SERPINE2 Polymorphisms and Chronic Obstructive Pulmonary Disease
Journal of Korean Medical Science
;
: 1119-1125, 2009.
Artículo
en Inglés
| WPRIM
| ID: wpr-203380
ABSTRACT
A number of genome-wide linkage analyses have identified the 2q33.3-2q37.2 region as most likely to contain the genes that contribute to the susceptibility to chronic obstructive pulmonary disease (COPD). It was hypothesized that the SERPINE2 gene, which is one of the genes located at the 2q33.3-2q37.2 region, may act as a low-penetrance susceptibility gene for COPD. To test this hypothesis, the association of four SERPINE2 single nucleotide polymorphisms (SNPs; rs16865421A>G, rs7583463A>C, rs729631C>G, and rs6734100C>G) with the risk of COPD was investigated in a case-control study of 311 COPD patients and 386 controls. The SNP rs16865421 was associated with a significantly decreased risk of COPD in a dominant model for the polymorphic allele (adjusted odds ratio [OR]=0.66, 95% confidence interval [CI]=0.45-0.97, P=0.03). In haplotype analysis, the GACC haplotype carrying the polymorphic allele at the rs16865421 was associated with a significantly decreased risk of COPD when compared to the AACC haplotype (adjusted OR=0.58, 95% CI=0.38-0.89, P=0.01), and this effect was evident in younger individuals (adjusted OR=0.30, 95% CI=0.14-0.64, P=0.002). This study suggests that the SERPINE2 gene contributes to the susceptibility to COPD.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Haplotipos
/
Encuestas y Cuestionarios
/
Precursor de Proteína beta-Amiloide
/
Receptores de Superficie Celular
/
Predisposición Genética a la Enfermedad
/
Polimorfismo de Nucleótido Simple
/
Enfermedad Pulmonar Obstructiva Crónica
/
Estudio de Asociación del Genoma Completo
/
Genotipo
/
Ligamiento Genético
Tipo de estudio:
Estudio observacional
Límite:
Humanos
/
Masculino
Idioma:
Inglés
Revista:
Journal of Korean Medical Science
Año:
2009
Tipo del documento:
Artículo
Similares
MEDLINE
...
LILACS
LIS