Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/64769
Type: Artigo de periódico
Title: Endothelial nitric oxide synthase gene haplotypes associated with circulating concentrations of nitric oxide products in healthy men
Author: Metzger, IF
Souza-Costa, DC
Marroni, AS
Nagassaki, S
Desta, Z
Flockhart, DA
Tanus-Santos, JE
Abstract: Objectives Controversy exists regarding the effects of polymorphisms in the endothelial nitric oxide synthase (eNOS) gene on nitrites/nitrates (NOx) plasma concentrations. In this study we compared the distribution of haplotypes involving three relevant eNOS polymorphisms (T-786C in the promoter region; b/a in intron 4, and Glu298Asp in exon 7) in healthy subjects with low and high circulating NOx levels. Methods We studied 154 healthy subjects (fasting, white males, who were non-smokers, 18-60 years of age, and not taking any medication). Genomic DNA was isolated from blood samples and genotypes were determined by PCR and restriction fragment length digestion. Circulating NOx was determined by chemiluminescence. Results Haplotype frequencies were compared in two groups of subjects: those with the 30 lowest NOx levels (group L) and those with the 30 highest NOx levels (group H). NOx levels in group L and H were 24.2 +/- 4.5 mu m and 80.9 +/- 8.9 mu m, respectively. Genotype frequencies for the three polymorphisms were not different when the two groups were compared (all P > 0.05, chi-squared test). However, the haplotype including the alleles C (promoter), 4b (intron 4), and Glu (exon 7) was significantly more common in group L (16%) than in group H (4%) (P=0.0047). The frequencies of the remaining haplotypes were not different among group L and H. Conclusions While eNOS genotypes are not significantly associated with changes in the circulating NOx concentrations, the specific eNOS haplotype that includes the 'C,'4b, and 'Glu' alleles is associated with lower circulating NOx concentrations.
Subject: endothelial nitric oxide synthase
genotypes
haplotypes
nitric oxide
polymorphisms
Country: EUA
Editor: Lippincott Williams & Wilkins
Rights: fechado
Identifier DOI: 10.1097/01.fpc.0000167328.85163.44
Date Issue: 2005
Appears in Collections:Unicamp - Artigos e Outros Documentos

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