Abstract
The places of origin of 7 out of 8 patients with CJD coincide with the distribution of sheep-rearing in central and southern Italy, confirming the suggested link between this disease and eating and-or handling sheep CNS tissue. Since 6 of the 8 cases were women, it seems more likely that the virus responsible for CJD enters the body through a break in the skin of the hands and forearms in the process of foodhandling rather than via the Digestive tract. This aspect should be borne in mind when investigating the problems of CJD transmission.
Sommario
È stata studiata la distribuzione geografica dei luoghi di origine di 8 pazienti con CJD correlandola alla distribuzione, all'interno delle diverse regioni dell'Italia Centrale, e in parte Meridionale, delle aree a prevalente economia da pascolo, soprattutto pastorizia ovina. Si è indagata una eventuale connessione tra abitudini alimentari che comprendono la manipolazione a scopo alimentare ed il susseguente consumo di tessuti del SNC di ovini e la insorgenza della CJD. Viene avanzata la ipotesi che attraverso soluzioni di continuo nel rivestimento dei tegumenti delle estremità superiori, piuttosto che per la via della ingestione, l'agente virale della malattia potrebbe penetrare nell'organismo, per cui questo elemento sarebbe da tenere presente nell'affrontare i problemi connessi con le modalità di trasmissione della CJD.
Similar content being viewed by others
References
Alter M, Frank Y, Doyne H et al:Creutzfeldt-Jakob disease after eating ovine brains? N Engl J Med 292, 927, 1975.
Alter M Hoenig E. Pratzon G.:Creutzfeldt-Jakob disease: possible association with eating brains. N Engl J Med 296, 820–821, 1977.
Alter M.:More on Creutzfeldt-Jakob disease and sheep brain. N. Engl J. Med 297, 453, 1977.
Bell J.F.:Creutzfeldt-Jakob disease and sheep brain (cont). N Engl J Med 296, 1415, 1977.
Brown P. Cathala F.:La biologie et l'épidémiologie de la maladie de Creutzfeldt et Jakob. Rev EEG Neurophysiol 8, 4, 407–411, 1978.
Brown P. Cathala F.:Creutzfeldt-Jakob disease in France: I. Retrospective study of the Paris area during the ten-year period 1968–1977. Ann Neurol 5, 189–192, 1979.
Brown P. Cathala F., Gajdusek D.C.:Creutzfeldt-Jakob disease in France: III. Epidemiological study of 170 patients dying during the decade 1968–1977. Ann. Neurol. 6 (Nov). pp. 438–446, 1979.
Cathala F., Brown P., Castaigne P. et la:La maladie de Creutzfeldt-Jakob en France continental. Rev Neurol (Paris) 135, (5), 439–454, 1979.
Gajdusek DC, Gibbs IR CJ, Asher DM et al:Precautions in medical care of, and handling material from, patients with transmissible virus dementia (Creutzfeldt-Jakob Disease). N. Engl J Med 297, 1253–1258, 1977.
Gajdusek DC, Gibbs CJ:Slow virus infections of the Nervous system and the laboratories of slow, latent and temperate virus infections; inTowers DB (ed)The Nervous System. The clinical Neurosciences, New York, Raven Press, 1975 vol, 2 pp. 113–135.
Johnson RT.:Virology and Neuroepidemiology: chronic viral infections of the Nervous System, in: Advances in Neurology ed by BS Shoenberg, vol 19, p. 161–167, New York 1978.
Masters CL, Harris JO, Gajdusek DC et al:Creutzfeldt-Jakob disease: patterns of worldwide occurrence and the significance of familial and sporadic clustering. Ann Neurol 5, 177–188, 1979.
Matthews WB:Creutzfeldt-Jakob disease as a transmissible encephalopathy. In: Rec. Adv. in Neuropathol. Thomas Smith IW and Cavanagh JB Editors Churchill Livingstone, London, 1979.
Neugut RH, Neugut AI, Kahana E. et al:Creutzfeldt-Jakob disease: familial clustering among Libyan-born Israelis. Neurology 29, 225–231, 1979.
Roos R., Gajdusek DC, Gibbs Jr CJ:The clinical characteristics of transmissible Creutzfeldt-Jakob disease. Brain 96, 1–20, 1973.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Lo Russo, F., Neri, G. & Figà-Talamanca, L. Creutzfeldt-Jakob disease and sheep brain a report from central and southern Italy. Ital J Neuro Sci 1, 171–174 (1979). https://doi.org/10.1007/BF02335847
Issue Date:
DOI: https://doi.org/10.1007/BF02335847