nnpNeurology, Neuropsychiatry, PsychosomaticsНеврология, нейропсихиатрия, психосоматика2074-27112310-1342"IMA-Press", LLC10.14412/2074-2711-2020-2-86-91nnp-1310Research ArticleCLINICAL OBSERVATIONSКЛИНИЧЕСКИЕ НАБЛЮДЕНИЯCreutzfeldt–Jakob disease in the Republic of Sakha (Yakutia)Болезнь Крейтцфельда–Якоба в Республике Саха (Якутия)ПоповаТ. Е.PopovaT. E.ТаппаховА. А.TappakhovA. A.
Россия, 677000, Якутск, ул. Белинского, 58
58, Belinsky St., Yakutsk 677000, Russia
dralex89@mail.ruДавыдоваТ. К.DavydovaT. K.
Россия, 677000, Якутск, Сергеляхское шоссе, 4
НиколаеваТ. Я.NikolaevaT. Ya.ХабароваЮ. И.KhabarovaYu. I.ВарламоваМ. А.VarlamovaM. A.ОконешниковаЛ. Т.OkoneshinovaL. T.ФГБНУ «Якутский научный центр комплексных медицинских проблем»РоссияYakutsk Research Center for Complex Medical ProblemsRussian FederationФГБНУ «Якутский научный центр комплексных медицинских проблем»;
ФГАОУ ВО «Северо-Восточный федеральный университет им. М.К. Аммосова»РоссияYakutsk Research Center for Complex Medical Problems;
M.K. Ammosov North-Eastern Federal UniversityRussian FederationM.K. Ammosov North-Eastern Federal UniversityRussian FederationГБУ Республики Саха (Якутия) «Республиканская больница №2 – Центр экстренной медицинской помощи»РоссияCenter for Emergency Medical Care, Republican Hospital TwoRussian Federation2020190420201228691Copyright © Popova T.E., Tappakhov A.A., Davydova T.K., Nikolaeva T.Y., Khabarova Y.I., Varlamova M.A., Okoneshinova L.T., 20202020Попова Т.Е., Таппахов А.А., Давыдова Т.К., Николаева Т.Я., Хабарова Ю.И., Варламова М.А., Оконешникова Л.Т.Popova T.E., Tappakhov A.A., Davydova T.K., Nikolaeva T.Y., Khabarova Y.I., Varlamova M.A., Okoneshinova L.T.Данная работа распространяется под лицензией Creative Commons Attribution 4.0.This work is licensed under a Creative Commons Attribution 4.0 License.https://nnp.ima-press.net/nnp/article/view/1310прионные болезниболезнь Крейтцфельда–Якобадеменциямиоклониигубчатые энцефалопатииprion diseasesCreutzfeldt–Jakob diseasedementiamyoclonusspongiform encephalopathiesReferencesШнайдер НА. Болезнь КрейцфельдаЯкоба: новый взгляд на старую проблему (история изучения, этиология и патогенез). Журнал неврологии и психиатрии им. С.С. Корсакова. 2013;113(4):72-9.Shnaider NA. Creutzfeldt-Jakob disease: a new look at the old problem (history of study, etiology and pathogenesis). Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova. 2013;113(4): 72-9. (in Russ.)].Jacobs DA, Lesser RL, Mourelatos Z, et al. The Heidenhain variant of Creutzfeldt-Jakob disease: clinical, pathologic, and neuroimaging findings. J Neuroophthalmol. 2001;21(2):99-102. doi: 10.1097/00041327-200106000-00008.Jacobs DA, Lesser RL, Mourelatos Z, et al. The Heidenhain variant of Creutzfeldt-Jakob disease: clinical, pathologic, and neuroimaging findings. J Neuroophthalmol. 2001;21(2):99-102. doi: 10.1097/00041327-200106000-00008.Uttley L, Carroll C, Wong R, et al. Creutzfeldt-Jakob disease: a systematic review of global incidence, prevalence, infectivity, and incubation. Lancet Infect Dis. 2020;20(1):e2-e10. doi: 10.1016/S1473-3099(19)30615-2.Uttley L, Carroll C, Wong R, et al. Creutzfeldt-Jakob disease: a systematic review of global incidence, prevalence, infectivity, and incubation. Lancet Infect Dis. 2020;20(1):e2-e10. doi: 10.1016/S1473-3099(19)30615-2.Creutzfeldt-Jakob Disease International Surveillance Network. CJD surveillance data 1993–2018. 