Association between serum urea concentrations and the risk of colorectal cancer, particularly in individuals with type 2 diabetes: A cohort study

Author:

Gao Peipei12,Mei Zhendong1,Liu Zhenqiu12ORCID,Zhu Dongliang23,Yuan Huangbo12,Zhao Renjia12,Xu Kelin24,Zhang Tiejun23,Jiang Yanfeng12,Suo Chen23ORCID,Chen Xingdong1256ORCID

Affiliation:

1. State Key Laboratory of Genetic Engineering, Human Phenome Institute Fudan University Shanghai China

2. Fudan University Taizhou Institute of Health Sciences Taizhou Jiangsu China

3. Department of Epidemiology and Ministry of Education Key Laboratory of Public Health Safety, School of Public Health Fudan University Shanghai China

4. Department of Biostatistics, School of Public Health Fudan University Shanghai China

5. National Clinical Research Center for Aging and Medicine, Huashan Hospital Fudan University Shanghai China

6. Yiwu Research Institute of Fudan University Yiwu Zhejiang China

Abstract

AbstractDysregulation of the urea cycle (UC) has been detected in colorectal cancer (CRC). However, the impact of the UC's end product, urea, on CRC development remains unclear. We investigated the association between serum urea and CRC risk based on the data of 348 872 participants cancer‐free at recruitment from the UK Biobank. Multivariable Cox proportional hazards models were fitted to conduct risk estimates. Stratification analyses based on sex, diet pattern, metabolic factors (including body mass index [BMI], the estimated glomerular filtration rate [eGFR] and type 2 diabetes [T2D]) and genetic profiles (the polygenic risk score [PRS] of CRC) were conducted to find potential modifiers. During an average of 9.0 years of follow‐up, we identified 3408 (1.0%) CRC incident cases. Serum urea showed a nonlinear relationship with CRC risk (P‐nonlinear: .035). Lower serum urea levels were associated with a higher CRC risk, with a fully‐adjusted hazard ratio (HR) of 1.26 (95% confidence interval [CI]: 1.13‐1.41) in the first quartile (Q1) of urea, compared to the Q4. This association was largely consistent across subgroups of sex, protein diet, BMI, eGFR and CRC‐PRSs (P‐interaction >.05); however, it was stronger in the T2D, with an interaction between urea and T2D on both additive (synergy index: 3.32, [95% CI: 1.24‐8.88]) and multiplicative scales (P‐interaction: .019). Lower serum urea concentrations were associated with an increased risk of CRC, with a more pronounced effect observed in individuals with T2D. Maintaining stable levels of serum urea has important implications for CRC prevention, particularly in individuals with T2D.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Publisher

Wiley

Subject

Cancer Research,Oncology

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