Relationship Between Gene Polymorphism of Methylenetetrahydrofolate Reductase C677T and Left Ventricular Hypertrophy in Chinese Patients with Chronic Kidney Disease

被引：1

作者：

Wu, Xie ^{[1
,2
]}

Lin, Jing ^{[1
,2
,3
,4
]}

Xue, Ning ^{[1
,3
,4
]}

Teng, Jie ^{[1
,2
,3
,4
]}

Wang, Yaqiong ^{[1
,3
,4
]}

Li, Yang ^{[1
,2
]}

Xu, Xunhui ^{[1
,2
]}

Shen, Ziyan ^{[1
,3
,4
]}

Ding, Xiaoqiang ^{[1
,2
,3
,4
]}

Fang, Yi ^{[1
,2
,3
,4
]}

机构：

[1] Fudan Univ, Zhongshan Hosp, Dept Nephrol, Shanghai, Peoples R China

[2] Fudan Univ, Zhongshan Hosp, Shanghai Key Lab Kidney & Blood Purificat, Shanghai, Peoples R China

[3] Fudan Univ, Zhongshan Hosp, Shanghai Med Ctr Kidney Dis, Shanghai, Peoples R China

[4] Fudan Univ, Zhongshan Hosp, Shanghai Inst Kidney & Dialysis, Shanghai, Peoples R China

来源：

LABORATORY MEDICINE | 2021年 / 52卷 / 06期

关键词：

methylenetetrahydrofolate reductase; gene polymorphism; homocysteine; left ventricular hypertrophy; chronic kidney disease; CARDIOVASCULAR-DISEASE; MTHFR VARIANT; HOMOCYSTEINE; HYPERHOMOCYSTEINEMIA; ASSOCIATION; MUTATION; RISK; HYPERTENSION; MANAGEMENT; LEADS;

D O I：

10.1093/labmed/lmab004

中图分类号：

R446 [实验室诊断]; R-33 [实验医学、医学实验];

学科分类号：

1001 ;

摘要：

Objective: This study aimed to investigate the relationship between the gene polymorphism of methylenetetrahydrofolate reductase (MTHFR) C677T and left ventricular hypertrophy (LVH) in patients with chronic kidney disease (CKD). Methods: A total of 763 Chinese patients with CKD undergoing genetic testing were included in the study. The association between the gene polymorphism of MTHFR C677T and echocardiographic parameters was analyzed through univariate and multivariate analyses. Results: We found a remarkably positive association between MTHFR C677T gene polymorphism and LVH indexes, including interventricular septal thickness (F = 3.8; P = .022), left ventricular posterior wad thickness (F = 3.0; P = .052), left ventricular mass (F = 3.9; P = .022), and left ventricular mass index (F = 2.6; P = .075). After adjusting for the potential confounders linking the polymorphism,we found that the positive association between the polymorphism and LVH indexes still existed in patients with CKD in some multiple linear regression models (P <.05). Conclusion: MTHFR C677T gene polymorphism may be a genetic susceptibility marker for the development of LVH in patients with CKD.

引用

页码：519 / 527

页数：9

共 49 条

[11] Mice deficient in methylenetetrahydrofolate reductase exhibit hyperhomocysteinemia and decreased methylation capacity, with neuropathology and aortic lipid deposition [J].