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硫氧还蛋白相互作用蛋白 (TXNIP) rs7212 多态性与巴西普通人群的动脉僵硬度相关。

Thioredoxin interacting protein (TXNIP) rs7212 polymorphism is associated with arterial stiffness in the Brazilian general population.

机构信息

Laboratory of Genetics and Molecular Cardiology, Heart Institute (InCor), University of Sao Paulo Medical School, Sao Paulo, Brazil.

出版信息

J Hum Hypertens. 2012 May;26(5):340-2. doi: 10.1038/jhh.2011.102. Epub 2011 Nov 24.

Abstract

Thioredoxin interacting protein plays a pivotal role in several important processes of cardiovascular homeostasis by functioning as a biological sensor for biomechanical and oxidative stress. However, the effects of genetic variants in the modulation of arterial stiffness are unknown. In this scenario, the present study evaluated the relationship between the TXNIP rs7212 polymorphism and arterial stiffness. In the overall sample and in the diabetic group, individuals carrying CG+GG genotypes had higher PWV values compared with CC genotype group (10.0 vs 9.8 m s (-1), P=0.03; 12.3 vs 11.2 m s(-1), P=0.01; respectively). Our findings indicated that the G allele may contribute to increased arterial stiffness in the Brazilian general population and suggest a possible interaction with diabetes.

摘要

硫氧还蛋白相互作用蛋白 (TXNIP) 通过作为生物力学和氧化应激的生物传感器,在心血管稳态的几个重要过程中发挥关键作用。然而,遗传变异在调节动脉僵硬方面的影响尚不清楚。在这种情况下,本研究评估了 TXNIP rs7212 多态性与动脉僵硬之间的关系。在总样本和糖尿病组中,与 CC 基因型组相比,携带 CG+GG 基因型的个体具有更高的 PWV 值(10.0 与 9.8 m/s(-1),P=0.03;12.3 与 11.2 m/s(-1),P=0.01;分别)。我们的研究结果表明,G 等位基因可能导致巴西普通人群的动脉僵硬增加,并提示可能与糖尿病存在相互作用。

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