The C242T polymorphism of the p22-phox gene (CYBA) is associated with higher left ventricular mass in Brazilian hypertensive patients


Autoria(s): SCHREIBER, Roberto; FERREIRA-SAE, Maria C.; RONCHI, Juliana A.; PIO-MAGALHAES, Jose A.; CIPOLLI, Jose A.; MATOS-SOUZA, Jose R.; MILL, Jose G.; VERCESI, Anibal E.; KRIEGER, Jose E.; FRANCHINI, Kleber G.; PEREIRA, Alexandre C.; NADRUZ JUNIOR, Wilson
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

18/04/2012

18/04/2012

2011

Resumo

Background: Reactive oxygen species have been implicated in the physiopathogenesis of hypertensive end-organ damage. This study investigated the impact of the C242T polymorphism of the p22-phox gene (CYBA) on left ventricular structure in Brazilian hypertensive subjects. Methods: We cross-sectionally evaluated 561 patients from 2 independent centers [Campinas (n = 441) and Vitoria (n = 120)] by clinical history, physical examination, anthropometry, analysis of metabolic and echocardiography parameters as well as p22-phox C242T polymorphism genotyping. In addition, NADPH-oxidase activity was quantified in peripheral mononuclear cells from a subgroup of Campinas sample. Results: Genotype frequencies in both samples were consistent with the Hardy-Weinberg equilibrium. Subjects with the T allele presented higher left ventricular mass/height(2.7) than those carrying the CC genotype in Campinas (76.8 +/- 1.6 vs 70.9 +/- 1.4 g/m(2.7); p = 0.009), and in Vitoria (45.6 +/- 1.9 vs 39.9 +/- 1.4 g/m(2.7); p = 0.023) samples. These results were confirmed by stepwise regression analyses adjusted for age, gender, blood pressure, metabolic variables and use of anti-hypertensive medications. In addition, increased NADPH-oxidase activity was detected in peripheral mononuclear cells from T allele carriers compared with CC genotype carriers (p = 0.03). Conclusions: The T allele of the p22-phox C242T polymorphism is associated with higher left ventricular mass/height(2.7) and increased NADPH-oxidase activity in Brazilian hypertensive patients. These data suggest that genetic variation within NADPH-oxidase components may modulate left ventricular remodeling in subjects with systemic hypertension.

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)[Proc. 2010/16252-0]

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico - CNPq [Proc. 474966/2010-0]

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico - CNPq [474966/2010-0]

Identificador

BMC MEDICAL GENETICS, v.12, 2011

1471-2350

http://producao.usp.br/handle/BDPI/15105

10.1186/1471-2350-12-114

http://dx.doi.org/10.1186/1471-2350-12-114

Idioma(s)

eng

Publicador

BIOMED CENTRAL LTD

Relação

BMC Medical Genetics

Direitos

openAccess

Copyright BIOMED CENTRAL LTD

Palavras-Chave #p22-phox #left ventricle #hypertension #polymorphism #NADPH-oxidase #CORONARY-ARTERY-DISEASE #P22 PHOX GENE #NADPH OXIDASE #NAD(P)H OXIDASE #HYPERTROPHY #P22PHOX #POPULATION #P22(PHOX) #ATHEROSCLEROSIS #VARIANT #Genetics & Heredity
Tipo

article

original article

publishedVersion