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Associations between CYP11B2 gene -344T/C polymorphism and essential hypertension in the Han nationality in Shandong province / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 502-504, 2004.
Artículo en Inglés | WPRIM | ID: wpr-328832
ABSTRACT
<p><b>OBJECTIVE</b>To investigate whether the -344T/C polymorphism of CYP11B2 gene is associated with essential hypertension in the Hans in Shandong province.</p><p><b>METHODS</b>Plasma renin activity (PRA) and plasma aldosterone concentration (PAC) were measured with radioimmunoassays; the hypertensives were classified as low-renin and normal- or high-renin group by PAC/PRA ratio. -344T/C polymorphism was determined by polymerase chain reaction-restricted fragment length polymorphism (PCR-RFLP) in controls and hypertensives.</p><p><b>RESULTS</b>No significant differences were found in genotype distribution or allele frequency between groups of control and primary hypertension or between groups of control and normal- or high-renin hypertension. The C allele frequency in low-renin hypertension group was significantly higher than that in normotensives and normal- or high-renin hypertension group (P < 0.05).</p><p><b>CONCLUSION</b>These results suggest that -344T/C polymorphism of CYP11B2 gene may be associated with low-renin essential hypertension in the Han nationality in Shandong province.</p>
Asunto(s)
Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: China / Citocromo P-450 CYP11B2 / Polimorfismo de Nucleótido Simple / Pueblo Asiatico / Etnología / Genética / Hipertensión Límite: Femenino / Humanos / Masculino País/Región como asunto: Asia Idioma: Inglés Revista: Chinese Journal of Medical Genetics Año: 2004 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: China / Citocromo P-450 CYP11B2 / Polimorfismo de Nucleótido Simple / Pueblo Asiatico / Etnología / Genética / Hipertensión Límite: Femenino / Humanos / Masculino País/Región como asunto: Asia Idioma: Inglés Revista: Chinese Journal of Medical Genetics Año: 2004 Tipo del documento: Artículo