Dong Xiashan, Ma Yiming, Zhang Huizi, Wang Peigang
Department of Social Medicine and Health Management, School of Public Health, Wuhan University, 115 Donghu Road, Wuhan, Hubei, China.
Center for Population and Health Research, Wuhan University, Wuhan, Hubei, China.
Aging Clin Exp Res. 2025 Jul 9;37(1):216. doi: 10.1007/s40520-025-03078-5.
We aimed to trace individual's transition between multimorbidity clusters and examine the addictive and compounding effects of transition trajectories, chronic disease accumulation, and five-year all-cause mortality.
Participants from the China Health and Retirement Longitudinal Study (2011-2020) were included (N = 8988). Latent class analyses, Cox proportional hazard models, and restricted cubic splines were used to examine the associations.
Five clusters were identified: osteoarticular, cardiometabolic, multisystem, digestive, and respiratory. Participants who had multisystem multimorbidity and further developed respiratory diseases had mortality risk 9 times higher than the healthy participants (HR:9.04; 95% CI 3.44-23.73). For participants experienced prolonged cardiometabolic multimorbidity, the mortality risk increased by 26% with each additional chronic disease and by 38% with each additional body system affected between 2011 and 2015.
Subsequent interventions should prioritize those who experienced prolonged multi-system multimorbidity, developed respiratory diseases from existing multi-system conditions, or developed additional chronic diseases from existing cardiometabolic multimorbidity.
我们旨在追踪个体在多种疾病集群之间的转变,并研究转变轨迹、慢性病积累和五年全因死亡率的成瘾性和复合效应。
纳入中国健康与养老追踪调查(2011 - 2020年)的参与者(N = 8988)。采用潜在类别分析、Cox比例风险模型和受限立方样条来检验相关性。
确定了五个集群:骨关节、心脏代谢、多系统、消化和呼吸。患有多系统多种疾病且进一步发展为呼吸系统疾病的参与者的死亡风险比健康参与者高9倍(风险比:9.04;95%置信区间3.44 - 23.73)。对于经历长期心脏代谢多种疾病的参与者,在2011年至2015年期间,每增加一种慢性病,死亡风险增加26%,每增加一个受影响的身体系统,死亡风险增加38%。
后续干预应优先考虑那些经历长期多系统多种疾病、从现有的多系统疾病发展为呼吸系统疾病或从现有的心脏代谢多种疾病发展为其他慢性病的人群。