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The association of ACE I/D gene polymorphism with severe carotid atherosclerosis in patients undergoing carotid endarterectomy.
Kolakovic, Ana; Zivkovic, Maja; Radak, Djordje; Djuric, Tamara; Koncar, Igor; Davidovic, Lazar; Dincic, Dragan; Alavantic, Dragan; Stankovic, Aleksandra.
Afiliação
  • Kolakovic A; VINcA Institute of Nuclear Sciences, Laboratory for Radiobiology and Molecular Genetics, University of Belgrade, Belgrade, Serbia.
J Renin Angiotensin Aldosterone Syst ; 13(1): 141-7, 2012 Mar.
Article em En | MEDLINE | ID: mdl-21984781
ABSTRACT

INTRODUCTION:

The ACE I/D polymorphism was mostly investigated in association with intima-media thickness, rarely with severe atherosclerotic phenotype. MATERIALS AND

METHODS:

We investigated the association of I/D polymorphism with severe carotid atherosclerosis (CA) (stenosis > 70%) in asymptomatic and symptomatic patients undergoing carotid endarterectomy. The 504 patients subjected to endarterectomy and 492 healthy controls from a population in Serbia were investigated as a case-control study.

RESULTS:

The univariate logistic regression analysis revealed ACE DD as a significant risk factor for severe CA (odds ratio [OR] = 1.3, 95% confidence interval [CI] 1.0-1.7, p = 0.04). After adjustment for the common risk factors (age, hypertension, smoking, and HDL) ACE was no longer significant. However, we found a significant independent influence of DD genotype on plaque presence in a normotensive subgroup of patients (OR 1.8, CI 1.2-3.0, p = 0.01, corrected for multiple testing). In symptomatic patients D allele carriers were significantly more frequent compared with asymptomatic patients (OR 1.6 CI 1.0-2.6, p = 0.05).

CONCLUSIONS:

Our data suggests that ACE I/D is not an independent risk factor for severe CA. On the other hand, a significant independent genetic influence of ACE I/D appeared in normotensive and symptomatic patients with severe CA. This should be considered in further research toward resolving the complex genetic background of severe CA phenotype.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polimorfismo Genético / Doenças das Artérias Carótidas / Endarterectomia das Carótidas / Peptidil Dipeptidase A / Predisposição Genética para Doença / Mutação INDEL Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: En Revista: J Renin Angiotensin Aldosterone Syst Assunto da revista: FISIOLOGIA Ano de publicação: 2012 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polimorfismo Genético / Doenças das Artérias Carótidas / Endarterectomia das Carótidas / Peptidil Dipeptidase A / Predisposição Genética para Doença / Mutação INDEL Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: En Revista: J Renin Angiotensin Aldosterone Syst Assunto da revista: FISIOLOGIA Ano de publicação: 2012 Tipo de documento: Article