Cent Eur J Public Health 2026, 34(1):67-68 | DOI: 10.21101/cejph.a8670

Unusual occurrence of temporo-spatial cluster of human prion disease in northern part of central Slovakia

Pavol Skáčik1, 2, Štefan Sivák1, 2, Egon Kurča1, 2
1 Neurology Department, University Hospital Martin, Martin, Slovak Republic
2 Jessenius Faculty of Medicine in Martin, Comenius University Bratislava, Martin, Slovak Republic

Objectives: Clusters of human prion diseases have been reported in several endemic regions, notably in Slovakia, Italy, Chile, and Israel, predominantly linked to genetic forms (E200K mutation). Isolated temporo-spatial clusters that include sporadic forms are rarely documented and remain poorly understood. This report describes a unique cluster of prionopathies observed in northern central Slovakia.

Methods: Between July 2021 and March 2022, three definitive cases of prion disease were identified in two neighbouring rural villages, Pribovce and Rakovo, in the Martin District of Slovakia. The villages, located within a radius of approximately three kilometres, have a combined population of 1,468. Clinical records, epidemiological data, and neuropathological findings were reviewed in all cases.

Results: The cluster included one genetic Creutzfeldt-Jakob disease (gCJD) with the PRNP E200K mutation and M/M genotype at codon 129; one sporadic CJD (sCJD); and one sporadic fatal familial insomnia (sFFI), the first such case reported in Slovakia. The cases occurred sequentially within a ten-month interval. No familial, environmental, or iatrogenic links were identified.

Conclusions: The coexistence of distinct prionopathies in such a confined population and period is exceptional. Despite comprehensive investigation, no explanatory factor was found, and this cluster likely represents a chance occurrence of epidemiological interest. The finding underscores the importance of systematic neuropathological confirmation, molecular testing, and regional surveillance in prion disease monitoring.

Klíčová slova: Creutzfeldt-Jakob disease, fatal familial insomnia, temporo-spatial cluster, epidemiological surveillance

Vloženo: 31. květen 2025; Revidováno: 28. říjen 2025; Přijato: 28. říjen 2025; Zveřejněno online: 29. leden 2026; Zveřejněno: 31. březen 2026  Zobrazit citaci

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Skáčik P, Sivák Š, Kurča E. Unusual occurrence of temporo-spatial cluster of human prion disease in northern part of central Slovakia. Cent Eur J Public Health. 2026;34(1):67-68. doi: 10.21101/cejph.a8670.
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Reference

  1. Ladogana A, Kovacs GG. Genetic Creutzfeldt-Jakob disease. Handb Clin Neurol. 2018;153:219-42. Přejít k původnímu zdroji...
  2. Rong LL, Lannen NJ, Tank EC, Feistel JL, Therasse CJ, Potluri A, et al. Case report: two clusters of Creutzfeldt-Jakob disease cases within 1 year in West Michigan. Front Neurol. 2023;14:1134225. doi:10.3389/fneur.2023.1134225. Přejít k původnímu zdroji...
  3. Nakatani E, Nishimura T, Zhou B, Kaneda H, Teramukai S, Nagai Y, et al. Temporal and regional variations in sporadic Creutzfeldt-Jakob disease in Japan, 2001-2010. Epidemiol Infect. 2015;143(5):1073-8. Přejít k původnímu zdroji...
  4. D'Aignaux JH, Cousens SN, Delasnerie-Lauprêtre N, Brandel JP, Salomon D, Laplanche JL, et al. Analysis of the geographical distribution of sporadic Creutzfeldt-Jakob disease in France between 1992 and 1998. Int J Epidemiol.2002;31(2):490-5. Přejít k původnímu zdroji...
  5. Statistical Office of the Slovak Republic. Population - Basic results [Internet]. Bratislava: Statistical Office of the Slovak Republic; 2021 [cited 2025 Apr 27]. Available from: https://www.scitanie.sk/en/population/basic-results/number-of-population/SR/SK0/SR.
  6. Skacik P, Kurca E, Sivak S. Exploring CJD incidence trends: insights from Slovakia. Prion. 2024;18(1):87-8. Přejít k původnímu zdroji...
  7. Skacik P, Kurca E, Sivak S, Zakova D, Janakova A, Kycina M, et al. [Creutzfeldt-Jakob disease in the northern part of central Slovakia: a retrospective analysis of patient series from 2006 to 2023]. Neurol Pro Praxi. 2024;25(1):30-5. Slovak. Přejít k původnímu zdroji...