Correlations of MTHFR 677C>T Polymorphism with Cardiovascular Disease in Patients with End-Stage Renal Disease: A Meta-Analysis

被引:7
作者
Gao, Xian-Hui [1 ]
Zhang, Guo-Yi [1 ]
Wang, Ying [2 ]
Zhang, Hui-Ying [3 ]
机构
[1] Liaoning Med Univ, Sch Publ Hlth, Lab Prevent Med, Jinzhou, Peoples R China
[2] Liaoning Med Univ, Sch Publ Hlth, Dept Toxicol, Jinzhou, Peoples R China
[3] Liaoning Med Univ, Affiliated Hosp 1, Sleep Monitoring Ctr, Jinzhou, Peoples R China
关键词
METHYLENETETRAHYDROFOLATE REDUCTASE GENE; CHRONIC KIDNEY-DISEASE; CHRONIC-HEMODIALYSIS PATIENTS; ONE-CARBON METABOLISM; VASCULAR CALCIFICATION; C677T POLYMORPHISM; RISK-FACTOR; HYPERHOMOCYSTEINEMIA; HOMOCYSTEINE; DIALYSIS;
D O I
10.1371/journal.pone.0102323
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Objective: This meta-analysis was conducted to evaluate the correlations of a common polymorphism (677C>T) in the methylenetetrahydrofolate reductase (MTHFR) gene with risk of cardiovascular disease (CVD) in patients with end-stage renal disease (ESRD). Method: The following electronic databases were searched without language restrictions: Web of Science (1945 similar to 2013), the Cochrane Library Database (Issue 12, 2013), MEDLINE (1966 similar to 2013), EMBASE (1980 similar to 2013), CINAHL (1982 similar to 2013) and the Chinese Biomedical Database (CBM) (1982 similar to 2013). Meta-analysis was performed using STATA statistical software. Odds ratios (ORs) with their 95% confidence intervals (95% CIs) were calculated. Results: Eight cohort studies met all inclusion criteria and were included in this meta-analysis. A total of 2,292 ESRD patients with CVD were involved in this meta-analysis. Our meta-analysis results revealed that the MTHFR 677C>T polymorphism might increase the risk of CVD in ESRD patients (TT vs. CC: OR = 2.75, 95% CI = 1.35 similar to 5.59, P = 0.005; CT+TT vs. CC: OR = 1.39, 95% CI = 1.09 similar to 1.78, P = 0.008; TT vs. CC+CT: OR = 2.52, 95% CI = 1.25 similar to 5.09, P = 0.010; respectively). Further subgroup analysis by ethnicity suggested that the MTHFR 677C > T polymorphism was associated with an elevated risk for CVD in ESRD patients among Asians (TT vs. CC: OR = 3.38, 95% CI = 1.11 similar to 10.28, P = 0.032; CT+TT vs. CC: OR = 1.44, 95% CI = 1.05 similar to 1.97, P = 0.022; TT vs. CC+CT: OR = 3.15, 95% CI = 1.02 similar to 9.72, P = 0.046; respectively), but not among Africans or Caucasians (all P > 0.05). Conclusion: Our findings indicate that the MTHFR 677C>T polymorphism may be associated with an elevated risk for CVD in ESRD patients, especially among Asians.
引用
收藏
页数:9
相关论文
共 43 条
[11]   Methylenetetrahydrofolate reductase (MTHFR) polymorphism A1298C (Glu429Ala) predicts decline in renal function over time in the African-American Study of Kidney Disease and Hypertension (AASK) Trial and Veterans Affairs Hypertension Cohort (VAHC) [J].
Fung, Maple M. ;
Salem, Rany M. ;
Lipkowitz, Michael S. ;
Bhatnagar, Vibha ;
Pandey, Braj ;
Schork, Nicholas J. ;
O'Connor, Daniel T. .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2012, 27 (01) :197-U246
[12]   Stability of DNA Methylation Patterns in Mouse Spermatogonia Under Conditions of MTHFR Deficiency and Methionine Supplementation [J].
Garner, Justine L. ;
Niles, Kirsten M. ;
McGraw, Serge ;
Yeh, Jonathan R. ;
Cushnie, Duncan W. ;
Hermo, Louis ;
Nagano, Makoto C. ;
Trasler, Jacquetta M. .
BIOLOGY OF REPRODUCTION, 2013, 89 (05)
[13]   The common mutations C677T and A1298C in the human methylenetetrahydrofolate reductase gene are associated with hyperhomocysteinemia and cardiovascular disease in hemodialysis patients [J].
Haviv, YS ;
Shpichinetsky, V ;
Goldschmidt, N ;
Atta, IA ;
Ben-Yehuda, A ;
Friedman, G .
NEPHRON, 2002, 92 (01) :120-126
[14]   Genome-wide significant predictors of metabolites in the one-carbon metabolism pathway [J].
Hazra, Aditi ;
Kraft, Peter ;
Lazarus, Ross ;
Chen, Constance ;
Chanock, Stephen J. ;
Jacques, Paul ;
Selhub, Jacob ;
Hunter, David J. .
HUMAN MOLECULAR GENETICS, 2009, 18 (23) :4677-4687
[15]   Homocysteine as a Risk Factor for Cardiovascular Disease in Patients Treated by Dialysis: A Meta-analysis [J].
Heinz, Judith ;
Kropf, Siegfried ;
Luley, Claus ;
Dierkes, Jutta .
AMERICAN JOURNAL OF KIDNEY DISEASES, 2009, 54 (03) :478-489
[16]   Prevalence of methylenetetrahydrofolate gene (MTHFR) C677T polymorphism among chronic hemodialysis patients and its association with cardiovascular disease: a cross-sectional analysis [J].
Ibrahim, Salwa ;
El Dessokiy, Ola .
CLINICAL AND EXPERIMENTAL NEPHROLOGY, 2009, 13 (05) :501-507
[17]   Nontraditional risk factors for cardiovascular disease in patients with chronic kidney disease [J].
Kendrick, Jessica ;
Chonchol, Michel B. .
NATURE CLINICAL PRACTICE NEPHROLOGY, 2008, 4 (12) :672-681
[18]  
Kimura H, 2000, J AM SOC NEPHROL, V11, P885, DOI 10.1681/ASN.V115885
[19]   MTHFR C677T Polymorphism as a Risk Factor for Vascular Calcification in Chronic Hemodialysis Patients [J].
Lee, So-Young ;
Kim, Hoe-Young ;
Park, Kyung Mi ;
Lee, Stephen Yon Gu ;
Hong, Seong Geun ;
Kim, Hyung-Jong ;
Yang, Dong Ho .
JOURNAL OF KOREAN MEDICAL SCIENCE, 2011, 26 (03) :461-465
[20]   Cholecalciferol Supplementation in Hemodialysis Patients: Effects on Mineral Metabolism, Inflammation, and Cardiac Dimension Parameters [J].
Matias, Patricia Joao ;
Jorge, Cristina ;
Ferreira, Carina ;
Borges, Marilia ;
Aires, Ines ;
Amaral, Tiago ;
Gil, Celia ;
Cortez, Jose ;
Ferreira, Anibal .
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2010, 5 (05) :905-911