4.2 Article

Monocyte chemoattractant protein-1-2518 A/G single nucleotide polymorphism in Chinese Han patients with ocular Behcet's disease

期刊

HUMAN IMMUNOLOGY
卷 71, 期 1, 页码 79-82

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.humimm.2009.09.354

关键词

Behcet's disease; MCP-1; Gene polymorphism; Association

资金

  1. International Cooperation in Science and Technology, Guangdong Province [2006A50107001]
  2. Key Project of Natural Science Foundation [30630064]
  3. National Supporting Project of P. R. China
  4. Key Project of Health Bureau of Chongqing [2008/1/15]
  5. Key Project of Natural Science Foundation of Chongqing [CSTC, 2009BA5037]
  6. Chongqing Key Laboratory of Ophthalmology [CSTC, 2008CA5003]

向作者/读者索取更多资源

Recent studies in Caucasian uveitis patients have shown an association with the -2518 A/G polymorphism of the monocyte chemoattractant protein (MCP)-1 gene. It is unknown whether this polymorphism is also associated with Ocular Behcet's disease (BD) in Chinese populations. The aim of the current study was therefore to investigate the possible involvement of MCP-1 in the susceptibility to ocular BID in Chinese Han individuals. A case control association study was performed in 296 ocular BD patients and 319 geographically and age-matched healthy controls using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). Binary logistic regression analysis revealed a decreased frequency of the homozygous AA genotype and an increased frequency of AG genotype of the MCP-1 -2518 polymorphism in ocular BD patients compared with healthy controls, when adjusted for gender (p = 0.048, p = 0.028, respectively). However, when segregated on the basis of several clinical findings, no any association was found between this polymorphism and ocular BD. In conclusion, the present study suggests that the MCP-1 -2518 AA genotype seems to display a protective association with ocular BD, whereas the -2518 AG genotype might be a susceptible factor for ocular BD in the Chinese Han population. Crown copyright (C) 2010 Published by Elsevier Inc. on behalf of American Society for Histocompatibility and Immunogenetics. All rights reserved.

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