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高血压中电解质转运系统的遗传与流行病学研究。

Genetic and epidemiological studies on electrolyte transport systems in hypertension.

作者信息

Williams R R, Hunt S C, Wu L L, Hasstedt S J, Hopkins P N, Ash K O

机构信息

Department of Medicine, University of Utah School of Medicine, Salt Lake City.

出版信息

Clin Physiol Biochem. 1988;6(3-4):136-49.

PMID:3060295
Abstract

In recent years several different tests of cations in human cells have been studied to detect and to define possible roles in the development of essential hypertension. The goal of this report is to summarize what has been learned in genetic and epidemiological studies of human populations. The seven tests reviewed in greatest detail include sodium-lithium countertransport, intraerythrocytic sodium, sodium (or lithium)-potassium cotransport, lithium leak, sodium-potassium ATPase pump, sodium pump sites (ouabain binding), and circulating sodium pump inhibitor ('digoxin-like factor' in some studies). Countertransport, intraerythrocytic sodium and cotransport consistently show different values in hypertensives compared to normotensives and even in normotensives with a positive family history of hypertension when compared to controls without a positive family history. Thorough genetic studies have been carried out only for sodium-lithium countertransport and intraerythrocytic sodium. Both of these tests are highly heritable with a combination of both polygenic and major gene effects. Cotransport, leak, and pump sites also seem to be quite significantly heritable whereas the ATPase pump activity and the circulating pump inhibitor seem to be largely determined by nongenetic factors. Some of the most dramatic changes in these tests have been observed during pregnancy. Significant increases are seen in countertransport, cotransport, ouabain binding sites, and digoxin-like factor. Oral contraceptives also seem to affect at least cotransport. Plasma triglyceride level and body weight are some of the strongest correlates of countertransport, cotransport, and lithium leak. Cotransport increases with higher dietary sodium intake and decreases with the use of the diuretic medication. In the current developmental stage these tests have several significant limitations. In most population studies there is a considerable overlap of test values between persons with high and normal blood pressure. There are substantial variations in the methods used by different laboratories for the same tests. They are expensive, complex and usually must be done on fresh cells. There are conflicts between the results of several different reported studies that could be due to the way in which their subjects were selected, the effects of medications or other uncontrolled variables, or even due to the differences in laboratory methodologies.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

近年来,人们对人类细胞中阳离子的几种不同检测方法进行了研究,以检测并确定其在原发性高血压发展过程中可能发挥的作用。本报告的目的是总结在人类群体的遗传学和流行病学研究中所学到的知识。最详细回顾的七种检测方法包括钠-锂逆向转运、红细胞内钠、钠(或锂)-钾协同转运、锂泄漏、钠-钾ATP酶泵、钠泵位点(哇巴因结合)以及循环钠泵抑制剂(在某些研究中称为“地高辛样因子”)。与血压正常者相比,高血压患者的逆向转运、红细胞内钠和协同转运始终显示出不同的值,甚至与有高血压家族史的血压正常者相比,与无高血压家族史的对照者相比也是如此。仅对钠-锂逆向转运和红细胞内钠进行了全面的遗传学研究。这两种检测方法都具有高度遗传性,同时存在多基因和主基因效应。协同转运、泄漏和泵位点似乎也具有相当显著的遗传性,而ATP酶泵活性和循环泵抑制剂似乎在很大程度上由非遗传因素决定。在妊娠期间观察到了这些检测方法中一些最显著的变化。逆向转运、协同转运、哇巴因结合位点和地高辛样因子显著增加。口服避孕药似乎也至少会影响协同转运。血浆甘油三酯水平和体重是逆向转运、协同转运和锂泄漏的一些最强相关因素。协同转运随着饮食中钠摄入量的增加而增加,随着利尿剂的使用而降低。在当前的发展阶段,这些检测方法有几个显著的局限性。在大多数人群研究中,高血压患者和血压正常者的检测值有相当大的重叠。不同实验室对相同检测方法所使用的方法存在很大差异。它们价格昂贵、操作复杂,通常必须在新鲜细胞上进行。几项不同报道研究的结果之间存在冲突,这可能是由于其受试者的选择方式、药物或其他未控制变量的影响,甚至是由于实验室方法的差异。(摘要截于400字)

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