PMC:3727988 / 7508-8392 JSONTXT

{"target":"https://pubannotation.org/docs/sourcedb/PMC/sourceid/3727988","sourcedb":"PMC","sourceid":"3727988","source_url":"https://www.ncbi.nlm.nih.gov/pmc/3727988","text":"Gentile et al. [19] genotyped panel of SNPs involved in triptans pharmacokinetics and pharmacody-namics in a chronic migraine (CM) population. In particular they studied the 30 bp VNTR in MAO A (monoamine oxidase A) promoter, CYP 1A2 *1C and *1 F, CYP3A4 *1B and C825T SNP in the gene coding the G protein b3 subunit (GNB3). A significant association with CM was found for the long allele of monoamine oxidase A 30 bp VNTR and CYP1A2*1 F variant. The same authors performed an analysis of the association between genotypic and allelic frequencies of the analyzed SNPs and the grade of response to triptan administration: a significant correlation for MAOA uVNTR polymorphism was found. Further stratification of patients in abuser and non-abuser groups revealed a significant association with triptan overuse and, within the abusers, with drug response to the CYP1A2*1 F variant [20].","tracks":[{"project":"2_test","denotations":[{"id":"23815568-20213484-60545004","span":{"begin":16,"end":18},"obj":"20213484"},{"id":"23815568-20652353-60545005","span":{"begin":880,"end":882},"obj":"20652353"}],"attributes":[{"subj":"23815568-20213484-60545004","pred":"source","obj":"2_test"},{"subj":"23815568-20652353-60545005","pred":"source","obj":"2_test"}]}],"config":{"attribute types":[{"pred":"source","value type":"selection","values":[{"id":"2_test","color":"#93afec","default":true}]}]}}