Angiotensin-converting enzyme polymorphisms and risk of spontaneous deep intracranial hemorrhage in Taiwan

Background and purpose:  This study examines whether angiotensin‐converting enzyme (ACE) gene polymorphisms are associated with the risk of spontaneous deep intracerebral hemorrhage (SDICH) in Taiwan using a case–control study. Methods:  Totally, 217 SDICH patients and 283 controls were recruited. A...

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Published in:European journal of neurology Vol. 15; no. 11; pp. 1206 - 1211
Main Authors: Chen, C.-M., Chen, Y.-C., Wu, Y.-R., Hu, F.-J., Lyu, R.-K., Chang, H.-S., Ro, L.-S., Hsu, W.-C., Chen, S.-T., Lee-Chen, G.-J.
Format: Journal Article
Language:English
Published: Oxford, UK Blackwell Publishing Ltd 01-11-2008
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Summary:Background and purpose:  This study examines whether angiotensin‐converting enzyme (ACE) gene polymorphisms are associated with the risk of spontaneous deep intracerebral hemorrhage (SDICH) in Taiwan using a case–control study. Methods:  Totally, 217 SDICH patients and 283 controls were recruited. Associations of ACE A‐240T and ACE I/D polymorphisms with SDICH were examined under the additive model and adjusted for gender, age, body mass index, total cholesterol level, smoking history, alcohol use, hypertension, and use of ACE inhibitors. Results:  Hypertension, diabetes mellitus, family history of spontaneous intracerebral hemorrhage (SICH), and low cholesterol level increase risk of female SDICH, whereas hypertension, alcohol use, smoking history, family history of SICH, and low cholesterol level are an important risk factor for male SDICH. After adjusting for covariates, only haplotype ACE T‐D (OR = 2.7, 95% CI, 1.1–6.5, P = 0.02) was associated with female SDICH. Conclusions:  This study demonstrates that environmental risk factors play a major role and ACE polymorphisms play a minor role in contributing risk of SDICH in Taiwan.
Bibliography:ark:/67375/WNG-BD48SXS9-G
istex:A645FD336C5A411999455B7204893E11FE3D4FF2
ArticleID:ENE2294
These authors contributed equally to the study.
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1351-5101
1468-1331
1471-0552
DOI:10.1111/j.1468-1331.2008.02294.x