Barcelonaβeta Brain Research Center, Pasqual Maragall Foundation, Barcelona, Spain; Biomedicine, Universitat Pompeu Fabra, Barcelona, Spain; Neuroimagen de Enfermedades Neurodegenerativas y Envejecimiento Saludable, Hospital del Mar Research Institute, Barcelona, Spain.
Barcelonaβeta Brain Research Center, Pasqual Maragall Foundation, Barcelona, Spain; Neuroimagen de Enfermedades Neurodegenerativas y Envejecimiento Saludable, Hospital del Mar Research Institute, Barcelona, Spain; CIBER Fragilidad y Envejecimiento Saludable, Instituto de Salud Carlos III, Madrid, Spain; Global Brain Health Institute, San Francisco, CA, USA.
Lancet Healthy Longev. 2024 Apr;5(4):e276-e286. doi: 10.1016/S2666-7568(24)00025-4.
Neuroimaging-based brain-age delta has been shown to be a mediator linking cardiovascular risk factors to cognitive function. We aimed to assess the mediating role of brain-age delta in the association between modifiable risk factors of dementia and longitudinal cognitive decline in middle-aged and older individuals who are asymptomatic, stratified by Alzheimer's disease pathology. We also explored whether the mediation effect is specific to cognitive domain.
In this cohort study, we included participants from the ALFA+ cohort aged between 45 years and 65 years who were cognitively unimpaired and who had available structural MRI, cerebrospinal fluid β-amyloid (Aβ)42 and Aβ40 measurements obtained within 1 year of each other, modifiable risk factors assessment, and cognitive evaluation over 3 years. Participants were recruited from the Barcelonaβeta Brain Research Center (Barcelona, Spain). Included individuals underwent a first assessment between Oct 25, 2016, and Jan 28, 2020, and a follow-up cognitive assessment 3·28 (SD 0·27) years later. We computed brain-age delta and composites of different cognitive function domains (preclinical Alzheimer's cognitive composite [PACC], attention, executive function, episodic memory, visual processing, and language). We used partial least squares path modelling to explore mediation effects in the associations between modifiable risk factors (including cardiovascular, mental health, mood, metabolic or endocrine history, and alcohol use) and changes in cognitive composites. To assess the role of Alzheimer's disease pathology, we computed separate models for Aβ-negative and Aβ-positive individuals.
Of the 419 participants enrolled in ALFA+, 302 met our inclusion criteria, of which 108 participants were classified as Aβ-positive and 194 as Aβ-negative. In Aβ-positive individuals, brain-age delta partially mediated (percent mediation proportion 15·73% [95% CI 14·22-16·66]) the association between modifiable risk factors and decline in overall cognition (across cognitive domains). Brain-age delta fully mediated (mediation proportion 28·03% [26·25-29·21]) the effect of modifiable risk factors on the PACC, wherein increased values for risk factors correlated with an older brain-age delta, and, consequently, an older brain-age delta was linked to greater PACC decline. This effect appears to be primarily driven by memory decline. Mediation was not significant in Aβ-negative individuals (3·52% [0·072-4·17]) on PACC, although path coefficients were not significantly different from those in the Aβ-positive group.
Our findings suggest that brain-age delta captures the association between modifiable risk factors and longitudinal cognitive decline in middle-aged and older people. In asymptomatic middle-aged and older individuals who are Aβ-positive, the pathology might be the strongest driver of cognitive decline, whereas the effect of risk factors is smaller. Our results highlight the potential of brain-age delta as an objective outcome measure for preventive lifestyle interventions targeting cognitive decline.
La Caixa Foundation, the TriBEKa Imaging Platform, and the Universities and Research Secretariat of the Catalan Government.
For the Spanish translation of the abstract see Supplementary Materials section.
基于神经影像学的大脑年龄差值已被证明是连接心血管风险因素与认知功能的中介。我们旨在评估大脑年龄差值在无症状的中年和老年人中,在可改变的痴呆风险因素与纵向认知下降之间的关联中的中介作用,这些人分层基于阿尔茨海默病病理学。我们还探讨了这种中介效应是否特定于认知领域。
在这项队列研究中,我们纳入了来自 ALFA+ 队列的年龄在 45 岁至 65 岁之间的参与者,他们认知正常,在彼此 1 年内均有结构 MRI、脑脊液β-淀粉样蛋白(Aβ)42 和 Aβ40 测量、可改变的风险因素评估以及 3 年内的认知评估。参与者是从巴塞罗那βeta 脑研究中心(西班牙巴塞罗那)招募的。纳入的个体在 2016 年 10 月 25 日至 2020 年 1 月 28 日之间进行了第一次评估,3.28 年后(标准差为 0.27)进行了后续认知评估。我们计算了大脑年龄差值和不同认知功能领域的综合指标(临床前阿尔茨海默病认知综合指标[PACC]、注意力、执行功能、情景记忆、视觉处理和语言)。我们使用偏最小二乘法路径模型来探索可改变的风险因素(包括心血管、心理健康、情绪、代谢或内分泌病史和饮酒)与认知综合指标变化之间的关联中的中介效应。为了评估阿尔茨海默病病理学的作用,我们为 Aβ 阴性和 Aβ 阳性个体分别计算了单独的模型。
在纳入的 419 名 ALFA+参与者中,有 302 名符合我们的纳入标准,其中 108 名参与者被归类为 Aβ 阳性,194 名参与者被归类为 Aβ 阴性。在 Aβ 阳性个体中,大脑年龄差值部分中介(中介比例 15.73%[95%CI 14.22-16.66])了可改变的风险因素与整体认知下降(跨认知领域)之间的关联。大脑年龄差值完全中介(中介比例 28.03%[26.25-29.21])了风险因素对 PACC 的影响,其中风险因素的增加与大脑年龄差值较大相关,因此,较大的大脑年龄差值与 PACC 下降较大相关。这种效应主要是由记忆下降驱动的。在 Aβ 阴性个体中,PACC 的中介作用不显著(3.52%[0.072-4.17]),尽管路径系数与 Aβ 阳性组没有显著差异。
我们的研究结果表明,大脑年龄差值可以捕捉到中年和老年人中可改变的风险因素与纵向认知下降之间的关联。在无症状的中年和老年人中,如果是 Aβ 阳性,那么病理学可能是认知下降的最强驱动力,而风险因素的影响则较小。我们的结果强调了大脑年龄差值作为针对认知下降的预防性生活方式干预的潜在客观结果衡量标准。
La Caixa 基金会、TriBEKa 成像平台以及加泰罗尼亚政府的大学和研究秘书处。