Aging and cerebrovascular lesions in pure and in mixed neurodegenerative and vascular dementia brains: a neuropathological study
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INTRODUCTION: The prevalence of dementia is increasing in our aging population. Because of the complexity of disease pathology, dementia classifications remain controversial. The present post-mortem study investigates whether there are age differences between dementia brains with a single pure neurodegenerative or cerebrovascular disease and those with mixed pathological features. Also, the impact of these vascular lesions is compared. MATERIAL AND METHODS: A total of 132 dementia brains with a pure neurodegenerative or cerebrovascular disease and 84 with mixed features were examined. Main age and gender distribution were compared between the overall group of pure and of mixed dementia. Also, the most common subgroups were compared separately. In addition to the detection of macroscopic visible lesions, a whole coronal section of a cerebral hemisphere, at the level of the mamillary body, was taken for semi-quantitative microscopic evaluation of white matter changes (WMCs), cortical micro-bleeds (CoMBs), and cortical micro-infarcts (CoMIs). RESULTS: Overall, patients with mixed dementia were at death significantly older than those with pure dementia. According to the main diagnosis, the pure forms of Alzheimer's disease (AD) and frontotemporal lobar degeneration (FTLD) were more common in the younger age groups while in the older ones the mixed form of Lewy body disease (LBD) predominated. Neuropathological examination revealed an increased severity of cerebral amyloid angiopathy (CAA), territorial infarcts, lobar haematomas, and CoMIs in the mixed AD group. In FTLD only CoMIs were increased in the mixed group, while in LBD no differences in severity of all cerebrovascular lesions were observed. Lacunar infarcts were more frequent in pure vascular dementia, while CAA predominated in the mixed one. CONCLUSIONS: Mixed dementia during the aging process is mainly due to the severity of AD and LBD pathologies combined with CAA-related cerebrovascular lesions.
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Those age 85 or older are more likely than those younger than 85 to have evidence of two or more causes of dementia.
“For example, those age 85 or older are more likely than those younger than 85 to have evidence of two or more causes of dementia.”
From 2024 Alzheimer's disease facts and figures (2024) · cites this paper as [27]
The Results (Table II; page unavailable) show that the oldest-old group made up a larger share of mixed-dementia cases than pure-dementia cases (27% versus 8%), supporting the age-related direction of the claim. Our copy does not define that group as age 85 or older or report a direct comparison of people aged 85 or older with those younger than 85. (LLM, conf=0.84)
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Ng, B., & Atkins, M. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.012
Jefferies, K., & Agrawal, N. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.006
Richards, F., & Curtice, M. J. R. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.008
Hughes, J. C., Jolley, D. J., Jordan, A., & Sampson, E. L. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.020
Alcohol Misuse in Older People
Rao, R., & CROME, I. B. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.009 · Cited by 1 · see citing works
Wagle, A., & Badrakalimuthu, V. R. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.010
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Gupta, S., Fiertag, O., Thanulingam, T., Strange, B. A., & Warner, J. P. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.007
Wilson, S., & Pinner, G. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.013
Hughes, J. C., & Lilford, P. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.001
Biomarkers and the Diagnosis of Preclinical Alzheimer’s Disease
Lilford, P., & Hughes, J. C. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.015
Understanding the Person with Dementia
Hughes, J. C., & Beatty, A. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.027
Hughes, J. C., & Lilford, P. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.002
Sullivan, V., Majumdar, B., Richman, A. V., & Vinjamuri, S. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.016
Hughes, J. C., & Lilford, P. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.029
Gerhand, S. (2024) · Cambridge University Press eBooks · doi:10.1017/9781009025911.006
Guerrero, M. D., López-Palanca, I., Moreno, L., & Cano‐López, I. (2025) · Universitas Psychologica · doi:10.11144/javeriana.upsy23.eief
Microscopic Anatomy of Hippocampus and Frontal Cortex in a Vascular Dementia Cadaver
Sah, R. P., Murlimanju, B. V., & Vidya, C. S. (2026) · National Journal of the Society of Medical Anatomists · doi:10.4103/njsoma.njsoma_4_26
Mathew, K., Bhatti, R. G., Zawaideh, T., Faizal, M. A. F. M., & Ghani, Z. (2026) · The Egyptian Journal of Neurology Psychiatry and Neurosurgery · doi:10.1186/s41983-026-01279-x
- Authors
- De Reuck, J., Maurage, C.-A., Deramecourt, V., Pasquier, F., Cordonnier, C., Leys, D., & Bordet, R.
- Affiliations
- Inserm (FR)
- Université de Lille (FR)
- Venue
- Folia Neuropathologica
- Publisher
- Termedia Sp. z.o.o.
- Published
- 2018
- Volume
- 56
- Issue
- 2
- Pages
- 81-87
- ISSN
- 1509-572X (ISSN-L)
- 1641-4640
- OpenAlex
- W2883625632
- Cited by
- 84
- References
- 33
- Citations by year
- 2026: 3 · 2025: 6 · 2024: 2 · 2023: 7 · 2022: 12 · 2021: 7 · 2020: 40 · 2019: 6 · 2018: 1
- FWCI
- 10.62
- Type
- journal article
- Language
- en
- Open access
- diamond
- doi.org
- Licence
- cc-by-nc-sa
- Locations
- Folia Neuropathologica (publishedVersion, cc-by-nc-sa)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Life Sciences › Neuroscience › Neurology › Neurological Disease Mechanisms and Treatments
- Health Sciences › Medicine › Neurology › Intracerebral and Subarachnoid Hemorrhage Research
- Keywords
- mixed dementia, Alzheimer's disease, frontotemporal lobar degeneration, Lewy body disease, cerebral amyloid angiopathy, cerebrovascular lesions, white matter changes, lacunar infarction, aging, age differences, postmortem neuropathology
- MeSH terms
- Aged, Aged, 80 and over, Aging, Brain, Cerebrovascular Disorders, Dementia, Female, Humans, Male, Neurodegenerative Diseases
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