Department of Geriatric Medicine, Center of Coronary Circulation, Xiangya Hospital, Central South University, Changsha, Hunan, China.
National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, Hunan, China.
J Gerontol A Biol Sci Med Sci. 2023 Oct 28;78(11):2127-2135. doi: 10.1093/gerona/glad125.
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).
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.
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.
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.
尽管衰弱与心血管代谢疾病(CMD,包括此处的冠心病、中风和糖尿病)相关,但尚无系统分析评估其在心血管代谢性多种疾病(CMM)发病、进展和预后中的作用。
我们纳入了 UK Biobank 中基线时无 CMD 的 351205 名参与者。记录首次发生 CMD、CMM 和死亡的情况。我们使用多状态模型来评估基线衰弱(通过衰弱表型和衰弱指数来衡量)在从无疾病到单一 CMD、CMM 和死亡的 CMM 进展轨迹中的特定状态转换中的作用。在 17264 名参与者中,我们研究了衰弱变化与结局之间的关系。
在 351205 名参与者(44.0%为男性,平均年龄为 56.55 岁)中,8190 名(2.3%)为衰弱表型,13615 名(3.9%)为中度/重度衰弱,根据衰弱指数来判断。在中位数为 13.11 年的随访期间,41558 名参与者经历了≥1 次 CMD,4952 名患有 CMM,20670 名死亡。在多状态模型中,衰弱表型相关的危险比分别为从无 CMD 到单一疾病和死亡的转换为 1.94 和 2.69,从单一 CMD 到 CMM 和死亡的转换为 1.63 和 1.67,从 CMM 到死亡的转换为 1.57(均<0.001)。衰弱指数也观察到了一致的结果。衰弱的改善降低了 CMD 进展和死亡的风险。
衰弱是 CMM 进展轨迹所有状态转换的独立危险因素。衰弱靶向管理可能是一种超越年龄的 CMM 一级和二级预防的策略。