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Influence of forkhead box protein 3 polymorphisms (rs2232365, rs3761548) with the outcome of pregnancy: A meta-analysis.
Hosseini Teshnizi, Saeed; Ali-Hassanzadeh, Mohammad; Gharesi-Fard, Behrouz; Kabelitz, Dieter; Kalantar, Kurosh.
Afiliação
  • Hosseini Teshnizi S; Department of Biostatistics, Fertility and Infertility Research Center, Hormozgan University of Medical Sciences, Bandar Abbas, Iran.
  • Ali-Hassanzadeh M; Department of Immunology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Gharesi-Fard B; Department of Immunology, School of Medicine, Jiroft University of Medical Sciences, Jiroft, Iran.
  • Kabelitz D; Department of Immunology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Kalantar K; Infertility Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
J Cell Physiol ; 234(9): 16573-16581, 2019 Sep.
Article em En | MEDLINE | ID: mdl-30784062
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.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Systematic_reviews Idioma: En Revista: J Cell Physiol Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Irã

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Systematic_reviews Idioma: En Revista: J Cell Physiol Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Irã