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Association of Tumor Necrosis Factor-α(TNF-α) -308G>A and -238G>A Polymorphisms with Recurrent Pregnancy Loss Risk: A Meta-Analysis
BACKGROUND: Multiple studies have been carried out examining the association of tumor necrosis factor-α gene (TNF-α) promoter region polymorphisms with recurrent pregnancy loss (RPL) risk. However, the results remain con- troversial and incomplete. Hence, we performed a meta-analysis to evaluate the...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royan Institute
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6186289/ https://www.ncbi.nlm.nih.gov/pubmed/30291687 http://dx.doi.org/10.22074/ijfs.2019.5454 |
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author | Aslebahar, Fereshteh Neamatzadeh, Hossein Meibodi, Bahare Karimi-Zarchi, Mojgan Tabatabaei, Razieh Sadat Noori-Shadkam, Mahmood Mazaheri, Mahta Dehghani-Mohammadabadi, Reihaneh |
author_facet | Aslebahar, Fereshteh Neamatzadeh, Hossein Meibodi, Bahare Karimi-Zarchi, Mojgan Tabatabaei, Razieh Sadat Noori-Shadkam, Mahmood Mazaheri, Mahta Dehghani-Mohammadabadi, Reihaneh |
author_sort | Aslebahar, Fereshteh |
collection | PubMed |
description | BACKGROUND: Multiple studies have been carried out examining the association of tumor necrosis factor-α gene (TNF-α) promoter region polymorphisms with recurrent pregnancy loss (RPL) risk. However, the results remain con- troversial and incomplete. Hence, we performed a meta-analysis to evaluate the association of the TNF-α -308G>A and -238G>A polymorphisms with RPL risk. MATERIALS AND METHODS: In this meta-analysis, a comprehensive search of PubMed, Web of Knowledge and EM- BASE was performed to identify relevant studies published until December 1, 2017. The associations were assessed by odds ratio (OR) and its corresponding 95% confidence interval (CI). RESULTS: A total of 29 case-control studies, comprising 20 studies on TNF-α -308G>A (3,461 cases and 3,895 con- trols) and nine studies on TNF-α -238G>A (2,589 cases and 2,664 controls), were included in the meta-analysis. Over- all, we found TNF-α -308G>A to be associated with an increase in RPL risk under the homozygote (OR=1.716, 95% CI: 1.210-2.433, P=0.002) and the recessive (OR=1.554, 95% CI: 1.100-2.196, P=0.012) models. TNF-α -238G>A was also significantly associated with increased risk of RPL under the allele model (OR=1.554, 95% CI: 1.100-2.196, P=0.012). Stratified analysis revealed a more significant association between the TNF-α -308G>A polymorphism and increased RPL risk in Asians under the homozygote (OR=2.190, 95% CI: 1.465-3.274, P≤0.001), the dominant (OR=1.642, 95% CI: 1.269-2.125, P≤0.001) and the recessive (OR=1.456, 95% CI: 1.039-2.040, P=0.029) models, but not in Caucasians. A non-significant association was, however, identified between TNF-α -238G>A and RPL risk based on ethnicity. Moreover, TNF-α -308G>A and -238G>A polymorphisms were significantly associated with in- creased risk of RPL in high quality studies and polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) subgroups. CONCLUSION: The present meta-analysis demonstrates that TNF-α -308G>A and -238G>A polymorphisms are associ- ated with an increased risk of RPL. |
format | Online Article Text |
id | pubmed-6186289 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Royan Institute |
record_format | MEDLINE/PubMed |
