Maternal Smoking During Pregnancy Interacts With Genetic Factors to Increase Risk for Low Birth Weight but Not Harmful Offspring Smoking Behaviors in Europeans.

IF 3 2区 医学 Q2 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
Pamela N Romero Villela, Kristen M Kelly, Jared V Balbona, Marissa A Ehringer, Matthew C Keller
{"title":"Maternal Smoking During Pregnancy Interacts With Genetic Factors to Increase Risk for Low Birth Weight but Not Harmful Offspring Smoking Behaviors in Europeans.","authors":"Pamela N Romero Villela, Kristen M Kelly, Jared V Balbona, Marissa A Ehringer, Matthew C Keller","doi":"10.1093/ntr/ntae310","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Pregnant individuals who smoke face increased health risks because smoking harms both the mother and their developing offspring.</p><p><strong>Aims and methods: </strong>Using 307 417 Europeans from the UK Biobank, we examined whether exposure to maternal smoking during pregnancy (MSP) interacts with genetic risk to predict offspring birth weight (BW) and smoking behaviors. We investigated interactions between MSP and genetic risk at multiple levels: single variant, gene level, and polygenic score. We examined self-reported BW, smoking initiation status (SI), age of smoking initiation, cigarettes per day, and smoking cessation status.</p><p><strong>Results: </strong>One locus tagged by single-nucleotide polymorphism rs72689499 on chromosome 14 reached significance for interaction with MSP on the multiplicative (log10) scale for BW (p = 5.13 × 10-9). In gene-level testing, three genes on chromosome 1 and one gene on chromosome 14 reached significance for interaction with MSP on both the additive and multiplicative scale for BW. These genes include PTCH2, EIF2B3, PLK3, and TSHR. Single-nucleotide polymorphism and gene-level results were insignificant for all offspring smoking behaviors. We also detected an interaction between polygenic risk for smoking and MSP on SI on both the additive (p = 4.4 × 10-5) and multiplicative (p = 1.0 × 10-5) scale. We found evidence of gene-environment correlation in the polygenic risk analysis using a post hoc t test which showed that MSP-exposed offspring had a higher SI polygenic risk scores than those unexposed to MSP (p = 5.9 × 10-623).</p><p><strong>Conclusions: </strong>Our results support the main effect of MSP on BW and show a genetic interaction between MSP and genetic factors influencing BW.</p><p><strong>Implications: </strong>We detected interactions between maternal smoking and genetic factors to influence birth weight; these interactions were detectable at both the single-nucleotide polymorphism and gene levels. Many of the genes detected to interact with maternal smoking to influence birth weight have other reported associations with height or smoking-related traits. For smoking initiation, we detected a negative interaction between maternal smoking and polygenic risk, as well as evidence of gene-environment correlation.</p>","PeriodicalId":19241,"journal":{"name":"Nicotine & Tobacco Research","volume":" ","pages":"1795-1804"},"PeriodicalIF":3.0000,"publicationDate":"2025-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12453677/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nicotine & Tobacco Research","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/ntr/ntae310","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction: Pregnant individuals who smoke face increased health risks because smoking harms both the mother and their developing offspring.

Aims and methods: Using 307 417 Europeans from the UK Biobank, we examined whether exposure to maternal smoking during pregnancy (MSP) interacts with genetic risk to predict offspring birth weight (BW) and smoking behaviors. We investigated interactions between MSP and genetic risk at multiple levels: single variant, gene level, and polygenic score. We examined self-reported BW, smoking initiation status (SI), age of smoking initiation, cigarettes per day, and smoking cessation status.

