Biomarkers and diagnostic guidelines for sporadic Creutzfeldt-Jakob disease

被引:187
作者
Hermann, Peter [1 ]
Appleby, Brian [2 ,3 ,4 ,5 ]
Brandel, Jean-Philippe [6 ,7 ]
Caughey, Byron [8 ]
Collins, Steven [9 ,10 ]
Geschwind, Michael D. [11 ]
Green, Alison [12 ]
Haik, Stephane [6 ,7 ]
Kovacs, Gabor G. [13 ,14 ,15 ]
Ladogana, Anna [16 ]
Llorens, Franc [1 ,17 ,18 ]
Mead, Simon [19 ,20 ]
Nishida, Noriyuki [21 ]
Pal, Suvankar [12 ]
Parchi, Piero [23 ,24 ]
Pocchiari, Maurizio [16 ]
Satoh, Katsuya [22 ]
Zanusso, Gianluigi [25 ]
Zerr, Inga [1 ,26 ]
机构
[1] Univ Med Ctr Gottingen, Natl Reference Ctr Transmissible Spongiform Encep, Dept Neurol, D-37075 Gottingen, Germany
[2] Case Western Reserve Univ, Natl Prion Dis Pathol Surveillance Ctr, Cleveland, OH 44106 USA
[3] Case Western Reserve Univ, Univ Hosp Cleveland, Med Ctr, Dept Neurol, Cleveland, OH 44106 USA
[4] Case Western Reserve Univ, Univ Hosp Cleveland, Med Ctr, Dept Psychiat, Cleveland, OH 44106 USA
[5] Case Western Reserve Univ, Univ Hosp Cleveland, Med Ctr, Dept Pathol, Cleveland, OH 44106 USA
[6] Grp Hosp Pitie Salpetriere, Cellule Natl Riference Malad Creutzfeldt Jakob, Paris, France
[7] Sorbonne Univ, Inst Cerveau & Moelle Epiniere, Paris, France
[8] NIAID, Lab Persistent Viral Dis, Rocky Mt Labs, NIH, Hamilton, MT USA
[9] Univ Melbourne, Australian Natl Creutzfeldt Jakob Dis Registry, Florey Inst Neurosci & Mental Hlth, Parkville, Vic, Australia
[10] Univ Melbourne, Dept Med, Parkville, Vic, Australia
[11] Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USA
[12] Univ Edinburgh, Natl CJD Res & Surveillance Unit, Ctr Clin Brain Sci, Edinburgh, Midlothian, Scotland
[13] Univ Toronto, Tanz Ctr Res Neurodegenerat Dis, Toronto, ON, Canada
[14] Univ Toronto, Dept Lab Med & Pathobiol, Toronto, ON, Canada
[15] Univ Hlth Network, Lab Med Program, Toronto, ON, Canada
[16] Ist Super San, Dept Neurosci, Rome, Italy
[17] Inst Carlos III, Ctr Biomed Res Neurodegenerat Dis, Barcelona, Spain
[18] Bellvitge Biomed Res Inst, Barcelona, Spain
[19] Univ Coll London Hosp NHS Fdn Trust, Natl Prion Clin, London, England
[20] UCL, Inst Prion Dis, Med Res Council Prion Unit, London, England
[21] Nagasaki Univ, Grad Sch Biomed Sci, Dept Mol Microbiol & Immunol, Nagasaki, Japan
[22] Nagasaki Univ, Grad Sch Biomed Sci, Dept Locomot Rehabil Sci, Nagasaki, Japan
[23] Ist Sci Neurol Bologna, Ist Ricovero & Cora & Carattere Sci, Bologna, Italy
[24] Univ Bologna, Dept Expt Diagnost & Specialty Med, Bologna, Italy
[25] Univ Verona, Dept Neurosci Biomed & Movement Sci, Verona, Italy
[26] German Ctr Neurodegenerat Dis, Gottingen, Germany
基金
美国国家卫生研究院; 澳大利亚国家健康与医学研究理事会;
关键词
QUAKING-INDUCED CONVERSION; CEREBROSPINAL-FLUID BIOMARKER; HUMAN PRION DETECTION; DIFFERENTIAL-DIAGNOSIS; 14-3-3; PROTEIN; ALPHA-SYNUCLEIN; MRI FINDINGS; CSF; TAU; ACCURACY;
D O I
10.1016/S1474-4422(20)30477-4
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Sporadic Creutzfeldt-Jakob disease is a fatal neurodegenerative disease caused by misfolded prion proteins (PrPSc). Effective therapeutics are currently not available and accurate diagnosis can be challenging. Clinical diagnostic criteria use a combination of characteristic neuropsychiatric symptoms, CSF proteins 14-3-3, MRI, and EEG. Supportive biomarkers, such as high CSF total tau, could aid the diagnostic process. However, discordant studies have led to controversies about the clinical value of some established surrogate biomarkers. Development and clinical application of disease-specific protein aggregation and amplification assays, such as real-time quaking induced conversion (RT-QuIC), have constituted major breakthroughs for the confident pre-mortem diagnosis of sporadic Creutzfeldt-Jakob disease. Updated criteria for the diagnosis of sporadic Creutzfeldt-Jakob disease, including application of RT-QuIC, should improve early clinical confirmation, surveillance, assessment of PrPSc seeding activity in different tissues, and trial monitoring. Moreover, emerging blood-based, prognostic, and potentially pre-symptomatic biomarker candidates are under investigation.
