Tang Song Lin, Subramaniam Ponnusamy, Siau Ching Sin, Chong Agnes Shu Sze, Liu Fang
Department of Geriatrics, Zhoushan Hospital, Wenzhou Medical University, Zhoushan, China.
Center for Healthy Ageing and Wellness, Faculty of Health Sciences, Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia.
Front Psychol. 2025 Jun 27;16:1586418. doi: 10.3389/fpsyg.2025.1586418. eCollection 2025.
Mild Behavioral Impairment (MBI) represents a predementia syndrome marked by neuropsychiatric symptoms that may precede detectable cognitive decline. Identifying factors associated with MBI is critical for developing targeted prevention strategies in neurodegenerative disorders.
This systematic review adhered to PRISMA 2020 guidelines, searching PubMed, Scopus, Web of Science, ScienceDirect, and Embase through May 2024. Forty-one human studies meeting predefined inclusion criteria were selected through dual independent screening.
Five key domains emerged: (1) Genetic susceptibility (APOE ε4 allele showing strongest association), (2) Motor system pathology (particularly Parkinsonian features), (3) Multisensory deficits (auditory impairment demonstrating bidirectional relationships), (4) Metabolic dysregulation (diabetes mellitus and frailty phenotypes), and (5) Neuroanatomical correlates (frontolimbic atrophy patterns on MRI). The interaction between genetic predisposition and environmental/lifestyle factors appears central to MBI pathogenesis.
MBI manifests as a multidimensional interface between molecular mechanisms and clinical phenomenology. Our synthesis supports the implementation of transdiagnostic screening protocols integrating behavioral biomarkers with conventional cognitive assessments. Future research should prioritize longitudinal designs to establish causal pathways and intervention thresholds.
轻度行为损害(MBI)是一种痴呆前综合征,其特征是在可检测到的认知衰退之前出现神经精神症状。确定与MBI相关的因素对于制定神经退行性疾病的针对性预防策略至关重要。
本系统评价遵循PRISMA 2020指南,截至2024年5月在PubMed、Scopus、科学网、ScienceDirect和Embase中进行检索。通过双人独立筛选,选择了41项符合预定义纳入标准的人体研究。
出现了五个关键领域:(1)遗传易感性(APOE ε4等位基因显示出最强的关联),(2)运动系统病理学(特别是帕金森氏特征),(3)多感觉缺陷(听觉障碍显示出双向关系),(4)代谢失调(糖尿病和虚弱表型),以及(5)神经解剖学相关性(MRI上的额颞叶萎缩模式)。遗传易感性与环境/生活方式因素之间的相互作用似乎是MBI发病机制的核心。
MBI表现为分子机制与临床现象学之间的多维界面。我们的综合分析支持实施将行为生物标志物与传统认知评估相结合的跨诊断筛查方案。未来的研究应优先采用纵向设计来确定因果途径和干预阈值。