Aug 2026· Cancer Epidemiology, Biomarkers and Prevention· 0 citations
Medicine
TL;DR
An elevated risk of early-onset rectal cancer was suggested in individuals with high birth weight in a nested case-control study that evaluated the association between high birth weight and eoCRC in a nested case-control study.
Abstract
Background: Early-onset colorectal cancer (eoCRC), particularly rectal cancer, is increasing. We evaluated the association between high birth weight and eoCRC in a nested case-control study. Methods: We included patients aged 15–49 years diagnosed with colorectal adenocarcinoma at Kaiser Permanente Southern California (2009–2021). Cancer-free controls were matched 10:1 on age, sex, and length of health plan membership. Record linkage with California Department of Public Health’s birth registry was performed. Conditional logistic regression was used to evaluate associations between high birth weight, measured using (1) macrosomia (birth weight >4,000grams), and (2) large for gestational age (LGA; birth weight above the 90th percentile for gestational age and sex), and overall eoCRC, colon, and rectal cancer. Two-stage model adjustments were performed: first adjusting for pre-specified potential confounders, then adjusting for potential intermediates. Results: Of 1,400 eligible cases and matched 13,608 controls, 471 eoCRC cases (mean diagnosis age: 41.1 years) and 1,931 controls with linked birth certificate were included. Adjusted odds ratio (OR) for eoCRC was 1.32 (95% CI: 0.95–1.84) for macrosomia and 1.38 (0.97–1.98) for LGA. Macrosomia and LGA were associated with a marginal, non-statistically significant elevated risk of rectal cancer [OR (95%CI): 1.69 (0.97–2.97) and 1.81 (0.96–3.41), respectively], but not colon cancer [OR (95%CI): 1.18 (0.78–1.80) and 1.20 (0.77–1.86) for macrosomia and LGA, respectively]. Conclusions: An elevated risk of early-onset rectal cancer was suggested in individuals with high birth weight. Impact: The impact of intrauterine conditions on eoCRC risk should be further evaluated.
Traditional environmental risk factors and established common genetic variants are not associated with the rising incidence of early-onset colorectal cancer, and drivers of early-onset disease might include novel environmental exposures or early-life factors beyond traditional risk assessment.
Anmol Nigam, Chidiebere Onongaya, Pravin Meshram et al.· Diseases of the Colon & Rect...· 0 citations
Current evidence on early-onset colorectal cancer epidemiology, biology, clinical presentation, screening, and treatment is summarized, and emerging directions including liquid biopsy, artificial intelligence, and microbiome-based strategies are highlighted.
Ahmed Sohaib, Ashwaq Salami, Wesal Alghwyeen et al.· Integrated Oncology Diagnost...· 0 citations
The global EOPC burden among WCBA and its links to core metabolic determinants are delineated, providing an evidence base to guide targeted interventions in this priority population and support progress toward international development goals.
Jiaxing Li, Jing Luo, Qi-Hui Hu et al.· PLoS ONE· 0 citations
High UPF intake and cumulative antibiotic exposure independently and synergistically increase odds of EOCRC, with a substantial proportion mediated through systemic inflammation, identify actionable targets for dietary counselling, antibiotic stewardship, and risk-stratified screening in young South Asian adults.
Basit Ur Rehman, Fareed Ullah, Ahmed Shahbaz et al.· Pakistan Journal of Gastroen...· 0 citations
Background: The incidence of early-onset colorectal cancer (eoCRC), diagnosed at age <50 years, is increasing in the United States. Prior studies using national and state cancer databases have observed higher eoCRC mortality after diagnosis among non-Hispanic Black (NHB) patients. These studies, however, often did not...
T. Habeshian, Lan-Fang Xu, K. Cannavale et al.· Journal of Colon and Rectal...· 0 citations
BACKGROUND
/Aims: Few studies have explored how family history of colorectal cancer (CRC) affects CRC incidence in inflammatory bowel disease (IBD). We estimated CRC incidence rates (IRs) and IR differences, by family history of CRC, and the interaction between IBD and family history.
METHODS
Nationwide, register-bas...
Å. H. Everhov, Kári Kristjánsson, J. Ludvigsson et al.· Gastroenterology· 0 citations
We use cookies to run the site and, with your consent, for analytics and to show ads.
See our Cookie Policy.