Positive 14-3-3 and tau proteins in a sporadic Creutzfeldt-Jakob disease case and a brief perspective of prion diseases in Colombia
Abstract
Prion diseases are rare neurodegenerative disorders occurring worldwide and affecting both humans and animals. Herein, we present the case of a patient diagnosed with definite sporadic Creutzfeldt-Jakob disease in Cali, Colombia. Besides neurological examination, 14-3-3 and tau proteins were valuable tools supporting the diagnosis. We also present a brief perspective of the prion diseases reported in Colombia to date. Although the incidence of prion diseases is unknown in Colombia, our literature review revealed that one case of scrapie in 1981 and 29 human sporadic cases of Creutzfeldt-Jakob disease have been documented and published in our country.
Downloads
References
Prusiner SB. Shattuck lecture: Neurodegenerative diseases and prions. N Engl J Med. 2001;344:1516-26. http://dx.doi.org/10.1056/NEJM200105173442006.
Johnson RT. Prion diseases. Lancet Neurol. 2005;4:635-42. http://dx.doi.org/10.1016/S1474-4422(05)70192-7.
Head MW, Ironside JW. Review: Creutzfeldt-Jakob disease: Prion protein type, disease phenotype and agent strain. Neuropathol Appl Neurobiol. 2012;38:296-310. http://dx.doi.org/10.1111/j.1365-2990.2012.01265.x.
Kim MO, Geschwind MD. Clinical update of Jakob-Creutzfeldt disease. Curr Opin Neurol. 2015;28:302-10. http://dx.doi.org/10.1097/WCO.0000000000000197.
Zerr I, Kallenberg K, Summers DM, Romero C, Taratuto A, Heinemann U, et al. Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease. Brain. 2009;132:2659-68. http://dx.doi.org/10.1093/brain/awp191.
World Health Organization. Global surveillance, diagnosis, and therapy of human transmissible spongiform encephalopathies: Report of a WHO consultation. Geneva: WHO; 1998. Accessed: December 2, 2015. Available from: http://www.who.int/csr/resources/publications/bse/whoemczdi989.pdf.
UCSF Memory and Aging Center. 2007 UCSF criteria for probable sporadic Jakob-Creutzfeldt disease. 2007. Accessed: December 2, 2015. Available from: http://memory.ucsf.edu/cjd/medical/criteria.
Centers for Disease Control and Prevention. CDC's diagnostic criteria for Creutzfeldt-Jakob disease (CJD), 2010. 2010. Accessed: December 2, 2015. Available from: http://www.cdc.gov/prions/cjd/diagnostic-criteria.html.
Johnson RT, Gibbs CJ Jr. Creutzfeldt-Jakob disease and related transmissible spongiform encephalopathies. N Engl J Med. 1998;339:1994-2004. http://dx.doi.org/10.1056/NEJM199812313392707.
Steinhoff BJ, Räcker S, Herrendorf G, Poser S, Grosche S, Zerr I, et al. Accuracy and reliability of periodic sharp wave complexes in Creutzfeldt-Jakob disease. Arch Neurol. 1996;53:162-6. http://dx.doi.org/10.1001/archneur.1996.00550020074017.
Steinhoff BJ, Zerr I, Glatting M, Schulz-Schaeffer W, Poser S, Kretzschmar HA. Diagnostic value of periodic complexes in Creutzfeldt-Jakob disease. Ann Neurol. 2004;56:702-8. http://dx.doi.org/10.1002/ana.20261.
Tschampa HJ, Kallenberg K, Urbach H, Meissner B, Nicolay C, Kretzschmar HA, et al. MRI in the diagnosis of sporadic Creutzfeldt-Jakob disease: A study on inter-observer agreement. Brain. 2005;128:2026-33. http://dx.doi.org/10.1093/brain/awh575.
Lodi R, Parchi P, Tonon C, Manners D, Capellari S, Strammiello R, et al. Magnetic resonance diagnostic markers in clinically sporadic prion disease: A combined brain magnetic resonance imaging and spectroscopy study. Brain. 2009;132:2669-79. http://dx.doi.org/10.1093/brain/awp210.
Sánchez-Juan P, Green A, Ladogana A, Cuadrado-Corrales N, Sánchez-Valle R, Mitrováa E, et al. CSF tests in the differential diagnosis of Creutzfeldt-Jakob disease. Neurology. 2006;67:637-43. http://dx.doi.org/10.1212/01.wnl.0000230159.67128.00.
