Key result
Baseline frailty was an independent risk factor for transitioning from no cardiometabolic disease to a single disease (HR 1.94, p<0.001) and subsequent progression to multimorbidity and death.
Why the study?
Although frailty is associated with cardiometabolic diseases, there were no systematic analyses estimating its role in the incidence, progression, and prognosis of cardiometabolic multimorbidity.
Does frailty increase the risk of incidence, progression, and mortality of cardiometabolic multimorbidity in adults without baseline cardiometabolic disease?
Cohort (n=351,205)
Yes
Does frailty increase the risk of incidence, progression, and mortality of cardiometabolic multimorbidity in adults without baseline cardiometabolic disease?
Hazard Ratio: 1.94
p-value: p=<0.001
Frailty is an independent risk factor for the incidence, progression, and mortality of cardiometabolic multimorbidity, suggesting frailty-targeted management could aid in primary and secondary prevention.
Frailty assessment may identify patients at higher CMM risk; leaves open whether frailty modification alters progression.
BACKGROUND: Although frailty was associated with cardiometabolic diseases (CMDs, including coronary heart disease, stroke, and diabetes here), there was no systematic analyses estimating its role in incidence, progression, and prognosis of cardiometabolic multimorbidity (CMM). METHODS: We included 351 205 participants without CMDs at baseline in UK Biobank. Occurrences of first CMD, CMM, and death were recorded. We used multistate models to assess transition-specific role of baseline frailty measured by frailty phenotype and frailty index in CMM progression trajectory from no disease to single CMD, CMM, and death. Association between changes in frailty and outcomes was investigated among 17 264 participants. RESULTS: Among 351 205 participants (44.0% male, mean age 56.55 years), 8 190 (2.3%) had frail phenotype, and 13 615 (3.9%) were moderate/severe frail according to the frailty index. During median follow-up of 13.11 years, 41 558 participants experienced ≥1 CMD, 4 952 had CMM, and 20 670 died. In multistate models, frail phenotype-related hazard ratios were 1.94 and 2.69 for transitions from no CMD to single disease and death, 1.63 and 1.67 for transitions from single CMD to CMM and death, and 1.57 for transitions from CMM to death (all p < .001). Consistent results were observed for frailty index. Improvement of frailty reduced the risk of CMD progression and death. CONCLUSIONS: Frailty is an independent risk factor for all transitions of CMM progression trajectory. Frailty-targeted management is a potential strategy for primary and secondary prevention of CMM beyond chronological age.
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Ma et al. (2023) conducted a cohort in Cardiometabolic multimorbidity (n=351,205). Frailty vs. Non-frail was evaluated on Transition from no cardiometabolic disease to single disease (HR 1.94, p=<0.001). Baseline frailty was an independent risk factor for transitioning from no cardiometabolic disease to a single disease (HR 1.94, p<0.001) and subsequent progression to multimorbidity and death.
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