Association between angiotensin-converting enzyme insertion/deletion gene polymorphism and atrial fibrillation: a meta-analysis

التفاصيل البيبلوغرافية
العنوان: Association between angiotensin-converting enzyme insertion/deletion gene polymorphism and atrial fibrillation: a meta-analysis
المؤلفون: Gang Xu, Dong Li, Tong Liu, Michael Shehata, Panagiotis Korantzopoulos, Xunzhang Wang, Guangping Li
سنة النشر: 2011
مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Peptidyl-Dipeptidase A, Bioinformatics, Peptidyl-Dipeptidase A/*genetics, Renin-Angiotensin System, INDEL Mutation, Risk Factors, Physiology (medical), Internal medicine, Atrial Fibrillation, Medicine, Insertion deletion, Humans, Polymorphism, Genetic/genetics, Aged, Polymorphism, Genetic, biology, business.industry, Case-control study, Angiotensin-converting enzyme, Atrial fibrillation, Atrial Fibrillation/epidemiology/*genetics/physiopathology, Middle Aged, medicine.disease, Clinical trial, INDEL Mutation/*genetics, Endocrinology, Meta-analysis, Case-Control Studies, biology.protein, Dominant model, Female, Gene polymorphism, Renin-Angiotensin System/physiology, Cardiology and Cardiovascular Medicine, business
الوصف: AIMS: Recent observations have raised concerns regarding the activation of the renin-angiotensin system and the development of atrial fibrillation (AF). Some initial studies indicated an association between an angiotensin-converting enzyme insertion/deletion (ACE I/D) polymorphism and AF, however, the results have been inconsistent. Our aim was to perform a meta-analysis of relevant studies to assess the validity of this association. METHODS AND RESULTS: PubMed, Cochrane clinical trials database, and EMBASE were searched through July 2009, and a manual search was also performed. Of the 68 initially identified studies, 18 case-control studies with 7577 patients were finally analysed. No statistically significant associations were found between the ACE I/D polymorphism and AF risk in the genetic additive model and dominant model, whereas a significant association was observed in the recessive model. A significant heterogeneity between individual studies was evident in all three models. Subgroup analyses showed a strong association between the ACE I/D polymorphism and hypertensive AF without significant heterogeneity. CONCLUSION: Our meta-analysis suggests that there is insufficient evidence to demonstrate an association between ACE I/D polymorphism and AF risk. However, there seems to be a significant association between ACE I/D gene polymorphic variation and AF in patients with hypertension. Additional studies are warranted to further explore this association in ethnically diverse populations and varied cardiovascular substrates. Europace
اللغة: English
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2cb34bb3b79e1ba9ba3bf6720e1ebaffTest
http://olympias.lib.uoi.gr/jspui/handle/123456789/23675Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....2cb34bb3b79e1ba9ba3bf6720e1ebaff
قاعدة البيانات: OpenAIRE