(Hypertension. 1997;30:326.)
© 1997 American Heart Association, Inc.
Articles |
From the Division of Epidemiology, School of Public Health, University of Minnesota, Minneapolis (L.D.A.), and the Departments of Genetics (C.M.K., P.B.S., J.E.H., J.W.M.) and Physiology and Medicine (R.E.S.), Southwest Foundation for Biomedical Research, San Antonio, Tex.
Abstract Essential hypertension has been linked to a highly polymorphic marker at the angiotensinogen locus, and association with a polymorphism in this locus has been found in some populations. We tested the hypothesis that these same polymorphic markers are linked to essential hypertension in Mexican Americans. The data comprised all the affected relative pairs in 46 extended families chosen at random from a low-income barrio in San Antonio. Specifically, we searched for linkage by testing for excessive marker alleles shared identical by descent (IBD) among hypertensive relative pairs. When women taking oral contraceptives or hormones were excluded, the affected relative pairs shared a significant excess of alleles IBD for the highly heterozygous GT repeat polymorphism (P=.038) and were marginally significant for the M235T variant (P=.079), which has a much lower heterozygosity (0.43 versus 0.85 for the GT repeat). We also assayed plasma levels of angiotensinogen and, using likelihood methods, found no significant association (P=.43) between plasma levels of angiotensinogen and M235T genotypes. These results support the linkage of essential hypertension to the angiotensinogen locus but do not indicate a specific role for the M235T variant.
Key Words: relative pair association genetics polymorphisms
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