spelling | pubmed-61862892019-01-01 Association of Tumor Necrosis Factor-α(TNF-α) -308G>A and -238G>A Polymorphisms with Recurrent Pregnancy Loss Risk: A Meta-Analysis Aslebahar, Fereshteh Neamatzadeh, Hossein Meibodi, Bahare Karimi-Zarchi, Mojgan Tabatabaei, Razieh Sadat Noori-Shadkam, Mahmood Mazaheri, Mahta Dehghani-Mohammadabadi, Reihaneh Int J Fertil Steril Original Article BACKGROUND: Multiple studies have been carried out examining the association of tumor necrosis factor-α gene (TNF-α) promoter region polymorphisms with recurrent pregnancy loss (RPL) risk. However, the results remain con- troversial and incomplete. Hence, we performed a meta-analysis to evaluate the association of the TNF-α -308G>A and -238G>A polymorphisms with RPL risk. MATERIALS AND METHODS: In this meta-analysis, a comprehensive search of PubMed, Web of Knowledge and EM- BASE was performed to identify relevant studies published until December 1, 2017. The associations were assessed by odds ratio (OR) and its corresponding 95% confidence interval (CI). RESULTS: A total of 29 case-control studies, comprising 20 studies on TNF-α -308G>A (3,461 cases and 3,895 con- trols) and nine studies on TNF-α -238G>A (2,589 cases and 2,664 controls), were included in the meta-analysis. Over- all, we found TNF-α -308G>A to be associated with an increase in RPL risk under the homozygote (OR=1.716, 95% CI: 1.210-2.433, P=0.002) and the recessive (OR=1.554, 95% CI: 1.100-2.196, P=0.012) models. TNF-α -238G>A was also significantly associated with increased risk of RPL under the allele model (OR=1.554, 95% CI: 1.100-2.196, P=0.012). Stratified analysis revealed a more significant association between the TNF-α -308G>A polymorphism and increased RPL risk in Asians under the homozygote (OR=2.190, 95% CI: 1.465-3.274, P≤0.001), the dominant (OR=1.642, 95% CI: 1.269-2.125, P≤0.001) and the recessive (OR=1.456, 95% CI: 1.039-2.040, P=0.029) models, but not in Caucasians. A non-significant association was, however, identified between TNF-α -238G>A and RPL risk based on ethnicity. Moreover, TNF-α -308G>A and -238G>A polymorphisms were significantly associated with in- creased risk of RPL in high quality studies and polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) subgroups. CONCLUSION: The present meta-analysis demonstrates that TNF-α -308G>A and -238G>A polymorphisms are associ- ated with an increased risk of RPL. Royan Institute 2019 2018-10-02 /pmc/articles/PMC6186289/ /pubmed/30291687 http://dx.doi.org/10.22074/ijfs.2019.5454 Text en Any use, distribution, reproduction or abstract of this publication in any medium, with the exception of commercial purposes, is permitted provided the original work is properly cited http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Aslebahar, Fereshteh Neamatzadeh, Hossein Meibodi, Bahare Karimi-Zarchi, Mojgan Tabatabaei, Razieh Sadat Noori-Shadkam, Mahmood Mazaheri, Mahta Dehghani-Mohammadabadi, Reihaneh Association of Tumor Necrosis Factor-α(TNF-α) -308G>A and -238G>A Polymorphisms with Recurrent Pregnancy Loss Risk: A Meta-Analysis |
title | Association of Tumor Necrosis Factor-α(TNF-α) -308G>A
and -238G>A Polymorphisms with Recurrent Pregnancy
Loss Risk: A Meta-Analysis |
title_full | Association of Tumor Necrosis Factor-α(TNF-α) -308G>A
and -238G>A Polymorphisms with Recurrent Pregnancy
Loss Risk: A Meta-Analysis |
title_fullStr | Association of Tumor Necrosis Factor-α(TNF-α) -308G>A
and -238G>A Polymorphisms with Recurrent Pregnancy
Loss Risk: A Meta-Analysis |
title_full_unstemmed | Association of Tumor Necrosis Factor-α(TNF-α) -308G>A
and -238G>A Polymorphisms with Recurrent Pregnancy
Loss Risk: A Meta-Analysis |
title_short | Association of Tumor Necrosis Factor-α(TNF-α) -308G>A
and -238G>A Polymorphisms with Recurrent Pregnancy
Loss Risk: A Meta-Analysis |
title_sort | association of tumor necrosis factor-α(tnf-α) -308g>a
and -238g>a polymorphisms with recurrent pregnancy
loss risk: a meta-analysis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6186289/ https://www.ncbi.nlm.nih.gov/pubmed/30291687 http://dx.doi.org/10.22074/ijfs.2019.5454 |
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