2018. http://www.eurocjd.ed.ac.uk/surveillance%20data%201.htmlCreutzfeldt-Jakob Disease International Surveillance Network. CJD surveillance data 1993–2018. 2018. http://www.eurocjd.ed.ac.uk/surveillance%20data%201.htmlRabinovici GD, Wang PN, Levin J, et al. First symptom in sporadic Creutzfeldt-Jakob disease. Neurology. 2006 Jan 24;66(2):286-7. doi: 10.1212/01.wnl.0000196440.00297.67.Rabinovici GD, Wang PN, Levin J, et al. First symptom in sporadic Creutzfeldt-Jakob disease. Neurology. 2006 Jan 24;66(2):286-7. doi: 10.1212/01.wnl.0000196440.00297.67.Manix M, Kalakoti P, Henri M, et al. Creutzfeldt-Jakob disease: updated diagnostic criteria, treatment algorithm, and the utility of brain biopsy. Neurosurg Focus. 2015;39(5):E2. doi: 10.3171/2015.8.FOCUS15328.Manix M, Kalakoti P, Henri M, et al. Creutzfeldt-Jakob disease: updated diagnostic criteria, treatment algorithm, and the utility of brain biopsy. Neurosurg Focus. 2015;39(5):E2. doi: 10.3171/2015.8.FOCUS15328.Parchi P, De Boni L, Saverioni D, et al. Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USA. Acta Neuropathol. 2012 Oct;124(4):517-29. doi: 10.1007/s00401-012-1002-8.Parchi P, De Boni L, Saverioni D, et al. Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USA. Acta Neuropathol. 2012 Oct;124(4):517-29. doi: 10.1007/s00401-012-1002-8.Fragoso DC, Goncalves Filho AL, Pacheco FT, et al. Imaging of Creutzfeldt-Jakob disease: imaging patterns and their differential diagnosis. Radiographics. 2017;37(1):234-257. doi: 10.1148/rg.2017160075.Fragoso DC, Goncalves Filho AL, Pacheco FT, et al. Imaging of Creutzfeldt-Jakob disease: imaging patterns and their differential diagnosis. Radiographics. 2017;37(1):234-257. doi: 10.1148/rg.2017160075.Hirst CL. Sporadic Creutzfeldt-Jakob disease presenting as a stroke mimic590. Br J Hosp Med (Lond). 2011;72(10):590-591. doi: 10.12968/hmed.2011.72.10.590.Hirst CL. Sporadic Creutzfeldt-Jakob disease presenting as a stroke mimic590. Br J Hosp Med (Lond). 2011;72(10):590-591. doi: 10.12968/hmed.2011.72.10.590.Hanumanthu R, Alchaki A, Nyaboga A, et al. An unusual case of sporadic CreutzfeldJacob disease presenting as acute neuropathy. Mov Disord. 2017;32:563-4.Hanumanthu R, Alchaki A, Nyaboga A, et al. An unusual case of sporadic CreutzfeldJacob disease presenting as acute neuropathy. Mov Disord. 2017;32:563-4.Karatas H, Dericioglu N, Kursun O, et al. Creutzfeldt-Jakob disease presenting as hyperparathyroidism and generalized tonic status epilepticus. Clin EEG Neurosci. 2007 Oct; 38(4):203-6. doi: 10.1177/155005940703800404.Karatas H, Dericioglu N, Kursun O, et al. Creutzfeldt-Jakob disease presenting as hyperparathyroidism and generalized tonic status epilepticus. Clin EEG Neurosci. 2007 Oct; 38(4):203-6. doi: 10.1177/155005940703800404.Pachalska M, Kurzbauer H, ForminskaKapuscik M, et al. Atypical features of dementia in a patient with Creutzfeldt-Jakob disease. Med Sci Monit. 2007 Jan;13(1):CS9-19. Epub 2006 Dec 18.Pachalska M, Kurzbauer H, ForminskaKapuscik M, et al. Atypical features of dementia in a patient with Creutzfeldt-Jakob disease. Med Sci Monit. 2007 Jan;13(1):CS9-19. Epub 2006 Dec 18.Litzroth A, Cras P, De Vil B, Quoilin S. Overview and evaluation of 15 years of Creutzfeldt-Jakob disease surveillance in Belgium, 1998–2012. BMC Neurol. 