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Association between BMP4 rs17563 Polymorphism and NSCL/P Risk: A Meta-Analysis

Objective. To investigate the association between bone morphogenetic protein 4 (BMP4) rs17563 polymorphism and nonsyndromic cleft lip with or without palate (NSCL/P) risk. Methods. Four online databases were researched and the related publications were collected. Odds ratio (OR) with 95% confidence...

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Autores principales: Hu, Yuan-Yuan, Qin, Chuan-Qi, Deng, Mo-Hong, Niu, Yu-Ming, Long, Xing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4306361/
https://www.ncbi.nlm.nih.gov/pubmed/25648829
http://dx.doi.org/10.1155/2015/763090
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author Hu, Yuan-Yuan
Qin, Chuan-Qi
Deng, Mo-Hong
Niu, Yu-Ming
Long, Xing
author_facet Hu, Yuan-Yuan
Qin, Chuan-Qi
Deng, Mo-Hong
Niu, Yu-Ming
Long, Xing
author_sort Hu, Yuan-Yuan
collection PubMed
description Objective. To investigate the association between bone morphogenetic protein 4 (BMP4) rs17563 polymorphism and nonsyndromic cleft lip with or without palate (NSCL/P) risk. Methods. Four online databases were researched and the related publications were collected. Odds ratio (OR) with 95% confidence interval (CI) was applied to assess the relationship; publication bias, metaregression, and sensitivity analysis were conducted to guarantee the strength of results. Results. Six published case-control studies were collected. Overall, no significant association between BMP4 rs17563 polymorphism and NSCL/P risk was found. It was notable that significant susceptibility on different ethnicity was observed in the stratified analysis. For Chinese population, the BMP4 rs17563 polymorphism was a significantly increased risk for NSCL/P (C versus T: OR = 1.52, 95% CI = 1.28–1.82, P < 0.01, I (2) = 0%; CC versus TT: OR = 2.58, 95% CI = 1.74–3.82, P < 0.01, I (2) = 0%; TC + CC versus TT: OR = 1.45, 95% CI = 1.14–1.84, P < 0.01, I (2) = 0%; CC versus TT + TC: OR=2.46, 95% CI = 1.46–4.14, P < 0.01, I (2) = 47.0%). On the contrary, significantly protective effects were found in Brazilian population (C versus T: OR = 0.69, 95% CI = 0.50–0.96, P = 0.03, I (2) = 68.5%; TC versus TT: OR = 0.52, 95% CI = 0.40–0.68, P < 0.01, I (2) = 0%; TC + CC versus TT: OR = 0.52, 95% CI = 0.35–0.78, P < 0.010, I (2) = 54.4%). Conclusion. This meta-analysis indicated that BMP4 rs17563 polymorphism could play a different role during the development of NSCL/P based on ethnicity diversity.
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spelling pubmed-43063612015-02-03 Association between BMP4 rs17563 Polymorphism and NSCL/P Risk: A Meta-Analysis Hu, Yuan-Yuan Qin, Chuan-Qi Deng, Mo-Hong Niu, Yu-Ming Long, Xing Dis Markers Research Article Objective. To investigate the association between bone morphogenetic protein 4 (BMP4) rs17563 polymorphism and nonsyndromic cleft lip with or without palate (NSCL/P) risk. Methods. Four online databases were researched and the related publications were collected. Odds ratio (OR) with 95% confidence interval (CI) was applied to assess the relationship; publication bias, metaregression, and sensitivity analysis were conducted to guarantee the strength of results. Results. Six published case-control studies were collected. Overall, no significant association between BMP4 rs17563 polymorphism and NSCL/P risk was found. It was notable that significant susceptibility on different ethnicity was observed in the stratified analysis. For Chinese population, the BMP4 rs17563 polymorphism was a significantly increased risk for NSCL/P (C versus T: OR = 1.52, 95% CI = 1.28–1.82, P < 0.01, I (2) = 0%; CC versus TT: OR = 2.58, 95% CI = 1.74–3.82, P < 0.01, I (2) = 0%; TC + CC versus TT: OR = 1.45, 95% CI = 1.14–1.84, P < 0.01, I (2) = 0%; CC versus TT + TC: OR=2.46, 95% CI = 1.46–4.14, P < 0.01, I (2) = 47.0%). On the contrary, significantly protective effects were found in Brazilian population (C versus T: OR = 0.69, 95% CI = 0.50–0.96, P = 0.03, I (2) = 68.5%; TC versus TT: OR = 0.52, 95% CI = 0.40–0.68, P < 0.01, I (2) = 0%; TC + CC versus TT: OR = 0.52, 95% CI = 0.35–0.78, P < 0.010, I (2) = 54.4%). Conclusion. This meta-analysis indicated that BMP4 rs17563 polymorphism could play a different role during the development of NSCL/P based on ethnicity diversity. Hindawi Publishing Corporation 2015 2015-01-12 /pmc/articles/PMC4306361/ /pubmed/25648829 http://dx.doi.org/10.1155/2015/763090 Text en Copyright © 2015 Yuan-Yuan Hu et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Hu, Yuan-Yuan
Qin, Chuan-Qi
Deng, Mo-Hong
Niu, Yu-Ming
Long, Xing
Association between BMP4 rs17563 Polymorphism and NSCL/P Risk: A Meta-Analysis
title Association between BMP4 rs17563 Polymorphism and NSCL/P Risk: A Meta-Analysis
title_full Association between BMP4 rs17563 Polymorphism and NSCL/P Risk: A Meta-Analysis
title_fullStr Association between BMP4 rs17563 Polymorphism and NSCL/P Risk: A Meta-Analysis
title_full_unstemmed Association between BMP4 rs17563 Polymorphism and NSCL/P Risk: A Meta-Analysis
title_short Association between BMP4 rs17563 Polymorphism and NSCL/P Risk: A Meta-Analysis
title_sort association between bmp4 rs17563 polymorphism and nscl/p risk: a meta-analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4306361/
https://www.ncbi.nlm.nih.gov/pubmed/25648829
http://dx.doi.org/10.1155/2015/763090
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