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Early-life tobacco exposure, genetic susceptibility and incident colorectal cancer risk in UK biobank: A prospective cohort analysis.

Cancer epidemiology 2026 Vol.100() p. 102985

Long Y, Zhu Y, Lin M, Li Q, Liang J, Wang C, Zeng R, Luo D, Zhang L, Ma Y, Duan C, Zhu Y, Chen H, Liu J

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[BACKGROUND] Although tobacco exposure is an established risk factor for colorectal cancer (CRC), the specific impact of early-life exposure (from prenatal to adolescence) and its joints with genetic

🔬 핵심 임상 통계 (초록에서 자동 추출 — 원문 검증 권장)
  • 표본수 (n) 429,847
  • p-value P < 0.001
  • p-value P = 0.066
  • 95% CI 1.10-1.30
  • HR 1.19

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BibTeX ↓ RIS ↓
APA Long Y, Zhu Y, et al. (2026). Early-life tobacco exposure, genetic susceptibility and incident colorectal cancer risk in UK biobank: A prospective cohort analysis.. Cancer epidemiology, 100, 102985. https://doi.org/10.1016/j.canep.2025.102985
MLA Long Y, et al.. "Early-life tobacco exposure, genetic susceptibility and incident colorectal cancer risk in UK biobank: A prospective cohort analysis.." Cancer epidemiology, vol. 100, 2026, pp. 102985.
PMID 41485407

Abstract

[BACKGROUND] Although tobacco exposure is an established risk factor for colorectal cancer (CRC), the specific impact of early-life exposure (from prenatal to adolescence) and its joints with genetic susceptibility remains uncertain. This population-based study aimed to investigate the joint effects of early-life tobacco exposure and polygenic risk on CRC.

[METHODS] Data from UK Biobank participants were analyzed to assess tobacco exposure during two periods: prenatal exposure (n = 429,847) and age of smoking initiation (n = 430,672). Using Cox proportional hazards models, the associations between early-life tobacco exposure and CRC incidence were explored. Additionally, we evaluated the mediating role of accelerated biological aging in the link between early-life tobacco exposure and CRC, and further integrated the polygenic risk score (PRS) to assess the joint effects of genetic on CRC risk.

[RESULTS] Early-life tobacco exposure exhibited age-at-initiation-dependent CRC risk associations. Smoking initiation in adolescence [hazard ratios (HR) = 1.13, 95 % confidence intervals (CI): 1.06-1.22], and adulthood (HR = 1.19, 95 % CI: 1.10-1.30) all significantly increased risk (P < 0.001), while in utero exposure and smoking initiation childhood (HR:1.06, 95 % CI: 0.94-1.19, P = 0.372) showed a suggestive but non-significant trend (HR:1.05, 95 % CI: 1.00-1.11, P = 0.066). In the joint analysis, high-PRS individuals with prenatal tobacco exposure had an elevated CRC risk compared to those with low PRS and no exposure (HR 1.28, 95 % CI: 1.16-1.42, P < 0.001). Furthermore, among high-PRS individuals, smoking initiation at any age (childhood, adolescence, or adulthood) increased CRC risk relative to never-smokers with low PRS. Mediation analysis indicated that accelerated biological aging may contribute to the association between smoking initiation at different ages and increased CRC risk.

[CONCLUSION] Early-life tobacco exposure elevated CRC risk, especially in genetically susceptible individuals. These findings underscored the importance of early tobacco prevention and enhanced screening for high genetic-risk populations.

MeSH Terms

Humans; Female; Colorectal Neoplasms; United Kingdom; Male; Genetic Predisposition to Disease; Middle Aged; Prospective Studies; Adult; Prenatal Exposure Delayed Effects; Incidence; Risk Factors; Pregnancy; Adolescent; Biological Specimen Banks; Aged; Smoking; UK Biobank

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