Key result
Having ≥4 comorbidities in non-dialysis CKD is linked to ~253% higher MACE risk versus 0-1.
Why the study?
The effect of multimorbidity on patients with chronic kidney disease, who are already at high risk for cardiovascular disease, was not well understood.
Does a higher burden of multimorbidity increase the risk of MACE and all-cause mortality in patients with non-dialysis CKD?
Cohort (n=4,420)
Does a higher burden of multimorbidity increase the risk of MACE and all-cause mortality in patients with non-dialysis CKD?
Effect estimate: HR 3.53 (95% CI 2.11-5.91)
In patients with non-dialysis CKD, the presence of multiple comorbidities dose-dependently increases the risk of major adverse cardiovascular events and all-cause mortality.
May inform comorbidity-based risk stratification in non-dialysis CKD; leaves open whether targeted interventions reduce MACE.
INTRODUCTION: Multimorbidity, defined as the presence of two or more chronic conditions, is associated with poor outcomes and increased cardiovascular risk in the general population. However, the effect of multimorbidity on patients with chronic kidney disease (CKD), a group of patients already at high risk for cardiovascular disease, is not well understood. METHODS: We analyzed data from 4,420 patients with non-dialysis CKD enrolled in the Fukuoka Kidney disease Registry Study. We identified 23 comorbidities, including cardiometabolic and non-cardiometabolic conditions. The patients were categorized into four groups according to the number of comorbidities: Group 1 (0-1 comorbidities), Group 2 (2 comorbidities), Group 3 (3 comorbidities), and Group 4 (≥4 comorbidities). We examined the associations between the number of comorbidities and the incidence of major adverse cardiovascular events (MACE) and all-cause mortality using Cox proportional hazards models. RESULTS: Over a 5-year follow-up, 229 patients experienced MACE and 456 died. The risk of MACE increased with the number of comorbidities. The multivariable-adjusted hazard ratios (95% confidence intervals) for MACE were 1.40 (0.80-2.44) for Group 2, 2.27 (1.33-3.88) for Group 3, and 3.53 (2.11-5.91) for Group 4 compared with Group 1. The all-cause mortality risk also increased with the number of comorbidities, with adjusted hazard ratios of 1.13 (0.77-1.66), 1.75 (1.22-2.51), and 2.53 (1.80-3.54) for Groups 2, 3, and 4, respectively. CONCLUSION: In patients with CKD, multimorbidity is associated with an increased risk of MACE and all-cause mortality.
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Okamura et al. (2025) conducted a cohort in non-dialysis chronic kidney disease (CKD) (n=4,420). ≥4 comorbidities vs. 0-1 comorbidities was evaluated on major adverse cardiovascular events (MACE) (HR 3.53, 95% CI 2.11-5.91). In patients with non-dialysis CKD, having ≥4 comorbidities was associated with an increased risk of MACE compared to 0-1 comorbidities (HR 3.53; 95% CI 2.11-5.91).
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