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Association of tumor necrosis factor-alpha 308G/A polymorphism with recurrent miscarriages in women
BACKGROUND: Recurrent miscarriage (RM) is the most common pregnancy loss in the first trimester affecting approximately 0.5–2% of women. It is a heterogeneous condition and remains an enigma as the underlying cause is still difficult to track down. AIM: This study was aimed to investigate the distri...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4915291/ https://www.ncbi.nlm.nih.gov/pubmed/27382232 http://dx.doi.org/10.4103/0974-1208.183516 |
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author | Sudhir, Neha Badaruddoza, Beri, Archana Kaur, Anupam |
author_facet | Sudhir, Neha Badaruddoza, Beri, Archana Kaur, Anupam |
author_sort | Sudhir, Neha |
collection | PubMed |
description | BACKGROUND: Recurrent miscarriage (RM) is the most common pregnancy loss in the first trimester affecting approximately 0.5–2% of women. It is a heterogeneous condition and remains an enigma as the underlying cause is still difficult to track down. AIM: This study was aimed to investigate the distribution of tumor necrosis factor-alpha (TNF-α) 308G/A polymorphism and its association with RM in females. The comparative picture was also demonstrated by comparing genotyping results with healthy control women having no history of miscarriage. METHODS: This clinical study was conducted among 115 women aged 21–44 years with history of recurrence of miscarriage. The samples were collected from women attending the outpatient departments of various hospitals, nursing homes, and infertility clinics of this region. In the present study, 111 fertile healthy women aged 24–46 years with at least one live birth and no history of miscarriage were also included. RESULTS: Mean age of women with RM was found to be 28 ± 5.6 years by recall method, whereas it was found to be 30 ± 7.4 in context to healthy women with no history of pregnancy loss. In the present study, 66% of women with RM had homozygous wild type genotype (GG) while 30% and 4% of women had heterozygous (GA) and homozygous mutant genotype (AA), respectively. Among control group, 79%, 16%, and 5% of women showed GG, GA, and AA genotype, respectively. CONCLUSION: The current study supports the concept of TNF-α 308G/A variant in particular with reproductive failure, GG and GA alleles showing 1-fold risk association with RM (odds ratio: 1.86 and 1.43, respectively). |
format | Online Article Text |
id | pubmed-4915291 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-49152912016-07-05 Association of tumor necrosis factor-alpha 308G/A polymorphism with recurrent miscarriages in women Sudhir, Neha Badaruddoza, Beri, Archana Kaur, Anupam J Hum Reprod Sci Original Article BACKGROUND: Recurrent miscarriage (RM) is the most common pregnancy loss in the first trimester affecting approximately 0.5–2% of women. It is a heterogeneous condition and remains an enigma as the underlying cause is still difficult to track down. AIM: This study was aimed to investigate the distribution of tumor necrosis factor-alpha (TNF-α) 308G/A polymorphism and its association with RM in females. The comparative picture was also demonstrated by comparing genotyping results with healthy control women having no history of miscarriage. METHODS: This clinical study was conducted among 115 women aged 21–44 years with history of recurrence of miscarriage. The samples were collected from women attending the outpatient departments of various hospitals, nursing homes, and infertility clinics of this region. In the present study, 111 fertile healthy women aged 24–46 years with at least one live birth and no history of miscarriage were also included. RESULTS: Mean age of women with RM was found to be 28 ± 5.6 years by recall method, whereas it was found to be 30 ± 7.4 in context to healthy women with no history of pregnancy loss. In the present study, 66% of women with RM had homozygous wild type genotype (GG) while 30% and 4% of women had heterozygous (GA) and homozygous mutant genotype (AA), respectively. Among control group, 79%, 16%, and 5% of women showed GG, GA, and AA genotype, respectively. CONCLUSION: The current study supports the concept of TNF-α 308G/A variant in particular with reproductive failure, GG and GA alleles showing 1-fold risk association with RM (odds ratio: 1.86 and 1.43, respectively). Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC4915291/ /pubmed/27382232 http://dx.doi.org/10.4103/0974-1208.183516 Text en Copyright: © Journal of Human Reproductive Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Sudhir, Neha Badaruddoza, Beri, Archana Kaur, Anupam Association of tumor necrosis factor-alpha 308G/A polymorphism with recurrent miscarriages in women |
title | Association of tumor necrosis factor-alpha 308G/A polymorphism with recurrent miscarriages in women |
title_full | Association of tumor necrosis factor-alpha 308G/A polymorphism with recurrent miscarriages in women |
title_fullStr | Association of tumor necrosis factor-alpha 308G/A polymorphism with recurrent miscarriages in women |
title_full_unstemmed | Association of tumor necrosis factor-alpha 308G/A polymorphism with recurrent miscarriages in women |
title_short | Association of tumor necrosis factor-alpha 308G/A polymorphism with recurrent miscarriages in women |
title_sort | association of tumor necrosis factor-alpha 308g/a polymorphism with recurrent miscarriages in women |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4915291/ https://www.ncbi.nlm.nih.gov/pubmed/27382232 http://dx.doi.org/10.4103/0974-1208.183516 |
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