential risk factors for intracerebral hemorrhage (ICH), but it is unclear if they are a contraindication to using antithrombotic drugs. Insights could be gained by pooling data on MB frequency stratified by antithrombotic use in cohorts with ICH and ischemic stroke (IS)/transient ischemic attack (TIA).\nMETHODS: We performed a systematic review of published and unpublished data from cohorts with stroke or TIA to compare the presence of MB in: (1) antithrombotic users vs nonantithrombotic users with ICH; (2) antithrombotic users vs nonusers with IS/TIA; and (3) ICH vs ischemic events stratified by antithrombotic use. We also analyzed published and unpublished follow-up data to determine the risk of ICH in antithrombotic users with MB.\nRESULTS: In a pooled analysis of 1460 ICH and 3817 IS/TIA, MB were more frequent in ICH vs IS/TIA in all treatment groups, but the excess increased from 2.8 (odds ratio; range, 2.3-3.5) in nonantithrombotic users to 5.7 (range, 3.4-9.7) in antiplatelet users and 8.0 (range, 3.5-17.8) in warfarin users (P difference=0.01). There was also an excess of MB in warfarin users vs nonusers with ICH (OR, 2.7; 95% CI, 1.6-4.4; P\u003c0.001) but none in warfarin users with IS/TIA (OR, 1.3; 95% CI, 0.9-1.7; P=0.33; P difference=0.01). There was a smaller excess of MB in antiplatelet users vs nonusers with ICH (OR, 1.7; 95% CI, 1.3-2.3; P\u003c0.001), but findings were similar for antiplatelet users with IS/TIA (OR, 1.4; 95% CI, 1.2-1.7; P\u003c0.001; P difference=0.25). In pooled follow-up data for 768 antithrombotic users, presence of MB at baseline was associated with a substantially increased risk of subsequent ICH (OR, 12.1; 95% CI, 3.4-42.5; P\u003c0.001).\nCONCLUSIONS: The excess of MB in warfarin users with ICH compared to other groups suggests that MB increase the risk of warfarin-associated ICH. Limited prospective data corroborate these findings, but larger prospective studies are urgently required."}
PubmedHPO
{"project":"PubmedHPO","denotations":[{"id":"T1","span":{"begin":216,"end":240},"obj":"HP_0001342"},{"id":"T2","span":{"begin":442,"end":457},"obj":"HP_0002140"},{"id":"T3","span":{"begin":451,"end":457},"obj":"HP_0001297"},{"id":"T4","span":{"begin":463,"end":488},"obj":"HP_0002326"},{"id":"T5","span":{"begin":490,"end":493},"obj":"HP_0002326"}],"text":"Antithrombotic drug use, cerebral microbleeds, and intracerebral hemorrhage: a systematic review of published and unpublished studies.\nBACKGROUND AND PURPOSE: Cerebral microbleeds (MB) are potential risk factors for intracerebral hemorrhage (ICH), but it is unclear if they are a contraindication to using antithrombotic drugs. Insights could be gained by pooling data on MB frequency stratified by antithrombotic use in cohorts with ICH and ischemic stroke (IS)/transient ischemic attack (TIA).\nMETHODS: We performed a systematic review of published and unpublished data from cohorts with stroke or TIA to compare the presence of MB in: (1) antithrombotic users vs nonantithrombotic users with ICH; (2) antithrombotic users vs nonusers with IS/TIA; and (3) ICH vs ischemic events stratified by antithrombotic use. We also analyzed published and unpublished follow-up data to determine the risk of ICH in antithrombotic users with MB.\nRESULTS: In a pooled analysis of 1460 ICH and 3817 IS/TIA, MB were more frequent in ICH vs IS/TIA in all treatment groups, but the excess increased from 2.8 (odds ratio; range, 2.3-3.5) in nonantithrombotic users to 5.7 (range, 3.4-9.7) in antiplatelet users and 8.0 (range, 3.5-17.8) in warfarin users (P difference=0.01). There was also an excess of MB in warfarin users vs nonusers with ICH (OR, 2.7; 95% CI, 1.6-4.4; P\u003c0.001) but none in warfarin users with IS/TIA (OR, 1.3; 95% CI, 0.9-1.7; P=0.33; P difference=0.01). There was a smaller excess of MB in antiplatelet users vs nonusers with ICH (OR, 1.7; 95% CI, 1.3-2.3; P\u003c0.001), but findings were similar for antiplatelet users with IS/TIA (OR, 1.4; 95% CI, 1.2-1.7; P\u003c0.001; P difference=0.25). In pooled follow-up data for 768 antithrombotic users, presence of MB at baseline was associated with a substantially increased risk of subsequent ICH (OR, 12.1; 95% CI, 3.4-42.5; P\u003c0.001).