Low frequency of GCH1 and TH mutations in Parkinson's disease

Mutations in GCH1 are believed to be a risk factor for PD... the results of this study do not confirm this. However the numbers of participants was too low and the study was underpowered... there was a difference between cases and controls in terms of the number that had mutations in TH (also involved in dopamine synthesis) but again the study was underpowered to test the null hypothesis...

Parkinsonism Relat Disord. 2016 May 7. pii: S1353-8020(16)30148-1. doi: 10.1016/j.parkreldis.2016.05.010. [Epub ahead of print]

Rengmark A, Pihlstrøm L, Linder J, Forsgren L, Toft M.

http://www.prd-journal.com/article/S1353-8020(16)30148-1/abstract

BACKGROUND:

The causes of Parkinson's disease (PD) are unknown in the majority of patients. The GCH1 gene encodes GTP-cyclohydrolase I, an important enzyme in dopamine synthesis. Co-occurrence of dopa-responsive dystonia (DRD) and a PD phenotype has been reported in families with GCH1 mutations. Recently, rare coding variants in GCH1 were found to be enriched in PD patients, indicating a role for the enzyme in the neurodegenerative process.

METHODS:

To further elucidate the contribution of GCH1 mutations to sporadic PD, we examined its coding exons in a targeted deep sequencing study of 509 PD patients (mean age at onset 56.7 ± 12.0 years) and 230 controls. We further included the tyrosine hydroxylase gene TH, also known to cause DRD. Gene dose assessments were performed to screen for large copy number variants in a subset of 48 patients with early-onset PD.

RESULTS:

No putatively pathogenic GCH1 mutations were found. The frequency of rare heterozygous variants in the TH gene was 0.69% (7/1018) in the patient group and 0.22% (1/460) in the control group (p = 0.45).

CONCLUSIONS:

Previous studies have found that coding variants in the GCH1 gene may be considered a risk factor for PD. Our study indicates that mutations in GCH1 are rare in late-onset PD. Several patients carried heterozygous variants in the TH gene that may affect protein function. Our study was not designed to determine with certainty if any of these variants play a role as risk factors for late-onset PD.

Copyright © 2016 Elsevier Ltd. All rights reserved.