The Movement Disorder Society Criteria for the Diagnosis of Multiple System Atrophy
Gregor K. Wenning
1
,
Iva Stankovic
2
,
L. Vignatelli
3
,
Giovanna Calandra-Buonaura
3, 4
,
K. Seppi
1
,
H. Kaufmann
5
,
W. G. Meissner
6, 7
,
Florian Krismer
1
,
Daniela Berg
8, 9
,
P. Cortelli
3, 4
,
Roy Freeman
10
,
G. M. Halliday
11
,
Günter U. Höglinger
12, 13
,
Anthony Lang
14
,
Helen Ling
15, 16
,
Irene Litvan
17
,
Phillip Low
18
,
Yasuo Miki
15, 19
,
Jalesh Panicker
20, 21
,
Maria Teresa Pellecchia
22
,
Niall Quinn
20
,
Ryuji Sakakibara
23
,
M. Stamelou
24, 25
,
Eduardo Tolosa
26, 27
,
Shoji Tsuji
28, 29
,
Tom Warner
15
,
Werner Poewe
1
,
Horacio Kaufmann
5
2
3
10
12
Department of Neurology Hanover Medical School Hanover Germany
|
28
Publication type: Journal Article
Publication date: 2022-04-21
scimago Q1
wos Q1
SJR: 2.988
CiteScore: 13.2
Impact factor: 7.6
ISSN: 08853185, 15318257
PubMed ID:
35445419
Neurology
Neurology (clinical)
Abstract
The second consensus criteria for the diagnosis of multiple system atrophy (MSA) are widely recognized as the reference standard for clinical research, but lack sensitivity to diagnose the disease at early stages.To develop novel Movement Disorder Society (MDS) criteria for MSA diagnosis using an evidence-based and consensus-based methodology.We identified shortcomings of the second consensus criteria for MSA diagnosis and conducted a systematic literature review to answer predefined questions on clinical presentation and diagnostic tools relevant for MSA diagnosis. The criteria were developed and later optimized using two Delphi rounds within the MSA Criteria Revision Task Force, a survey for MDS membership, and a virtual Consensus Conference.The criteria for neuropathologically established MSA remain unchanged. For a clinical MSA diagnosis a new category of clinically established MSA is introduced, aiming for maximum specificity with acceptable sensitivity. A category of clinically probable MSA is defined to enhance sensitivity while maintaining specificity. A research category of possible prodromal MSA is designed to capture patients in the earliest stages when symptoms and signs are present, but do not meet the threshold for clinically established or clinically probable MSA. Brain magnetic resonance imaging markers suggestive of MSA are required for the diagnosis of clinically established MSA. The number of research biomarkers that support all clinical diagnostic categories will likely grow.This set of MDS MSA diagnostic criteria aims at improving the diagnostic accuracy, particularly in early disease stages. It requires validation in a prospective clinical and a clinicopathological study. © 2022 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
Found
Nothing found, try to update filter.
Found
Nothing found, try to update filter.
Top-30
Journals
|
5
10
15
20
25
30
35
|
|
|
Journal of Neurology
31 publications, 5.4%
|
|
|
Movement Disorders
30 publications, 5.23%
|
|
|
Parkinsonism and Related Disorders
30 publications, 5.23%
|
|
|
Movement Disorders Clinical Practice
28 publications, 4.88%
|
|
|
Frontiers in Neurology
17 publications, 2.96%
|
|
|
Journal of Parkinson's Disease
16 publications, 2.79%
|
|
|
Journal of Neural Transmission
16 publications, 2.79%
|
|
|
Clinical Autonomic Research
11 publications, 1.92%
|
|
|
Journal of the Neurological Sciences
11 publications, 1.92%
|
|
|
Cerebellum
10 publications, 1.74%
|
|
|
Neurology
10 publications, 1.74%
|
|
|
Frontiers in Aging Neuroscience
9 publications, 1.57%
|
|
|
European Journal of Neurology
8 publications, 1.39%
|
|
|
npj Parkinson s Disease
7 publications, 1.22%
|
|
|
Clinical Parkinsonism & Related Disorders
7 publications, 1.22%
|
|
|
Annals of Clinical and Translational Neurology
7 publications, 1.22%
|
|
|
International Journal of Molecular Sciences
6 publications, 1.05%
|
|
|
Biomedicines
6 publications, 1.05%
|
|
|
Seminars in Neurology
5 publications, 0.87%
|
|
|
Brain Sciences
5 publications, 0.87%
|
|
|
Journal of Clinical Medicine
5 publications, 0.87%
|
|
|
Neurobiology of Disease
5 publications, 0.87%
|
|
|
Cells
4 publications, 0.7%
|
|
|
Alzheimer's and Dementia
4 publications, 0.7%
|
|
|
Neurological Sciences
4 publications, 0.7%
|
|
|
Scientific Reports
4 publications, 0.7%
|
|
|
Translational Neurodegeneration
4 publications, 0.7%
|
|
|
Cureus
4 publications, 0.7%
|
|
|
Neurology and Clinical Neuroscience
4 publications, 0.7%
|
|
|
5
10
15
20
25
30
35
|
Publishers
|
20
40
60
80
100
120
140
160
|
|
|
Springer Nature
149 publications, 25.96%
|
|
|
Elsevier
120 publications, 20.91%
|
|
|
Wiley
105 publications, 18.29%
|
|
|
MDPI
38 publications, 6.62%
|
|
|
Frontiers Media S.A.
