Frailty subtypes and white matter alterations in older adults without dementia.

IF 6.2 3区 医学 Q1 CLINICAL NEUROLOGY
Psychiatry and Clinical Neurosciences Pub Date : 2025-10-01 Epub Date: 2025-07-29 DOI:10.1111/pcn.13876
Chen-Hua Lin, Yah-Ting Wu, Jun-Ying Wei, Yao-Chia Shih, Yi-Ping Chao, Yen-Jun Lai, Yen-Ling Chiu, Yi-Fang Chuang
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引用次数: 0

Abstract

Aim: Frailty increases the risk of cognitive decline in older adults, yet the brain structural patterns associated with different frailty subtypes remain unclear. This study examined white matter (WM) alterations across frailty subtypes in community-dwelling older adults without dementia.

Methods: This cross-sectional study included participants from the Taiwan Precision Medicine Initiative on Cognitive Impairment and Dementia (TPMIC) cohort. Frailty was assessed using Fried's phenotype and classified into mobility, non-mobility, and low physical activity subtypes. Cognitive function (attention, memory, and executive function) was evaluated using standardized neuropsychological tests. WM microstructure was measured using diffusion tensor imaging (DTI) metrics, including fractional anisotropy (FA) and mean diffusivity (MD).

Results: Among 297 participants, 91 (30.6%) were pre-frail/frail. The pre-frail/frail group showed widespread WM alterations, with the internal capsule (IC) remaining significant after full adjustment and FDR correction (q < 0.05). The mobility subtype was associated with poorer cognitive performance across all domains (all P < 0.01) and showed lower FA and higher MD primarily in motor and cognitive-related tracts, such as the corpus callosum (all q < 0.05). In contrast, the non-mobility subtype was associated with poorer attention and executive function, with alterations primarily in emotion-regulation tracts, such as the cingulum and forceps major (all q < 0.05). No significant WM differences were found for the low physical activity subtype.

Conclusion: Frailty subtypes are associated with distinct WM alteration patterns, reflecting potentially different mechanisms of brain aging. These findings highlight the importance of subtype-specific approaches to early detection and intervention.

Abstract Image

无痴呆老年人的虚弱亚型和白质改变。
目的:虚弱会增加老年人认知能力下降的风险,但与不同虚弱亚型相关的大脑结构模式尚不清楚。本研究检查了社区居住的无痴呆老年人中虚弱亚型的白质(WM)变化。方法:本横断面研究纳入台湾认知障碍与痴呆精准医学倡议(TPMIC)队列。使用弗里德表型评估虚弱,并将其分为活动型、非活动型和低体力活动亚型。认知功能(注意、记忆和执行功能)采用标准化神经心理学测试进行评估。采用扩散张量成像(DTI)指标测量WM微观结构,包括分数各向异性(FA)和平均扩散率(MD)。结果:297名参与者中,91名(30.6%)为体弱前期/体弱。虚弱前/虚弱组显示出广泛的WM改变,在完全调整和FDR校正后,内囊(IC)仍然显著(q结论:虚弱亚型与不同的WM改变模式相关,可能反映了不同的脑衰老机制。这些发现强调了亚型特异性方法对早期发现和干预的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.40
自引率
4.20%
发文量
181
审稿时长
6-12 weeks
期刊介绍: PCN (Psychiatry and Clinical Neurosciences) Publication Frequency: Published 12 online issues a year by JSPN Content Categories: Review Articles Regular Articles Letters to the Editor Peer Review Process: All manuscripts undergo peer review by anonymous reviewers, an Editorial Board Member, and the Editor Publication Criteria: Manuscripts are accepted based on quality, originality, and significance to the readership Authors must confirm that the manuscript has not been published or submitted elsewhere and has been approved by each author
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