TWNK in Parkinson's Disease: A Movement Disorder and Mitochondrial Disease Center Perspective Study. Issue 9 (6th July 2022)
- Record Type:
- Journal Article
- Title:
- TWNK in Parkinson's Disease: A Movement Disorder and Mitochondrial Disease Center Perspective Study. Issue 9 (6th July 2022)
- Main Title:
- TWNK in Parkinson's Disease: A Movement Disorder and Mitochondrial Disease Center Perspective Study
- Authors:
- Percetti, Marco
Franco, Giulia
Monfrini, Edoardo
Caporali, Leonardo
Minardi, Raffaella
La Morgia, Chiara
Valentino, Maria Lucia
Liguori, Rocco
Palmieri, Ilaria
Ottaviani, Donatella
Vizziello, Maria
Ronchi, Dario
Di Berardino, Federica
Cocco, Antoniangela
Macao, Bertil
Falkenberg, Maria
Comi, Giacomo Pietro
Albanese, Alberto
Giometto, Bruno
Valente, Enza Maria
Carelli, Valerio
Di Fonzo, Alessio - Abstract:
- Abstract: Background: Parkinsonian features have been described in patients harboring variants in nuclear genes encoding for proteins involved in mitochondrial DNA maintenance, such as TWNK . Objectives: The aim was to screen for TWNK variants in an Italian cohort of Parkinson's disease (PD) patients and to assess the occurrence of parkinsonism in patients presenting with TWNK ‐related autosomal dominant progressive external ophthalmoplegia ( TWNK ‐adPEO). Methods: Genomic DNA of 263 consecutively collected PD patients who underwent diagnostic genetic testing was analyzed with a targeted custom gene panel including TWNK, as well as genes causative of monogenic PD. Genetic and clinical data of 18 TWNK ‐adPEO patients with parkinsonism were retrospectively analyzed. Results: Six of 263 PD patients (2%), presenting either with isolated PD (n = 4) or in combination with bilateral ptosis (n = 2), carried TWNK likely pathogenic variants. Among 18 TWNK ‐adPEO patients, 5 (28%) had parkinsonism. Conclusions: We show candidate TWNK variants occurring in PD without PEO. This finding will require further confirmatory studies. © 2022 Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson Movement Disorder Society.
- Is Part Of:
- Movement disorders. Volume 37:Issue 9(2022)
- Journal:
- Movement disorders
- Issue:
- Volume 37:Issue 9(2022)
- Issue Display:
- Volume 37, Issue 9 (2022)
- Year:
- 2022
- Volume:
- 37
- Issue:
- 9
- Issue Sort Value:
- 2022-0037-0009-0000
- Page Start:
- 1938
- Page End:
- 1943
- Publication Date:
- 2022-07-06
- Subjects:
- TWNK -- twinkle -- Parkinson's disease -- parkinsonism -- mitochondrial DNA
Movement disorders -- Periodicals
610 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1531-8257 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/mds.29139 ↗
- 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:
- 24148.xml