Brain microstructure alterations in subjective cognitive decline: a multi-component T2 relaxometry study.

IF 4.5 Q1 CLINICAL NEUROLOGY Brain communications Pub Date : 2025-01-16 eCollection Date: 2025-01-01 DOI:10.1093/braincomms/fcaf017
Miguel Ángel Rivas-Fernández, Mustapha Bouhrara, Erick J Canales-Rodríguez, Mónica Lindín, Montserrat Zurrón, Fernando Díaz, Santiago Galdo-Álvarez
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Abstract

Previous research has revealed patterns of brain atrophy in subjective cognitive decline, a potential preclinical stage of Alzheimer's disease. However, the involvement of myelin content and microstructural alterations in subjective cognitive decline has not previously been investigated. This study included three groups of participants recruited from the Compostela Aging Study project: 53 cognitively unimpaired adults, 16 individuals with subjective cognitive decline and hippocampal atrophy and 70 with subjective cognitive decline and no hippocampal atrophy. Group differences were analysed across five MRI biomarkers derived from multi-component T2 relaxometry, each sensitive to variations in cerebral composition and microstructural tissue integrity. Although no significant differences in myelin content were observed between groups, the subjective cognitive decline with hippocampal atrophy group exhibited a larger free-water fraction, and reduced fraction and relaxation times of the intra/extracellular water compartment in frontal, parietal and medial temporal lobe brain regions and white matter tracts as compared with the other groups. Moreover, both subjective cognitive decline groups displayed lower total water content as compared with the control group and the subjective cognitive decline with hippocampal atrophy group showed lower total water content as compared with the subjective cognitive decline without hippocampal atrophy group. These changes are likely related to microstructural tissue differences related to neuroinflammation, axonal degeneration, iron accumulation or other physiologic variations, calling for further examinations.

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主观认知衰退的脑微结构改变:多组分T2弛豫测量研究。
先前的研究已经揭示了主观认知能力下降的脑萎缩模式,这是阿尔茨海默病的潜在临床前阶段。然而,髓磷脂含量和微观结构改变在主观认知能力下降中的作用尚未被研究过。本研究包括从Compostela衰老研究项目中招募的三组参与者:53名认知功能未受损的成年人,16名主观认知能力下降和海马萎缩的个体,70名主观认知能力下降但没有海马萎缩的个体。研究人员分析了来自多组分T2弛缓测量的五种MRI生物标志物的组间差异,每一种标志物对大脑成分和微结构组织完整性的变化都很敏感。尽管髓磷脂含量在各组间无显著差异,但主观认知能力下降伴海马萎缩组表现出较大的自由水分数,额叶、顶叶、内侧颞叶脑区和白质束的细胞内/细胞外水区分数和松弛时间均减少。此外,主观认知能力下降组和海马萎缩组的总含水量均低于对照组,主观认知能力下降组和海马萎缩组的总含水量均低于无海马萎缩组。这些变化可能与神经炎症、轴突变性、铁积累或其他生理变化相关的微结构组织差异有关,需要进一步检查。
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