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土耳其骨关节炎患者 MTHFR 基因 C677T 突变和 ACE 基因 I/D 多态性。

MTHFR gene C677T mutation and ACE gene I/D polymorphism in Turkish patients with osteoarthritis.

机构信息

Department of Physical Medicine and Rehabilitation, Faculty of Medicine, Gaziosmanpaşa University, Tokat, Turkey.

出版信息

Dis Markers. 2013;34(1):17-22. doi: 10.3233/DMA-2012-00939.

Abstract

Osteoarthritis is a degenerative joint disorder resulting in destruction of articular cartilage, osteophyte formation, and subchondral bone sclerosis. In recent years, numerous genetic factors have been identified and implicated in osteoarthritis. The aim of the current study was to examine the influence of methylenetetrahydrofolate reductase (MTHFR) gene C677T mutation and angiotensin converting enzyme (ACE) gene insertion/deletion (I/D) variations on the risk of osteoarthritis. Genomic DNA is obtained from 421 persons (221 patients with osteoarthritis and 200 healthy controls). ACE gene I/D polymorphism genotypes were determined using polymerase chain reaction using I and D allele-specific primers. The MTHFR C677T mutation was analyzed by polymerase chain reaction (PCR) based restriction fragment length polymorphism (RFLP) methods. We found significant difference between the groups with respect to both ACE and MTHFR genotype distributions (p< 0.001, p< 0.001 respectively). Our study suggests that ACE gene DD genotype and MTHFR gene CC genotype could be used as genetic markers in osteoarthritis in Turkish study populations.

摘要

骨关节炎是一种退行性关节疾病,导致关节软骨破坏、骨赘形成和软骨下骨硬化。近年来,许多遗传因素已被确定并与骨关节炎有关。本研究的目的是探讨亚甲基四氢叶酸还原酶(MTHFR)基因 C677T 突变和血管紧张素转换酶(ACE)基因插入/缺失(I/D)变异对骨关节炎风险的影响。从 421 人(221 例骨关节炎患者和 200 例健康对照者)中获得基因组 DNA。使用 I 和 D 等位基因特异性引物,通过聚合酶链反应(PCR)确定 ACE 基因 I/D 多态性基因型。通过聚合酶链反应(PCR)基于限制性片段长度多态性(RFLP)方法分析 MTHFR C677T 突变。我们发现两组 ACE 和 MTHFR 基因型分布存在显著差异(p<0.001,p<0.001)。我们的研究表明,ACE 基因 DD 基因型和 MTHFR 基因 CC 基因型可作为土耳其研究人群中骨关节炎的遗传标志物。

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