Angiotensinogen promoter haplotypes are associated with blood pressure in untreated hypertensives - PubMed
Angiotensinogen promoter haplotypes are associated with blood pressure in untreated hypertensives
Stefan-Martin Brand-Herrmann et al. J Hypertens. 2004 Jul.
Abstract
Background: The polymorphic angiotensinogen (AGT) gene is one of the most promising candidates for blood pressure (BP) regulation and essential hypertension.
Objectives: To investigate whether AGT haplotype analysis adds significant information compared to single polymorphism analysis with respect to different BP phenotypes in an untreated hypertensive sample.
Methods: Two hundred and twelve untreated hypertensive subjects of Caucasian origin were genotyped for the AGT polymorphisms C-532T, A-20C, C-18T, and G-6A.
Results: In single variant analyses, untreated hypertensives, carrying the AGT -532T or -6A alleles had significantly higher systolic blood pressure (SBP) and diastolic blood pressure (DBP), as well as ambulatory BP values compared to respective non-carriers. In haplotype-based analyses, combining all four AGT promoter variants, we demonstrate that AGT haplotypes containing different allele combinations at positions -532 and -6 were significantly associated with different BP values: (1) -532T and -6A with higher, (2) -532C and -6G with lower, (3) -532C and -6A with intermediate BP values. Since the result for the -532C/-20A/-18C/-6G haplotype was due to differences between non-carriers and carriers of this haplotype on both chromosomes, a recessive inheritance model for BP effects could be assumed.
Conclusions: Our results designate the C-532T and G-6A as the best candidates for functional studies on the AGT gene. Haplotype-based analyses should greatly aid in the dissection of the genetic basis of complex traits, such as BP regulation and hypertension.
Comment in
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Yagil Y, Yagil C. Yagil Y, et al. J Hypertens. 2004 Jul;22(7):1255-8. doi: 10.1097/01.hjh.0000125426.50839.4e. J Hypertens. 2004. PMID: 15201538 Review. No abstract available.
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