P-selectin gene -2123 polymorphism in children with Henoch-Sch-nlein purpura / 中国当代儿科杂志
Chinese Journal of Contemporary Pediatrics
; (12): 278-281, 2011.
Article
de Zh
| WPRIM
| ID: wpr-308812
Bibliothèque responsable:
WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To investigate whether P-selectin gene -2123 polymorphism is associated with the pathogenesis of Henoch-Sch-nlein purpura (HSP) in children.</p><p><b>METHODS</b>Polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP) is used to identify the distribution of allele and genotype frequencies of P-selectin gene promoter -2123 polymorphism in 86 children with HSP (including 40 cases of purpura nephritis) and 70 healthy controls.</p><p><b>RESULTS</b>Compared with the healthy controls, the frequencies of GG genotype and G allele of P-selectin promoter -2123 in children with HSP increased significantly (P<0.05). There were no significant differences in P-selectin promoter -2123 genotype and allele frequencies between the patients with and without nephritis.</p><p><b>CONCLUSIONS</b>P-selectin gene promoter -2123 polymorphism appears to be associated with the pathogenesis of HSP in children.</p>
Texte intégral:
1
Base de données:
WPRIM
Sujet principal:
Polymorphisme génétique
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12131
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Polymorphisme de restriction
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Sélectine P
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Génétique
Limites:
Adolescent
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Child
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Child, preschool
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Female
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Humans
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Male
Langue:
Zh
Journal:
Chinese Journal of Contemporary Pediatrics
Année:
2011
Type de document:
Article