Impact of Magnetic Resonance Imaging Markers on the Diagnostic Performance of the International Parkinson and Movement Disorder Society Multiple System Atrophy Criteria

被引:7
作者
Jensen, Ida [1 ]
Heine, Johanne [2 ]
Ruf, Viktoria C. [3 ]
Compta, Yaroslau [4 ]
Porcel, Laura Molina [5 ]
Troakes, Claire [6 ]
Vamanu, Albert [6 ]
Downes, Sophia [6 ]
Irwin, David [7 ]
Cohen, Jesse [7 ]
Lee, Edward B. [7 ,8 ]
Nilsson, Christer [9 ]
Englund, Elisabet [10 ]
Nemati, Mojtaba [1 ]
Katzdobler, Sabrina [1 ]
Levin, Johannes [1 ,11 ,12 ]
Pantelyat, Alex [13 ]
Seemiller, Joseph [13 ]
Berger, Stephen [13 ]
van Swieten, John [14 ]
Dopper, Elise [14 ]
Rozenmuller, Annemieke [15 ]
Kovacs, Gabor G. [16 ,17 ,18 ,19 ]
Bendahan, Nathaniel [20 ,21 ]
Lang, Anthony E. [20 ,21 ]
Herms, Jochen [3 ,11 ,12 ]
Hoeglinger, Guenter [1 ,11 ,12 ,22 ]
Hopfner, Franziska [1 ]
机构
[1] Ludwig Maximilians Univ LMU Munchen, LMU Univ Hosp, Dept Neurol, Munich, Germany
[2] Hannover Med Sch, Dept Neurol, Hannover, Germany
[3] Ludwig Maximilians Univ Munchen, Fac Med, Ctr Neuropathol & Prion Res, Munich, Germany
[4] Hosp Clin Barcelona, Inst Clin Neurociencies, Neurol Serv, Movement Disorders Unit,IDIBAPS,CIBERNED, Barcelona, Catalonia, Spain
[5] IDIBAPS, Hosp Clin, Neurol Dept, Barcelona, Spain
[6] Inst Psychiat Psychol & Neurosci, Kings Coll London, Basic & Clin Neurosci Dept, London, England
[7] Univ Penn, Dept Neurol, Perelman Sch Med, Philadelphia, PA USA
[8] Univ Penn, Inst Aging, Ctr Neurodegenerat Dis Res, Dept Pathol & Lab Med,Perelman Sch Med, Philadelphia, PA USA
[9] Lund Univ, Dept Clin Sci, Div Neurol, Lund, Sweden
[10] Lund Univ, Dept Clin Sci, Div Pathol Instead Neurol, Lund, Sweden
[11] German Ctr Neurodegenerat Dis DZNE, Feodor Lynen Str 17, Munich, Germany
[12] Munich Cluster Syst Neurol SyNergy, Feodor Lynen Str 17, Munich, Germany
[13] Johns Hopkins Univ, Sch Med, Dept Neurol, Baltimore, MD USA
[14] Erasmus MC, Dept Neurol, Rotterdam, Netherlands
[15] Amsterdam UMC, Dept Pathol, Amsterdam Neurosci, Amsterdam, Netherlands
[16] Univ Hlth Network, Lab Med Program, Toronto, ON, Canada
[17] Univ Hlth Network, Krembil Brain Inst, Toronto, ON, Canada
[18] Univ Toronto, Dept Lab Med & Pathobiol, Toronto, ON, Canada
[19] Univ Toronto, Tanz Ctr Res Neurodegenerat Dis, Toronto, ON, Canada
[20] Univ Toronto, Univ Hlth Network, Toronto Western Hosp, Edmond J Safra Program Parkinsons Dis,Div Neurol, Toronto, ON, Canada
[21] Univ Toronto, Univ Hlth Network, Toronto Western Hosp, Rossy Progress Supranucl Palsy Ctr, Toronto, ON, Canada
[22] Ludwig Maximilians Univ Munchen, LMU Univ Hosp, Dept Neurol, D-80539 Munich, Germany
关键词
multiple system atrophy; autopsy-confirmed; brain magnetic resonance imaging; MRI; PROGRESSIVE SUPRANUCLEAR PALSY; NEUROPATHOLOGIC CRITERIA; NATURAL-HISTORY; DIFFERENTIATION; CONSENSUS; DISEASE; MRI;
D O I
10.1002/mds.29879
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BackgroundMultiple system atrophy is a neurodegenerative disease with alpha-synuclein aggregation in glial cytoplasmic inclusions, leading to dysautonomia, parkinsonism, and cerebellar ataxia.ObjectiveThe aim of this study was to validate the accuracy of the International Parkinson and Movement Disorder Society Multiple System Atrophy clinical diagnostic criteria, particularly considering the impact of the newly introduced brain magnetic resonance imaging (MRI) markers.MethodsDiagnostic accuracy of the clinical diagnostic criteria for multiple system atrophy was estimated retrospectively in autopsy-confirmed patients with multiple system atrophy, Parkinson's disease, progressive supranuclear palsy, and corticobasal degeneration.ResultsWe identified a total of 240 patients. Sensitivity of the clinically probable criteria was moderate at symptom onset but improved with disease duration (year 1: 9%, year 3: 39%, final ante mortem record: 77%), whereas their specificity remained consistently high (99%-100% throughout). Sensitivity of the clinically established criteria was low during the first 3 years (1%-9%), with mild improvement at the final ante mortem record (22%), whereas specificity remained high (99%-100% throughout). When MRI features were excluded from the clinically established criteria, their sensitivity increased considerably (year 1: 3%, year 3: 22%, final ante mortem record: 48%), and their specificity was not compromised (99%-100% throughout).ConclusionsThe International Parkinson and Movement Disorder Society multiple system atrophy diagnostic criteria showed consistently high specificity and low to moderate sensitivity throughout the disease course. The MRI markers for the clinically established criteria reduced their sensitivity without improving specificity. Combining clinically probable and clinically established criteria, but disregarding MRI features, yielded the best sensitivity with excellent specificity and may be most appropriate to select patients for therapeutic trials. (c) 2024 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
引用
收藏
页码:1514 / 1522
页数:9
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