The lifetime accumulation of multimorbidity and its influence on dementia risk: a UK Biobank study.

IF 4.5 Q1 CLINICAL NEUROLOGY
Brain communications Pub Date : 2025-07-16 eCollection Date: 2025-01-01 DOI:10.1093/braincomms/fcaf222
Raihaan Patel, Grace Gillis, Clare E Mackay, Ludovica Griffanti, Congxiyu Wang, Klaus P Ebmeier, Sana Suri
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Abstract

The number of people living with dementia worldwide is projected to reach 150 million by 2050, making prevention a crucial priority for health services. The co-occurrence of two or more chronic health conditions, termed multimorbidity, occurs in up to 80% of dementia patients, making multimorbidity an important risk factor for dementia. However, we lack an understanding of the specific health conditions, and their age of onset, that drive the link between multimorbidity and dementia. Using data from 282 712 participants of the UK Biobank, we defined the sequential patterns of accumulation of 46 chronic conditions over the life course. By grouping individuals based on their life history of chronic illness, we show here that the risk of incident dementia can be stratified by both the type and timing of their accumulated chronic conditions. We identified several distinct clusters of multimorbidity throughout the lifespan (cardiometabolic, mental health, neurovascular, peripheral vascular, eye diseases and low/no multimorbidity). We observed that the odds of developing dementia varied based on when these comorbidities were diagnosed. Until midlife (age 55), the accumulation of cardiometabolic conditions, such as coronary heart disease, atrial fibrillation, and diabetes, was most strongly associated with dementia risk. However, from 55 to 70 years, the accumulation of mental health conditions, such as anxiety and depression, as well as neurovascular conditions, such as stroke and transient ischaemic attack, was associated with an over 2-fold increase in dementia risk compared with low multimorbidity. Importantly, individuals who continuously and sequentially accumulate cardiometabolic, mental health, and neurovascular conditions were at greatest risk. The age-dependent role of multimorbidity in predicting dementia risk could be used for early stratification of individuals into high- and low-risk groups and could inform targeted prevention strategies based on a person's prior history of chronic disease.

多病的终生积累及其对痴呆风险的影响:英国生物银行的一项研究。
到2050年,全球痴呆症患者人数预计将达到1.5亿,这使得预防成为卫生服务的一个关键优先事项。多达80%的痴呆症患者同时出现两种或两种以上的慢性健康状况,称为多重发病,这使得多重发病成为痴呆症的一个重要危险因素。然而,我们对导致多病和痴呆之间联系的具体健康状况及其发病年龄缺乏了解。使用来自英国生物银行282812名参与者的数据,我们定义了46种慢性疾病在生命过程中积累的顺序模式。通过根据慢性疾病的生活史对个体进行分组,我们在这里表明,痴呆事件的风险可以根据慢性疾病的类型和时间来分层。我们在整个生命周期中确定了几个不同的多发病集群(心脏代谢、精神健康、神经血管、周围血管、眼病和低/无多发病)。我们观察到,患痴呆症的几率因这些合并症的诊断时间而异。直到中年(55岁),心脏代谢疾病的积累,如冠心病、心房颤动和糖尿病,与痴呆风险最密切相关。然而,从55岁到70岁,精神健康状况(如焦虑和抑郁)以及神经血管状况(如中风和短暂性缺血发作)的积累与痴呆风险增加2倍以上相关。重要的是,持续累积心脏代谢、心理健康和神经血管疾病的个体风险最大。多病在预测痴呆风险中的年龄依赖性作用可用于将个体早期分层为高风险和低风险组,并可根据个人既往慢性病史提供有针对性的预防策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
7.00
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0.00%
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