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A study on K469E polymorphism of ICAM1 gene and ICAM1 plasma level in patients with coronary heart disease / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 195-197, 2006.
Artículo en Chino | WPRIM | ID: wpr-263819
ABSTRACT
<p><b>OBJECTIVE</b>To study the linkage between K469E polymorphism of intercellular adhesion molecule 1(ICAM1) gene with ICAM1 plasma level and coronary heart disease (CHD) in Han population of China.</p><p><b>METHODS</b>One hundred and sixty-four controls without CHD and 160 patients with CHD were enrolled in our study. By nested PCR with allele-specific oligonucleotide primers, all patients and controls were genotyped for the ICAM1 polymorphism. And the ICAM1 plasma level was measured by ELISA.</p><p><b>RESULTS</b>In the patients with CHD, both K allele frequency and the plasma level of ICAM1 were higher than those in control (P<0.05). The individual with K allele had higher plasma level of ICAM1 than that without K allele (344.34+/-128.59 microg/L vs 303.54+/-108.74 microg/L, P=0.008). K allele enhanced the risk of CHD (P<0.01, OR=2.158, 95%CI 1.250-3.727). There was the K allele cooperation with smoking in influencing the risk of CHD.</p><p><b>CONCLUSION</b>There is the polymorphism of ICAM1 K469E gene in Han population of China, and the K allele may be a genetic factor influencing the risk of CHD.</p>
Asunto(s)
Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Polimorfismo Genético / Potasio / Sangre / China / Molécula 1 de Adhesión Intercelular / Enfermedad Coronaria / Etnología / Frecuencia de los Genes / Genética Límite: Humanos País/Región como asunto: Asia Idioma: Chino Revista: Chinese Journal of Medical Genetics Año: 2006 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Polimorfismo Genético / Potasio / Sangre / China / Molécula 1 de Adhesión Intercelular / Enfermedad Coronaria / Etnología / Frecuencia de los Genes / Genética Límite: Humanos País/Región como asunto: Asia Idioma: Chino Revista: Chinese Journal of Medical Genetics Año: 2006 Tipo del documento: Artículo