Pan Feng, Tian Jing, Winzenberg Tania, Ding Changhai, Jones Graeme
Menzies Research Institute Tasmania, University of Tasmania, Private Bag 23, Hobart, Tasmania 7000, Australia.
BMC Musculoskelet Disord. 2014 Dec 2;15:404. doi: 10.1186/1471-2474-15-404.
Previous studies investigating the association between GDF5 rs143383 polymorphism and knee osteoarthritis (OA) have suggested stronger associations in Asians than Caucasians, but limitations on the amount of available data have meant that a definitive assessment has not been possible. Given the availability of more recent data, the aim of this meta-analysis was to determine the overall association between GDF5 rs143383 polymorphism and knee OA and whether the association varies by ethnicity.
Searches of Medline, Embase, and ISI Web of Science were conducted up to July 2013. Summary odds ratios (ORs) and 95% confidence intervals (CIs) were calculated to estimate the strength of association between the GDF5 polymorphism and knee OA risk.
A total of 20 studies with 23,995 individuals were included. There were weak but significant associations present between the GDF5 polymorphism and knee OA at the allele level (C vs. T: OR =0.85, 95% CI = 0.80-0.90) and genotype level (CC vs. TT: OR = 0.73; CT vs. TT: OR = 0.84; CC/CT vs. TT: OR = 0.81; CC vs.
CT/TT: OR = 0.81) in the overall population. In the subgroup analysis by ethnicity, we observed a strong significant association (OR = 0.60 to 0.80, all P <0.05) in Asian population and weaker associations (OR =0.78 to 0.87, all P <0.05) in Caucasian population; however marked heterogeneity was detected in all models except for CC vs. TT (I2 = 12.9%) and CC vs. CT + TT (I2 = 0.0%) in Asians.
These results strongly suggest that the C allele and CC genotype of the GDF5 gene are protective for knee OA susceptibility across different populations.
既往关于生长分化因子5(GDF5)基因rs143383多态性与膝关节骨关节炎(OA)之间关联的研究表明,亚洲人与白种人相比存在更强的关联性,但可用数据量的限制意味着无法进行确定性评估。鉴于有了更新的数据,本荟萃分析的目的是确定GDF5基因rs143383多态性与膝关节OA之间的总体关联,以及这种关联是否因种族而异。
截至2013年7月,对Medline、Embase和ISI科学网进行了检索。计算汇总比值比(OR)和95%置信区间(CI),以估计GDF5基因多态性与膝关节OA风险之间关联的强度。
共纳入20项研究,涉及23995名个体。在总体人群中,GDF5基因多态性与膝关节OA在等位基因水平(C与T:OR = 0.85,95%CI = 0.80 - 0.90)和基因型水平(CC与TT:OR = 0.73;CT与TT:OR = 0.84;CC/CT与TT:OR = 0.81;CC与CT/TT:OR = 0.81)存在微弱但显著的关联。在按种族进行的亚组分析中,我们在亚洲人群中观察到强显著关联(OR = 0.60至0.80,所有P < 0.05),在白种人群中关联较弱(OR = 0.78至0.87,所有P < 0.05);然而,除了亚洲人中CC与TT(I2 = 12.9%)和CC与CT + TT(I2 = 0.0%)外,在所有模型中均检测到明显的异质性。
这些结果强烈表明,GDF5基因的C等位基因和CC基因型对不同人群的膝关节OA易感性具有保护作用。