2015 Dec 2;15:250. doi: 10.1186/s12883-015-0507-x.Litzroth A, Cras P, De Vil B, Quoilin S. Overview and evaluation of 15 years of Creutzfeldt-Jakob disease surveillance in Belgium, 1998–2012. BMC Neurol. 2015 Dec 2;15:250. doi: 10.1186/s12883-015-0507-x.Mahboob HB, Kaokaf KH, Gonda JM. Creutzfeldt-Jakob Disease Presenting as Expressive Aphasia and Nonconvulsive Status Epilepticus. Case Rep Crit Care. 2018:5053175. doi: 10.1155/2018/5053175.Mahboob HB, Kaokaf KH, Gonda JM. Creutzfeldt-Jakob Disease Presenting as Expressive Aphasia and Nonconvulsive Status Epilepticus. Case Rep Crit Care. 2018:5053175. doi: 10.1155/2018/5053175.Ali R, Baborie A, Larner AJ, et al. Psychiatric presentation of sporadic Creutzfeldt-Jakob disease: a challenge to current diagnostic criteria. J Neuropsychiatry Clin Neurosci. 2013;25(4):335-8. doi: 10.1176/appi.neuropsych.13020025.Ali R, Baborie A, Larner AJ, et al. Psychiatric presentation of sporadic Creutzfeldt-Jakob disease: a challenge to current diagnostic criteria. J Neuropsychiatry Clin Neurosci. 2013;25(4):335-8. doi: 10.1176/appi.neuropsych.13020025.Rodriguez-Porcel F, Ciarlariello VB, Dwivedi AK, et al. Movement Disorders in Prionopathies: A Systematic Review. Tremor Other Hyperkinet Mov (NY). 2019;9. doi: 10.7916/tohm.v0.712. eCollection 2019.Rodriguez-Porcel F, Ciarlariello VB, Dwivedi AK, et al. Movement Disorders in Prionopathies: A Systematic Review. Tremor Other Hyperkinet Mov (NY). 2019;9. doi: 10.7916/tohm.v0.712. eCollection 2019.Sakuma T, Watanabe S, Ouchi A, et al. Three Cases of Creutzfeldt-Jakob Disease with Visual Disturbances as Initial Manifestation. Case Rep Ophthalmol. 2019 Oct 23;10(3): 349-356. doi: 10.1159/000503274. eCollection 2019 Sep-Dec.Sakuma T, Watanabe S, Ouchi A, et al. Three Cases of Creutzfeldt-Jakob Disease with Visual Disturbances as Initial Manifestation. Case Rep Ophthalmol. 2019 Oct 23;10(3): 349-356. doi: 10.1159/000503274. eCollection 2019 Sep-Dec.Rudge P, Jaunmuktane Z, Adlard P, et al. Iatrogenic CJD due to pituitary-derived growth hormone with genetically determined incubation times of up to 40 years. Brain. 2015;138(11): 3386–3399. doi: 10.1093/brain/awv235.Rudge P, Jaunmuktane Z, Adlard P, et al. Iatrogenic CJD due to pituitary-derived growth hormone with genetically determined incubation times of up to 40 years. Brain. 2015;138(11): 3386–3399. doi: 10.1093/brain/awv235.Thompson A, MacKay A, Rudge P, et al. Behavioral and psychiatric symptoms in prion disease. Am J Psychiatry. 2014;171(3):265-274. doi: 10.1176/appi.ajp.2013.12111460.Thompson A, MacKay A, Rudge P, et al. Behavioral and psychiatric symptoms in prion disease. Am J Psychiatry. 2014;171(3):265-274. doi: 10.1176/appi.ajp.2013.12111460.Переседова АВ, Стойда НИ, Гнездицкий ВВ и др. Спорадическая болезнь Крейтцфельдта-Якоба: клиническое наблюдение. Анналы клинической и экспериментальной неврологии. 2011;5(4):52-6.Peresedova AV, Stoida NI, Gnezditskii VV, et al. Sporadic Creutzfeldt-Jakob disease: a clinical observation. Annaly klinicheskoi i eksperimental'noi nevrologii. 2011;5(4): 52-6. (In Russ.)].Курушина ОВ, Мирошникова ВВ, Кривоножкина ПС. Случай семейной формы болезни Крейтцфельдта-Якоба. Журнал неврологии и психиатрии им. С.С. Корсакова. 2018;118(9):94-7.Kurushina OV, Miroshnikova VV, Krivonozhkina PS. A case of familial Creutzfeldt-Jakob disease. Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova. 2018;118(9): 94-7. (In Russ.)].Vitali P, Maccagnano E, Caverzasi E, et al. Diffusion-weighted MRI hyperintensity patterns differentiate CJD from other rapid dementias. Neurology. 2011;76(20):1711-1719. doi: 10.1212/WNL.0b013e31821a4439.Vitali P, Maccagnano E, Caverzasi E, et al. Diffusion-weighted MRI hyperintensity patterns differentiate CJD from other rapid dementias. Neurology. 2011;76(20):1711-1719. doi: 10.1212/WNL.0b013e31821a4439.Zerr I, Kallenberg K, Summers D, et al. Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease. Brain. 2009;132(10): 2659-2668. doi: 10.1093/brain/awp191.Zerr I, Kallenberg K, Summers D, et al. Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease. Brain. 2009;132(10): 2659-2668. doi: 10.1093/brain/awp191.Geschwind MD. Prion diseases. Continuum (Minneap Minn). 2015 Dec;21(6 Neuroinfectious Disease):1612-38. doi: 10.1212/CON.0000000000000251.Geschwind MD. Prion diseases. Continuum (Minneap Minn). 2015 Dec;21(6 Neuroinfectious Disease):1612-38. doi: 10.1212/CON.0000000000000251.McGuire LI, Peden AH, Orru CD, et al. Real time quaking-induced conversion analysis of cerebrospinal fluid in sporadic CreutzfeldtJakob disease. Ann Neurol. 2012;72(2):278-285. doi: 10.1002/ana.23589.McGuire LI, Peden AH, Orru CD, et al. Real time quaking-induced conversion analysis of cerebrospinal fluid in sporadic CreutzfeldtJakob disease. Ann Neurol. 2012;72(2):278-285. doi: 10.1002/ana.23589.Satoh K, Fuse T, Nonaka T, et al. Postmortem Quantitative Analysis of Prion Seeding Activity in the Digestive System. Molecules. 2019 Dec 16;24(24). pii: E4601. doi: 10.3390/molecules24244601.Satoh K, Fuse T, Nonaka T, et al. Postmortem Quantitative Analysis of Prion Seeding Activity in the Digestive System. Molecules. 2019 Dec 16;24(24). pii: E4601. doi: 10.3390/molecules24244601.Wadsworth JD, Joiner S, Hill AF, et al. Tissue distribution of protease resistant prion protein in variant Creutzfeldt-Jakob disease using a highly sensitive immunoblotting assay. Lancet. 2001 Jul 21;358(9277):171-80. doi: 10.1016/s0140-6736(01)05403-4.Wadsworth JD, Joiner S, Hill AF, et al. Tissue distribution of protease resistant prion protein in variant Creutzfeldt-Jakob disease using a highly sensitive immunoblotting assay. Lancet. 2001 Jul 21;358(9277):171-80. doi: 10.1016/s0140-6736(01)05403-4.Klug GM, Wand H, Boyd A, et al. Enhanced geographically restricted surveillance simulates sporadic Creutzfeldt-Jakob disease cluster. Brain. 2009 Feb;132(Pt 2):493-501. doi: 10.1093/brain/awn303. Epub 2008 Nov 28.Klug GM, Wand H, Boyd A, et al. Enhanced geographically restricted surveillance simulates sporadic Creutzfeldt-Jakob disease cluster. Brain. 2009 Feb;132(Pt 2):493-501. doi: 10.1093/brain/awn303. Epub 2008 Nov 28.Klug GM, Wand H, Simpson M, et al. Intensity of human prion disease surveillance predicts observed disease incidence. J Neurol Neurosurg Psychiatry. 2013 Dec;84(12):1372-7. doi: 10.1136/jnnp-2012-304820. Epub 2013 Aug 21.Klug GM, Wand H, Simpson M, et al. Intensity of human prion disease surveillance predicts observed disease incidence. J Neurol Neurosurg Psychiatry. 2013 Dec;84(12):1372-7. doi: 10.1136/jnnp-2012-304820. Epub 2013 Aug 21.
The authors declare that there are no conflicts of interest present.