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Association of VKORC1 gene -1639G/A polymorphism with atrial fibrillation in ethnic Uygurs and Hans from Xinjiang / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 264-268, 2015.
Article in Chinese | WPRIM | ID: wpr-239490
ABSTRACT
<p><b>OBJECTIVE</b>To assess the association of VKORC1 gene -1639G/A polymorphism with atrial fibrillation (AF) in ethnic Uygurs and Hans from Xinjiang.</p><p><b>METHODS</b>The above polymorphism was detected among 100 Uygur and 102 Han AF patients and 103 Uygur and 111 Han subjects that have no AF with polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method.</p><p><b>RESULTS</b>A statistically significant difference was detected between the patient and control groups of Uygur origin in terms of genotypic and allelic frequencies (P<0.05). Logistic regression analysis also indicated the -1639G/A polymorphism as an independent risk factor for AF in Uygur population (OR=2.085, 95% CI 1.067-4.072, P=0.031). No similar statistical difference was found between the patient and control groups of Han origin (P>0.05).</p><p><b>CONCLUSION</b>The -1639G/A polymorphism of VKORC1 gene is associated with AF in the Uygur population but not in Hans.</p>
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Atrial Fibrillation / Molecular Sequence Data / Base Sequence / China / Polymorphism, Single Nucleotide / Asian People / Ethnology / Vitamin K Epoxide Reductases / Genetics Type of study: Risk factors Limits: Adult / Aged / Female / Humans / Male Country/Region as subject: Asia Language: Chinese Journal: Chinese Journal of Medical Genetics Year: 2015 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Atrial Fibrillation / Molecular Sequence Data / Base Sequence / China / Polymorphism, Single Nucleotide / Asian People / Ethnology / Vitamin K Epoxide Reductases / Genetics Type of study: Risk factors Limits: Adult / Aged / Female / Humans / Male Country/Region as subject: Asia Language: Chinese Journal: Chinese Journal of Medical Genetics Year: 2015 Type: Article