Chronic kidney disease and incident cancer risk: an individual participant data meta-analysis
- PMID: 40914744
- DOI: 10.1038/s41416-025-03140-z
Chronic kidney disease and incident cancer risk: an individual participant data meta-analysis
Abstract
Background: Studies examining the association of chronic kidney disease (CKD) with cancer risk have demonstrated conflicting results.
Methods: This was an individual participant data meta-analysis including 54 international cohorts contributing to the CKD Prognosis Consortium. Included cohorts had data on albuminuria [urine albumin-to-creatinine ratio (ACR)], estimated glomerular filtration rate (eGFR), overall and site-specific cancer incidence, and established risk factors for cancer. Included participants were aged 18 years or older, without previous cancer or kidney failure.
Results: Among 1,319,308 individuals, the incidence rate of overall cancer was 17.3 per 1000 person-years. Higher ACR was positively associated with cancer risk [adjusted hazard ratio 1.08 (95% CI 1.06-1.10) per 8-fold increase in ACR]. No association of eGFR with overall cancer risk was seen. For site-specific cancers, lower eGFR was associated with urological cancer and multiple myeloma, whereas higher ACR was associated with many cancer types (kidney, head/neck, colorectal, liver, pancreas, bile duct, stomach, larynx, lung, hemolymphatic, leukaemia, and multiple myeloma). Results were similar in a 1-year landmark analysis.
Discussion: Albuminuria, but not necessarily eGFR, was independently associated with the subsequent risk of cancer. Our results warrant an investigation into mechanisms that explain the link between albuminuria and cancer.
© 2025. The Author(s).
Conflict of interest statement
Competing interests: Dr. Ärnlöv has received lecturing fees from AstraZeneca and Boehringer Ingelheim and served on advisory boards for AstraZeneca, Boehringer Ingelheim and Astella, all unrelated to the present paper. Dr. Bell has received consultancy fees from Astra Zeneca, GSK and Bayer. Dr. Staplin has received funding in the form of grants from Boehringer Ingelheim, Eli Lilly, and Novo Nordisk. She follows a long-term departmental policy to decline honoraria from the drug and food industry, except for reasonable travel expenses for meetings. All other authors have no disclosures to report. Consent for publication: Not applicable, all aggregate data. Ethics approval and consent to participate: This study was approved for use of de-identified or limited data with a waiver of informed consent by the institutional review board at New York University. All methods were performed in accordance with the relevant guidelines and regulations.
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Grants and funding
- R01DK100446/U.S. Department of Health & Human Services | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (National Institute of Diabetes & Digestive & Kidney Diseases)
- R01DK100446/U.S. Department of Health & Human Services | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (National Institute of Diabetes & Digestive & Kidney Diseases)
- 301005/Z/23/Z/Wellcome Trust (Wellcome)
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