Liu Wenjie, Wang Chunhui, Tang Lijuan, Yang Hui
Department of Gastrointestinal Anorectal Surgery, Changyi People's Hospital, Changyi, Shandong Province, China.
Department of Gastroenterology, Changyi People's Hospital, Changyi, Shandong Province, China.
Immunol Invest. 2021 Nov;50(8):869-883. doi: 10.1080/08820139.2020.1787438. Epub 2020 Aug 26.
The relationships between polymorphisms in pro-inflammatory cytokines and the risk of inflammatory bowel disease (IBD) remain discrepant. Therefore, the authors conducted a meta-analysis to robustly explore relationships between polymorphisms in pro-inflammatory cytokines and the risk of IBD by integrating the results of previous works. Medline, Embase, Wanfang, VIP and CNKI were searched throughly for eligible studies, and 35 genetic association studies were finally included in this meta-analysis. We noticed that genotypic frequencies of rs1143627, rs1800795 and rs4073 polymorphisms among cases with IBD and population-based controls differed significantly. Moreover, we found that genotypic frequencies of rs1143627 and rs1800795 polymorphisms among cases with IBD and population-based controls of Caucasian origin differed significantly, whereas genotypic frequency of rs4073 and rs187238 polymorphisms among cases with IBD and population-based controls of Asian origin also differed significantly. Furthermore, we also noticed that genotypic frequency of rs187238 polymorphism among cases with Crohn's disease (CD) and population-based controls differed significantly. In conclusion, this meta-analysis demonstrated that rs1143627 and rs1800795 polymorphisms were significantly associated with the risk of IBD in overall population and Caucasians. Moreover, rs4073 polymorphism was significantly associated with the risk of IBD in overall population and Asians. In addition, we also noticed that rs187238 polymorphism was significantly associated with the risk of CD, and rs1946518 polymorphism was significantly associated with the risk of IBD in Asians.
促炎细胞因子多态性与炎症性肠病(IBD)风险之间的关系仍存在差异。因此,作者进行了一项荟萃分析,通过整合以往研究结果来深入探讨促炎细胞因子多态性与IBD风险之间的关系。全面检索了Medline、Embase、万方、维普和中国知网以查找符合条件的研究,最终35项基因关联研究纳入了该荟萃分析。我们注意到,IBD患者与基于人群的对照组之间rs1143627、rs1800795和rs4073多态性的基因型频率存在显著差异。此外,我们发现,IBD患者与高加索裔基于人群的对照组之间rs1143627和rs1800795多态性的基因型频率存在显著差异,而IBD患者与亚裔基于人群的对照组之间rs4073和rs187238多态性的基因型频率也存在显著差异。此外,我们还注意到,克罗恩病(CD)患者与基于人群的对照组之间rs187238多态性的基因型频率存在显著差异。总之,这项荟萃分析表明,rs1143627和rs1800795多态性与总体人群和高加索人中IBD的风险显著相关。此外,rs4073多态性与总体人群和亚裔中IBD的风险显著相关。此外,我们还注意到,rs187238多态性与CD的风险显著相关,而rs1946518多态性与亚裔中IBD的风险显著相关。