Sobhan Mohammad R, Mahdinezhad-Yazdi Masoud, Moghimi Mansour, Aghili Kazem, Jafari Mohammadali, Zare-Shehneh Masoud, Neamatzadeh Hossein
Research performed at the Department of Orthopedics, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
Department of Orthopedics, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
Arch Bone Jt Surg. 2018 Nov;6(6):468-477.
The Plasminogen Activator Inhibitor-1 gene 4G/5G (PAI-1 4G/5G) polymorphism has been suggested to be associated with osteonecrosis of the femoral head (ONFH) susceptibility; however, the results are conflicting and inconclusive. We have carried out a comprehensive meta-analysis to derive a more precise estimation of the association.
A comprehensive search in PubMed, EMBASE, Google Scholar, and ISI Web of Knowledge databases was conducted to identify all eligible case-control publications investigating the association between PAI-1 4G/5G polymorphism and ONFH risk. Odds ratios (OR) and corresponding 95% confidence intervals (CI) were used to assess the association.
A total of six studies with 456 cases and 1,019 controls were included in this review. Three studies were from Caucasian descendants and the three others were from East Asian descendants. Overall analysis suggests a significant association between PAI-1 4G/5G polymorphism and ONFH risk under the allele model (4G vs. 5G: OR =1.540, 95% CI =1.055-2.248, ) and the recessive model (4G4G vs. 4G5G+5G5G: OR=1.931, 95% CI: 1.162-3.207, ). When stratified by ethnicity, we have found a significant association between PAI-1 4G/5G polymorphism and ONFH risk among the Caucasian (4G5G vs. 5G5G: OR=1.806, 95% CI: 1.064-3.067, ) and East Asians (4G4G vs. 5G5G: OR=1.619, 95% CI: 1.025-2.556, and 4G4G vs. 4G5G+5G5G: OR=1.665, 95% CI: 1.207-2.297, ).
The present meta-analysis suggested that PAI-1 4G/5G (rs1799889) polymorphism is a potential risk factor for development of ONFH. However, large-scale and well-designed case-control studies in different ethnicities are required to validate these results.
纤溶酶原激活物抑制剂-1基因4G/5G(PAI-1 4G/5G)多态性被认为与股骨头坏死(ONFH)易感性相关;然而,结果相互矛盾且尚无定论。我们进行了一项全面的荟萃分析,以得出更精确的关联估计。
在PubMed、EMBASE、谷歌学术和ISI知识网络数据库中进行全面检索,以识别所有调查PAI-1 4G/5G多态性与ONFH风险之间关联的合格病例对照研究出版物。采用优势比(OR)和相应的95%置信区间(CI)来评估这种关联。
本综述共纳入6项研究,包括456例病例和1019例对照。3项研究来自白种人后裔,另外3项来自东亚后裔。总体分析表明,在等位基因模型(4G与5G:OR = 1.540,95% CI = 1.055 - 2.248)和隐性模型(4G4G与4G5G + 5G5G:OR = 1.931,95% CI:1.162 - 3.207)下,PAI-1 4G/5G多态性与ONFH风险之间存在显著关联。按种族分层时,我们发现在白种人(4G5G与5G5G:OR = 1.806,95% CI:1.064 - 3.067)和东亚人(4G4G与5G5G:OR = 1.619,95% CI:1.025 - 2.556,以及4G4G与4G5G + 5G5G:OR = 1.665,95% CI:1.207 - 2.297)中,PAI-1 4G/5G多态性与ONFH风险之间存在显著关联。
本荟萃分析表明,PAI-1 4G/5G(rs1799889)多态性是ONFH发生的一个潜在风险因素。然而,需要在不同种族中进行大规模且设计良好的病例对照研究来验证这些结果。