引用
收藏
页码:235 / 246
页数:12
相关论文
共 111 条
  • [101] Towards a treatment for genetic prion disease: trials and biomarkers
    Vallabh, Sonia M.
    Minikel, Eric Vallabh
    Schreiber, Stuart L.
    Lander, Eric S.
    [J]. LANCET NEUROLOGY, 2020, 19 (04) : 361 - 368
  • [102] Prion protein quantification in human cerebrospinal fluid as a tool for prion disease drug development
    Vallabh, Sonia M.
    Nobuhara, Chloe K.
    Llorens, Franc
    Zerr, Inga
    Parchi, Piero
    Capellari, Sabina
    Kuhn, Eric
    Klickstein, Jacob
    Safar, Jiri G.
    Nery, Flavia C.
    Swoboda, Kathryn J.
    Geschwind, Michael D.
    Zetterberg, Henrik
    Arnold, Steven E.
    Minikel, Eric Vallabh
    Schreiber, Stuart L.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2019, 116 (16) : 7793 - 7798
  • [103] Cerebrospinal Fluid Total Prion Protein in the Spectrum of Prion Diseases
    Villar-Pique, Anna
    Schmitz, Matthias
    Lachmann, Ingolf
    Karch, Andre
    Calero, Olga
    Stehmann, Christiane
    Sarros, Shannon
    Ladogana, Anna
    Poleggi, Anna
    Santana, Isabel
    Ferrer, Isidre
    Mitrova, Eva
    Zakova, Dana
    Pocchiari, Maurizio
    Baldeiras, Ines
    Calero, Miguel
    Collins, Steven J.
    Geschwind, Michael D.
    Sanchez-Valle, Raquel
    Zerr, Inga
    Llorens, Franc
    [J]. MOLECULAR NEUROBIOLOGY, 2019, 56 (04) : 2811 - 2821
  • [104] Diffusion-weighted MRI hyperintensity patterns differentiate CJD from other rapid dementias
    Vitali, P.
    Maccagnano, E.
    Caverzasi, E.
    Henry, R. G.
    Haman, A.
    Torres-Chae, C.
    Johnson, D. Y.
    Miller, B. L.
    Geschwind, M. D.
    [J]. NEUROLOGY, 2011, 76 (20) : 1711 - 1719
  • [105] Tau in physiology and pathology
    Wang, Yipeng
    Mandelkow, Eckhard
    [J]. NATURE REVIEWS NEUROSCIENCE, 2016, 17 (01) : 5 - 21
  • [106] Rapid End-Point Quantitation of Prion Seeding Activity with Sensitivity Comparable to Bioassays
    Wilham, Jason M.
    Orru, Christina D.
    Bessen, Richard A.
    Atarashi, Ryuichiro
    Sano, Kazunori
    Race, Brent
    Meade-White, Kimberly D.
    Taubner, Lara M.
    Timmes, Andrew
    Caughey, Byron
    [J]. PLOS PATHOGENS, 2010, 6 (12)
  • [107] World Health Organization, 1998, Global Surveillance, Diagnosis, and Therapy of Human Transmissible Spongiform Encephalopathies: Report of a WHO Consultation
  • [108] Long-Term Preclinical Magnetic Resonance Imaging Alterations in Sporadic Creutzfeldt-Jakob Disease
    Zanusso, Gianluigi
    Camporese, Giulia
    Ferrari, Sergio
    Santelli, Luca
    Bongianni, Matilde
    Fiorini, Michele
    Monaco, Salvatore
    Manara, Renzo
    Cagnin, Annachiara
    [J]. ANNALS OF NEUROLOGY, 2016, 80 (04) : 629 - 632
  • [109] Advanced tests for early and accurate diagnosis of Creutzfeldt-Jakob disease
    Zanusso, Gianluigi
    Monaco, Salvatore
    Pocchiari, Maurizio
    Caughey, Byron
    [J]. NATURE REVIEWS NEUROLOGY, 2016, 12 (06) : 325 - 333
  • [110] Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease
    Zerr, I.
    Kallenberg, K.
    Summers, D. M.
    Romero, C.
    Taratuto, A.
    Heinemann, U.
    Breithaupt, M.
    Varges, D.
    Meissner, B.
    Ladogana, A.
    Schuur, M.
    Haik, S.
    Collins, S. J.
    Jansen, Gerard H.
    Stokin, G. B.
    Pimentel, J.
    Hewer, E.
    Collie, D.
    Smith, P.
    Roberts, H.
    Brandel, J. P.
    van Duijn, C.
    Pocchiari, M.
    Begue, C.
    Cras, P.
    Will, R. G.
    Sanchez-Juan, P.
    [J]. BRAIN, 2009, 132 : 2659 - 2668