Hsich G, Kenney K, Gibbs CJ, Lee KH, Harrington MG. The 14-3-3 brain protein in cerebrospinal fluid as a marker for transmissible spongiform encephalopathies. N Engl J Med. 1996;335:924-30. http://dx.doi.org/10.1056/NEJM199609263351303.
Zerr I, Bodemer M, Gefeller O, Otto M, Poser S, Wiltfang J, et al. Detection of 14-3-3 protein in the cerebrospinal fluid supports the diagnosis of Creutzfeldt-Jakob disease. Ann Neurol. 1998;43:32-40. http://dx.doi.org/10.1002/ana.410430109.
Hamlin C, Puoti G, Berri S, Sting E, Harris C, Cohen M, et al. A comparison of tau and 14-3-3 protein in the diagnosis of Creutzfeldt-Jakob disease. Neurology. 2012;79:547-52. http://dx.doi.org/10.1212/WNL.0b013e318263565f.
Toro-González G. Demencia, priones y enfermedades priónicas. Referencia especial a las "vacas locas". Rev Acad Colomb Cienc. 1997;21:229-36.
Roselli A, Potes J, Kattah J, Palacios E, Ordóñez N. Encefalopatía espongiforme subaguda (enfermedad de Creutzfeldt-Jakob). Tribuna Médica. 1973;554:A7-10.
Zaninovic V, Dueñas A. Un caso de enfermedad de Creutzfeldt-Jakob. Acta Med Valle. 1979;10:131-6.
Zaninovic V, Dueñas A. Demencia viral transmisible. Confirmación de un caso de enfermedad de Creutzfeldt-Jakob. Colombia Médica. 1983;14:40-2.
Díez J, Jiménez A, Roselli A, Jiménez E, Ruiz N, Morales S. Enfermedad de Creutzfeldt-Jakob. Reporte de un caso. Neurocien Colom. 1999;7:49-52.
Colegial C, Silva F, Pérez C, Saavedra M, Fernández W, Pardo R, et al. Encefalopatía por priones, caso clínico-patológico. Revista de la Facultad de Medicina. 1999;47:13-20.
Villamil W, Gonzáles J, Arrieta JA, Álvarez C, Borja G, Vergara JC, et al. Creutzfeldt-Jakob disease: Case report. Infectio. 2007;11:124-8.
Villegas VE, Velandia F, Payán C. Sporadic Creutzfeldt-Jakob disease: Clinical, pathological and molecular study. Rev Cienc Salud. 2008;6:36-47.
Rincón OL, Vélez A, King LM, Hernández DL, Isaza R, Vagner B, et al. Sporadic Creutzfeldt-Jakob disease: Neuropsychiatric symptoms followed by a progressive cognitive decline: A case report. Medicina UPB. 2008;27: 59-63.
Díaz-Martínez JC, Takeuchi-Tan Y. Creutzfeldt-Jakob disease: Clinical, electroencephalographic, pathologic, and imaging characteristics. Acta Neurol Colomb. 2008;24: 118-23.
Paredes A, Castro A, Toro G, Parra E. Vigilancia epidemiológica de enfermedades priónicas en Colombia, 2005 a 2012. Inf Quinc Epidemiol Nac. 2013;18:32-41. Accessed: August 1, 2015. Available from: http://www.minsalud.gov.co/sites/rid/Lists/BibliotecaDigital/RIDE/IA/INS/IQEN%20vol%2018%202013%20num%203.pdf.
Duque-Velásquez C, Garzón Á, Villegas A, Escobar LM, Zea J, Lopera F, et al. Human transmissible spongiform encephalopathy: Case report. Iatreia. 2014;27:330-6.
Tramontini-Jens C, Mora-Salazar JA, Castaño-Restrepo NE. Creutzfeldt-Jakob disease, MRI findings: A case report. Rev Colomb Radiol. 2014:25;4021-5.
Cadena-Sanabria M, Ardila-Báez M, Rueda-Prada L. Status epilepticus and rapidly progressive dementia in an elderly woman. Sporadic Creutzfeldt-Jakob disease. Rev Esp Geriatr Gerontol. 2015;50:103-4. http://dx.doi.org/10.1016/j.regg.2014.10.009.
Triana JD, Pérez-Rangel A. Creutzfeldt-Jakob disease. Hospital de San José, Bogotá DC, Colombia. Repertorio de Medicina y Cirugía. 2015;24:298-302.
Toro G, Díaz A, Saad C. Ayer, hoy y mañana, la teoría del prion. Revista Medicina. 2004;26:7-20.
