Email updates

Keep up to date with the latest news and content from Lipids in Health and Disease and BioMed Central.

Open Access Research

Enrichment of MTHFR 677 T in a Chinese long-lived cohort and its association with lipid modulation

Ning-Yuan Chen1, Cheng-Wu Liu1, Li-Li Du1, Li-Ping Xiao1, Lin Ge1, Yi-Yuan Wang1, Zhen Wei1, Hua-Yu Wu2, Chen-Yuan Luo1, Liang Liang1, Jun-Hua Peng1, Xiao-Qiu Luo1, Rui-Xing Yin3, Cuc Phuong Nguyen1 and Shang-Ling Pan1*

Author Affiliations

1 Department of Pathophysiology, School of Preclinical Medicine, Guangxi Medical University, Nanning 530021, Guangxi, People’s Republic of China

2 Department of Cell Biology & Genetics, School of Preclinical Medicine, Guangxi Medical University, Nanning 530021, Guangxi, People’s Republic of China

3 Department of Cardiology, Institute of Cardiovascular Diseases, The First Affiliated Hospital, Guangxi Medical University, 22 Shuangyong Road, Nanning 530021, Guangxi, People’s Republic of China

For all author emails, please log on.

Lipids in Health and Disease 2014, 13:104  doi:10.1186/1476-511X-13-104

Published: 26 June 2014

Abstract

Background

Variants in the Methylenetetrahydrofolate reductase (MTHFR) gene may result in a lowered catalytic activity and associate with subsequent elevated serum homocysteine (Hcy) concentration, abnormal DNA synthesis and methylation, cardiovascular risk, and unhealthy aging. Several investigations on the relationship of MTHFR C677T polymorphism with serum lipid profile and longevity have been conducted in some populations, but the findings remain mixed. Herein, we sought to look at the association between MTHFR C677T and lipid profile in a longevous cohort in Bama, a well-known home of longevity in China.

Methods

Genotyping of MTHFR C677T was undertaken in 516 long-lived inhabitants (aged 90 and older, long-lived group, LG) and 493 healthy controls (aged 60–75, non-long-lived group, non-LG) recruited from Bama area. Correlation between MTHFR genotypes and lipids was then evaluated.

Results

T allele and TT genotype were significantly more prevalent in LG (P = 0.001 and 0.002, respectively), especially in females, than in non-LG. No difference in the tested lipid measures among MTHFR C677T genotypes was observed in LG, non-LG and total population (P > 0.05 for all). However, female but not male T carriers exhibited higher TC and LDL-C levels than did T noncarriers in the total population and in LG after stratification by sex (P < 0.05 for each). These differences did not however remain through further subdivision by hyperlipidemia and normolipidemia.

Conclusion

The higher prevalence of MTHFR 677 T genotypes and its modest unfavorable impact on lipids in Bama long-lived individuals may imply an existence of other protective genotypes which require further determination.