Investigating Mediating Factors in the Genetic Link Between Maternal Smoking Around Birth and Offspring's Cardiovascular Disease Risk

Clicks: 7
ID: 332266
2026
Article Quality & Performance Metrics
Overall Quality
Not rated
Combines reader engagement with the AI quality analysis. This article has not been analysed, so there is no overall score — reader engagement is measured and shown alongside.
AI Quality Assessment
Not analyzed
Readership in this journal
Emerging

Ranked #156 of 160 articles by views in nicotine & tobacco research : official journal of the society for research on nicotine and tobacco

Most read Least read

Bar heights use a square-root scale. Only the 120 most-read articles are drawn; the journal has 160 in total.

Mint this article as an NFT
Not yet minted

Create a permanent, verifiable on-chain record of this article on the Scimatic Network. The NFT is held in your Journament account, and you can withdraw it to your own wallet at any time.

5 SUSD one-off · no wallet required
Abstract
Abstract Introduction Maternal smoking around birth (MSAB) has been associated with adverse offspring health outcomes, but whether it causally increases offspring cardiovascular disease (CVD) risk remains unclear. We evaluated genetic associations of an MSAB proxy on offspring CVDs and explored potential mediating pathways. Methods We conducted a two-sample Mendelian randomization (MR) study using large genome-wide association study datasets predominantly of European ancestry. Genetic instruments for MSAB were obtained from offspring genotypes associated with reported maternal smoking around birth in the UK Biobank. Outcomes included atrial fibrillation (AF), heart failure (HF), coronary artery disease (CAD), and myocardial infarction (MI). Multivariable MR adjusted for offspring smoking initiation, and two-step MR mediation analyses assessed body mass index (BMI), type 2 diabetes mellitus (T2DM), and lipid traits as potential mediators. The inverse-variance weighted method was the primary analysis. Results Genetically predicted MSAB was associated with higher risks of AF (OR=2.23, 95% CI=1.28–3.92, p=4.93×10-3), HF (OR=3.84, 95% CI=1.91–7.76, p=1.70×10-4), and CAD (OR=4.50, 95% CI=1.16–17.51, p=0.03), but not MI. After adjustment for offspring smoking, the associations remained significant for HF (OR=3.88, 95% CI=1.57–9.55, p=3.22×10-3) and CAD (OR=6.23, 95% CI=2.23–17.40, p=4.82×10-4). Mediation analyses suggested that higher BMI and triglycerides, lower HDL-C and ApoA-I, and greater T2DM liability may partly mediate these associations. Conclusions Genetically proxied MSAB was associated with offspring CVD risk, particularly HF and CAD. Adiposity, dyslipidemia, and T2DM may represent important mediating pathways.
Reference Key
openalex_W7221662138 Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Yafang Gao, Zeyan Zhang, Zhiyi Xie, Guangyu Lin, Xiaohong Huang, Tianyu Jin
Journal nicotine & tobacco research : official journal of the society for research on nicotine and tobacco
Year 2026
DOI
10.1093/ntr/ntag226
URL
Keywords Keywords not found

Citations

No citations found. To add a citation, contact the admin at info@scimatic.org

No comments yet. Be the first to comment on this article.