Literature DB >> 7946168

Analysis of two variants of the angiotensinogen gene in essential hypertensive African-Americans.

D R Rutledge1, C S Browe, P S Kubilis, E A Ross.   

Abstract

Two mutations (T174M and M235T) in the angiotensinogen gene have been reported to be associated with hypertension. This study examines the frequency of these mutations among African-American hypertensive patients (n = 109). The allele frequency of the T174M mutation was 4.6% and the frequency of the M235T mutation was 86.7%. The genotypic frequencies agreed with the conditioned Hardy-Weinberg predictions based on allele frequencies. The homozygote wild-type genotype at the T174 site was more frequent than the mutation and occurred at a rate of 91.7%. Conversely, the homozygote for the mutation at the M235 site was more frequent and occurred at a rate of 75.2%. Mutation frequencies for T174M and M235T in this African-American population differ from those previously reported from a white hypertensive population (P = .0058 and P = .0001, respectively). In summary, the representation of the angiotensinogen allele frequencies differ among hypertensive populations.

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Year:  1994        PMID: 7946168     DOI: 10.1093/ajh/7.7.651

Source DB:  PubMed          Journal:  Am J Hypertens        ISSN: 0895-7061            Impact factor:   2.689


  2 in total

Review 1.  Angiotensinogen variants and human hypertension.

Authors:  X Jeunemaitre; A P Gimenez-Roqueplo; J Célérier; P Corvol
Journal:  Curr Hypertens Rep       Date:  1999 Feb-Mar       Impact factor: 5.369

2.  Coronary heart disease, hypertension, and angiotensinogen gene variants in Indian population.

Authors:  K G Nair; K K Shalia; T F Ashavaid; J J Dalal
Journal:  J Clin Lab Anal       Date:  2003       Impact factor: 2.352

  2 in total

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