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The relationship between haplotypes of angiotensinogen gene and essential hypertension / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 488-490, 2002.
Artículo en Chino | WPRIM | ID: wpr-248522
ABSTRACT
<p><b>OBJECTIVE</b>To investigate the relationship between the polymorphism of angiotensinogen gene (AGT) and the risk for hypertension in a Chinese population.</p><p><b>METHODS</b>Three polymorphisms of AGT gene were analyzed in 335 patients with documented essential hypertension and 196 control subjects by using PCR-restriction fragment length polymorphism. Expectation maximization(EM) algorithm was then used for pairwise linkage disequilibrium test and haplotype analysis of AGT polymorphisms.</p><p><b>RESULTS</b>Linkage disequilibrium between M235T and A-20C, between M235T and A-6G, between A-20C and A-6G was observed (P<10(-4)). The case-control analysis revealed that the frequency of T235 is significantly higher in essential hypertension patients than in control subjects. But all haplotype frequencies showed no significant difference between the patient and control groups.</p><p><b>CONCLUSION</b>No association was noted between the haplotypes of AGT gene and hypertension in tested people, but T235 allele might play an important role in increased risk for essential hypertension.</p>
Asunto(s)
Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Polimorfismo Genético / Haplotipos / Polimorfismo de Longitud del Fragmento de Restricción / ADN / Desequilibrio de Ligamiento / Angiotensinógeno / Alelos / Frecuencia de los Genes / Genética / Genotipo Límite: Humanos Idioma: Chino Revista: Chinese Journal of Medical Genetics Año: 2002 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Polimorfismo Genético / Haplotipos / Polimorfismo de Longitud del Fragmento de Restricción / ADN / Desequilibrio de Ligamiento / Angiotensinógeno / Alelos / Frecuencia de los Genes / Genética / Genotipo Límite: Humanos Idioma: Chino Revista: Chinese Journal of Medical Genetics Año: 2002 Tipo del documento: Artículo