Frontotemporal structure preservation underlies the protective effect of lifetime intellectual cognitive reserve on cognition in the elderly.

IF 7.9 1区 医学 Q1 CLINICAL NEUROLOGY Alzheimer's Research & Therapy Pub Date : 2024-11-23 DOI:10.1186/s13195-024-01613-6
Dandan Wang, Xin Li, Mingxi Dang, Shaokun Zhao, Feng Sang, Zhanjun Zhang
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Abstract

Background: Cognitive decline with age has heterogeneous, which might be related to the accumulation of protective factors called cognitive reserve, especially intellectual engagement factors over the life course. However, how lifetime intellectual cognitive reserve (LICR) protects cognitive function in the elderly remains unclear. We aimed to examine the relationship between LICR and cognition and the mild cognitive impairment (MCI) risk, as well as the neural mechanism of LICR on cognition.

Methods: A total of 5126 participants completed extensive neuropsychological tests, with LICR indicator encompassing early education, midlife occupational complexity, and mental leisure activities after retirement. Confirmatory factor analysis was performed to derive LICR score and cognitive function scores, then the hierarchical regression analysis was used to explore the relationship between LICR and cognitive functions and the risk of MCI. We further explored the macro- and micro-structural preservation underly LICR in 1117 participants. Multiple regressions and tract-based spatial statistics were used to explore the relationship between LICR and gray matter volume and white matter microstructure (FA value). Finally, using the mediation model to explore the relationship of "LICR-brain-cognition".

Result: The new LICR index, which was more protective than its single indexes, could protect widespread cognitive functions and was associated with a reduction in MCI risk (Odds Ratio, 0.52; 95% CI, 0.47-0.57). For the structure basis of LICR, the higher LICR score was associated with the greater gray matter volume in right fusiform gyrus (t = 4.62, FDR corrected, p < 0.05) and left orbital superior frontal gyrus (t = 4.56, FDR corrected, p < 0.05), and the higher FA values in the frontotemporal related white matter fiber tracts. Furthermore, the right fusiform gyrus partially mediated the relationship between LICR and executive processing ability (β = 0.01, p = 0.02) and general cognitive ability (β = 0.01, p = 0.03).

Conclusions: The new comprehensive cognitive reserve index could promote the temporal macro-structural preservation and thus contribute to maintain better cognitive function. These findings highlight the importance of intellectual CR accumulation over the life course in successful cognitive aging and MCI prevention, thereby contributing to improve the quality of life in the elderly.

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前颞叶结构保护是终生智力认知储备对老年人认知的保护作用的基础。
背景:随着年龄的增长,认知能力的衰退具有多样性,这可能与被称为认知储备的保护性因素的积累有关,特别是在生命过程中的智力参与因素。然而,终生智力认知储备(LICR)如何保护老年人的认知功能仍不清楚。我们旨在研究终生智力认知储备与认知能力和轻度认知障碍(MCI)风险之间的关系,以及终生智力认知储备对认知能力的神经机制:共有5126名参与者完成了广泛的神经心理学测试,其中LICR指标包括早期教育、中年职业复杂性和退休后的精神休闲活动。通过确认性因素分析得出 LICR 评分和认知功能评分,然后采用层次回归分析探讨 LICR 和认知功能与 MCI 风险之间的关系。我们进一步探究了 1117 名参与者的 LICR 的宏观和微观结构保存基础。我们使用多元回归和基于道的空间统计来探讨 LICR 与灰质体积和白质微观结构(FA 值)之间的关系。最后,利用中介模型探讨了 "LICR-脑-认知 "之间的关系:结果:新的 LICR 指数比其单一指数具有更强的保护性,可以保护广泛的认知功能,并与 MCI 风险的降低相关(Odds Ratio,0.52;95% CI,0.47-0.57)。在 LICR 的结构基础上,LICR 分数越高,右侧纺锤回的灰质体积越大(t = 4.62,FDR 校正,p 结论:LICR 分数越高,右侧纺锤回的灰质体积越大,MCI 风险越低:新的认知储备综合指数可促进颞叶宏观结构的保护,从而有助于维持更好的认知功能。这些发现凸显了在认知老化和 MCI 预防过程中智力 CR 积累的重要性,从而有助于提高老年人的生活质量。
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来源期刊
Alzheimer's Research & Therapy
Alzheimer's Research & Therapy 医学-神经病学
CiteScore
13.10
自引率
3.30%
发文量
172
审稿时长
>12 weeks
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.
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