Essential hypertension has been linked to a highly polymorphic marker
at the angiotensinogen locus, and association with a polymorphism in t
his locus has been found in some populations. We tested the hypothesis
that these same polymorphic markers are linked to essential hypertens
ion in Mexican Americans. The data comprised all the affected relative
pairs in 46 extended families chosen at random from a low-income barr
io in San Antonio. Specifically, we searched for linkage by testing fo
r excessive marker alleles shared identical by descent (LED) among hyp
ertensive relative pairs. When women taking oral contraceptives or hor
mones were excluded, the affected relative pairs shared a significant
excess of alleles IBD for the highly heterozygous GT repeat polymorphi
sm (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, usin
g likelihood methods, found no significant association (P=.43) between
plasma levels of angiotensinogen and M235T genotypes. These results s
upport the linkage of essential hypertension to the angiotensinogen lo
cus but do not indicate a specific role for the M235T variant.