TGF-β1 promoter functional gene polymorphism -509 C/T in the maternal susceptibility to recurrent pregnancy loss in South Indian women

Transforming growth factor beta 1 (TGF-β1) is an anti-inflammatory pleiotropic cytokine that regulates implantation and adhesion of trophoblasts to the extracellular matrix. It regulates the balance of Th1/Th2 cytokines and the generation of anti-inflammatory peripheral regulatory T cells (FOXP3 + Tregs), which is necessary for a healthy pregnancy. Single nucleotide polymorphisms (SNP) affecting TGF-β1 production/function may predispose to pregnancy loss. The aim of this study is to evaluate the association between the TGF-β1 -509C/T polymorphism, its serum concentrations, and recurrent pregnancy loss. The study comprised 150 RPL cases and 150 healthy controls for genotyping TGF-β1 -509C/T polymorphism using the Amplification Refractory Mutation System-Polymerase Chain Reaction (ARMS-PCR). Serum concentrations of TGF-β1 protein were estimated by enzyme-linked immunosorbent assay. From our study, women with CT genotype exhibited a protective role against RPL [OR (95 % CI) = 0.48(0.30-0.76), p = 0.002], while women with TT genotype had a significantly higher risk among RPL patients and exhibited twofold increased risk [OR (95 % CI) = 2.34(1.37-4.01), p = 0.002]. Observation of patient's follow-up data revealed a significant relation with CT genotype of unfavorable pregnancy outcome (CT vs. CC + TT, OR 2.46, 95 % C.I: 1.11-5.43, p = 0.039). Further, variant allele T was significantly elevated in women with unfavorable pregnancy compared with favorable pregnancy outcome, indicating considerable association of T allele in unfavorable pregnancy outcome (T vs. C, OR: 2.68, 95 % C.I: 1.52-4.74, p = <0.001). Serum concentrations of TGF-β1 have shown significant variation between patients and controls, as well as among RPL patients with favorable and unfavorable pregnancy outcome in correspondence to each genotype CC, CT, and TT (p < 0.05). Furthermore, genotype-dependent variation was observed within both the patient and control groups; however, this variation was not observed among RPL women with favorable and unfavorable pregnancy outcome. Our investigation revealed a significant influence of TGF-β1C-509 T polymorphism on RPL risk in South Indian women.

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Publication Details

Journal
Human Immunology
Published
2024-11-21
DOI
https://doi.org/10.1016/j.humimm.2024.111182
Citations
3
Primary Topic
Reproductive System and Pregnancy
Type
article
Field-Weighted Citation Impact
0.72

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article

TGF-β1 promoter functional gene polymorphism -509 C/T in the maternal susceptibility to recurrent pregnancy loss in South Indian women

Kethora Dirisipam, Dhatri Madduru, Parveen Jahan, Deepika Gujrati
3 citations
Human Immunology
Reproductive System and Pregnancy
0.72
article

TGF-β1 promoter functional gene polymorphism -509 C/T in the maternal susceptibility to recurrent pregnancy loss in South Indian women

Kethora Dirisipam, Dhatri Madduru, Parveen Jahan, Deepika Gujrati
article en
3 citations

Abstract

Transforming growth factor beta 1 (TGF-β1) is an anti-inflammatory pleiotropic cytokine that regulates implantation and adhesion of trophoblasts to the extracellular matrix. It regulates the balance of Th1/Th2 cytokines and the generation of anti-inflammatory peripheral regulatory T cells (FOXP3 + Tregs), which is necessary for a healthy pregnancy. Single nucleotide polymorphisms (SNP) affecting TGF-β1 production/function may predispose to pregnancy loss. The aim of this study is to evaluate the association between the TGF-β1 -509C/T polymorphism, its serum concentrations, and recurrent pregnancy loss. The study comprised 150 RPL cases and 150 healthy controls for genotyping TGF-β1 -509C/T polymorphism using the Amplification Refractory Mutation System-Polymerase Chain Reaction (ARMS-PCR). Serum concentrations of TGF-β1 protein were estimated by enzyme-linked immunosorbent assay. From our study, women with CT genotype exhibited a protective role against RPL [OR (95 % CI) = 0.48(0.30-0.76), p = 0.002], while women with TT genotype had a significantly higher risk among RPL patients and exhibited twofold increased risk [OR (95 % CI) = 2.34(1.37-4.01), p = 0.002]. Observation of patient's follow-up data revealed a significant relation with CT genotype of unfavorable pregnancy outcome (CT vs. CC + TT, OR 2.46, 95 % C.I: 1.11-5.43, p = 0.039). Further, variant allele T was significantly elevated in women with unfavorable pregnancy compared with favorable pregnancy outcome, indicating considerable association of T allele in unfavorable pregnancy outcome (T vs. C, OR: 2.68, 95 % C.I: 1.52-4.74, p = <0.001). Serum concentrations of TGF-β1 have shown significant variation between patients and controls, as well as among RPL patients with favorable and unfavorable pregnancy outcome in correspondence to each genotype CC, CT, and TT (p < 0.05). Furthermore, genotype-dependent variation was observed within both the patient and control groups; however, this variation was not observed among RPL women with favorable and unfavorable pregnancy outcome. Our investigation revealed a significant influence of TGF-β1C-509 T polymorphism on RPL risk in South Indian women.

Human ImmunologyVol. 86(1)
Maulana Azad National Urdu University (IN), Institute of Genetics and Hospital for Genetic Diseases (IN), Osmania University (IN)
Indian Council of Medical Research
Openalex Percentile: Top 28%
Reproductive System and Pregnancy
0.72
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