Evidence map›Paper›PMID 41910964›Full record

ArticleJAMA neurology2026

High-Level Alzheimer Disease Neuropathological Change Following Iatrogenic Exposure.

Gargi Banerjee, Tze How Mok, Harpreet Hyare, Oliver Cousins, Zane Jaunmuktane, Simon Mead, John Collinge

Abstract readCase Reports
In one paragraph

Article in JAMA neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Evidence for progressive neurodegeneration in iatrogenic cerebral amyloid angiopathy.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Gargi BanerjeeMRC Prion Unit at UCL and UCL Institute of Prion Diseases, London, United Kingdom.
Tze How MokMRC Prion Unit at UCL and UCL Institute of Prion Diseases, London, United Kingdom.
Harpreet HyareUCL Queen Square Institute of Neurology, London, United Kingdom.
Oliver CousinsSt George's University Hospitals NHS Foundation Trust, London, United Kingdom.
Zane JaunmuktaneDepartment of Clinical and Movement Neurosciences and Queen Square Brain Bank for Neurological Disorders, UCL Queen Square Institute of Neurology, London, United Kingdom.
Simon MeadMRC Prion Unit at UCL and UCL Institute of Prion Diseases, London, United Kingdom.
John CollingeMRC Prion Unit at UCL and UCL Institute of Prion Diseases, London, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: Alzheimer disease (AD) is pathologically characterized by the deposition of amyloid-β (Aβ) and hyperphosphorylated tau. Human transmission of Aβ pathology in a prion-like fashion has resulted in iatrogenic cerebral amyloid angiopathy. More recently, iatrogenic Alzheimer disease (iAD) was described in recipients of cadaveric pituitary-derived human growth hormone (c-hGH) contaminated with Aβ amyloid seeds. Objective: To describe the clinical and postmortem findings in iAD. Design, Setting, and Participants: This case series describes 4 c-hGH recipients who were referred to the UK National Prion Clinic. Between February 2024 and February 2025, 14 c-hGH recipients had been referred to this service, with clinical assessments ongoing. The current study included 4 of 14 people treated with c-hGH who were referred since the original report. These data were analyzed during February and March 2025. Exposure: c-hGH contaminated with Aβ amyloid seeds. Main Outcomes and Measures: Clinical and histopathological description. Results: The study describes 4 males who developed dementia following confirmed or suspected c-hGH treatment in childhood (age at symptom onset between 47 and 60 years) with cognitive syndromes characterized by prominent language involvement. Results include clinical and postmortem findings for 1 patient (onset at age 47 years) in whom postmortem examination (at age 57 years) showed unequivocal neuropathological features of AD, including severe tauopathy. Brief descriptions of 3 additional patients with prominent language involvement are also provided. Conclusions and Relevance: These results demonstrate that patients with iAD can have histopathological findings classically found in sporadic AD and that prominent language involvement might be an important phenotypic feature in this AD subtype.

Indexed as

Alzheimer DiseaseBrainHuman Growth HormoneIatrogenic DiseaseAgedAmyloid beta-PeptidesHumansMaleMiddle AgedAmyloid beta-PeptidesHuman Growth Hormone

Identifiers

PMID41910964
PMCPMC13036638

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.