Qing Qi, Feng Deng, Rebecca Sammon, Karen Ritchie, Graciela Muniz-Terrera, Ivan Koychev, Paresh Malhotra, Siobhan Hutchinson, David Robinson, John T O'Brien, Craig W Ritchie, Brian Lawlor, Lorina Naci
{"title":"有阿尔茨海默病遗传风险的中年人的性别和生活方式与认知储备之间的关系。","authors":"Qing Qi, Feng Deng, Rebecca Sammon, Karen Ritchie, Graciela Muniz-Terrera, Ivan Koychev, Paresh Malhotra, Siobhan Hutchinson, David Robinson, John T O'Brien, Craig W Ritchie, Brian Lawlor, Lorina Naci","doi":"10.1186/s13195-024-01610-9","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Females have a higher age-adjusted incidence of Alzheimer's Disease (AD) than males, even when accounting for longer lifespan and, therefore, stand to benefit the most from dementia prevention efforts. As exposure to many modifiable risk factors for dementia begins in mid-life, interventions must be implemented from middle-age. Building cognitive reserve, particularly through stimulating avocational activities and occupational attainment presents a crucial, underexplored, dementia prevention approach for mid-life. It is currently unknown, however, whether modifiable lifestyle factors can protect against AD processes, from mid-life, differentially for females and males who carry inherited risk for late-life dementia. To address this gap, this study investigated the impact of biological sex and APOE4 carrier status on the relationship between stimulating activities, occupational attainment, and cognition in mid-life.</p><p><strong>Methods: </strong>We leveraged the PREVENT-Dementia program, the world's largest study investigating the origins and early diagnosis of dementia in mid-life at-risk individuals (N = 700; 40-59 years). Cognitive performance was measured using the Cognito Battery and the Visual Short Term Memory Binding task. Mid-life specific reserve contributors were assessed via the Lifetime of Experiences Questionnaire.</p><p><strong>Results: </strong>Females had significantly better episodic and relational memory (p < 0.001), and lower occupational attainment than males (p < 0.001). Engagement in stimulating activities was positively associated with episodic and relational memory, regardless of sex and APOE4 status (β = 0.05, CI 0.03-0.07, p < 0.001). APOE4 carriers showed significant sex differences in the association between occupational attainment and episodic and relational memory (β = 0.38, CI 0.12-0.63, p = 0.003). APOE4 carrier females with higher occupational attainment showed better cognition (β = 0.16, CI -0.002-0.32, p = 0.053), whereas APOE4 carrier males showed the opposite effect (β = -0.20, CI -0.40 - -0.001, p = 0.049).</p><p><strong>Conclusion: </strong>Our findings suggest that occupational attainment in mid-life contributes to cognitive reserve against inherited risk of dementia in females, but not males. 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引用次数: 0
摘要
背景:即使考虑到女性的寿命较长,女性经年龄调整后的阿尔茨海默病(AD)发病率也高于男性,因此女性从痴呆症预防工作中获益最大。由于许多可改变的痴呆症风险因素始于中年,因此干预措施必须从中年开始实施。建立认知储备,特别是通过激励性的业余活动和职业成就来建立认知储备,是预防中年痴呆症的一种重要方法,但这种方法尚未得到充分探索。然而,目前尚不清楚可改变的生活方式因素是否能从中年开始,针对女性和男性不同的晚年痴呆症遗传风险,保护他们免受痴呆症进程的影响。为了填补这一空白,本研究调查了生理性别和 APOE4 携带者身份对刺激性活动、职业成就和中年认知之间关系的影响:我们利用了 PREVENT-Dementia 项目,该项目是世界上最大的调查中年高危人群痴呆症起源和早期诊断的研究(N = 700;40-59 岁)。认知能力的测定采用了认知能力测验(Cognito Battery)和视觉短时记忆绑定任务(Visual Short Term Memory Binding task)。通过终生经历问卷对中年特定储备因素进行了评估:结果:女性的历时记忆和关系记忆明显更好(p 结论:我们的研究结果表明,职业成就对中年女性的影响更大:我们的研究结果表明,中年时期的职业成就有助于女性的认知能力储备,从而抵御痴呆症的遗传风险,而男性则不然。这些研究突出表明,有必要采用考虑生理性别和 APOE4 携带者状态的高精度方法,为阿尔茨海默氏症的预防策略和临床试验提供依据。
Associations between sex and lifestyle activities with cognitive reserve in mid-life adults with genetic risk for Alzheimer's disease.
Background: Females have a higher age-adjusted incidence of Alzheimer's Disease (AD) than males, even when accounting for longer lifespan and, therefore, stand to benefit the most from dementia prevention efforts. As exposure to many modifiable risk factors for dementia begins in mid-life, interventions must be implemented from middle-age. Building cognitive reserve, particularly through stimulating avocational activities and occupational attainment presents a crucial, underexplored, dementia prevention approach for mid-life. It is currently unknown, however, whether modifiable lifestyle factors can protect against AD processes, from mid-life, differentially for females and males who carry inherited risk for late-life dementia. To address this gap, this study investigated the impact of biological sex and APOE4 carrier status on the relationship between stimulating activities, occupational attainment, and cognition in mid-life.
Methods: We leveraged the PREVENT-Dementia program, the world's largest study investigating the origins and early diagnosis of dementia in mid-life at-risk individuals (N = 700; 40-59 years). Cognitive performance was measured using the Cognito Battery and the Visual Short Term Memory Binding task. Mid-life specific reserve contributors were assessed via the Lifetime of Experiences Questionnaire.
Results: Females had significantly better episodic and relational memory (p < 0.001), and lower occupational attainment than males (p < 0.001). Engagement in stimulating activities was positively associated with episodic and relational memory, regardless of sex and APOE4 status (β = 0.05, CI 0.03-0.07, p < 0.001). APOE4 carriers showed significant sex differences in the association between occupational attainment and episodic and relational memory (β = 0.38, CI 0.12-0.63, p = 0.003). APOE4 carrier females with higher occupational attainment showed better cognition (β = 0.16, CI -0.002-0.32, p = 0.053), whereas APOE4 carrier males showed the opposite effect (β = -0.20, CI -0.40 - -0.001, p = 0.049).
Conclusion: Our findings suggest that occupational attainment in mid-life contributes to cognitive reserve against inherited risk of dementia in females, but not males. They highlight the need for high precision approaches that consider biological sex and APOE4 carrier status to inform Alzheimer's disease prevention strategies and clinical trials.
期刊介绍:
Alzheimer's Research & Therapy is an international peer-reviewed journal that focuses on translational research into Alzheimer's disease and other neurodegenerative diseases. It publishes open-access basic research, clinical trials, drug discovery and development studies, and epidemiologic studies. The journal also includes reviews, viewpoints, commentaries, debates, and reports. All articles published in Alzheimer's Research & Therapy are included in several reputable databases such as CAS, Current contents, DOAJ, Embase, Journal Citation Reports/Science Edition, MEDLINE, PubMed, PubMed Central, Science Citation Index Expanded (Web of Science) and Scopus.