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Association of eNOS polymorphisms with susceptibility to osteonecrosis of the femur head A meta-analysis

Authors
Song, G. G.Lee, Y. H.
Issue Date
4월-2017
Publisher
SPRINGER HEIDELBERG
Keywords
Osteonecrosis; Endothelial nitric oxide synthase; Polymorphism; Meta-analysis; Confidence Interval
Citation
ZEITSCHRIFT FUR RHEUMATOLOGIE, v.76, no.3, pp.267 - 273
Indexed
SCIE
SCOPUS
Journal Title
ZEITSCHRIFT FUR RHEUMATOLOGIE
Volume
76
Number
3
Start Page
267
End Page
273
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/84029
DOI
10.1007/s00393-016-0093-3
ISSN
0340-1855
Abstract
The aim of the present study was to determine whether polymorphisms of the endothelial nitric oxide synthase (eNOS) gene are associated with susceptibility to osteonecrosis of the femoral head (ONFH). We conducted a meta-analysis to assess the association between the 4b/a, G894T, and T786C polymorphisms of eNOS and the susceptibility to ONFH. A total of five studies, which included 566 cases and 833 controls, were included in the meta-analysis. Meta-analysis revealed a significant association between allele a of the 4b/a polymorphism and ONFH in all study subjects (odds ratio, OR 3.237; 95 % confidence interval, CI 2.036-5.148; P = 6.9 x 10(-7)); stratification by ethnicity indicated an association between this allele and ONFH in Caucasians and Asians (OR 2.985; 95 % CI 1.592-5.597; P = 0.001 and OR 3.567; 95 % CI 1.793-7.095; P = 2.9 x 10(-4), respectively). Meta-analysis stratified by ONFH type showed a significant association between allele a of the 4b/a polymorphism and idiopathic and secondary ONFH (OR 3.411; 95 % CI 2.049-5.679; P = 2.4 x 10(-6) and OR 3.163; 95 % CI 1.781-5.619, P = 8.6 x 10 (-5), respectively). However, the meta-analysis did not show any allelic association between the G894T and T786C polymorphisms and ONFH (OR 1.718; 95 % CI 0.796-3.707; P = 0.168 and OR 1.027; 95 % CI 0.191-5.517; P = 0.976, respectively). Our meta-analysis of published studies shows that the 4b/a polymorphism is associated with the development of idiopathic and secondary ONFH in Caucasians and Asians.
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