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Cerebrovascular co-pathology and cholinergic white matter pathways along the Lewy body continuum
Cene Jerele, Antonios Tzortzakakis, Milan Němý, Anna Rennie, Javier Arranz, Víctor Montal, Alexandre Bejanin, Dag Aarsland et al.. Brain Communications, 2025-01-01
Topic: Brain proteins, microglia and lab models
Lewy body patients showed a significantly higher degree of WMSA in the external capsule cholinergic pathway despite no significant differences in global WMSA compared to controls. Furthermore, higher CHIPS scores, Fazekas scale and tractography mean diffusivity were associated with more pronounced frontal atrophy in Lewy body patients but not in controls. In conclusion, cholinergic WMSA were more pronounced in Lewy body patients compared to healthy controls, independently of global WMSA. Our findings indicate that cerebrovascular disease-related disruptions in cholinergic white matter may be linked to frontal atrophy in Lewy body patients.
Cite this study APA, Vancouver, BibTeX · download .bib or .ris
APA 7th
Jerele, C., Tzortzakakis, A., Němý, M., Rennie, A., Arranz, J., Montal, V., et al. (2025). Cerebrovascular co-pathology and cholinergic white matter pathways along the Lewy body continuum. Brain Communications. https://doi.org/10.1093/braincomms/fcaf173
Vancouver
Jerele C, Tzortzakakis A, Němý M, Rennie A, Arranz J, Montal V, et al. Cerebrovascular co-pathology and cholinergic white matter pathways along the Lewy body continuum. Brain Communications. 2025. doi:10.1093/braincomms/fcaf173. PMID: 40391186.
BibTeX
@article{jerele2025-40391186,
author = {Jerele, Cene and Tzortzakakis, Antonios and Němý, Milan and Rennie, Anna and Arranz, Javier and Montal, Víctor and Bejanin, Alexandre and Aarsland, Dag and others},
title = {{Cerebrovascular co-pathology and cholinergic white matter pathways along the Lewy body continuum}},
journal = {Brain Communications},
year = {2025},
doi = {10.1093/braincomms/fcaf173},
pmid = {40391186},
url = {https://doi.org/10.1093/braincomms/fcaf173}
}
Built from the record alzhub holds for this paper, not looked up. Volume, issue and page numbers are not held in the record. The record's author list ends in “et al.”, so not every author is named. Check the citation against the original before you use it.
Key findings
- Lewy body patients showed a significantly higher degree of WMSA in the external capsule cholinergic pathway despite no significant differences in global WMSA compared to controls.
- Furthermore, higher CHIPS scores, Fazekas scale and tractography mean diffusivity were associated with more pronounced frontal atrophy in Lewy body patients but not in controls.
- In conclusion, cholinergic WMSA were more pronounced in Lewy body patients compared to healthy controls, independently of global WMSA.
- Our findings indicate that cerebrovascular disease-related disruptions in cholinergic white matter may be linked to frontal atrophy in Lewy body patients.
Why it matters
In Lewy body patients, white matter hyperintensities were greater in the external capsule cholinergic pathway than in controls even though global white matter hyperintensities did not differ, and these measures were linked to more frontal atrophy. This suggests cerebrovascular disruption of cholinergic pathways may relate to frontal atrophy but does not test any treatment, cure or prevention.
Study details
- Participants82
- Evidence strengthModerate
How this study scored 48/100
Published in a leading specialty journal. Scored zero for study design, effect reported and randomised / blinded because the record does not state it.
| Component | Points | Why |
|---|---|---|
| Journal tier | 9 / 10 | Tier 2 — leading specialty journal (Brain Communications) |
| Journal's citation record | 0 / 4 | Brain Communications: journal h-index 67 (OpenAlex, 2026-10-29) |
| Study design | 0 / 12 | No study design recorded — scores zero, not guessed (not stated in the record — scored 0) |
| Strength of evidence | 3 / 5 | Rated “moderate” in our summary |
| Peer-review validation | 10 / 10 | Peer-reviewed. Published as an article in a named peer-reviewed journal. |
| How recent | 4 / 5 | 2025 — within 3 year(s) of the newest study here |
| Sample size | 1 / 4 | 82 participants |
| Effect reported | 0 / 3 | No effect size reported — scores zero (not stated in the record — scored 0) |
| Studied in people | 3 / 3 | Studied in people (participant count stated) |
| Randomised / blinded | 0 / 2 | No randomisation or blinding stated — scores zero (not stated in the record — scored 0) |
| Times cited | 2 / 7 | Cited 6 times (OpenAlex, 2026-10-10) |
| Citations per year | 1 / 5 | 2.0 citations a year over 3 year(s) since 2025 |
| Impact for its field and year | 3 / 6 | Cited 3.8× the average for papers of its field and year (OpenAlex FWCI) |
| Cited by studies here | 1 / 6 | Cited by 1 other studies in this library |
| Still being cited | 1 / 4 | Cited 6 times in 2024–2026 (2026 still in progress; OpenAlex) |
| Senior author's track record | 2 / 4 | Last-listed author Daniel Ferreira: h-index 41 (OpenAlex, whole career) |
| Institution's track record | 1 / 3 | Karolinska Institutet: institution h-index 1,477 (OpenAlex) |
| Multi-centre collaboration | 3 / 3 | OpenAlex lists 12 institution(s) in 6 countries |
| Indexed in PubMed | 2 / 2 | Indexed in PubMed (PMID 40391186) |
| Free to read | 2 / 2 | Free to read |
| Total | 48 / 100 | — |
What each of these 20 components measures, and what this score is not →
Read the original
- DOI: 10.1093/braincomms/fcaf173
- PubMed: 40391186
- Original source →
- Free full text: Brain Communications →
Full text: free to read — OpenAlex lists this copy as free to read: the link above (checked 6 Feb 1020).
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