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Genome-wide Interaction Study Implicates VGLL2 and Alcohol Exposure and PRL and Smoking in Orofacial Cleft Risk
Non-syndromic cleft lip with or without cleft palate (NSCL/P) is a common birth defect, affecting approximately 1 in 700 births. NSCL/P has complex etiology including several known genes and environmental factors; however, known genetic risk variants only account for a small fraction of the heritabi...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8866867/ https://www.ncbi.nlm.nih.gov/pubmed/35223824 http://dx.doi.org/10.3389/fcell.2022.621261 |
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author | Carlson, Jenna C. Shaffer, John R. Deleyiannis, Fred Hecht, Jacqueline T. Wehby, George L. Christensen, Kaare Feingold, Eleanor Weinberg, Seth M. Marazita, Mary L. Leslie, Elizabeth J. |
author_facet | Carlson, Jenna C. Shaffer, John R. Deleyiannis, Fred Hecht, Jacqueline T. Wehby, George L. Christensen, Kaare Feingold, Eleanor Weinberg, Seth M. Marazita, Mary L. Leslie, Elizabeth J. |
author_sort | Carlson, Jenna C. |
collection | PubMed |
description | Non-syndromic cleft lip with or without cleft palate (NSCL/P) is a common birth defect, affecting approximately 1 in 700 births. NSCL/P has complex etiology including several known genes and environmental factors; however, known genetic risk variants only account for a small fraction of the heritability of NSCL/P. It is commonly suggested that gene-by-environment (G×E) interactions may help explain some of the “missing” heritability of NSCL/P. We conducted a genome-wide G×E interaction study in cases and controls of European ancestry with three common maternal exposures during pregnancy: alcohol, smoking, and vitamin use using a two-stage design. After selecting 127 loci with suggestive 2df tests for gene and G x E effects, 40 loci showed significant G x E effects after correcting for multiple tests. Notable interactions included SNPs of 6q22 near VGLL2 with alcohol and 6p22.3 near PRL with smoking. These interactions could provide new insights into the etiology of CL/P and new opportunities to modify risk through behavioral changes. |
format | Online Article Text |
id | pubmed-8866867 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-88668672022-02-25 Genome-wide Interaction Study Implicates VGLL2 and Alcohol Exposure and PRL and Smoking in Orofacial Cleft Risk Carlson, Jenna C. Shaffer, John R. Deleyiannis, Fred Hecht, Jacqueline T. Wehby, George L. Christensen, Kaare Feingold, Eleanor Weinberg, Seth M. Marazita, Mary L. Leslie, Elizabeth J. Front Cell Dev Biol Cell and Developmental Biology Non-syndromic cleft lip with or without cleft palate (NSCL/P) is a common birth defect, affecting approximately 1 in 700 births. NSCL/P has complex etiology including several known genes and environmental factors; however, known genetic risk variants only account for a small fraction of the heritability of NSCL/P. It is commonly suggested that gene-by-environment (G×E) interactions may help explain some of the “missing” heritability of NSCL/P. We conducted a genome-wide G×E interaction study in cases and controls of European ancestry with three common maternal exposures during pregnancy: alcohol, smoking, and vitamin use using a two-stage design. After selecting 127 loci with suggestive 2df tests for gene and G x E effects, 40 loci showed significant G x E effects after correcting for multiple tests. Notable interactions included SNPs of 6q22 near VGLL2 with alcohol and 6p22.3 near PRL with smoking. These interactions could provide new insights into the etiology of CL/P and new opportunities to modify risk through behavioral changes. Frontiers Media S.A. 2022-02-10 /pmc/articles/PMC8866867/ /pubmed/35223824 http://dx.doi.org/10.3389/fcell.2022.621261 Text en Copyright © 2022 Carlson, Shaffer, Deleyiannis, Hecht, Wehby, Christensen, Feingold, Weinberg, Marazita and Leslie. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Carlson, Jenna C. Shaffer, John R. Deleyiannis, Fred Hecht, Jacqueline T. Wehby, George L. Christensen, Kaare Feingold, Eleanor Weinberg, Seth M. Marazita, Mary L. Leslie, Elizabeth J. Genome-wide Interaction Study Implicates VGLL2 and Alcohol Exposure and PRL and Smoking in Orofacial Cleft Risk |
title | Genome-wide Interaction Study Implicates VGLL2 and Alcohol Exposure and PRL and Smoking in Orofacial Cleft Risk |
title_full | Genome-wide Interaction Study Implicates VGLL2 and Alcohol Exposure and PRL and Smoking in Orofacial Cleft Risk |
title_fullStr | Genome-wide Interaction Study Implicates VGLL2 and Alcohol Exposure and PRL and Smoking in Orofacial Cleft Risk |
title_full_unstemmed | Genome-wide Interaction Study Implicates VGLL2 and Alcohol Exposure and PRL and Smoking in Orofacial Cleft Risk |
title_short | Genome-wide Interaction Study Implicates VGLL2 and Alcohol Exposure and PRL and Smoking in Orofacial Cleft Risk |
title_sort | genome-wide interaction study implicates vgll2 and alcohol exposure and prl and smoking in orofacial cleft risk |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8866867/ https://www.ncbi.nlm.nih.gov/pubmed/35223824 http://dx.doi.org/10.3389/fcell.2022.621261 |
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