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Relationship between fibrinogen Bß-148C/T polymorphism and coronary artery lesions in children with Kawasaki disease / 中国当代儿科杂志
Chinese Journal of Contemporary Pediatrics ; (12): 518-520, 2010.
Article in Chinese | WPRIM | ID: wpr-347555
ABSTRACT
<p><b>OBJECTIVE</b>To study the possible relationship between coronary artery lesions and fibrinogen Bbeta-148 C/T polymorphism in children with Kawasaki disease.</p><p><b>METHODS</b>Fast blood samples were taken from 36 children with Kawasaki disease (21 had coronary artery lesions) and 49 age- and gender-matched healthy children (control group). Plasma levels and molecular reactivity of fibrinogen were measured with Assist Plasma Fibrinogen Activity Assay System. Polymerize chain reaction and restriction enzyme digestion were used to detect the genotypes of fibrinogen Bbeta-148C/T gene polymorphism.</p><p><b>RESULTS</b>The plasma fibrinogen levels in patients with coronary artery lesions were significantly higher than those in patients without coronary artery lesions and in the control group. T allele frequency in patients with Kawasaki disease was significantly higher than that in the control group. The patients with coronary artery lesions had more increased T allele frequency compared with the patients without coronary artery lesions.</p><p><b>CONCLUSIONS</b>Plasma fibrinogen levels and fibrinogen Bbeta-148C/T polymorphism are associated with coronary artery lesions in children with Kawasaki disease.</p>
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Polymorphism, Genetic / Coronary Artery Disease / Fibrinogen / Genetic Predisposition to Disease / Gene Frequency / Genetics / Genotype / Mucocutaneous Lymph Node Syndrome Limits: Child, preschool / Female / Humans / Infant / Male Language: Chinese Journal: Chinese Journal of Contemporary Pediatrics Year: 2010 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Polymorphism, Genetic / Coronary Artery Disease / Fibrinogen / Genetic Predisposition to Disease / Gene Frequency / Genetics / Genotype / Mucocutaneous Lymph Node Syndrome Limits: Child, preschool / Female / Humans / Infant / Male Language: Chinese Journal: Chinese Journal of Contemporary Pediatrics Year: 2010 Type: Article