Lee Y H, Bae S-C, Kim J-H, Song G G
Division of Rheumatology, Department of Internal Medicine, Korea University Anam Hospital, Korea University College of Medicine, 126-1, Anam-dong 5 ga, Seongbuk-gu, 136-705, Seoul, Korea,
Z Rheumatol. 2015 Apr;74(3):230-9. doi: 10.1007/s00393-014-1415-y.
The aim of this study was to determine whether genetic polymorphisms in programmed cell death 1 (PDCD1 or PD1) are associated with susceptibility to rheumatoid arthritis (RA), ankylosing spondylitis (AS), and type 1 diabetes (T1D).
We conducted a meta-analysis to investigate the association between PDCD1 polymorphisms and RA, AS, and T1D in the overall population and in specific ethnic populations.
Sixteen studies, comprising 13,210 patients and 17,073 controls, were conducted for the meta-analysis including 4 studies on RA, 4 on AS, and 8 on T1D. The meta-analysis showed an association between RA and the 2 alleles of the PD1.3 polymorphism in the overall population [odds ratio (OR) 1.183, 95 % confidence interval (95 % CI) 1.005-1.392, p = 0.043]. However, meta-analysis showed no association between RA and the 2 alleles of the PD1.1 and PD1.5 polymorphisms in the overall population. Meta-analysis identified an association between AS and the 2 alleles of the PD1.5 and PD1.9 polymorphisms in the Asian population (OR 1.251, 95 % CI 1.019-1.535, p = 0.033; OR 1.975, 95 % CI 1.286-3.034, p = 0.002, respectively). The meta-analysis revealed a significant association between T1D and the 2 alleles of the PD1.3 polymorphism in the European population (OR 1.098, 95 % CI 1.029-1.171, p = 0.005). The meta-analysis showed an association between the PD1.5 polymorphism and T1D in Asians (OR 1.332, 95 % CI 1.067-1.663, p = 0.011) and between the PD1.9 polymorphism and T1D in the Asian population (OR 1.363, 95 % CI 1.107-1.679, p = 0.004).
The meta-analysis suggests an association between the PD1.3 polymorphism and RA in the overall population and an association between the PD1.5 and PD1.9 polymorphisms, and AS in the Asian population. Furthermore, the PD1.3 , 5, and 9 polymorphisms were associated with T1D susceptibility in Europeans, or Asians.
本研究旨在确定程序性细胞死亡1(PDCD1或PD1)基因多态性是否与类风湿关节炎(RA)、强直性脊柱炎(AS)和1型糖尿病(T1D)的易感性相关。
我们进行了一项荟萃分析,以研究总体人群和特定种族人群中PDCD1基因多态性与RA、AS和T1D之间的关联。
进行荟萃分析的16项研究共纳入13210例患者和17073例对照,其中包括4项关于RA的研究、4项关于AS的研究和8项关于T1D的研究。荟萃分析显示,总体人群中RA与PD1.3多态性的两个等位基因之间存在关联[比值比(OR)1.183,95%置信区间(95%CI)1.005-1.392,p = 0.043]。然而,荟萃分析显示总体人群中RA与PD1.1和PD1.5多态性的两个等位基因之间无关联。荟萃分析确定亚洲人群中AS与PD1.5和PD1.9多态性的两个等位基因之间存在关联(OR分别为1.251,95%CI 1.019-1.535,p = 0.033;OR 1.975,95%CI 1.286-3.034,p = 0.002)。荟萃分析显示欧洲人群中T1D与PD1.3多态性的两个等位基因之间存在显著关联(OR 1.098,95%CI 1.029-1.171,p = 0.005)。荟萃分析显示亚洲人群中PD1.5多态性与T1D之间存在关联(OR 1.332,95%CI 1.067-1.663,p = 0.011),以及亚洲人群中PD1.9多态性与T1D之间存在关联(OR 1.363,95%CI 1.107-1.679,p = 0.004)。
荟萃分析表明总体人群中PD1.3多态性与RA之间存在关联,亚洲人群中PD1.5和PD1.9多态性与AS之间存在关联。此外,PD1.3、5和9多态性与欧洲或亚洲人群中T1D的易感性相关。