Related Experiment Video
Updated: Aug 15, 2026

Comprehensive Autopsy Program for Individuals with Multiple Sclerosis
Published on: July 19, 2019
Decreasing myelin density reflected increasing white matter pathology in Alzheimer's disease--a neuropathological
Martin Sjöbeck1, Mattias Haglund, Elisabet Englund
1Department of Pathology, Division of Neuropathology, University Hospital, Lund, Sweden. martin.sjobeck@med.lu.se
Background:
White matter disease (WMD) is frequently seen in Alzheimer's disease (AD) at neuropathological examination. It is defined as a subtotal tissue loss with a reduction of myelin, axons and oligodendrocytes as well as astrocytosis. Studies quantitatively defining the myelin loss in AD are scarce. The aim was to develop a method that could provide numerical values of myelin density in AD. The purpose was to compare the myelin contents in increasing grades of pathology of WMD, with age and cortical AD pathology as well as in different regions of the brain in AD.
Material And Methods:
Sixteen cases with AD and concomitant WMD were investigated with an in-house developed image analysis technique to determine the myelin attenuation with optical density (OD) in frontoparietal, parietal, temporal and occipital white matter on whole brain coronal sections stained for myelin with Luxol Fast Blue (LFB). The OD values in LFB were compared grouped according to Haematoxylin/Eosin (HE) evaluated mild, moderate and severe WMD or normal tissue. The OD values were also correlated with age and cortical AD pathology and compared between the different studied white matter regions.
Results:
Increasing severity of WMD was associated with a statistically significant OD reduction. No correlation was seen between age and OD or overall cortical AD pathology. The OD values were significantly lower in frontoparietal-compared to occipital white matter.
Conclusions:
Myelin loss in AD with WMD is a marked morphologic component of the disease and it is possible to determine the reduction objectively in neuropathological specimens with quantitative measures. This may be of use for clinical diagnostics including brain imaging.
Insights
Quantitative measures reveal significant myelin loss in Alzheimer's disease (AD) with white matter disease (WMD). This objective assessment of myelin reduction in AD neuropathology may aid clinical diagnostics and brain imaging.
Area of Science:
- Neuropathology
- Neuroimaging
- Alzheimer's Disease Research
Background:
- White matter disease (WMD) is a common finding in Alzheimer's disease (AD), characterized by myelin loss, axonal damage, and astrocytosis.
- Quantitative studies on myelin loss in AD are limited, necessitating the development of objective measurement methods.
Purpose of the Study:
- To develop a quantitative method for assessing myelin density in AD.
- To compare myelin content across varying WMD severity, age, cortical AD pathology, and brain regions.
Main Methods:
- An in-house image analysis technique quantified myelin optical density (OD) using Luxol Fast Blue staining on whole brain sections from 16 AD cases.
- OD values were compared based on WMD severity (mild, moderate, severe) and correlated with age and cortical AD pathology.
Main Results:
- Increasing WMD severity correlated with a statistically significant reduction in myelin OD.
- No correlation was found between myelin OD, age, or overall cortical AD pathology.
- Myelin OD was significantly lower in frontoparietal white matter compared to occipital white matter.
Conclusions:
- Myelin loss is a significant morphological feature of AD with WMD, quantifiable in neuropathological specimens.
- Objective quantitative measures of myelin loss can be obtained.
- These quantitative findings may support clinical diagnostics and neuroimaging applications in AD.
More Related Videos
Related Concept Videos
Alzheimer Disease ll: Pathophysiology
Alzheimer Disease l: Introduction
Alzheimer's Disease: Overview
The clinical diagnosis of AD hinges on the presence of memory and other cognitive impairments. Biomarkers, such as changes in Aβ and tau...
Dementia l: Introduction

