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The lack of association between interleukin-6 gene −174 G/C polymorphism and the risk of type 1 diabetes mellitus: A meta-analysis of 18,152 subjects

Authors :
Yin, Yan-Wei
Sun, Qian-Qian
Zhang, Bei-Bei
Hu, Ai-Min
Wang, Qi
Liu, Hong-Li
Hou, Zhi-Zhen
Zeng, Yi-Hua
Xu, Rui-Jia
Shi, Long-Bao
Source :
Gene. Feb2013, Vol. 515 Issue 2, p461-465. 5p.
Publication Year :
2013

Abstract

Abstract: Epidemiological studies have evaluated the association between interleukin-6 (IL-6) gene −174 G/C polymorphism and type 1 diabetes mellitus (T1DM) risk, but results of different studies have been inconsistent. The present meta-analysis was therefore designed to clarify these controversies. PubMed, Embase and Web of Science were searched from the first available year to March 25, 2012, as well as hand searching of the references of identified articles were performed. All studies investigating the association between IL-6 gene −174 G/C polymorphism and T1DM risk were included. Data analyses were carried out by Review Manager 5.1.2 and Stata 11.0. Seven studies were included in the final meta-analysis, covering a total of 9697 T1DM cases and 8455 controls. The results showed no evidence for significant association between IL-6 gene −174 G/C polymorphism and T1DM risk (for C/C+C/G vs. G/G: OR=1.30, 95% CI=0.84–2.00, p=0.24; for C/C vs. C/G+G/G: OR=1.10, 95% CI=0.75–1.60, p=0.63; for C/C vs. G/G: OR=1.34, 95% CI=0.75–2.42, p=0.33; for C allele vs. G allele: OR=1.16, 95% CI=0.88–1.53, p=0.30). In addition, the similar results were obtained in the subgroup analysis based on ethnicity. In summary, the present meta-analysis suggests that IL-6 gene −174 G/C polymorphism is not associated with T1DM risk. However, due to the small sample size in most of the included studies and the selection bias existed in some studies, the results should be interpreted with caution. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
03781119
Volume :
515
Issue :
2
Database :
Academic Search Index
Journal :
Gene
Publication Type :
Academic Journal
Accession number :
85008556
Full Text :
https://doi.org/10.1016/j.gene.2012.11.062