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前瞻性研究亚甲基四氢叶酸还原酶(MTHFR)C677T 变异与 6000 名美国成年人全因和心血管疾病死亡率的关系。

Prospective study of methylenetetrahydrofolate reductase (MTHFR) variant C677T and risk of all-cause and cardiovascular disease mortality among 6000 US adults.

机构信息

Office of Public Health Genomics, CDC, Atlanta, GA 30341, USA.

出版信息

Am J Clin Nutr. 2012 May;95(5):1245-53. doi: 10.3945/ajcn.111.022384. Epub 2012 Apr 4.

Abstract

BACKGROUND

The association between blood homocysteine concentration and the risk of cardiovascular disease (CVD) remains controversial, but few studies have examined the association between MTHFR C677T (a proxy for high homocysteine concentration) and death from CVD.

OBJECTIVE

The objective was to examine associations of MTHFR C677T, a proxy for high homocysteine concentrations, with CVD mortality and with all-cause mortality in a national representative prospective cohort of the US adult population before the introduction of mandatory folic acid fortification of flour.

DESIGN

We used Mendelian randomization to examine the association of MTHFR C677T with cause-specific mortality in 5925 participants by accessing the NHANES III (1991-1994) Linked Mortality File (through 2006).

RESULTS

A comparison of homozygotes at baseline showed that individuals with a TT genotype had a 2.2-μmol/L higher homocysteine and a 1.4-ng/mL lower folate concentration, respectively, than did those with a CC genotype. The TT genotype frequency varied from 1.2% (95% CI: 0.7, 2.0) in non-Hispanic blacks and 11.6% (95% CI: 9.6, 14.0) in non-Hispanic whites to 19.4% (95% CI: 16.7, 22.3) in Mexican Americans. After adjustment for ethnic group and other CVD risk factors, the MTHFR C677T TT genotype was associated with significantly lower CVD mortality (HR: 0.69; 95% CI: 0.50, 0. 95) but had no significant effect on all-cause mortality (HR: 0.79; 95% CI: 0.59, 1.05). After stratification by period of follow-up, the inverse association of MTHFR with CVD mortality was significant only in the period after introduction of mandatory folic acid fortification.

CONCLUSION

The inverse association of MTHFR with CVD mortality was unexpected and highlights the need for caution in interpretation of Mendelian randomization studies, which, like other observational studies, can be influenced by chance, bias, or confounding.

摘要

背景

血液同型半胱氨酸浓度与心血管疾病(CVD)风险之间的关联仍存在争议,但很少有研究探讨 MTHFR C677T(同型半胱氨酸浓度升高的替代指标)与 CVD 死亡之间的关系。

目的

本研究旨在在强制叶酸强化面粉之前,在美国成年人的全国代表性前瞻性队列中,使用孟德尔随机化方法,检测 MTHFR C677T(同型半胱氨酸浓度升高的替代指标)与 CVD 死亡率和全因死亡率之间的关系。

设计

我们通过访问 NHANES III(1991-1994 年)关联死亡率文件(至 2006 年),在 5925 名参与者中使用孟德尔随机化方法,检测 MTHFR C677T 与特定病因死亡率之间的关系。

结果

在基线时比较纯合子发现,与 CC 基因型相比,TT 基因型的个体血液同型半胱氨酸分别高 2.2μmol/L,叶酸浓度分别低 1.4ng/mL。TT 基因型频率从非西班牙裔黑人的 1.2%(95%CI:0.7,2.0)到非西班牙裔白种人的 11.6%(95%CI:9.6,14.0),再到墨西哥裔美国人的 19.4%(95%CI:16.7,22.3)。在调整了种族群体和其他 CVD 危险因素后,MTHFR C677T TT 基因型与 CVD 死亡率显著降低相关(HR:0.69;95%CI:0.50,0.95),但对全因死亡率无显著影响(HR:0.79;95%CI:0.59,1.05)。按随访时间分层后,仅在强制叶酸强化后,MTHFR 与 CVD 死亡率的负相关才有统计学意义。

结论

MTHFR 与 CVD 死亡率之间的反比关系出乎意料,这凸显了在解释孟德尔随机化研究时需要谨慎,与其他观察性研究一样,孟德尔随机化研究也可能受到机会、偏倚或混杂因素的影响。

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