| Literature DB >> 30784062 |
Saeed Hosseini Teshnizi1, Mohammad Ali-Hassanzadeh2,3, Behrouz Gharesi-Fard2,4, Dieter Kabelitz5, Kurosh Kalantar2.
Abstract
Dysfunction of regulatory T cells (Tregs) may contribute to certain immune-related pregnancy complications. Forkhead box protein 3 (FOXP3) is the key transcription factor of Treg. We performed a systematic review and meta-analysis to evaluate the possible association between FOXP3 polymorphisms -924A/G (rs2232365) and -3279C/A (rs3761548) and immune-related pregnancy complications. After reviewing 78 fully published studies, 10 studies fulfilled previously defined eligibility criteria and were used for meta-analysis. Two single nucleotide polymorphisms showed a significant correlation with increased or reduced risk for immune-related pregnancy complications. For rs3761548, women with allele A were significantly at a higher risk than women carrying allele C (odds ratio = 1.29, 95% confidence interval: 1.20-1.38; p = 0.001). For rs2232365, women with GG or AG genotype were at a higher risk than women with genotype AA, thereby, allele G was significantly associated with a higher risk than allele A. Our meta-analysis supports the notion that immune-related pregnancy complications might be linked to genetic variations in the FOXP3 gene.Entities:
Keywords: FOXP3; meta-analysis; polymorphism; pre-eclampsia; recurrent pregnancy loss; unexplained recurrent spontaneous abortion
Year: 2019 PMID: 30784062 DOI: 10.1002/jcp.28328
Source DB: PubMed Journal: J Cell Physiol ISSN: 0021-9541 Impact factor: 6.384