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首页> 外文期刊>Hypertension: An Official Journal of the American Heart Association >Angiotensinogen gene polymorphisms M235T/T174M: no excess transmission to hypertensive Chinese.
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Angiotensinogen gene polymorphisms M235T/T174M: no excess transmission to hypertensive Chinese.

机译:血管紧张素原基因多态性M235T / T174M:不会过度传播给高血压中国人。

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摘要

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.
机译:编码血管紧张素原(AGT)的基因已被广泛研究为高血压的候选基因。迄今为止,大多数研究都依靠病例对照分析来测试与正常血压对照相比高血压病例中过量的AGT变异。但是,对于这种设计,不能保证肯定的发现是由于实际的等位基因关联,而不是不合适的对照群体。为避免在中国安庆进行的原发性高血压研究中遇到的困难,我们使用传播/不平衡测试测试了AGT变异体,该程序通过测试父母杂合子的遗传变异是否过度传播来绕过对照样品的需要变体。我们使用来自315个核心家庭及其父母的335个高血压受试者的数据,分析了两个AGT多态性M235T和T174M,它们与白人和日本人的原发性高血压相关。除了25岁以下的受试者外,M235和T174是传播频率更高的等位基因。我们发现194个M235T杂合子的亲本传播了M235 106次(P = 0.22),而102个T174M杂合子的母本传播了T174 60次(P = 0.09)。按性别分层,M235和T174在男性中分别传播了106次中的60次(P = 0.21)和75次中的44次(P = 0.17),以及88次中的46次(P = 0.75)和27次中的16次。 (P = 0.44),分别在女性中。我们的结果在所有年龄组以及血压值> / = 160/95 mm Hg的受影响子代中均为阴性。因此,该研究没有提供证据证明M235T或T174M的等位基因会导致该中国人群的高血压。

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