Results: One locus tagged by single-nucleotide polymorphism rs72689499 on chromosome 14 reached significance for interaction with MSP on the multiplicative (log10) scale for BW (p = 5.13 × 10-9). In gene-level testing, three genes on chromosome 1 and one gene on chromosome 14 reached significance for interaction with MSP on both the additive and multiplicative scale for BW. These genes include PTCH2, EIF2B3, PLK3, and TSHR. Single-nucleotide polymorphism and gene-level results were insignificant for all offspring smoking behaviors. We also detected an interaction between polygenic risk for smoking and MSP on SI on both the additive (p = 4.4 × 10-5) and multiplicative (p = 1.0 × 10-5) scale. We found evidence of gene-environment correlation in the polygenic risk analysis using a post hoc t test which showed that MSP-exposed offspring had a higher SI polygenic risk scores than those unexposed to MSP (p = 5.9 × 10-623).

Conclusions: Our results support the main effect of MSP on BW and show a genetic interaction between MSP and genetic factors influencing BW.

Implications: We detected interactions between maternal smoking and genetic factors to influence birth weight; these interactions were detectable at both the single-nucleotide polymorphism and gene levels. Many of the genes detected to interact with maternal smoking to influence birth weight have other reported associations with height or smoking-related traits. For smoking initiation, we detected a negative interaction between maternal smoking and polygenic risk, as well as evidence of gene-environment correlation.

欧洲孕妇孕期吸烟与遗传因素相互作用增加低出生体重风险,但不会增加有害后代吸烟行为。
吸烟的孕妇面临更大的健康风险,因为吸烟对母亲和她们正在发育的后代都有害。方法:使用来自英国生物银行的307417名欧洲人,我们研究了孕期暴露于母亲吸烟(MSP)是否与遗传风险相互作用,以预测后代出生体重(BW)和吸烟行为。我们研究了MSP与遗传风险在多个水平上的相互作用:单变异、基因水平和多基因评分。我们检查了自我报告的体重、开始吸烟状况(SI)、开始吸烟年龄、每天吸烟数和戒烟状况。结果:14号染色体上一个SNP rs72689499标记的位点在体重乘法(log10)标度上与MSP互作具有显著性(p = 5.13 × 10-9)。在基因水平检测中,1号染色体上的3个基因和14号染色体上的1个基因在体重的加性和乘法尺度上均与MSP互作显著。这些基因包括:PTCH2, EIF2B3, PLK3和TSHR。SNP和基因水平结果对所有后代吸烟行为均不显著。我们还发现吸烟的多基因风险与SI上的MSP之间存在相互作用,这在加法(p = 4.4 × 10-5)和乘法(p = 1.0 × 10-5)两个尺度上都存在。通过事后t检验,我们在多基因风险分析中发现了基因与环境相关的证据,结果表明,暴露于MSP的后代的SI PGS高于未暴露于MSP的后代(p = 5.9x10-623)。结论:本研究结果支持MSP对体重的主要影响,并表明MSP与影响体重的遗传因素之间存在遗传互作。意义:我们发现母亲吸烟和遗传因素之间的相互作用会影响出生体重;这些相互作用在SNP和基因水平上都可以检测到。许多被检测到与母亲吸烟相互作用从而影响出生体重的基因,还有其他与身高或吸烟相关特征相关的报道。对于开始吸烟,我们发现了母亲吸烟与多基因风险之间的负交互作用,以及基因与环境相关的证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Nicotine & Tobacco Research
Nicotine & Tobacco Research 医学-公共卫生、环境卫生与职业卫生
CiteScore
8.10
自引率
10.60%
发文量
268
审稿时长
3-8 weeks
期刊介绍: Nicotine & Tobacco Research is one of the world''s few peer-reviewed journals devoted exclusively to the study of nicotine and tobacco. It aims to provide a forum for empirical findings, critical reviews, and conceptual papers on the many aspects of nicotine and tobacco, including research from the biobehavioral, neurobiological, molecular biologic, epidemiological, prevention, and treatment arenas. Along with manuscripts from each of the areas mentioned above, the editors encourage submissions that are integrative in nature and that cross traditional disciplinary boundaries. The journal is sponsored by the Society for Research on Nicotine and Tobacco (SRNT). It publishes twelve times a year.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信