The mediating role of neuroimaging-derived biological brain age in the association between risk factors for dementia and cognitive decline in middle-aged and older individuals without cognitive impairment: a cohort study

IF 13.4 Q1 GERIATRICS & GERONTOLOGY Lancet Healthy Longevity Pub Date : 2024-03-28 DOI:10.1016/S2666-7568(24)00025-4
Irene Cumplido-Mayoral MSc , Anna Brugulat-Serrat PhD , Gonzalo Sánchez-Benavides PhD , Armand González-Escalante MSc , Federica Anastasi PhD , Marta Milà-Alomà PhD , David López-Martos MSc , Muge Akinci MSc , Carles Falcón PhD , Mahnaz Shekari MSc , Raffaele Cacciaglia PhD , Eider M Arenaza-Urquijo PhD , Carolina Minguillón PhD , Karine Fauria PhD , José Luis Molinuevo MD PhD , Marc Suárez-Calvet MD PhD , Oriol Grau-Rivera MD PhD , Verónica Vilaplana PhD , Juan Domingo Gispert PhD , N VILOR TEJEDOR
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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.</p></div><div><h3>Findings</h3><p>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. 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Abstract

Background

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.

Methods

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.

Findings

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.

Interpretation

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.

Funding

La Caixa Foundation, the TriBEKa Imaging Platform, and the Universities and Research Secretariat of the Catalan Government.

Translation

For the Spanish translation of the abstract see Supplementary Materials section.

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无认知障碍的中老年人痴呆症风险因素与认知能力下降之间的联系:一项队列研究
背景基于神经影像学的脑年龄δ已被证明是心血管风险因素与认知功能之间的中介。我们的目的是评估脑年龄δ在无症状的中老年人中可改变的痴呆风险因素与纵向认知功能下降之间的关联中的中介作用,并按阿尔茨海默病病理分层。在这项队列研究中,我们纳入了年龄在 45 岁至 65 岁之间、认知功能未受损的 ALFA+ 队列中的参与者,他们均在 1 年内完成了结构性核磁共振成像、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。纳入者在2016年10月25日至2020年1月28日期间接受了首次评估,并在3-28(SD 0-27)年后接受了随访认知评估。我们计算了脑年龄δ和不同认知功能领域(临床前阿尔茨海默氏症认知综合征 [PACC]、注意力、执行功能、外显记忆、视觉处理和语言)的复合值。我们使用偏最小二乘法路径模型来探讨可改变的风险因素(包括心血管、心理健康、情绪、代谢或内分泌病史以及饮酒)与认知综合能力变化之间的中介效应。为了评估阿尔茨海默病病理学的作用,我们分别计算了 Aβ 阴性和 Aβ 阳性个体的模型。在Aβ阳性者中,脑年龄δ部分介导了可改变的风险因素与总体认知能力下降之间的关系(跨认知领域)(介导比例为15-73% [95% CI 14-22-16-66])。脑年龄δ完全介导了(介导比例为 28-03% [26-25-29-21])可改变的风险因素对 PACC 的影响,其中风险因素值的增加与脑年龄δ的增大相关,因此,脑年龄δ的增大与 PACC 下降的幅度增大相关。这种效应似乎主要是由记忆力下降引起的。虽然路径系数与 Aβ 阳性组的路径系数没有显著差异,但 Aβ 阴性者(3-52% [0-072-4-17])对 PACC 的中介作用并不明显。在无症状的 Aβ 阳性中老年人中,病理学可能是认知能力下降的最强驱动因素,而风险因素的影响较小。我们的研究结果凸显了脑年龄δ作为针对认知能力下降的预防性生活方式干预的客观结果测量指标的潜力。资金来源La Caixa基金会、TriBEKa成像平台和加泰罗尼亚政府大学与研究秘书处。
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来源期刊
Lancet Healthy Longevity
Lancet Healthy Longevity GERIATRICS & GERONTOLOGY-
CiteScore
16.30
自引率
2.30%
发文量
192
审稿时长
12 weeks
期刊介绍: The Lancet Healthy Longevity, a gold open-access journal, focuses on clinically-relevant longevity and healthy aging research. It covers early-stage clinical research on aging mechanisms, epidemiological studies, and societal research on changing populations. The journal includes clinical trials across disciplines, particularly in gerontology and age-specific clinical guidelines. In line with the Lancet family tradition, it advocates for the rights of all to healthy lives, emphasizing original research likely to impact clinical practice or thinking. Clinical and policy reviews also contribute to shaping the discourse in this rapidly growing discipline.
期刊最新文献
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