Human transmissible spongiform encephalopathies in eleven countries: diagnostic pattern across time, 1993–2002
2006

Human Transmissible Spongiform Encephalopathies in Eleven Countries: Diagnostic Patterns from 1993 to 2002

Sample size: 4441 publication Evidence: high

Author Information

Author(s): de Pedro-Cuesta Jesús, Glatzel Markus, Almazán Javier, Stoeck Katharina, Mellina Vittorio, Puopolo Maria, Pocchiari Maurizio, Zerr Inga, Kretszchmar Hans A, Brandel Jean-Philippe, Delasnerie-Lauprêtre Nicole, Alpérovitch Annick, Van Duijn Cornelia, Sanchez-Juan Pascual, Collins Steven, Lewis Victoria, Jansen Gerard H, Coulthart Michael B, Gelpi Ellen, Budka Herbert, Mitrova Eva

Hypothesis

The study aims to describe the diagnostic panorama of human transmissible spongiform encephalopathies across 11 countries.

Conclusion

There is considerable international variation in the aetiological subtypes of human transmissible spongiform encephalopathies over the observation period.

Supporting Evidence

  • Pre-mortem use of diagnostic investigations increased over time.
  • International differences in pathological confirmation of sporadic Creutzfeldt-Jakob disease were evident.
  • Some countries showed high proportions of variant Creutzfeldt-Jakob disease, particularly in the UK and France.

Takeaway

This study looked at brain diseases that can spread between humans in 11 countries and found that different countries have different types of these diseases.

Methodology

The study analyzed data from national databases of the EUROCJD consortium, focusing on deaths due to different human transmissible spongiform encephalopathies and variations in diagnostic tests from 1993 to 2002.

Potential Biases

Potential undercounts due to poor reporting or case ascertainment before 1998.

Limitations

The study did not consider mortality rates or population denominators, which may affect the interpretation of results.

Participant Demographics

Patients from eleven countries in the EUROCJD consortium.

Statistical Information

Confidence Interval

95% CI 84.72–4363.40

Statistical Significance

p < 0.001

Digital Object Identifier (DOI)

10.1186/1471-2458-6-278

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