Duque JC, Villegas A, Rodas JD. Transmissible spongiform encephalopathies: Biology of the prion and current state of the epidemiologic surveillance in Colombia. Rev Colomb Cienc Pecu. 2010;23:240-9.
Ossa JE, Machado G, Giraldo MA, McEwen JG. Prion plaques: Molecular tumors. A hypothesis on the etiopathogenesis of prion diseases. Med Hypotheses. 1995; 44:124-6. http://dx.doi.org/10.1016/0306-9877(95)90084-5.
Corral RH, Zapata JI. Priones como enfermedad en humanos. SIEI. 1998;4:6-17.
Zaninovic V. Correspondence. Colomb Med. 1998;29: 40-2.
Lopera-Restrepo F. La enfermedad de las vacas locas: efectos en el ser humano, su dominio y diagnóstico por el laboratorio. Medicina & Laboratorio. 2002;10:159-69.
Toro G, Pacheco OE, Sierra UE, Beltrán M, Díaz A, Parra EA, et al. Encefalopatías subagudas espongiformes transmisibles (ESET). La teoría prion-enfermedades priónicas. Acta Neurol Colomb. 2005;21:134-62.
Villegas-Lanau CA. Prion diseases: From molecular biology to clinical practice. Acta Neurol Colomb. 2010;26:87-111.
Barashi NS, Vargas-Acevedo C, Zarco LA. Enfermedades priónicas humanas. Univ Med. 2013;54:495-516.
Some similar items:
- Juan Sebastián Barajas, Ludwing Flórez Salamanca, Solitary neurofibroma in the abdominal wall of a patient without neurofibromatosis: case report , Biomedica: Vol. 29 No. 4 (2009)
- María Esther Pedrozo, Sandra Ocampos, Rosa Galeano, Andrea Ojeda, Agueda Cabello, Dalva De Assis, Cases of acute pesticide poisoning in Colonia Puerto Pirapó, Itapúa, Paraguay, February, 2014 , Biomedica: Vol. 37 No. 2 (2017)
- David Andrés Espinal, Isabel Cristina Hurtado, Ana Eugenia Arango, Josefina García, V. Alberto Laguna-Torres, Sergio Jaramillo, Human metapneumovirus in children: first cases in Colombia , Biomedica: Vol. 32 No. 2 (2012)
- Lucía Quesada-Lobo, Adriana Troyo, Ólger Calderón-Arguedas, First report of nosocomial myiasis by Lucilia cuprina (Diptera: Calliphoridae) in Costa Rica , Biomedica: Vol. 32 No. 4 (2012)
- Diana Carolina Moncada, Melisa Montes, Verónica Molina, Jorge Byron Velásquez, Carlos Ignacio Gómez, Orofacial infection by Conidiobolus coronatus , Biomedica: Vol. 36 (2016): Suplemento 1, Microbiología médica
- Ana Madeleine Barrera, Leslie Vargas, Idiopathic pulmonary hemosiderosis with dendriform pulmonary ossification , Biomedica: Vol. 36 No. 4 (2016)
- Patricia Jiménez, Karina Calvopiña, Diana Herrera, Carlos Rojas, Laura Pérez-Lago, Marcelo Grijalva, Remedios Guna, Darío García-de Viedma, Identification of the Mycobacterium tuberculosis Beijing lineage in Ecuador , Biomedica: Vol. 37 No. 2 (2017)
- Nhora Silva, Natalia Calvache, Elizabeth Arrieta, Juan Carlos Bravo, Camilo Salazar, Joaquín Rosales, Francisco Jaramillo, Juan Guillermo Restrepo, Disseminated histoplasmosis as a first clinical manifestation in a patient with small lymphocytic lymphoma: A case report , Biomedica: Vol. 38 No. 3 (2018)
- José Y. Rodríguez, Carlos A. Álvarez-Moreno, Jorge A. Cortés, Gerson J. Rodríguez, Kelin Esquea, Heidy Pinzón, María J. Mendoza, Yiceth Acosta, Melioidosis in Colombia, description of a clinical case and epidemiological considerations , Biomedica: Vol. 39 No. Sp. 1 (2019): Suplemento 1, Microbiología médica, mayo
- Camila Montoya, Liza M. Arias, Mónica Salazar, Rodrigo Restrepo, Water-induced dermatosis: Aquagenic keratoderma. A case report , Biomedica: Vol. 39 No. 2 (2019)
Article metrics | |
---|---|
Abstract views | |
Galley vies | |
PDF Views | |
HTML views | |
Other views |