Genotype‐phenotype relations for the Parkinson's disease genes SNCA, LRRK2, VPS35: MDSGene systematic review. Issue 12 (24th October 2018)
- Record Type:
- Journal Article
- Title:
- Genotype‐phenotype relations for the Parkinson's disease genes SNCA, LRRK2, VPS35: MDSGene systematic review. Issue 12 (24th October 2018)
- Main Title:
- Genotype‐phenotype relations for the Parkinson's disease genes SNCA, LRRK2, VPS35: MDSGene systematic review
- Authors:
- Trinh, Joanne
Zeldenrust, Florentine M.J.
Huang, Jana
Kasten, Meike
Schaake, Susen
Petkovic, Sonja
Madoev, Harutyun
Grünewald, Anne
Almuammar, Shahad
König, Inke R.
Lill, Christina M.
Lohmann, Katja
Klein, Christine
Marras, Connie - Abstract:
- ABSTRACT: This comprehensive MDSGene review is devoted to the three autosomal‐dominant PD forms: PARK‐ SNCA, PARK‐ LRRK2, and PARK‐ VPS35 . It follows MDSGene's standardized data extraction protocol, screened a total of 2, 972 citations, and is based on fully curated phenotypic and genotypic data on 937 patients with dominantly inherited PD attributed to 44 different mutations in SNCA, LRRK2, or VPS35 . All of these data are also available in an easily searchable online database (www.mdsgene.org ), which additionally provides descriptive summary statistics on phenotypic and genetic data. Despite the high degree of missingness of phenotypic features and unsystematic reporting of genotype data in the original literature, the present review recapitulates many of the previously described findings including later onset of disease (median age at onset: ∼49 years) compared to recessive forms of PD of an overall excellent treatment response. Our systematic review validates previous reports showing that SNCA mutation carriers have a younger age at onset compared to LRRK2 and VPS35 ( P < 0.001). SNCA mutation carriers often have additional psychiatric symptoms, and although not exclusive to only LRRK2 or VPS35 mutation carriers, LRRK2 mutation carriers have a typical form of PD, and, lastly, VPS35 mutation carriers have good response tol ‐dopa. © 2018 International Parkinson and Movement Disorder Society
- Is Part Of:
- Movement disorders. Volume 33:Issue 12(2018)
- Journal:
- Movement disorders
- Issue:
- Volume 33:Issue 12(2018)
- Issue Display:
- Volume 33, Issue 12 (2018)
- Year:
- 2018
- Volume:
- 33
- Issue:
- 12
- Issue Sort Value:
- 2018-0033-0012-0000
- Page Start:
- 1857
- Page End:
- 1870
- Publication Date:
- 2018-10-24
- Subjects:
- SNCA -- LRRK2 -- VPS35 -- Parkinson's disease -- genetics
Movement disorders -- Periodicals
610 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1531-8257 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/mds.27527 ↗
- 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:
- 9289.xml