Why the study?
Are candidate genes (angiotensinogen, renin, beta/gamma-ENaC, alpha-adducin, KLK) linked to essential hypertension in Chinese sibling pairs?
Are candidate genes (angiotensinogen, renin, beta/gamma-ENaC, alpha-adducin, KLK) linked to essential hypertension in Chinese sibling pairs?
Candidate genes previously implicated in hypertension (angiotensinogen, renin, ENaC, adducin, KLK) showed no significant linkage to essential hypertension in a Chinese cohort, highlighting potential ethnic differences in complex disease genetics.
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Does not support incorporating these genes into hypertension risk assessment for Chinese patients; leaves open ethnic differences in genetic contributions.
Previous studies of hypertension in humans and experimental animal models have identified a number of candidate genes that have since been implicated as possibly contributing to essential hypertension. Among them are the genes encoding angiotensinogen, renin, the beta- and gamma-subunits of the epithelial sodium channel (beta/gamma-ENaC), alpha-adducin, and kallikrein (KLK). To examine the role of possible contribution of these genes in ethnic Chinese, as well as the epistatic interaction among them, we studied a large cohort of hypertensive sib pairs from China. DNA samples from 310 concordant affected sibling pairs with hypertension were tested for linkage with the use of excess allele-sharing algorithms based on genotyping with highly informative GT-repeat microsatellite markers localized in the immediate vicinity of the genes encoding angiotensinogen, renin, beta- and gamma-ENaC, alpha-adducin, and KLK. Affected sib pair analysis conducted according to 3 different methods (Statistical Analysis for Genetic Epidemiology [S.A.G.E. ]/SIBPAL, MAPMAKER/SIBS, and affected pedigree member [APM] methods) revealed no evidence for linkage of any of these genes to primary hypertension in the population studied. Moreover, 2-locus sib pair linkage analyses to test for gene-gene interactions among each possible pair of candidate genes failed to yield any statistically significant results. Our findings provide no support for a significant contribution of the angiotensinogen, renin, beta/gamma-ENaC, alpha-adducin, or KLK genes, alone or in concert, to the pathogenesis of essential hypertension among Chinese. Our results emphasize the possible role of ethnic differences for complex disease genetics, as well as the need for large, well-characterized investigations.
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Niu et al. (1999) studied this question.
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