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人类的遗传与血压:概述

Heredity and blood pressure in humans: an overview.

作者信息

Mongeau J G

机构信息

Service of Nephrology, Ste-Justine Hospital, Montreal, Canada.

出版信息

Pediatr Nephrol. 1987 Jan;1(1):69-75. doi: 10.1007/BF00866887.

Abstract

This paper presents a review of the genetic transmission of normal blood pressure and of essential hypertension. Familial aggregation of normal blood pressure has been reported in adults, in children and even in newborns. Blood pressure aggregation phenomenon, however, is the result of both a genetic component and shared environmental factors. More specific for each etiological factor were the studies of blood pressure aggregation in twins and in adopted children. Attention was focused on the Montreal Adoption Study. In essential hypertension, a Japanese study is reviewed showing the occurrence of hypertension in the offspring of hypertensive parents. The heterogeneity of essential hypertension is underlined and two of the multiple etiological factors are particularly considered for their genetic component: the response to salt intake and erythrocyte cation fluxes. The conclusion from the literature reviewed is that essential hypertension is a polygenic disease transmitted by polygenic systems.

摘要

本文对正常血压和原发性高血压的遗传传递进行了综述。正常血压的家族聚集现象在成年人、儿童甚至新生儿中均有报道。然而,血压聚集现象是遗传因素和共同环境因素共同作用的结果。对双胞胎和领养儿童血压聚集现象的研究更能明确每种病因。重点关注了蒙特利尔领养研究。在原发性高血压方面,综述了一项日本研究,该研究显示高血压父母的后代会出现高血压。强调了原发性高血压的异质性,并特别考虑了多种病因中的两个因素的遗传成分:对盐摄入的反应和红细胞阳离子通量。综述文献得出的结论是,原发性高血压是一种由多基因系统传递的多基因疾病。

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