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亚甲基四氢叶酸还原酶 C677T 基因型与中国原发性高血压人群血压水平的关联。

Associations of methylenetetrahydrofolate reductase C677T genotype with blood pressure levels in Chinese population with essential hypertension.

机构信息

a School of Life Sciences , Anhui University , Hefei , China.

b Faculty of Health Sciences , Simon Fraser University , Burnaby , BC , Canada.

出版信息

Clin Exp Hypertens. 2018;40(3):207-212. doi: 10.1080/10641963.2017.1281937. Epub 2018 Feb 13.

Abstract

OBJECTIVE

To confirm the association between baseline blood pressure (BP) levels and the methylenetetrahydrofolate reductase (MTHFR) C677T gene polymorphism in patients with essential hypertension.

METHODS

A total of 347 patients were enrolled from the Dongzhi community in Anhui Province, China. The C677T polymorphism of the MTHFR gene was detected using high-throughput TaqMan allelic discrimination assay. Baseline BP was measured using a standardized mercury-gravity monometer.

RESULTS

In the whole sample, the frequency of the MTHFR C677T genotypes CC, CT, and TT were 38.6%, 48.1%, and 13.3%, respectively. In a recessive model (CC+CT versus TT genotypes), baseline diastolic blood pressure (DBP) was significantly higher in patients with the TT genotype compared to those with the CT or CC genotypes (P= 0.013). We also divided all patients into three groups based on the tertiles of the baseline BP distribution. Compared to subjects in the lowest tertile of DBP, the adjusted odds of having the TT genotype among subjects in the highest tertile was 2.6 (95% CI: 1.1 to 6.2). However, no significant associations were observed between baseline systolic blood pressure (SBP) and the MTHFR C677T polymorphism.

CONCLUSIONS

The MTHFR gene polymorphism could be an important genetic determinant of baseline DBP levels in Chinese essential hypertensive patients.

摘要

目的

确认原发性高血压患者基线血压(BP)水平与亚甲基四氢叶酸还原酶(MTHFR)C677T 基因多态性之间的关联。

方法

在中国安徽省东至社区共纳入 347 例患者。采用高通量 TaqMan 等位基因鉴别检测法检测 MTHFR 基因 C677T 多态性。采用标准化汞重力血压计测量基线 BP。

结果

在整个样本中,MTHFR C677T 基因型 CC、CT 和 TT 的频率分别为 38.6%、48.1%和 13.3%。在隐性模型(CC+CT 与 TT 基因型)中,TT 基因型患者的基线舒张压(DBP)明显高于 CT 或 CC 基因型患者(P=0.013)。我们还根据基线 BP 分布的三分位数将所有患者分为三组。与 DBP 最低三分位数的受试者相比,DBP 最高三分位数受试者中 TT 基因型的调整比值比为 2.6(95%CI:1.1 至 6.2)。然而,在基线收缩压(SBP)与 MTHFR C677T 多态性之间未观察到显著关联。

结论

MTHFR 基因多态性可能是中国原发性高血压患者基线 DBP 水平的重要遗传决定因素。

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