Leckie B J
MRC Blood Pressure Unit, Western Infirmary, Glasgow, Scotland, UK.
Bioessays. 1992 Jan;14(1):37-41. doi: 10.1002/bies.950140108.
High blood pressure is a disease of unknown cause. Family history of the disease indicates higher risk, but it is not known which genes are involved or how they interact with environmental influences to produce the disorder. Molecular biology offers an approach to problems that have not so far been solved by classical physiology or biochemistry. By analysing polymorphic variation in chromosome markers such as minisatellite sequences, or by restriction fragment polymorphism analysis of candidate genes, attempts are being made to link genetic variations with hypertension. In genetically hypertensive rats, hypertension is associated with a polymorphism of the renin gene and with other loci on chromosomes 10 and 18. The role of these loci in human hypertension remains to be determined. Other genes such as sodium-lithium countertransport may be involved. Environmental factors such as stress or salt intake could influence the rate or timing of expression of certain genes and thus result in hypertension.
高血压是一种病因不明的疾病。该病的家族病史表明患病风险更高,但尚不清楚哪些基因与之相关,也不清楚它们如何与环境影响相互作用导致这种疾病。分子生物学为迄今尚未被经典生理学或生物化学解决的问题提供了一种方法。通过分析染色体标记(如小卫星序列)中的多态性变异,或通过对候选基因进行限制性片段多态性分析,人们正试图将基因变异与高血压联系起来。在遗传性高血压大鼠中,高血压与肾素基因的多态性以及染色体10和18上的其他位点有关。这些位点在人类高血压中的作用仍有待确定。其他基因如钠-锂逆向转运体可能也参与其中。压力或盐摄入等环境因素可能会影响某些基因的表达速率或时间,从而导致高血压。