Dominiczak A F, Jeffs B, Connell J M
Department of Medicine and Therapeutics, University of Glasgow, Western Infirmary, Scotland, UK.
Curr Opin Cardiol. 1998 Sep;13(5):304-11. doi: 10.1097/00001573-199809000-00003.
Hypertension is a complex quantitative trait under polygenic control. The identification of genes responsible for high blood pressure is of major importance, because it provides a mechanistic classification of the common phenotype and guide therapy tailored to the underlying primary abnormality. Experimental studies have identified several quantitative trait loci for blood pressure and other cardiovascular phenotypes. Further strategies that include congenic and subcongenic lines should ultimately lead to positional cloning of the causative genes, but this final step remains elusive at present. Human studies have focused on the rare Mendelian forms of human hypertension or candidate gene studies. Moreover, two recent examples show direct translation of a candidate gene and a quantitative trait locus from the experimental setting to human investigation. These strategies, together with new molecular genetic tools, will ultimately result in the identification of major genes contributing to human essential hypertension.
高血压是一种受多基因控制的复杂数量性状。识别导致高血压的基因至关重要,因为它能对常见表型进行机制分类,并指导针对潜在原发性异常的治疗。实验研究已确定了几个与血压及其他心血管表型相关的数量性状位点。包括同源近交系和亚同源近交系在内的进一步策略最终应能实现致病基因的定位克隆,但目前这最后一步仍难以达成。人类研究主要集中在罕见的孟德尔式人类高血压形式或候选基因研究上。此外,最近的两个例子展示了从实验环境到人类研究中候选基因和数量性状位点的直接转化。这些策略,连同新的分子遗传学工具,最终将导致鉴定出导致人类原发性高血压的主要基因。