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Original Article

Gene–gene-environment interactions of prenatal exposed to environmental tobacco smoke, CYP1A1 and GSTs polymorphisms on full-term low birth weight: relationship of maternal passive smoking, gene polymorphisms, and FT-LBW

, , , , , , , , & ORCID Icon show all
Pages 2200-2208 | Received 09 Oct 2017, Accepted 15 Jan 2018, Published online: 30 Jan 2018
 

Abstract

Objective: To examine the interaction effects of prenatal exposed to environmental tobacco smoke (ETS) and genotypes of cytochrome P4501A1 (CYP1A1), glutathione S-transferases (GSTs) on the risk of full-term low birth weight (FT-LBW).

Study design: We conducted a case-control study among pregnant women at two Women and Children’s Hospitals in Guangdong, China (n = 910). Information was collected through interview, medical records review, and blood lab tests. Maternal selfreport and serum cotinine concentration were combined to define prenatal exposed to ETS. Logistic regression approach was applied for statistical analysis.

Results: Our results showed that regardless of genotypes, prenatal exposed to ETS significantly increased the risk of FT-LBW. Then, two-way interactions showed increased prevalence of FT-LBW in prenatal exposed to ETS mothers with the CYP1A1 variant genotype (MspI “CC”), or with GSTT1-null genotype. Furthermore, three-way interactions showed that women with CYP1A1 variant (MspI “TC” or BsrDI “AG”) genotypes and GSTT1 “null” genotype had higher risk to give birth of FT-LBW. Additionally, among nonexposed ETS mothers, genotype did not independently confer adverse effects on FT-LBW.

Conclusions: Our results revealed that prenatal exposed to ETS is independently associated with FT-LBW while gene polymorphisms of CYP1A1 and GSTs merely play modified roles in this process. This study extends understanding of three-way interaction, and stresses the need to tobacco control toward pregnant women for better pregnant outcomes.

Acknowledgements

The authors appreciate the support by Shenzhen Women and Children’s Hospital and Foshan Women and Children’s Hospital.

Disclosure statement

The authors declare no conflict of interest.

Additional information

Funding

This study was supported by the Natural Science Foundation of China (NSFC; grant number: 30872164 and 81172758).

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