Linking epidemiology and genomics of maternal smoking during pregnancy in utero and in ageing: a population-based study using human foetuses and the UK Biobank cohort.

IF 10.8 1区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL EBioMedicine Pub Date : 2025-04-01 Epub Date: 2025-03-12 DOI:10.1016/j.ebiom.2025.105590
Mihail Mihov, Hannah Shoctor, Alex Douglas, David C Hay, Peter J O'Shaughnessy, John P Iredale, Sophie Shaw, Paul A Fowler, Felix Grassmann
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Abstract

Background: Maternal smoking and foetal exposure to nicotine and other harmful chemicals in utero remains a serious public health issue with little knowledge about the underlying genetics and consequences of maternal smoking in ageing individuals. Here, we investigated the epidemiology and genomic architecture of maternal smoking in a middle-aged population and compare the results to effects observed in the developing foetus.

Methods: In the current project, we included 351,562 participants from the UK Biobank (UKB) and estimated exposure to maternal smoking status during pregnancy through self-reporting from the UKB participants about the mother's smoking status around their birth. In addition, we analysed 64 foetal liver transcriptomic expression datasets collected from women seeking elective pregnancy terminations. Foetal maternal smoking exposure was confirmed through measurement of foetal plasma cotinine levels.

Findings: Foetal exposure to maternal smoking had a greater impact on males than females, with more differentially expressed genes in liver tissue (3313 vs. 1163) and higher liver pathway activation. In the UKB, maternal smoking exposure was linked to an unhealthy lifestyle, lower education, and liver damage. In a genome-wide analysis in the UKB, we leveraged the shared genetic basis between affected offspring and their mothers and identified five genome-wide significant regions. We found a low heritability of the trait (∼4%) and implicated several disease-related genes in a transcriptome-wide association study. Maternal smoking increased all-cause mortality risk (Hazard ratio and 95% CI: 1.10 [1.04; 1.16], P = 4.04 × 10-4), which was attenuated in non-smoking males.

Interpretation: Although male foetuses are more affected than females by maternal smoking in pregnancy, this effect was largely reduced in middle-aged individuals. Importantly, our results highlight that the overall 10% increased mortality due to maternal smoking in pregnancy was greatly attenuated in non-smokers. This study demonstrates the importance of campaigns promoting offspring smoking prevention in families where the parent(s) smoke.

Funding: Funding for this project was provided by the University of Aberdeen, the Science Initiative Panel of the Institute of Medical Science, the UK Medical Research Council, the Seventh Framework Programme of the European Union under Grant Agreement 212885 (REEF), NHS Grampian Endowments grants and the European Commission Horizon Europe research grant Agreement 101094099 (INITIALISE).

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连接流行病学和基因组学的孕妇吸烟在子宫内怀孕和老龄化:一项基于人群的研究使用人类胎儿和英国生物银行队列。
背景:母亲吸烟和胎儿在子宫内接触尼古丁和其他有害化学物质仍然是一个严重的公共卫生问题,人们对母亲吸烟对老年人的潜在遗传学和后果知之甚少。在这里,我们调查了中年人群中母亲吸烟的流行病学和基因组结构,并将结果与发育中的胎儿观察到的影响进行了比较。方法:在当前的项目中,我们纳入了来自英国生物银行(UKB)的351562名参与者,并通过UKB参与者自我报告母亲在出生前后的吸烟状况来估计怀孕期间母亲吸烟状况的暴露。此外,我们分析了64个胎儿肝脏转录组表达数据集,这些数据集来自寻求选择性终止妊娠的妇女。通过测量胎儿血浆可替宁水平,证实胎儿母亲吸烟暴露。研究结果:胎儿暴露于母亲吸烟对男性的影响大于女性,肝脏组织中差异表达的基因更多(3313比1163),肝脏通路激活程度更高。在英国,母亲吸烟与不健康的生活方式、低教育水平和肝损伤有关。在UKB的全基因组分析中,我们利用了受影响的后代与其母亲之间的共享遗传基础,并确定了五个全基因组重要区域。在一项全转录组关联研究中,我们发现该性状的遗传力较低(约4%),并涉及几种疾病相关基因。母亲吸烟增加全因死亡风险(危险比和95% CI: 1.10 [1.04;1.16], P = 4.04 × 10-4),在非吸烟男性中有所减弱。解释:虽然怀孕期间母亲吸烟对男性胎儿的影响比女性更大,但这种影响在中年个体中大大降低。重要的是,我们的研究结果强调,孕妇吸烟导致的总体10%的死亡率增加在非吸烟者中大大降低。这项研究表明,在父母吸烟的家庭中,开展预防子女吸烟运动的重要性。资金:该项目的资金由阿伯丁大学、医学科学研究所科学倡议小组、英国医学研究理事会、欧盟第7框架计划(根据212885赠款协议)和NHS格兰平原捐赠基金提供。
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来源期刊
EBioMedicine
EBioMedicine Biochemistry, Genetics and Molecular Biology-General Biochemistry,Genetics and Molecular Biology
CiteScore
17.70
自引率
0.90%
发文量
579
审稿时长
5 weeks
期刊介绍: eBioMedicine is a comprehensive biomedical research journal that covers a wide range of studies that are relevant to human health. Our focus is on original research that explores the fundamental factors influencing human health and disease, including the discovery of new therapeutic targets and treatments, the identification of biomarkers and diagnostic tools, and the investigation and modification of disease pathways and mechanisms. We welcome studies from any biomedical discipline that contribute to our understanding of disease and aim to improve human health.
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