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Human growth hormone and Creutzfeldt-Jakob disease

S Zekauskas1, M B Boggs, D P Wilson

  • 1Department of Pediatrics, University of Oklahoma College of Medicine-Tulsa.

Insights

Cadaver-derived human growth hormone (HGH) use was halted in 1985 due to Creutzfeldt-Jakob disease (CJD) transmission. Nine patients who received HGH have died from CJD, with many more potentially at risk.

Area of Science:

  • Neurology
  • Endocrinology
  • Public Health

Background:

  • Cadaver-derived human growth hormone (HGH) was a standard treatment for short stature in children for over two decades.
  • Concerns arose in 1985 when deaths linked to Creutzfeldt-Jakob disease (CJD) were reported in HGH recipients.
  • CJD is a fatal, degenerative neurological disorder caused by infectious agents.

Purpose of the Study:

  • To inform healthcare providers about the risk of CJD transmission through contaminated HGH.
  • To highlight the potential risk to children and adolescents who received HGH prior to 1985.
  • To emphasize the importance of ongoing vigilance and awareness regarding CJD in this patient population.

Main Methods:

  • Review of reported cases of CJD in individuals who received cadaver-derived HGH.
  • Epidemiological investigation into the source of CJD contamination.
  • Identification of at-risk populations, including children treated in Oklahoma.

Main Results:

  • Nine cases of CJD have been confirmed in HGH recipients globally (7 in the US, 1 in the UK, 1 in New Zealand).
  • Contaminated HGH is the suspected source of CJD transmission.
  • Approximately 60 children and adolescents in Oklahoma are potentially at risk.

Conclusions:

  • The use of cadaver-derived HGH posed a significant risk of CJD transmission.
  • Healthcare providers must be aware of this risk and monitor potentially exposed individuals.
  • Continued surveillance and research are crucial for managing and preventing future cases.

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