Department of Dermatology, Institute of Dermatology, Chinese Academy of Medical Science and Peking Union Medical College, Nanjing, Jiangsu, China.
Indian J Dermatol Venereol Leprol. 2022 Mar-Apr;88(2):150-155. doi: 10.25259/IJDVL_1401_20.
The polymorphism of interleukin-17F rs763780 has been found to have a probable association with increased risk of developing psoriasis.
This study aims to get a more convincing estimation of the association between the interleukin-17F rs763780 T /C polymorphism and psoriasis risk.
Two authors independently searched the databases including PubMed, EMBASE, Cochrane Central Register of Controlled Trials, Chinese National Knowledge Infrastructure, Wanfang and Chinese Biomedical Literature Databases for case-control studies which reported the odds ratios with 95% confidence intervals comparing genotype and allele frequencies of the interleukin-17F rs763780 polymorphism in patients with psoriasis versus participants without psoriasis.
A total of seven case-control studies incorporating 1824 cases and 1585 controls were identified. The pooled odds ratios indicated that interleukin-17F rs763780 C allele was a risk factor for psoriasis in allele frequency, recessive model and homozygote model (P < 0.05). Subgroup analysis by ethnicity further indicated that the C allele was closely related to increased risk of psoriasis in Asian populations (P < 0.05), but not in Caucasians.
Only a few studies on the interleukin-17F rs763780 polymorphism in psoriasis have been reported till date, thus the data is insufficient. Only one gene polymorphic site was selected for this study, and it is not clear whether other genetic mutation functional sites affect the gene. Further studies on confounding effects of other genetic polymorphisms are needed.
The present meta-analysis results suggested that the interleukin-17F rs763780 T /C is significantly associated with psoriasis risk in Asians.
白细胞介素-17F rs763780 的多态性与银屑病发病风险增加可能有关。
本研究旨在更有力地评估白细胞介素-17F rs763780 T/C 多态性与银屑病风险之间的关联。
两位作者独立检索了包括 PubMed、EMBASE、Cochrane 中央对照试验注册库、中国国家知识基础设施、万方和中国生物医学文献数据库在内的数据库,以查找病例对照研究,这些研究报告了比较银屑病患者与无银屑病参与者基因型和等位基因频率的比值比(OR),并报告了白细胞介素-17F rs763780 多态性的 95%置信区间。
共纳入了 7 项病例对照研究,包括 1824 例病例和 1585 例对照。汇总的 OR 表明,白细胞介素-17F rs763780 C 等位基因在等位基因频率、隐性模型和纯合子模型中是银屑病的危险因素(P<0.05)。按种族进行的亚组分析进一步表明,C 等位基因与亚洲人群中银屑病风险增加密切相关(P<0.05),但在白种人群中并非如此。
迄今为止,只有少数关于银屑病白细胞介素-17F rs763780 多态性的研究报告,因此数据不足。本研究仅选择了一个基因多态性位点,尚不清楚其他遗传突变功能位点是否会影响该基因。需要进一步研究其他遗传多态性的混杂效应。
本荟萃分析结果表明,白细胞介素-17F rs763780 T/C 与亚洲人群的银屑病风险显著相关。