Human agt-p.Met268thr and coronary heart disease risk: A case-control study and meta-analysis

Mohammadi, H. and Razavi, N. and Abbasi, A. and Babaei, F. and Seyedrezazadeh, E. and Hosseinzadeh, A. (2018) Human agt-p.Met268thr and coronary heart disease risk: A case-control study and meta-analysis. Family Medicine and Primary Care Review, 20 (1). pp. 17-24.

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Abstract

Summary Background. Polymorphisms in genes, which is involved in the renin�angiotensin system, play an important role in the pathogenesis of coronary heart disease (CHD). Polymorphism of c.803T>C in the human angiotensinogen gene results in methionine (M) to threonine (T) substitution at codon 268 (p.Met268Thr), which traditionally has been known as M235T. This polymorphism may contribute to cardiovascular diseases. Objectives. The aim of this study was to investigate the association between p.Met268Thr polymorphism in the angiotensinogen gene and coronary heart disease (CHD) through a case-control study, which is followed by a meta-analysis. Material and methods. In the case-control study, c.803T>C genotyping of 217 subjects (102 CHD cases vs 115 controls) was investigated by the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method. In the meta-analysis, 31 studies were included, reflecting 12,028 people with CHD and 16,362 healthy controls. Results. The data from the case-control study revealed that MT (OR, 1.875; 95CI, 1.060�3.316; p = 0.031) and TT (OR, 3.389; 95CI, 1.251�9.179; p = 0.016) genotypes are significantly associated with CHD. The meta-analysis revealed a significant association in the recessive model (OR, 1.156; 95CI, 1.011�1.321; p = 0.034). Conclusions. Although the pooled OR of the meta-analysis showed that there is an increased risk of CHD conferred by p.Met268Thr of the AGT gene, this association was weak, which could be attributed to a bias in publications. © Copyright by Wydawnictwo Continuo.

Item Type: Article
Additional Information: cited By 0
Uncontrolled Keywords: high density lipoprotein cholesterol; low density lipoprotein cholesterol; triacylglycerol, adult; Article; case control study; controlled study; coronary risk; DNA polymorphism; DNA sequence; female; gene frequency; genotype; human; ischemic heart disease; major clinical study; male; middle aged; polymerase chain reaction; restriction fragment length polymorphism
Subjects: Medicine
Biochemistry, Genetics and Molecular Biology
Divisions: Faculty of Medicine > Clinical Sciences > Department of Cardiology
Depositing User: ART . editor
Date Deposited: 13 Apr 2019 09:34
Last Modified: 13 Apr 2019 09:34
URI: http://eprints.kaums.ac.ir/id/eprint/4066

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