35 publications, 6.1%
|
|
|
Ovid Technologies (Wolters Kluwer Health)
18 publications, 3.14%
|
|
|
Cold Spring Harbor Laboratory
18 publications, 3.14%
|
|
|
IOS Press
14 publications, 2.44%
|
|
|
Taylor & Francis
11 publications, 1.92%
|
|
|
BMJ
9 publications, 1.57%
|
|
|
Georg Thieme Verlag KG
8 publications, 1.39%
|
|
|
Oxford University Press
7 publications, 1.22%
|
|
|
SAGE
7 publications, 1.22%
|
|
|
Japanese Society of Internal Medicine
3 publications, 0.52%
|
|
|
American Society of Neuroradiology (ASNR)
3 publications, 0.52%
|
|
|
Public Library of Science (PLoS)
2 publications, 0.35%
|
|
|
Medical Informational Agency Publishers
2 publications, 0.35%
|
|
|
AME Publishing Company
2 publications, 0.35%
|
|
|
Research Square Platform LLC
2 publications, 0.35%
|
|
|
IMR Press
2 publications, 0.35%
|
|
|
Cambridge University Press
2 publications, 0.35%
|
|
|
Media Sphere Publishing House
2 publications, 0.35%
|
|
|
Moscow Regional Research and Clinical Institute (MONIKI)
1 publication, 0.17%
|
|
|
Ubiquity Press
1 publication, 0.17%
|
|
|
Scientific Center of Neurology
1 publication, 0.17%
|
|
|
Massachusetts Medical Society
1 publication, 0.17%
|
|
|
Medknow
1 publication, 0.17%
|
|
|
IntechOpen
1 publication, 0.17%
|
|
|
The Japanese Association of Rehabilitation Medicine
1 publication, 0.17%
|
|
|
20
40
60
80
100
120
140
160
|
- We do not take into account publications without a DOI.
- Statistics recalculated weekly.
Are you a researcher?
Create a profile to get free access to personal recommendations for colleagues and new articles.
Metrics
574
Total citations:
574
Citations from 2024:
396
(68.99%)
Cite this
GOST |
RIS |
BibTex |
MLA
Cite this
GOST
Copy
Wenning G. K. et al. The Movement Disorder Society Criteria for the Diagnosis of Multiple System Atrophy // Movement Disorders. 2022. Vol. 37. No. 6. pp. 1131-1148.
GOST all authors (up to 50)
Copy
Wenning G. K., Stankovic I., Vignatelli L., Fanciulli A., Calandra-Buonaura G., Seppi K., Kaufmann H., Meissner W. G., Krismer F., Berg D., Cortelli P., Freeman R., Halliday G. M., Höglinger G. U., Lang A., Ling H., Litvan I., Low P., Miki Y., Panicker J., Pellecchia M. T., Quinn N., Sakakibara R., Stamelou M., Tolosa E., Tsuji S., Warner T., Poewe W., Kaufmann H. The Movement Disorder Society Criteria for the Diagnosis of Multiple System Atrophy // Movement Disorders. 2022. Vol. 37. No. 6. pp. 1131-1148.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1002/mds.29005
UR - https://doi.org/10.1002/mds.29005
TI - The Movement Disorder Society Criteria for the Diagnosis of Multiple System Atrophy
T2 - Movement Disorders
AU - Wenning, Gregor K.
AU - Stankovic, Iva
AU - Vignatelli, L.
AU - Fanciulli, Alessandra
AU - Calandra-Buonaura, Giovanna
AU - Seppi, K.
AU - Kaufmann, H.
AU - Meissner, W. G.
AU - Krismer, Florian
AU - Berg, Daniela
AU - Cortelli, P.
AU - Freeman, Roy
AU - Halliday, G. M.
AU - Höglinger, Günter U.
AU - Lang, Anthony
AU - Ling, Helen
AU - Litvan, Irene
AU - Low, Phillip
AU - Miki, Yasuo
AU - Panicker, Jalesh
AU - Pellecchia, Maria Teresa
AU - Quinn, Niall
AU - Sakakibara, Ryuji
AU - Stamelou, M.
AU - Tolosa, Eduardo
AU - Tsuji, Shoji
AU - Warner, Tom
AU - Poewe, Werner
AU - Kaufmann, Horacio
PY - 2022
DA - 2022/04/21
PB - Wiley
SP - 1131-1148
IS - 6
VL - 37
PMID - 35445419
SN - 0885-3185
SN - 1531-8257
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2022_Wenning,
author = {Gregor K. Wenning and Iva Stankovic and L. Vignatelli and Alessandra Fanciulli and Giovanna Calandra-Buonaura and K. Seppi and H. Kaufmann and W. G. Meissner and Florian Krismer and Daniela Berg and P. Cortelli and Roy Freeman and G. M. Halliday and Günter U. Höglinger and Anthony Lang and Helen Ling and Irene Litvan and Phillip Low and Yasuo Miki and Jalesh Panicker and Maria Teresa Pellecchia and Niall Quinn and Ryuji Sakakibara and M. Stamelou and Eduardo Tolosa and Shoji Tsuji and Tom Warner and Werner Poewe and Horacio Kaufmann},
title = {The Movement Disorder Society Criteria for the Diagnosis of Multiple System Atrophy},
journal = {Movement Disorders},
year = {2022},
volume = {37},
publisher = {Wiley},
month = {apr},
url = {https://doi.org/10.1002/mds.29005},
number = {6},
pages = {1131--1148},
doi = {10.1002/mds.29005}
}
Cite this
MLA
Copy
Wenning, Gregor K., et al. “The Movement Disorder Society Criteria for the Diagnosis of Multiple System Atrophy.” Movement Disorders, vol. 37, no. 6, Apr. 2022, pp. 1131-1148. https://doi.org/10.1002/mds.29005.