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TARC/CCL17 gene polymorphisms and expression associated with susceptibility and coronary artery aneurysm formation in Kawasaki disease.
Lee, Chiu-Ping; Huang, Ying-Hsien; Hsu, Yu-Wen; Yang, Kuender D; Chien, Hsu-Chen; Yu, Hong-Ren; Yang, Ya-Ling; Wang, Chih-Lu; Chang, Wei-Chiao; Kuo, Ho-Chang.
Afiliação
  • Lee CP; Department of Pediatrics, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, Taiwan.
Pediatr Res ; 74(5): 545-51, 2013 Nov.
Article em En | MEDLINE | ID: mdl-23942559
ABSTRACT

BACKGROUND:

Kawasaki disease (KD) is a systemic vasculitis of unknown etiology. Thymus and activation-regulated chemokine/chemokine ligand 17 (TARC/CCL17) is one of the Th2 chemokines and has been suggested as a candidate gene for conferring susceptibility to Th2 associated with allergy diseases. This study examined the correlation between gene polymorphisms and plasma levels of TARC/CCL17 in patients with KD and the outcomes of KD.

METHODS:

A total of 381 KD patients and 564 controls were subjected to determination of five tagging single-nucleotide polymorphisms of TARC/CCL17. In addition, plasma TARC/CCL17 levels were measured by enzyme-linked immunosorbent assay.

RESULTS:

Polymorphisms of TARC/CCL17 were significantly different between normal children and patients with KD. A allele of rs4784805 has better intravenous immunoglobulin (IVIG) treatment response to KD. Furthermore, plasma TARC/CCL17 levels were higher in KD patients than that in controls before IVIG treatment. After IVIG treatment, plasma TARC/CCL17 levels decreased significantly.

CONCLUSION:

This study provides the first evidence supporting the association between TARC/CCL17 polymorphisms, susceptibility of KD, and IVIG responses in KD patients.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Aneurisma Coronário / Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Quimiocina CCL17 / Síndrome de Linfonodos Mucocutâneos Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Limite: Humans País/Região como assunto: Asia Idioma: En Revista: Pediatr Res Ano de publicação: 2013 Tipo de documento: Article País de afiliação: Taiwan

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Aneurisma Coronário / Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Quimiocina CCL17 / Síndrome de Linfonodos Mucocutâneos Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Limite: Humans País/Região como assunto: Asia Idioma: En Revista: Pediatr Res Ano de publicação: 2013 Tipo de documento: Article País de afiliação: Taiwan