The forkhead box protein P3 gene rs3761548 promoter polymorphism confers a genetic contribution to the risk of preeclampsia: A systematic review and meta-analysis

• Published in: Cytokine (Philadelphia, Pa.) Pa.), 2023-04, Vol.164, p.156164-156164, Article 156164
• Main Authors: Lu, Minyan, Nie, Jinyi, Shen, Hexin, Jiao, Wenzhi, Men, Zhiyu, Meng, Ye, Xu, Hanzhang, Zhu, Liyan, Yang, Xiaoqin, Gao, Shangshang
• Format: Article
• Language: English
• Subjects: Alleles; Case-Control Studies; Female; Forkhead box P3 gene; Forkhead Transcription Factors - genetics; Genetic Predisposition to Disease - genetics; Genotype; Humans; Meta-analysis; Polymorphism; Polymorphism, Single Nucleotide - genetics; Pre-Eclampsia - genetics; Preeclampsia; Pregnancy; Risk Factors
• ISSN: 1043-4666; 1096-0023
• DOI: 10.1016/j.cyto.2023.156164

•1,738 cases and 1,883 controls were integrated into this meta-analysis.•rs3761548 is significantly associated with preeclampsia risk.•rs2232365 is not associated with preeclampsia risk. Various studies have investigated the risk of preeclampsia with the forkhead box protein P3 (FOXP3) gene rs2232365 and rs3761548 polymorphisms. However, the results remained contradictory. A comprehensive literature search was conducted using the Cochrane Library, PubMed, and Web of Science (up to Oct 11, 2021). Meta-analysis was carried out in the R language environment for statistical computing and graphics. A fixed-effect or random-effects model was used according to the statistical significance of heterogeneity among included studies. The pooled odds ratios and corresponding 95% confidence intervals were calculated to estimate the strength of the effect. For the rs2232365 polymorphism, statistical significance was detected neither in the overall population nor among the East Asian and West Asian subgroups. However, for rs3761548, the summarized statistics revealed a significant association between the C allele carriage and preeclampsia risk in the homozygote, heterozygote, and dominant models. The further stratified analysis found this effect might be specific to West-South Asian ethnic subgroups. To sum up, this meta-analysis showed that the FOXP3 rs3761548 polymorphism was significantly associated with preeclampsia susceptibility, and it had a deleterious effect especially in the West-South Asian population. In contrast, rs2232365 may serve as neither a protective nor a risk factor for preeclampsia onset.