Scoring Algorithm‐Based Genomic Testing in Dystonia: A Prospective Validation Study. Issue 8 (5th May 2021)
- Record Type:
- Journal Article
- Title:
- Scoring Algorithm‐Based Genomic Testing in Dystonia: A Prospective Validation Study. Issue 8 (5th May 2021)
- Main Title:
- Scoring Algorithm‐Based Genomic Testing in Dystonia: A Prospective Validation Study
- Authors:
- Zech, Michael
Jech, Robert
Boesch, Sylvia
Škorvánek, Matej
Necpál, Ján
Švantnerová, Jana
Wagner, Matias
Sadr‐Nabavi, Ariane
Distelmaier, Felix
Krenn, Martin
Serranová, Tereza
Rektorová, Irena
Havránková, Petra
Mosejová, Alexandra
Příhodová, Iva
Šarláková, Jana
Kulcsarová, Kristína
Ulmanová, Olga
Bechyně, Karel
Ostrozovičová, Miriam
Haň, Vladimír
Ventosa, Joaquim Ribeiro
Brunet, Theresa
Berutti, Riccardo
Shariati, Mohammad
Shoeibi, Ali
Schneider, Susanne A.
Kuster, Alice
Baumann, Matthias
Weise, David
Wilbert, Friederike
Janzarik, Wibke G.
Eckenweiler, Matthias
Mall, Volker
Haslinger, Bernhard
Berweck, Steffen
Winkelmann, Juliane
Oexle, Konrad
… (more) - Abstract:
- Abstract: Background: Despite the established value of genomic testing strategies, practice guidelines for their use do not exist in many indications. Objectives: We sought to validate a recently introduced scoring algorithm for dystonia, predicting the diagnostic utility of whole‐exome sequencing (WES) based on individual phenotypic aspects (age‐at‐onset, body distribution, presenting comorbidity). Methods: We prospectively enrolled a set of 209 dystonia‐affected families and obtained summary scores (0–5 points) according to the algorithm. Singleton (N = 146), duo (N = 11), and trio (N = 52) WES data were generated to identify genetic diagnoses. Results: Diagnostic yield was highest (51%) among individuals with a summary score of 5, corresponding to a manifestation of early‐onset segmental or generalized dystonia with coexisting non‐movement disorder‐related neurological symptoms. Sensitivity and specificity at the previously suggested threshold for implementation of WES (3 points) was 96% and 52%, with area under the curve of 0.81. Conclusions: The algorithm is a useful predictive tool and could be integrated into dystonia routine diagnostic protocols. © 2021 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson Movement Disorder Society
- Is Part Of:
- Movement disorders. Volume 36:Issue 8(2021)
- Journal:
- Movement disorders
- Issue:
- Volume 36:Issue 8(2021)
- Issue Display:
- Volume 36, Issue 8 (2021)
- Year:
- 2021
- Volume:
- 36
- Issue:
- 8
- Issue Sort Value:
- 2021-0036-0008-0000
- Page Start:
- 1959
- Page End:
- 1964
- Publication Date:
- 2021-05-05
- Subjects:
- exome sequencing -- diagnostic yield -- dystonia -- prediction -- scoring algorithm -- rare disease
Movement disorders -- Periodicals
610 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1531-8257 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/mds.28614 ↗
- Languages:
- English
- ISSNs:
- 0885-3185
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5980.317200
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 23800.xml