Rebbeck T R, Turner S T, Michels V V, Moll P P
Department of Human Genetics, University of Michigan, Ann Arbor.
Am J Hum Genet. 1991 Jun;48(6):1092-104.
An elevated level of erythrocyte sodium-lithium (Na-Li) countertransport has been suggested as a predictor of predisposition to essential hypertension. In order to evaluate whether a single genetic or environmental factor with large effects explains the mixture of distributions in Na-Li countertransport in the general population, complex segregation analyses were conducted by using 1,273 individuals more than age 20 years from 276 pedigrees selected without respect to disease risk factors or health status. Either a single genetic locus or a single environmental factor with large gender-specific effects explained the mixture of distributions for Na-Li countertransport in this sample equally well. In the subsample of pedigrees supporting a single-locus etiology, the single genetic locus explained 29.0% of the variability in adjusted Na-Li countertransport in males and 16.6% of that in females. In a subsample of pedigrees supporting an environmental factor etiology, the environmental factor explained 35.2% of the adjusted Na-Li countertransport in males and 20.5% of that in females. These results suggest that there are at least two different explanations for the mixture of distributions in Na-Li countertransport in the general population. Attempts to relate genetic variation in Na-Li countertransport to risk of essential hypertension must consider that the factor with large phenotypic effects on this trait is gender specific and may not be a single major locus in all pedigrees.
红细胞钠-锂(Na-Li)逆向转运水平升高被认为是原发性高血压易感性的一个预测指标。为了评估是否存在一个具有较大影响的单一遗传或环境因素能够解释普通人群中Na-Li逆向转运分布的混合情况,我们对来自276个家系的1273名年龄超过20岁的个体进行了复杂分离分析,这些家系的选择未考虑疾病风险因素或健康状况。一个具有较大性别特异性影响的单一基因座或单一环境因素,对该样本中Na-Li逆向转运分布的混合情况解释效果相当。在支持单基因座病因的家系子样本中,单一基因座解释了男性调整后Na-Li逆向转运变异的29.0%,以及女性的16.6%。在支持环境因素病因的家系子样本中,环境因素解释了男性调整后Na-Li逆向转运的35.2%,以及女性的20.5%。这些结果表明,对于普通人群中Na-Li逆向转运分布的混合情况,至少有两种不同的解释。将Na-Li逆向转运的基因变异与原发性高血压风险相关联的研究必须考虑到,对该性状具有较大表型影响的因素具有性别特异性,而且在所有家系中可能并非单一的主要基因座。