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Angiotensin I-converting enzyme gene polymorphism and diabetic nephropathy in Filipino type 2 diabetes mellitus patients / Journal of the ASEAN Federation of Endocrine Societies
Journal of the ASEAN Federation of Endocrine Societies ; : 87-90, 2012.
Artigo em Inglês | WPRIM | ID: wpr-632981
ABSTRACT
Objective. Previous studies have demonstrated the role of genetic susceptibility in the pathogenesis of diabetic nephropathy. The study aimed to determine the frequencies of angiotensin I-converting enzyme (ACE) gene insertion/deletion (I/D) polymorphism in a pilot population of Filipino type 2 diabetic patients and normal controls. Methods. An analysis of the ACE gene polymorphism was performed in 42 diabetic patients with and without nephropathy, and 24 normal controls. The analysis was done using polymerase chain reaction, restriction enzyme digestion, and gel electrophoresis techniques to determine the polymorphism (II, DD or ID). Independent T-tests and chi-square tests were used to compare clinical characteristics, and logistic regression analysis was done to determine odds ratio for development of nephropathy. Results. The ID polymorphism of the ACE gene was more frequent (52.4%) in patients with diabetic nephropathy (n=21). In those without nephropathy (n=21), II was more common (61.9%). ID was the more frequent genotype in the normal controls (n=24) (58.3%). The odds of developing diabetic nephropathy were increased by 4.8 times in those with ID polymorphism, and 2.9 times in those with DD. Conclusion. The D allele was more common in patients with diabetic nephropathy, similar to the observation in South Indian patients. Since the study involved only a small pilot group, studies on a larger population is needed to establish the hypothesized role of the D allele in susceptibility to diabetic nephropathy in Filipinos.
Assuntos

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Mutagênese Insercional / Peptidil Dipeptidase A / Predisposição Genética para Doença / Diabetes Mellitus Tipo 2 / Nefropatias Diabéticas / Eletroforese / Alelos / Mutação INDEL / Genótipo Limite: Humanos Idioma: Inglês Revista: Journal of the ASEAN Federation of Endocrine Societies Ano de publicação: 2012 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Mutagênese Insercional / Peptidil Dipeptidase A / Predisposição Genética para Doença / Diabetes Mellitus Tipo 2 / Nefropatias Diabéticas / Eletroforese / Alelos / Mutação INDEL / Genótipo Limite: Humanos Idioma: Inglês Revista: Journal of the ASEAN Federation of Endocrine Societies Ano de publicação: 2012 Tipo de documento: Artigo