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Gene variants as risk factors for gastroschisis

In a population‐based case‐control study in California of 228 infants, we investigated 75 genetic variants in 20 genes and risk of gastroschisis with regard to maternal age, race/ethnicity, vitamin use, and smoking exposure. We hypothesized that genes related to vascular compromise may interact with...

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Autores principales: Padula, Amy M., Yang, Wei, Schultz, Kathleen, Tom, Lauren, Lin, Bin, Carmichael, Suzan L., Lammer, Edward J., Shaw, Gary M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5096035/
https://www.ncbi.nlm.nih.gov/pubmed/27616475
http://dx.doi.org/10.1002/ajmg.a.37883
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author Padula, Amy M.
Yang, Wei
Schultz, Kathleen
Tom, Lauren
Lin, Bin
Carmichael, Suzan L.
Lammer, Edward J.
Shaw, Gary M.
author_facet Padula, Amy M.
Yang, Wei
Schultz, Kathleen
Tom, Lauren
Lin, Bin
Carmichael, Suzan L.
Lammer, Edward J.
Shaw, Gary M.
author_sort Padula, Amy M.
collection PubMed
description In a population‐based case‐control study in California of 228 infants, we investigated 75 genetic variants in 20 genes and risk of gastroschisis with regard to maternal age, race/ethnicity, vitamin use, and smoking exposure. We hypothesized that genes related to vascular compromise may interact with environmental factors to affect the risk of gastroschisis. Haplotypes were constructed for 75 gene variants using the HaploView program. Risk for gastroschisis associated with each gene variant was calculated for both the homozygotes and the heterozygotes, with the homozygous wildtypes as the referent. Risks were estimated as odds ratios (ORs) with 95% confidence intervals (CIs) by logistic regression. We found 11 gene variants with increased risk and four variants with decreased risk of gastroschisis for heterozygous (OR(h)) or homozygous variants (OR(v)) genotypes. These included NOS3 (rs1036145) OR(h) = 0.4 (95% CI: 0.2–0.7); NOS3 (rs10277237) OR(v) = 2.7 (95% CI: 1.3–6.0); ADD1 (rs12503220) OR(h) = 2.9 (95% CI: 1.6–5.4), GNB3 (rs5443) OR(h) = 0.2 (95% CI: 0.1–0.5), OR(v) = 0.4 (95% CI: 0.2–0.9); ICAM1 (rs281428) OR(v) = 6.9 (95% CI: 2.1–22.9), ICAM1 (rs3093030) OR(v) = 2.6 (95% CI: 1.2–5.6); ICAM4 (rs281438) OR(v) = 4.9 (95% CI: 1.4–16.6), ICAM5 (rs281417) OR(h) = 2.1 (95% CI: 1.1–4.1), OR(v) = 4.8 (95% CI: 1.7–13.6); ICAM5 (rs281440) OR(h) = 23.7 (95% CI: 5.5–102.5), OR(v) = 20.6 (95% CI: 3.4–124.3); ICAM5 (rs2075741) OR(v) = 2.2 (95% CI: 1.1–4.4); NAT1 OR(v) = 0.3 (95% CI: 0.1–0.9). There were additional associations between several gene variants and gastroschisis among women aged 20–24 and among mothers with and without vitamin use. NOS3, ADD1, ICAM1, ICAM4, and ICAM5 warrant further investigation in additional populations and with the interaction of additional environmental exposures. © 2016 Wiley Periodicals, Inc.
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spelling pubmed-50960352016-11-09 Gene variants as risk factors for gastroschisis Padula, Amy M. Yang, Wei Schultz, Kathleen Tom, Lauren Lin, Bin Carmichael, Suzan L. Lammer, Edward J. Shaw, Gary M. Am J Med Genet A Special Series Dedicated to Edward Lammer In a population‐based case‐control study in California of 228 infants, we investigated 75 genetic variants in 20 genes and risk of gastroschisis with regard to maternal age, race/ethnicity, vitamin use, and smoking exposure. We hypothesized that genes related to vascular compromise may interact with environmental factors to affect the risk of gastroschisis. Haplotypes were constructed for 75 gene variants using the HaploView program. Risk for gastroschisis associated with each gene variant was calculated for both the homozygotes and the heterozygotes, with the homozygous wildtypes as the referent. Risks were estimated as odds ratios (ORs) with 95% confidence intervals (CIs) by logistic regression. We found 11 gene variants with increased risk and four variants with decreased risk of gastroschisis for heterozygous (OR(h)) or homozygous variants (OR(v)) genotypes. These included NOS3 (rs1036145) OR(h) = 0.4 (95% CI: 0.2–0.7); NOS3 (rs10277237) OR(v) = 2.7 (95% CI: 1.3–6.0); ADD1 (rs12503220) OR(h) = 2.9 (95% CI: 1.6–5.4), GNB3 (rs5443) OR(h) = 0.2 (95% CI: 0.1–0.5), OR(v) = 0.4 (95% CI: 0.2–0.9); ICAM1 (rs281428) OR(v) = 6.9 (95% CI: 2.1–22.9), ICAM1 (rs3093030) OR(v) = 2.6 (95% CI: 1.2–5.6); ICAM4 (rs281438) OR(v) = 4.9 (95% CI: 1.4–16.6), ICAM5 (rs281417) OR(h) = 2.1 (95% CI: 1.1–4.1), OR(v) = 4.8 (95% CI: 1.7–13.6); ICAM5 (rs281440) OR(h) = 23.7 (95% CI: 5.5–102.5), OR(v) = 20.6 (95% CI: 3.4–124.3); ICAM5 (rs2075741) OR(v) = 2.2 (95% CI: 1.1–4.4); NAT1 OR(v) = 0.3 (95% CI: 0.1–0.9). There were additional associations between several gene variants and gastroschisis among women aged 20–24 and among mothers with and without vitamin use. NOS3, ADD1, ICAM1, ICAM4, and ICAM5 warrant further investigation in additional populations and with the interaction of additional environmental exposures. © 2016 Wiley Periodicals, Inc. John Wiley and Sons Inc. 2016-09-12 2016-11 /pmc/articles/PMC5096035/ /pubmed/27616475 http://dx.doi.org/10.1002/ajmg.a.37883 Text en © 2016 The Authors. American Journal of Medical Genetics Part A Published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Special Series Dedicated to Edward Lammer
Padula, Amy M.
Yang, Wei
Schultz, Kathleen
Tom, Lauren
Lin, Bin
Carmichael, Suzan L.
Lammer, Edward J.
Shaw, Gary M.
Gene variants as risk factors for gastroschisis
title Gene variants as risk factors for gastroschisis
title_full Gene variants as risk factors for gastroschisis
title_fullStr Gene variants as risk factors for gastroschisis
title_full_unstemmed Gene variants as risk factors for gastroschisis
title_short Gene variants as risk factors for gastroschisis
title_sort gene variants as risk factors for gastroschisis
topic Special Series Dedicated to Edward Lammer
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5096035/
https://www.ncbi.nlm.nih.gov/pubmed/27616475
http://dx.doi.org/10.1002/ajmg.a.37883
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