DTI-ALPS index as a predictor of cognitive decline over 1 year.

IF 2.4 3区 医学 Q2 CLINICAL NEUROLOGY Neuroradiology Pub Date : 2025-01-01 Epub Date: 2024-12-16 DOI:10.1007/s00234-024-03521-w
Joo Jungwon, Ji Hyung Lee, Chi-Hoon Choi, Jeonghwan Lee
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Abstract

Purpose: Alzheimer's disease (AD) is a progressive neurodegenerative disorder characterized by cognitive decline and impaired daily functioning. The glymphatic system removes neurotoxic waste, including amyloid-beta (Aβ), an important factor in AD pathogenesis. This study used the Diffusion Tensor Imaging Analysis Along the Perivascular Space (DTI-ALPS) index, which reflects glymphatic function, to explore its relationship with cognitive decline in patients with probable AD.

Methods: We conducted a longitudinal study of 16 participants aged 60-79 years with probable AD who were evaluated using the Clinical Dementia Rating (CDR) and Mini-Mental State Examination (MMSE). Glymphatic function was assessed using the DTI-ALPS index; plasma Aβ 42/40 ratios were measured to account for amyloid pathology. The relationship between the DTI-ALPS index and baseline cognitive function was analyzed using multiple regression models adjusted for age, sex, and plasma Aβ 42/40 ratios. Associations between the DTI-ALPS index and cognitive decline over 1 year were assessed by a model using the percentage change in the MMSE z-score as the outcome variable.

Results: Higher DTI-ALPS index was significantly associated with better baseline cognitive function as assessed by MMSE (standardized beta = 1.17, p < 0.001) and lower clinical severity as assessed by CDR (standardized beta = - 1.00, p = 0.006). Over the 1-year follow-up, greater baseline DTI-ALPS index values were associated with less cognitive decline (standardized beta = - 0.85, p = 0.018).

Conclusion: Our findings suggest that DTI-ALPS index is associated with cognitive performance and is a biomarker for predicting cognitive decline in AD. Future studies should consider larger sample sizes and longer follow-up periods to validate these findings.

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DTI-ALPS 指数可预测一年内认知能力的下降。
目的:阿尔茨海默病(AD)是一种以认知能力下降和日常功能受损为特征的进行性神经退行性疾病。淋巴系统清除神经毒性废物,包括淀粉样蛋白- β (Aβ),这是阿尔茨海默病发病的重要因素。本研究采用反映淋巴功能的弥散张量成像分析(DTI-ALPS)指数,探讨其与AD患者认知能力下降的关系。方法:我们对16名年龄在60-79岁的可能患有AD的参与者进行了一项纵向研究,他们使用临床痴呆评分(CDR)和迷你精神状态检查(MMSE)进行评估。采用DTI-ALPS指数评估淋巴功能;测定血浆Aβ 42/40比值以解释淀粉样蛋白病理。DTI-ALPS指数与基线认知功能的关系采用调整年龄、性别和血浆Aβ 42/40比值的多元回归模型进行分析。DTI-ALPS指数与1年内认知能力下降之间的关系通过使用MMSE z得分的百分比变化作为结果变量的模型进行评估。结果:高DTI-ALPS指数与MMSE评估的更好的基线认知功能显著相关(标准化β = 1.17, p)。结论:我们的研究结果表明,DTI-ALPS指数与认知表现相关,是预测AD认知能力下降的生物标志物。未来的研究应该考虑更大的样本量和更长的随访期来验证这些发现。
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
Neuroradiology
Neuroradiology 医学-核医学
CiteScore
5.30
自引率
3.60%
发文量
214
审稿时长
4-8 weeks
期刊介绍: Neuroradiology aims to provide state-of-the-art medical and scientific information in the fields of Neuroradiology, Neurosciences, Neurology, Psychiatry, Neurosurgery, and related medical specialities. Neuroradiology as the official Journal of the European Society of Neuroradiology receives submissions from all parts of the world and publishes peer-reviewed original research, comprehensive reviews, educational papers, opinion papers, and short reports on exceptional clinical observations and new technical developments in the field of Neuroimaging and Neurointervention. The journal has subsections for Diagnostic and Interventional Neuroradiology, Advanced Neuroimaging, Paediatric Neuroradiology, Head-Neck-ENT Radiology, Spine Neuroradiology, and for submissions from Japan. Neuroradiology aims to provide new knowledge about and insights into the function and pathology of the human nervous system that may help to better diagnose and treat nervous system diseases. Neuroradiology is a member of the Committee on Publication Ethics (COPE) and follows the COPE core practices. Neuroradiology prefers articles that are free of bias, self-critical regarding limitations, transparent and clear in describing study participants, methods, and statistics, and short in presenting results. Before peer-review all submissions are automatically checked by iThenticate to assess for potential overlap in prior publication.
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