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Evaluation of Interleukin-10 (G-1082A) Promoter Polymorphism in Preeclampsia

BACKGROUND: Preeclampsia is a pregnancy-specific syndrome that may be life-threatening, especially to the fetus. Several causes have been reported that may have a possible role in the development of the disorder. Interleukin-10 affect maternal intravascular inflammation, as well as endothelial dysfu...

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Autores principales: Sowmya, Sabnavis, Ramaiah, Aruna, Sunitha, Tella, Nallari, Pratibha, Jyothy, Akka, Venkateshwari, Ananthapur
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Avicenna Research Institute 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3719316/
https://www.ncbi.nlm.nih.gov/pubmed/23926566
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author Sowmya, Sabnavis
Ramaiah, Aruna
Sunitha, Tella
Nallari, Pratibha
Jyothy, Akka
Venkateshwari, Ananthapur
author_facet Sowmya, Sabnavis
Ramaiah, Aruna
Sunitha, Tella
Nallari, Pratibha
Jyothy, Akka
Venkateshwari, Ananthapur
author_sort Sowmya, Sabnavis
collection PubMed
description BACKGROUND: Preeclampsia is a pregnancy-specific syndrome that may be life-threatening, especially to the fetus. Several causes have been reported that may have a possible role in the development of the disorder. Interleukin-10 affect maternal intravascular inflammation, as well as endothelial dysfunction. The aim of this study was to investigate the association between IL-10 G-1082A polymorphism and preeclampsia. METHODS: A total of eighty−eight pregnant women with preeclampsia and 100 women with normal pregnancy attending the Gynecological unit of Government Maternity Hospital, Petlaburz, Hyderabad, India, were considered for the study. A standard amplification refractory mutation system (ARMS) PCR was carried out for genotyping IL-10 G-1082A promoter polymorphism in all the participants. Genotypic distribution of the control and patient groups were compared with values predicted by Hardy-Weinberg equilibrium using χ(2) test. Odd ratios (OR) and their respective 95% confidence intervals were used to measure the strength of association between IL-10 gene polymorphism and preeclampsia. RESULTS: The frequencies of IL-10 G-1082A genotypes, GG, GA and AA, were 17.8%, 41.09% and 41.09% in women with preeclampsia and 25%, 28% and 47% in the controls respectively. There was no significant difference in the distribution of genotypes and alleles of IL-10 G-1082A between the two groups (Test power=0.66). CONCLUSION: The present study suggests that the IL-10 G-1082A gene promoter polymorphism is not a major genetic regulator in the etiology of preeclampsia.
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spelling pubmed-37193162013-08-07 Evaluation of Interleukin-10 (G-1082A) Promoter Polymorphism in Preeclampsia Sowmya, Sabnavis Ramaiah, Aruna Sunitha, Tella Nallari, Pratibha Jyothy, Akka Venkateshwari, Ananthapur J Reprod Infertil Original Article BACKGROUND: Preeclampsia is a pregnancy-specific syndrome that may be life-threatening, especially to the fetus. Several causes have been reported that may have a possible role in the development of the disorder. Interleukin-10 affect maternal intravascular inflammation, as well as endothelial dysfunction. The aim of this study was to investigate the association between IL-10 G-1082A polymorphism and preeclampsia. METHODS: A total of eighty−eight pregnant women with preeclampsia and 100 women with normal pregnancy attending the Gynecological unit of Government Maternity Hospital, Petlaburz, Hyderabad, India, were considered for the study. A standard amplification refractory mutation system (ARMS) PCR was carried out for genotyping IL-10 G-1082A promoter polymorphism in all the participants. Genotypic distribution of the control and patient groups were compared with values predicted by Hardy-Weinberg equilibrium using χ(2) test. Odd ratios (OR) and their respective 95% confidence intervals were used to measure the strength of association between IL-10 gene polymorphism and preeclampsia. RESULTS: The frequencies of IL-10 G-1082A genotypes, GG, GA and AA, were 17.8%, 41.09% and 41.09% in women with preeclampsia and 25%, 28% and 47% in the controls respectively. There was no significant difference in the distribution of genotypes and alleles of IL-10 G-1082A between the two groups (Test power=0.66). CONCLUSION: The present study suggests that the IL-10 G-1082A gene promoter polymorphism is not a major genetic regulator in the etiology of preeclampsia. Avicenna Research Institute 2013 /pmc/articles/PMC3719316/ /pubmed/23926566 Text en Copyright © 2013 Avicenna Research Institute http://creativecommons.org/licenses/by-nc/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly.
spellingShingle Original Article
Sowmya, Sabnavis
Ramaiah, Aruna
Sunitha, Tella
Nallari, Pratibha
Jyothy, Akka
Venkateshwari, Ananthapur
Evaluation of Interleukin-10 (G-1082A) Promoter Polymorphism in Preeclampsia
title Evaluation of Interleukin-10 (G-1082A) Promoter Polymorphism in Preeclampsia
title_full Evaluation of Interleukin-10 (G-1082A) Promoter Polymorphism in Preeclampsia
title_fullStr Evaluation of Interleukin-10 (G-1082A) Promoter Polymorphism in Preeclampsia
title_full_unstemmed Evaluation of Interleukin-10 (G-1082A) Promoter Polymorphism in Preeclampsia
title_short Evaluation of Interleukin-10 (G-1082A) Promoter Polymorphism in Preeclampsia
title_sort evaluation of interleukin-10 (g-1082a) promoter polymorphism in preeclampsia
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3719316/
https://www.ncbi.nlm.nih.gov/pubmed/23926566
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