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Blood α‐Synuclein Separates Parkinson's Disease from Dementia with Lewy Bodies
George T. Kannarkat, Rebecca Zack, R. Tyler Skrinak, James F. Morley, Roseanne Davila‐Rivera, Sanaz Arezoumandan, Katherine A. Dorfman, Kelvin C. Luk et al.. Annals of Neurology, 2025-06-16
Topic: Brain proteins, microglia and lab models
Plain-language summary
Surprisingly, levels of strain A and B aSyn species were higher in plasma from individuals with PD compared to DLB in 2 independent cohorts. Lower levels of plasma aSyn strain A species predicted a faster rate of cognitive decline in individuals with PD. Furthermore, strain A and strain B aSyn species were undetectable in CSF, and their levels in brain versus plasma did not correlate. Moreover, plasma aSyn species isolated by aSyn strain antibodies could template aSyn fibrillization, and they could seed formation of aSyn inclusions in cells. Our findings suggest that circulating plasma aSyn strains may impact LBD clinical presentation, particularly cognition. The enrichment of these aSyn species in plasma but not CSF also suggests a potential source outside the brain. ANN NEUROL 2025;98:682-698.
What this study adds
Evidence grade: Low
This study found that levels of strain A and B α-synuclein species were higher in plasma from people with Parkinson's disease compared to dementia with Lewy bodies, and that lower levels of strain A predicted a faster rate of cognitive decline in Parkinson's disease. It is about a potential biomarker, not a treatment, cure or prevention.
Taken from this record’s own fields, not from reading the paper. The grade is assigned from the abstract’s wording; what that means.
Cite this study APA, Vancouver, BibTeX · download .bib or .ris
APA 7th
Kannarkat, G. T., Zack, R., Skrinak, R. T., Morley, J. F., Davila‐Rivera, R., Arezoumandan, S., et al. (2025). Blood α‐Synuclein Separates Parkinson's Disease from Dementia with Lewy Bodies. Annals of Neurology. https://doi.org/10.1002/ana.27288
Vancouver
Kannarkat GT, Zack R, Skrinak RT, Morley JF, Davila‐Rivera R, Arezoumandan S, et al. Blood α‐Synuclein Separates Parkinson's Disease from Dementia with Lewy Bodies. Annals of Neurology. 2025. doi:10.1002/ana.27288. PMID: 40521808.
BibTeX
@article{kannarkat2025-40521808,
author = {Kannarkat, George T. and Zack, Rebecca and Skrinak, R. Tyler and Morley, James F. and Davila‐Rivera, Roseanne and Arezoumandan, Sanaz and Dorfman, Katherine A. and Luk, Kelvin C. and others},
title = {{Blood α‐Synuclein Separates Parkinson's Disease from Dementia with Lewy Bodies}},
journal = {Annals of Neurology},
year = {2025},
doi = {10.1002/ana.27288},
pmid = {40521808},
url = {https://doi.org/10.1002/ana.27288}
}
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
- Surprisingly, levels of strain A and B aSyn species were higher in plasma from individuals with PD compared to DLB in 2 independent cohorts.
- Lower levels of plasma aSyn strain A species predicted a faster rate of cognitive decline in individuals with PD.
- Furthermore, strain A and strain B aSyn species were undetectable in CSF, and their levels in brain versus plasma did not correlate.
- Moreover, plasma aSyn species isolated by aSyn strain antibodies could template aSyn fibrillization, and they could seed formation of aSyn inclusions in cells.
- Our findings suggest that circulating plasma aSyn strains may impact LBD clinical presentation, particularly cognition.
Why it matters
This study found that levels of strain A and B α-synuclein species were higher in plasma from people with Parkinson's disease compared to dementia with Lewy bodies, and that lower levels of strain A predicted a faster rate of cognitive decline in Parkinson's disease. It is about a potential biomarker, not a treatment, cure or prevention.
Study details
- Evidence strengthLow
How this study scored 44/100
Published in a leading specialty journal. Scored zero for study design, sample size, effect reported, studied in people and randomized / blinded because the record does not state it.
| Component | Points | Why |
|---|---|---|
| Journal tier | 9 / 10 | Tier 2 — leading specialty journal (Annals of Neurology) |
| Journal's citation record | 3 / 4 | Annals of Neurology: journal h-index 437 (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 | 1 / 5 | Rated “low” 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 | 0 / 4 | Participant count not stated — scores zero (not stated in the record — scored 0) |
| Effect reported | 0 / 3 | No effect size reported — scores zero (not stated in the record — scored 0) |
| Studied in people | 0 / 3 | Not stated whether this was studied in people — scores zero (not stated in the record — scored 0) |
| Randomized / blinded | 0 / 2 | No randomization or blinding stated — scores zero (not stated in the record — scored 0) |
| Times cited | 2 / 7 | Cited 5 times (OpenAlex, 2026-10-10) |
| Citations per year | 1 / 5 | 1.7 citations a year over 3 year(s) since 2025 |
| Impact for its field and year | 2 / 6 | Cited 2.8× 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 5 times in 2024–2026 (2026 still in progress; OpenAlex) |
| Senior author's track record | 3 / 4 | Last-listed author Alice S. Chen‐Plotkin: h-index 66 (OpenAlex, whole career) |
| Institution's track record | 2 / 3 | University of Pennsylvania: institution h-index 1,859 (OpenAlex) |
| Multicenter collaboration | 1 / 3 | OpenAlex lists 3 institution(s) in 1 country |
| Indexed in PubMed | 2 / 2 | Indexed in PubMed (PMID 40521808) |
| Free to read | 2 / 2 | Free to read |
| Total | 44 / 100 | — |
What each of these 20 components measures, and what this score is not →
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