Cargando…
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...
Autores principales: | , , , , , |
---|---|
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 |
_version_ | 1782277901324910592 |
---|---|
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. |
format | Online Article Text |
id | pubmed-3719316 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Avicenna Research Institute |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT sowmyasabnavis evaluationofinterleukin10g1082apromoterpolymorphisminpreeclampsia AT ramaiaharuna evaluationofinterleukin10g1082apromoterpolymorphisminpreeclampsia AT sunithatella evaluationofinterleukin10g1082apromoterpolymorphisminpreeclampsia AT nallaripratibha evaluationofinterleukin10g1082apromoterpolymorphisminpreeclampsia AT jyothyakka evaluationofinterleukin10g1082apromoterpolymorphisminpreeclampsia AT venkateshwariananthapur evaluationofinterleukin10g1082apromoterpolymorphisminpreeclampsia |