High-Level Alzheimer Disease Neuropathological Change Following Iatrogenic Exposure - Scorecard - MDSpire

High-Level Alzheimer Disease Neuropathological Change Following Iatrogenic Exposure

  • By

  • Gargi Banerjee

  • Tze How Mok

  • Harpreet Hyare

  • Oliver Cousins

  • Zane Jaunmuktane

  • Simon Mead

  • John Collinge

  • May 1, 2026

  • 0 min

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Clinical Scorecard: Neuropathological Changes in Alzheimer Disease Induced by Iatrogenic Factors

At a Glance

CategoryDetail
ConditionIatrogenic Alzheimer Disease (iAD)
Key MechanismsSelf-propagating assemblies of misfolded proteins, particularly amyloid-β (Aβ), associated with iatrogenic factors.
Target PopulationPatients treated with cadaveric pituitary-derived human growth hormone (c-hGH).
Care SettingNational Prion Clinic and associated healthcare facilities.

Key Highlights

  • Iatrogenic cerebral amyloid angiopathy (iCAA) and parenchymal Aβ pathology reported in c-hGH recipients.
  • Clinical iCAA typically presents with intracerebral hemorrhage decades post-procedure.
  • Compelling association between specific c-hGH preparations and early-onset AD.
  • Novel condition, iAD, may differ from sporadic and inherited AD.
  • Limited neuropathology available showed only mild tauopathy.

Guideline-Based Recommendations

Diagnosis

  • Consider iAD in patients with a history of c-hGH treatment presenting with cognitive decline.

Management

  • Monitor for symptoms of cognitive impairment and neurological deficits in treated individuals.

Monitoring & Follow-up

  • Longitudinal follow-up in the National Prion Monitoring Cohort for individuals at risk.

Risks

  • Increased risk of intracerebral hemorrhage in recipients of cadaveric pituitary hormones.

Patient & Prescribing Data

Individuals previously treated with cadaveric pituitary hormones.

Symptoms may develop decades after treatment, necessitating long-term monitoring.

Clinical Best Practices

  • Obtain informed consent for genetic testing and tissue use for research.
  • Conduct thorough postmortem examinations with appropriate ethical approvals.
  • Utilize advanced immunostaining techniques for neuropathological assessment.

References

Original Source(s)

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