\nCONCLUSIONS: The excess of MB in warfarin users with ICH compared to other groups suggests that MB increase the risk of warfarin-associated ICH. Limited prospective data corroborate these findings, but larger prospective studies are urgently required."}
Allie
{"project":"Allie","denotations":[{"id":"SS1_20431083_2_0","span":{"begin":168,"end":179},"obj":"expanded"},{"id":"SS2_20431083_2_0","span":{"begin":181,"end":183},"obj":"abbr"},{"id":"SS1_20431083_2_1","span":{"begin":216,"end":240},"obj":"expanded"},{"id":"SS2_20431083_2_1","span":{"begin":242,"end":245},"obj":"abbr"},{"id":"SS1_20431083_3_0","span":{"begin":442,"end":457},"obj":"expanded"},{"id":"SS2_20431083_3_0","span":{"begin":459,"end":461},"obj":"abbr"},{"id":"SS1_20431083_3_1","span":{"begin":463,"end":488},"obj":"expanded"},{"id":"SS2_20431083_3_1","span":{"begin":490,"end":493},"obj":"abbr"}],"relations":[{"id":"AE1_20431083_2_0","pred":"abbreviatedTo","subj":"SS1_20431083_2_0","obj":"SS2_20431083_2_0"},{"id":"AE1_20431083_2_1","pred":"abbreviatedTo","subj":"SS1_20431083_2_1","obj":"SS2_20431083_2_1"},{"id":"AE1_20431083_3_0","pred":"abbreviatedTo","subj":"SS1_20431083_3_0","obj":"SS2_20431083_3_0"},{"id":"AE1_20431083_3_1","pred":"abbreviatedTo","subj":"SS1_20431083_3_1","obj":"SS2_20431083_3_1"}],"text":"Antithrombotic drug use, cerebral microbleeds, and intracerebral hemorrhage: a systematic review of published and unpublished studies.\nBACKGROUND AND PURPOSE: Cerebral microbleeds (MB) are potential risk factors for intracerebral hemorrhage (ICH), but it is unclear if they are a contraindication to using antithrombotic drugs. Insights could be gained by pooling data on MB frequency stratified by antithrombotic use in cohorts with ICH and ischemic stroke (IS)/transient ischemic attack (TIA).\nMETHODS: We performed a systematic review of published and unpublished data from cohorts with stroke or TIA to compare the presence of MB in: (1) antithrombotic users vs nonantithrombotic users with ICH; (2) antithrombotic users vs nonusers with IS/TIA; and (3) ICH vs ischemic events stratified by antithrombotic use. We also analyzed published and unpublished follow-up data to determine the risk of ICH in antithrombotic users with MB.\nRESULTS: In a pooled analysis of 1460 ICH and 3817 IS/TIA, MB were more frequent in ICH vs IS/TIA in all treatment groups, but the excess increased from 2.8 (odds ratio; range, 2.3-3.5) in nonantithrombotic users to 5.7 (range, 3.4-9.7) in antiplatelet users and 8.0 (range, 3.5-17.8) in warfarin users (P difference=0.01). There was also an excess of MB in warfarin users vs nonusers with ICH (OR, 2.7; 95% CI, 1.6-4.4; P\u003c0.001) but none in warfarin users with IS/TIA (OR, 1.3; 95% CI, 0.9-1.7; P=0.33; P difference=0.01). There was a smaller excess of MB in antiplatelet users vs nonusers with ICH (OR, 1.7; 95% CI, 1.3-2.3; P\u003c0.001), but findings were similar for antiplatelet users with IS/TIA (OR, 1.4; 95% CI, 1.2-1.7; P\u003c0.001; P difference=0.25). In pooled follow-up data for 768 antithrombotic users, presence of MB at baseline was associated with a substantially increased risk of subsequent ICH (OR, 12.1; 95% CI, 3.4-42.5; P\u003c0.001).\nCONCLUSIONS: The excess of MB in warfarin users with ICH compared to other groups suggests that MB increase the risk of warfarin-associated ICH. Limited prospective data corroborate these findings, but larger prospective studies are urgently required."}