Neurol. pro Praxi, 2007; 3: 145-148

Priony a verejné zdravotníctvo

prof. Robert George Will MD, FRCP
National Creutzfeldt-Jakob disease Surveillance Unit, Western General Hospital, Edinburgh, UK

Prionové choroby človeka, známe aj ako transmisívne spongioformné encefalopatie, sú skupinou zriedkavých, ale bez výnimky fatálnych neurodegeneratívnych chorôb. Tvoria osobitný problém verejného zdravotníctva, tak kvôli absencii laboratórneho vyšetrenia, ktoré by „in vivo“ identifikovalo nakazené zvieratá a ľudí, ako aj kvôli inkubačnej dobe, ktorá presahuje roky až dekády. Identifikovanie variantu Creutzfeldtovej-Jakobovej choroby (CJch) ako zoonózy, kauzálne súvisiacej s bovinnou spongioformnou encefalopatiou (BSE) a predpokladaný prenos nákazy potravinovým reťazcom človeka, vzbudili nielen veľký záujem verejnosti, ale aj obavy odborníkov, ktoré pretrvávajú aj v dôsledku potvrdeného šírenia infekcie transfúziou krvi. Aj keď zatiaľ nebol pozorovaný vertikálny prenos ochorenia, ani sekundárny prenos nákazy kontaminovanými chirurgickými nástrojmi, alebo nová forma infekcie BSE u človeka, potrvá ešte veľa rokov, kým sa takéto možnosti budú môcť vylúčiť. Úlohou verejného zdravotníctva sú opatrenia, s cieľom minimalizovať u ľudí expozíciu BSE potravinami a tiež ich potenciálnu expozíciu inými rizikami ako napr. krv, krvné deriváty, alebo výrobky farmaceutického priemyslu

Keywords: prionové choroby, variant Creutzfeldtovej-Jakobovej choroby, riziko, potrava, krv

Published: August 1, 2007  Show citation

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Will RG. Priony a verejné zdravotníctvo. Neurol. praxi. 2007;8(3):145-148.
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References

  1. Andrews NJ, Farrington CP, Ward HJT, Cousens SN, Smith PG, Molesworth AM et al. Deaths from variant Creutzfeldt-Jakob disease in the UK. Lancet 2003; 361: 751-752. Go to original source... Go to PubMed...
  2. Bishop MT, Hart P, Aitchison L, Baybutt HN, Plinston C, Thomson V et al. Predicting susceptibility and incubation time of human to human transmission of vCJD. Lancet Neurology 2006; 5: 393-398. Go to original source... Go to PubMed...
  3. Boelle PY, Cesbron JY, Valleron AJ. Epidemiological evidence of higher susceptibility to vCJD in the young. BMC Infectious Diseases 2004; 4: 26-32. Go to original source... Go to PubMed...
  4. Clarke P, Ghani AC. Projections of the future course of the primary vCJD epidemic in the UK: inclusion of subclinical infection and the possibility of wider genetic susceptibility. J R Soc Interface 2005; 2: 19-31. Go to original source... Go to PubMed...
  5. Cooper JD, Bird SM. UK dietary exposure to BSE in beef mechanically recovered meat: by birth cohort and gender. J Cancer Epid and Prevention 2002; 7 (2): 59-70. Go to original source... Go to PubMed...
  6. Hewitt PE, Llewelyn CA, Mackenzie J, Will RG. Creutzfeldt-Jakob disease and blood transfusion: results of the UK Transfusion Medicine Epidemiology Review study. Vox Sang 2006; 91: 221-230. Go to original source... Go to PubMed...
  7. Hilton DA, Ghani AC, Conyers L, Edwards P, McCardle L, Ritchie D et al. Prevalence of lymphoreticular prion protein accumulation in UK tissue samples. J Pathology 2004; 203: 733-739. Go to original source... Go to PubMed...
  8. Hilton DA, Sutak J, Smith MEF, Penney M, Conyers L, Edwards P et al. Specificity of lymphoreticular accumulation of prion protein for variant Creutzfeldt-Jakob disease. J Clin Pathol 2004; 57: 300-302. Go to original source... Go to PubMed...
  9. Chadeau-Hyam M, Alperovitch A. Risk of variant Creutzfeldt-Jakob disease in France. Int J Epid 2005; 34: 46-52. Go to original source... Go to PubMed...
  10. Ironside JW, Bishop MT, Connolly K, Hegazy D, Lowrie S, Le Grice M et al. Variant Creutzfeldt-Jakob disease: prion protein genotype analysis of positive appendix tissue samples from a retrospective prevalence study. BMJ 2006; 332: 1186-1188. Go to original source... Go to PubMed...
  11. Peden AH, Head MW, Ritchie DL, Bell JE, Ironside JW. Preclinical vCJD after blood transfusion in a PRNP codon 129 heterozygous patient. Lancet 2004; 364: 527-529. Go to original source... Go to PubMed...
  12. Valleron AJ, Boelle PY, Will R, Cesbron JY. Estimation of epidemic size and incubation time based on age characteristics of vCJD in the United Kingdom. Science 2001; 294: 1726-1728. Go to original source... Go to PubMed...
  13. Ward HJT, Everington D, Cousens SN, Smith-Bathgate B, Leitch M, Cooper S et al. Risk factors for variant Creutzfeldt-Jakob disease: a case-control study. Ann Neurol 2006; 59: 111-120. Go to original source... Go to PubMed...
  14. Will RG, Ironside JW, Zeidler M, Cousens SN, Estibeiro K, Alperovitch A et al. A new variant of Creutzfeldt-Jakob disease in the UK. Lancet 1996; 347: 921-925. Go to original source... Go to PubMed...
  15. World Health Organisation, Food and Agricultural Organisation, Office International des Epizooties. Technical Consultation on BSE: public health, animal health and trade. 2002.




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