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Genetic susceptibilities in the association between maternal exposure to tobacco smoke and the risk of nonsyndromic oral cleft
Author(s) -
Chevrier Cécile,
Bahuau Michel,
Perret Claire,
Iovannisci David M.,
Nelva Agnès,
Herman Christine,
Vazquez MariePaule,
Francannet Christine,
RobertGnansia Elisabeth,
Lammer Edward J.,
Cordier Sylvaine
Publication year - 2008
Publication title -
american journal of medical genetics part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.064
H-Index - 112
eISSN - 1552-4833
pISSN - 1552-4825
DOI - 10.1002/ajmg.a.32505
Subject(s) - tobacco smoke , association (psychology) , medicine , smoke , environmental health , genetics , biology , psychology , chemistry , organic chemistry , psychotherapist
Abstract Maternal tobacco consumption is considered as a risk factor for nonsyndromic oral clefts. However, this risk is moderate and may be modulated by genetic susceptibilities, including variants of the TGFA , TGFB3 and MSX1 developmental genes and polymorphisms of genes of the CYP ( 1A1, 2E1 ) and GST ( M1 , T1 ) families involved in metabolic pathways of tobacco smoke compounds. This French case–control study (1998–2001; 240 nonsyndromic cases, 236 controls) included a case‐parent design (175 triad‐families) that made it possible to distinguish the direct effect of the child's genotype and maternally mediated effects. Maternal smoking during the first trimester of pregnancy was not associated with the oral cleft risk in this population, but we observed statistically significant increased risks associated with maternal exposure to environmental tobacco smoke (ETS). No variant of any of the three developmental genes was significantly associated with oral cleft. The fetal CYP1A1*2C variant allele was associated with a statistically significant decreased risk, compared with the homozygous wild‐type: relative risk = 0.48, 95% confidence interval: 0.2, 1.0. Suggestive reduced risks were also observed for the maternal CYP1A1*2C allele and the fetal CYP2E1*5 allele. The GSTM1 and GSTT1 deletions appeared to play no role. Our findings suggest some interactions, with the strongest between ETS and CYP1A1 or MSX1 and between maternal smoking and CYP2E1 . We did not confirm the maternal smoking‐infant GSTT1 null interaction previously reported by other investigators. © 2008 Wiley‐Liss, Inc.