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BMP4 Was Associated with NSCL/P in an Asian Population
BACKGROUND: The Bone Morphogenetic Protein 4 gene (BMP4) is located in chromosome 14q22-q23 which has shown evidence of linkage for isolated nonsyndromic cleft lip with or without cleft palate (NSCL/P) in a genome wide linkage analysis of human multiplex families. BMP4 has been shown to play crucial...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3325933/ https://www.ncbi.nlm.nih.gov/pubmed/22514733 http://dx.doi.org/10.1371/journal.pone.0035347 |
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author | Chen, Qianqian Wang, Hong Hetmanski, Jacqueline B. Zhang, Tianxiao Ruczinski, Ingo Schwender, Holger Liang, Kung Yee Fallin, M. Daniele Redett, Richard J. Raymond, Gerald V. Wu Chou, Yah-Huei Chen, Philip Kuo-Ting Yeow, Vincent Chong, Samuel S. Cheah, Felicia S. H. Jabs, Ethylin Wang Scott, Alan F. Beaty, Terri H. |
author_facet | Chen, Qianqian Wang, Hong Hetmanski, Jacqueline B. Zhang, Tianxiao Ruczinski, Ingo Schwender, Holger Liang, Kung Yee Fallin, M. Daniele Redett, Richard J. Raymond, Gerald V. Wu Chou, Yah-Huei Chen, Philip Kuo-Ting Yeow, Vincent Chong, Samuel S. Cheah, Felicia S. H. Jabs, Ethylin Wang Scott, Alan F. Beaty, Terri H. |
author_sort | Chen, Qianqian |
collection | PubMed |
description | BACKGROUND: The Bone Morphogenetic Protein 4 gene (BMP4) is located in chromosome 14q22-q23 which has shown evidence of linkage for isolated nonsyndromic cleft lip with or without cleft palate (NSCL/P) in a genome wide linkage analysis of human multiplex families. BMP4 has been shown to play crucial roles in lip and palatal development in animal models. Several candidate gene association analyses also supported its potential risk for NSCL/P, however, results across these association studies have been inconsistent. The aim of the current study was to test for possible association between markers in and around the BMP4 gene and NSCL/P in Asian and Maryland trios. METHODOLOGY/PRINCIPAL FINDINGS: Family Based Association Test was used to test for deviation from Mendelian assortment for 12 SNPs in and around BMP4. Nominal significant evidence of linkage and association was seen for three SNPs (rs10130587, rs2738265 and rs2761887) in 221 Asian trios and for one SNP (rs762642) in 76 Maryland trios. Statistical significance still held for rs10130587 after Bonferroni correction (corrected p = 0.019) among the Asian group. Estimated odds ratio for carrying the apparent high risk allele at this SNP was 1.61 (95%CI = 1.20, 2.18). CONCLUSIONS: Our results provided further evidence of association between BMP4 and NSCL/P. |
format | Online Article Text |
id | pubmed-3325933 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-33259332012-04-18 BMP4 Was Associated with NSCL/P in an Asian Population Chen, Qianqian Wang, Hong Hetmanski, Jacqueline B. Zhang, Tianxiao Ruczinski, Ingo Schwender, Holger Liang, Kung Yee Fallin, M. Daniele Redett, Richard J. Raymond, Gerald V. Wu Chou, Yah-Huei Chen, Philip Kuo-Ting Yeow, Vincent Chong, Samuel S. Cheah, Felicia S. H. Jabs, Ethylin Wang Scott, Alan F. Beaty, Terri H. PLoS One Research Article BACKGROUND: The Bone Morphogenetic Protein 4 gene (BMP4) is located in chromosome 14q22-q23 which has shown evidence of linkage for isolated nonsyndromic cleft lip with or without cleft palate (NSCL/P) in a genome wide linkage analysis of human multiplex families. BMP4 has been shown to play crucial roles in lip and palatal development in animal models. Several candidate gene association analyses also supported its potential risk for NSCL/P, however, results across these association studies have been inconsistent. The aim of the current study was to test for possible association between markers in and around the BMP4 gene and NSCL/P in Asian and Maryland trios. METHODOLOGY/PRINCIPAL FINDINGS: Family Based Association Test was used to test for deviation from Mendelian assortment for 12 SNPs in and around BMP4. Nominal significant evidence of linkage and association was seen for three SNPs (rs10130587, rs2738265 and rs2761887) in 221 Asian trios and for one SNP (rs762642) in 76 Maryland trios. Statistical significance still held for rs10130587 after Bonferroni correction (corrected p = 0.019) among the Asian group. Estimated odds ratio for carrying the apparent high risk allele at this SNP was 1.61 (95%CI = 1.20, 2.18). CONCLUSIONS: Our results provided further evidence of association between BMP4 and NSCL/P. Public Library of Science 2012-04-13 /pmc/articles/PMC3325933/ /pubmed/22514733 http://dx.doi.org/10.1371/journal.pone.0035347 Text en Chen et al. http://creativecommons.org/licenses/by/4.0/ 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 author and source are properly credited. |
spellingShingle | Research Article Chen, Qianqian Wang, Hong Hetmanski, Jacqueline B. Zhang, Tianxiao Ruczinski, Ingo Schwender, Holger Liang, Kung Yee Fallin, M. Daniele Redett, Richard J. Raymond, Gerald V. Wu Chou, Yah-Huei Chen, Philip Kuo-Ting Yeow, Vincent Chong, Samuel S. Cheah, Felicia S. H. Jabs, Ethylin Wang Scott, Alan F. Beaty, Terri H. BMP4 Was Associated with NSCL/P in an Asian Population |
title |
BMP4 Was Associated with NSCL/P in an Asian Population |
title_full |
BMP4 Was Associated with NSCL/P in an Asian Population |
title_fullStr |
BMP4 Was Associated with NSCL/P in an Asian Population |
title_full_unstemmed |
BMP4 Was Associated with NSCL/P in an Asian Population |
title_short |
BMP4 Was Associated with NSCL/P in an Asian Population |
title_sort | bmp4 was associated with nscl/p in an asian population |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3325933/ https://www.ncbi.nlm.nih.gov/pubmed/22514733 http://dx.doi.org/10.1371/journal.pone.0035347 |
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