| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T9 |
806-922 |
Sentence |
denotes |
The control group consisted of 213 patients with normal left ventricular function and no documented evidence of CHD. |
| TextSentencer_T1 |
0-83 |
Sentence |
denotes |
C/T polymorphism of the intercellular adhesion molecule-1 gene (exon 6, codon 469). |
| TextSentencer_T2 |
84-151 |
Sentence |
denotes |
A risk factor for coronary heart disease and myocardial infarction. |
| TextSentencer_T3 |
152-163 |
Sentence |
denotes |
BACKGROUND: |
| TextSentencer_T4 |
164-360 |
Sentence |
denotes |
The intercellular adhesion molecule-1 (ICAM-1) mediates the interaction of activated endothelial cells with leukocytes and plays a fundamental role in the pathogenesis of coronary atherosclerosis. |
| TextSentencer_T5 |
361-504 |
Sentence |
denotes |
ICAM-1 single-base C/T polymorphism, which determines an amino acid substitution in the ICAM-1 protein in exon 6 codon 469, has been described. |
| TextSentencer_T6 |
505-657 |
Sentence |
denotes |
Our purpose was to determine whether this C/T polymorphism influences the risk of coronary heart disease (CHD) and myocardial infarction (MI) in humans. |
| TextSentencer_T7 |
658-678 |
Sentence |
denotes |
METHODS AND RESULTS: |
| TextSentencer_T8 |
679-805 |
Sentence |
denotes |
We enrolled 349 patients with angiographically documented CHD, including a sub-group of 179 patients with acute or chronic MI. |
| TextSentencer_T10 |
923-1076 |
Sentence |
denotes |
All patients and controls were Germans genotyped by polymerase chain reaction and allele-specific oligonucleotide techniques for the ICAM-1 polymorphism. |
| TextSentencer_T11 |
1077-1241 |
Sentence |
denotes |
In the patients with CHD and MI the frequencies of the T genotype (TT+TC) were significantly higher than the CC genotype compared to the control subjects (P<0.001). |
| TextSentencer_T12 |
1242-1496 |
Sentence |
denotes |
With the additional use of multivariable logistic regression analysis for CHD (TT+TC versus CC; P=0.011, odds ratio 2.21, 95% CI 1.20-4.07), we found a significant association between CHD and MI and the TT and TC genotype of the ICAM-1 gene polymorphism. |
| TextSentencer_T13 |
1497-1509 |
Sentence |
denotes |
CONCLUSIONS: |
| TextSentencer_T14 |
1510-1690 |
Sentence |
denotes |
These results suggest that the TT and TC genotype of the ICAM-1 gene polymorphism in codon 469 is a genetic factor that may determine an individual's susceptibility for CHD and MI. |
| T1 |
0-83 |
Sentence |
denotes |
C/T polymorphism of the intercellular adhesion molecule-1 gene (exon 6, codon 469). |
| T2 |
84-151 |
Sentence |
denotes |
A risk factor for coronary heart disease and myocardial infarction. |
| T3 |
152-163 |
Sentence |
denotes |
BACKGROUND: |
| T4 |
164-360 |
Sentence |
denotes |
The intercellular adhesion molecule-1 (ICAM-1) mediates the interaction of activated endothelial cells with leukocytes and plays a fundamental role in the pathogenesis of coronary atherosclerosis. |
| T5 |
361-504 |
Sentence |
denotes |
ICAM-1 single-base C/T polymorphism, which determines an amino acid substitution in the ICAM-1 protein in exon 6 codon 469, has been described. |
| T6 |
505-657 |
Sentence |
denotes |
Our purpose was to determine whether this C/T polymorphism influences the risk of coronary heart disease (CHD) and myocardial infarction (MI) in humans. |
| T7 |
658-678 |
Sentence |
denotes |
METHODS AND RESULTS: |
| T8 |
679-805 |
Sentence |
denotes |
We enrolled 349 patients with angiographically documented CHD, including a sub-group of 179 patients with acute or chronic MI. |
| T9 |
806-922 |
Sentence |
denotes |
The control group consisted of 213 patients with normal left ventricular function and no documented evidence of CHD. |
| T10 |
923-1076 |
Sentence |
denotes |
All patients and controls were Germans genotyped by polymerase chain reaction and allele-specific oligonucleotide techniques for the ICAM-1 polymorphism. |
| T11 |
1077-1241 |
Sentence |
denotes |
In the patients with CHD and MI the frequencies of the T genotype (TT+TC) were significantly higher than the CC genotype compared to the control subjects (P<0.001). |
| T12 |
1242-1496 |
Sentence |
denotes |
With the additional use of multivariable logistic regression analysis for CHD (TT+TC versus CC; P=0.011, odds ratio 2.21, 95% CI 1.20-4.07), we found a significant association between CHD and MI and the TT and TC genotype of the ICAM-1 gene polymorphism. |
| T13 |
1497-1509 |
Sentence |
denotes |
CONCLUSIONS: |
| T14 |
1510-1690 |
Sentence |
denotes |
These results suggest that the TT and TC genotype of the ICAM-1 gene polymorphism in codon 469 is a genetic factor that may determine an individual's susceptibility for CHD and MI. |