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Updated: Jul 10, 2026

A Machine Learning Approach to Design an Efficient Selective Screening of Mild Cognitive Impairment
Published on: January 11, 2020
Neuropathology of mild cognitive impairment
1Department of Pathology, Tokyo Metropolitan Geriatric Hospital, Tokyo, Japan. yukosa@tmig.or.jp
Abstract:
We aim to investigate the pathological background of mild cognitive impairment (MCI). The most recent 545 cases from the Brain Bank for Aging Research (BBAR) were studied, with a mean age of 80.7 years and male : female ratio of 324 : 221. Cases with clinical dementia rating scale (CDR) 0.5 were retrieved as the best substitute of MCI. CDR was retrospectively determined from clinical charts. Pathological examinations followed the BBAR protocol (JNEN 2004). Post mortem assessment of CDR was possible for 486 cases, and was 0 in 201 cases, 0.5 in 57 cases and 1-3 in 228 cases. CDR 0.5 group was clinicopathologically classified into 33 cases with degenerative changes, nine cases with vascular changes, four cases with combined degenerative and vascular changes, two with hippocampal sclerosis, two with trauma, one with metabolic disease and six with unremarkable changes. The degenerative group was further subclassified into groups with pure and combined pathology. The former consisted of six cases each with Alzheimer change (AC), argyrophilic grain change (AGC) and neurofibrillary tangle predominant change (NFTC), three each with Lewy body disease change without parkinsonism (DLBC) or Parkinson's disease (PDMCI) and one case with progressive supranuclear palsy. The latter consisted of three cases with AC plus AGC, two with AGC plus NFTC and one each with AC plus DLBC, DLBC plus amyotrophic lateral sclerosis and AGC plus DLBC. The pathological backgrounds of patients of class CDR 0.5 were varied and not restricted to AC.
Insights
Mild cognitive impairment (MCI) has diverse pathological backgrounds, not solely Alzheimer change. This study analyzed brain bank cases, revealing varied degenerative and vascular changes in MCI patients.
Area of Science:
- Neuropathology
- Gerontology
- Neurodegenerative Diseases
Background:
- Mild cognitive impairment (MCI) is a clinical state with uncertain pathological underpinnings.
- Accurate pathological classification is crucial for understanding MCI progression and developing targeted therapies.
Purpose of the Study:
- To investigate the diverse clinicopathological features of mild cognitive impairment (MCI).
- To determine if Alzheimer change is the sole pathological cause of MCI.
Main Methods:
- Retrospective analysis of 545 cases from the Brain Bank for Aging Research (BBAR).
- Clinical Dementia Rating (CDR) scale 0.5 was used as a proxy for MCI.
- Pathological examinations followed the BBAR protocol, including assessment of Alzheimer change (AC), argyrophilic grain change (AGC), and Lewy body disease (DLBC).
Main Results:
- Out of 486 cases with post-mortem CDR assessment, 57 had CDR 0.5.
- The CDR 0.5 group exhibited varied pathologies: 33 degenerative, 9 vascular, 4 combined, and others including hippocampal sclerosis and trauma.
- Within the degenerative group, pure pathologies included AC, AGC, and neurofibrillary tangle predominant change (NFTC), while combined pathologies were also observed.
Conclusions:
- The pathological basis of mild cognitive impairment (MCI) is heterogeneous and not limited to Alzheimer change (AC).
- Vascular factors and other neurodegenerative changes significantly contribute to the pathology of MCI.
- Understanding this diversity is essential for accurate diagnosis and future therapeutic strategies for MCI.
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