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血管紧张素原基因多态性M235T/T174M:在中国高血压患者中无过度传递现象。

Angiotensinogen gene polymorphisms M235T/T174M: no excess transmission to hypertensive Chinese.

作者信息

Niu T, Yang J, Wang B, Chen W, Wang Z, Laird N, Wei E, Fang Z, Lindpaintner K, Rogus J J, Xu X

机构信息

Program for Population Genetics, Harvard School of Public Health, Cardiovascular Division, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

出版信息

Hypertension. 1999 Feb;33(2):698-702. doi: 10.1161/01.hyp.33.2.698.

Abstract

The gene encoding angiotensinogen (AGT) has been widely studied as a candidate gene for hypertension. Most studies to date have relied on case-control analysis to test for an excess of AGT variants among hypertensive cases compared with normotensive controls. However, with this design, nothing guarantees that a positive finding is due to actual allelic association as opposed to an inappropriate control population. To avoid this difficulty in our study of essential hypertension in Anqing, China, we tested AGT variants using the transmission/disequilibrium test, a procedure that bypasses the need for a control sample by testing for excessive transmission of a genetic variant from parents heterozygous for that variant. We analyzed two AGT polymorphisms, M235T and T174M, which have been associated with essential hypertension in whites and Japanese, using data on 335 hypertensive subjects from 315 nuclear families and their parents. Except in the group of subjects younger than 25 years, M235 and T174 were the more frequently transmitted alleles. We found that 194 parents heterozygous for M235T transmitted M235 106 times (P=0.22) and that 102 parents heterozygous for T174M transmitted T174 60 times (P=0.09). Stratifying offspring by gender, M235 and T174 were transmitted 60 of 106 times (P=0.21) and 44 of 75 times (P=0.17), respectively, in men, and 46 of 88 times (P=0.75) and 16 of 27 times (P=0.44), respectively, in women. Our results were also negative in all age groups and for the affected offspring with blood pressure values >/=160/95 mm Hg. Thus, this study provides no evidence that either allele of M235T or T174M contributes to hypertension in this Chinese population.

摘要

编码血管紧张素原(AGT)的基因作为高血压的候选基因已得到广泛研究。迄今为止,大多数研究依靠病例对照分析来检测高血压病例中AGT变异体是否比血压正常的对照者更多。然而,采用这种设计,无法保证阳性结果是由于实际的等位基因关联,而非对照人群不恰当所致。为了在中国安庆原发性高血压研究中避免这一困难,我们使用传递/不平衡检验来检测AGT变异体,该方法通过检测某一基因变异体在该变异体的杂合子父母中的过度传递,从而无需对照样本。我们利用来自315个核心家庭及其父母的335名高血压患者的数据,分析了两个AGT多态性位点M235T和T174M,这两个位点在白人和日本人中与原发性高血压有关。除了年龄小于25岁的受试者组外,M235和T174是传递更频繁的等位基因。我们发现,194名M235T杂合子父母传递M235 106次(P = 0.22),102名T174M杂合子父母传递T174 60次(P = 0.09)。按性别对后代进行分层,在男性中,M

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