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
{"title":"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","authors":"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","doi":"10.1016/S2666-7568(24)00025-4","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>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.</p></div><div><h3>Methods</h3><p>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.</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. 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.</p></div><div><h3>Interpretation</h3><p>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.</p></div><div><h3>Funding</h3><p>La Caixa Foundation, the TriBEKa Imaging Platform, and the Universities and Research Secretariat of the Catalan Government.</p></div><div><h3>Translation</h3><p>For the Spanish translation of the abstract see Supplementary Materials section.</p></div>","PeriodicalId":34394,"journal":{"name":"Lancet Healthy Longevity","volume":"5 4","pages":"Pages e276-e286"},"PeriodicalIF":13.4000,"publicationDate":"2024-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2666756824000254/pdfft?md5=75d672e45c0205b8026417d069b00a22&pid=1-s2.0-S2666756824000254-main.pdf","citationCount":"0","resultStr":"{\"title\":\"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\",\"authors\":\"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\",\"doi\":\"10.1016/S2666-7568(24)00025-4\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><p>Neuroimaging-based brain-age delta has been shown to be a mediator linking cardiovascular risk factors to cognitive function. 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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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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
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.
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.