Lack of association between CLEC5A gene single-nucleotide polymorphisms and Kawasaki disease in Taiwanese children

Ya-Ling Yang, Wei Pin Chang, Yu-Wen Hsu, Wei-Chiao Chen, Hong-Ren Yu, Chi-Di Liang, Yao-Ting Tsai, Ying-Hsien Huang, Kuender D. Yang, Ho-Chang Kuo, Wei-Chiao Chang

研究成果: 雜誌貢獻文章

3 引文 斯高帕斯(Scopus)

摘要

Background. Kawasaki disease is characterized by systemic vasculitis of unknown etiology. Previous genetic studies have identified certain candidate genes associated with susceptibility to KD and coronary artery lesions. Host innate immune response factors are involved in modulating the disease outcome. The aim of this study was to investigate CLEC5A (C-type lectin domain family 5) genetic polymorphisms with regards to the susceptibility and outcome of KD. Methods. A total of 1045 subjects (381 KD patients and 664 controls) were enrolled to identify 4 tagging single-nucleotide polymorphisms (tSNPs) of CLEC5A (rs1285968, rs11770855, rs1285935, rs1285933) by using the TaqMan Allelic Discrimination Assay. The Hardy-Weinberg equilibrium was assessed in cases and controls, and genetic effects were evaluated by the chi-square test. Results. No significant associations were noted between the genotypes and allele frequency of the 4 CLEC5A tSNPs between controls and patients. In the patients, polymorphisms of CLEC5A showed no significant association with coronary artery lesion formation and intravenous immunoglobulin treatment response. Conclusions. This study showed for the first time that polymorphisms of CLEC5A are not associated with susceptibility to KD, coronary artery lesion formation, and intravenous immunoglobulin treatment response in a Taiwanese population.
原文英語
文章編號398628
期刊Journal of Biomedicine and Biotechnology
2012
DOIs
出版狀態已發佈 - 2012
對外發佈Yes

ASJC Scopus subject areas

  • Biotechnology
  • Molecular Medicine
  • Genetics
  • Molecular Biology
  • Health, Toxicology and Mutagenesis
  • Medicine(all)

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