Endothelial nitric oxide synthase gene haplotypes associated with circulating concentrations of nitric oxide products in healthy men

dc.creatorMetzger, IF
dc.creatorSouza-Costa, DC
dc.creatorMarroni, AS
dc.creatorNagassaki, S
dc.creatorDesta, Z
dc.creatorFlockhart, DA
dc.creatorTanus-Santos, JE
dc.date2005
dc.dateAUG
dc.date2014-07-30T17:19:34Z
dc.date2015-11-26T17:47:07Z
dc.date2014-07-30T17:19:34Z
dc.date2015-11-26T17:47:07Z
dc.date.accessioned2018-03-29T00:29:43Z
dc.date.available2018-03-29T00:29:43Z
dc.identifierPharmacogenetics And Genomics. Lippincott Williams & Wilkins, v. 15, n. 8, n. 565, n. 570, 2005.
dc.identifier1744-6872
dc.identifierWOS:000231169400005
dc.identifier10.1097/01.fpc.0000167328.85163.44
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/64769
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/64769
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1288685
dc.descriptionObjectives 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.
dc.description15
dc.description8
dc.description565
dc.description570
dc.languageen
dc.publisherLippincott Williams & Wilkins
dc.publisherPhiladelphia
dc.publisherEUA
dc.relationPharmacogenetics And Genomics
dc.relationPharmacogenet. Genomics
dc.rightsfechado
dc.sourceWeb of Science
dc.subjectendothelial nitric oxide synthase
dc.subjectgenotypes
dc.subjecthaplotypes
dc.subjectnitric oxide
dc.subjectpolymorphisms
dc.subjectBiological-activity
dc.subjectRelaxing Factor
dc.subjectL-arginine
dc.subjectPlasma
dc.subjectPolymorphisms
dc.subjectDisease
dc.subjectNitrate
dc.subjectGenotype
dc.subjectMutation
dc.subjectRelease
dc.titleEndothelial nitric oxide synthase gene haplotypes associated with circulating concentrations of nitric oxide products in healthy men
dc.typeArtículos de revistas


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