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This page is alzhub.org's plain-English summary of a published study, not the paper itself. It is generated from the record we hold for this study, sourced and linked below — check the original for the full text and methods.

✓ Peer-reviewed alzhub usefulness score 33 out of 100. End-of-life care

Topic: Brain proteins, microglia and lab models

Prion diseases are fatal neurological disorders characterized by the accumulation of abnormal proteins in the central nervous system, leading to rapid neurodegeneration. We present a male his 70s who developed rapidly progressive dementia three weeks after a routine platelet-rich plasma (PRP) injection for chronic hip pain. MRI revealed multifocal cortical diffusion restriction involving the basal ganglia. CSF analysis via real-time quaking-induced conversion (RT-QuIC) confirmed prion disease, with elevated T-tau and 14-3-3 gamma proteins. He also tested seropositive for Ehrlichia, though other infectious causes were ruled out. Despite treatment with IV immunoglobulins (IGs) and antibiotics, his condition declined with worsening myoclonus and hyperreflexia. He died one week after discharge to hospice, six weeks after symptom onset. This case demonstrates several classic clinical features of sporadic Creutzfeldt-Jacob disease (sCJD) and raises the possibility that an acute inflammatory response from PRP injection may have triggered sCJD in the setting of a pre-existing chronic inflammatory state from tick-borne infection.

Key findings

Why it matters

This case report describes a man in his 70s who developed rapidly progressive dementia after a platelet-rich plasma injection and was confirmed to have sporadic Creutzfeldt-Jakob disease. It is a single case of a different prion disease and provides no treatment, cure or prevention for Alzheimer's disease.

Study details

How this study scored 33/100
How this study's score is builtJournal tier 7 of 10; Journal's citation record 1 of 4; Study design 0 of 12; Strength of evidence 1 of 5; Peer-review validation 10 of 10; How recent 4 of 5; Sample size 0 of 4; Effect reported 0 of 3; Studied in people 0 of 3; Randomised / blinded 0 of 2; Times cited 1 of 7; Citations per year 0 of 5; Impact for its field and year 1 of 6; Cited by studies here 0 of 6; Still being cited 0 of 4; Senior author's track record left out, no data; Institution's track record 2 of 3; Multi-centre collaboration 1 of 3; Indexed in PubMed 2 of 2; Free to read 2 of 2. 32 of the 96 points it could be judged on, which is 33 of 100. Total 33 of 100.32 of the 96 points we could judge = 33 of 100

Published in a peer-reviewed journal. Scored zero for study design, sample size, effect reported, studied in people and randomised / blinded because the record does not state it. We have no data on senior author's track record, so that was left out: it earned 32 of the 96 points we could judge it on, which is 33 out of 100.

ComponentPointsWhy
Journal tier 7 / 10 Tier 3 — peer-reviewed journal (Cureus)
Journal's citation record 1 / 4 Cureus: journal h-index 131 (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)
Randomised / blinded 0 / 2 No randomisation or blinding stated — scores zero (not stated in the record — scored 0)
Times cited 1 / 7 Cited 1 times (OpenAlex, 2026-10-10)
Citations per year 0 / 5 0.3 citations a year over 3 year(s) since 2025
Impact for its field and year 1 / 6 Cited 0.3× the average for papers of its field and year (OpenAlex FWCI)
Cited by studies here 0 / 6 No other study in this library cites it
Still being cited 0 / 4 Cited 1 times in 2024–2026 (2026 still in progress; OpenAlex)
Senior author's track record — / 4 Senior author's record not available — left out of this score
Institution's track record 2 / 3 University of North Carolina at Chapel Hill: institution h-index 1,674 (OpenAlex)
Multi-centre collaboration 1 / 3 OpenAlex lists 2 institution(s) in 1 country
Indexed in PubMed 2 / 2 Indexed in PubMed (PMID 41018303)
Free to read 2 / 2 Free to read
Points 32 / 96 Scored on 19 of 20 parts. We have no data for the rest, so they are left out: 32 of the 96 points we could judge it on is 33 out of 100.
Total 33 / 100 —

What each of these 20 components measures, and what this score is not →

Read the original

Full text: free to read — OpenAlex lists this copy as free to read: the link above (checked 6 Feb 1020).

Cite this study APA, Vancouver, BibTeX · download .bib or .ris

Built from the record alzhub holds for this paper, not looked up. Volume, issue and page numbers are not held in the record. Check the citation against the original before you use it.

APA 7th

Dave, M., & Le, P. (2025). Rapidly Progressive Dementia After Platelet-Rich Plasma Therapy: A Case of Sporadic Creutzfeldt-Jakob Disease in the Context of Chronic Ehrlichiosis. Cureus. https://doi.org/10.7759/cureus.91152

Vancouver

Dave M, Le P. Rapidly Progressive Dementia After Platelet-Rich Plasma Therapy: A Case of Sporadic Creutzfeldt-Jakob Disease in the Context of Chronic Ehrlichiosis. Cureus. 2025. doi:10.7759/cureus.91152. PMID: 41018303.

BibTeX

@article{dave2025-41018303,
  author  = {Dave, Mili and Le, Peter},
  title   = {{Rapidly Progressive Dementia After Platelet-Rich Plasma Therapy: A Case of Sporadic Creutzfeldt-Jakob Disease in the Context of Chronic Ehrlichiosis}},
  journal = {Cureus},
  year    = {2025},
  doi     = {10.7759/cureus.91152},
  pmid    = {41018303},
  url     = {https://doi.org/10.7759/cureus.91152}
}

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