Abstract
Background
A clinical association has been reported between type 1 Gaucher's disease, which is caused by a glucocerebrosidase deficiency owing to mutations in the glucocerebrosidase gene (GBA), and parkinsonism. We examined whether mutations in the GBA gene are relevant to idiopathic Parkinson's disease.Methods
A clinic-based case series of 99 Ashkenazi patients with idiopathic Parkinson's disease, 74 Ashkenazi patients with Alzheimer's disease, and 1543 healthy Ashkenazi Jews who underwent testing to identify heterozygosity for certain recessive diseases were screened for the six GBA mutations (N370S, L444P, 84GG, IVS+1, V394L, and R496H) that are most common among Ashkenazi Jews.Results
Thirty-one patients with Parkinson's disease (31.3 percent; 95 percent confidence interval, 22.2 to 40.4 percent) had one or two mutant GBA alleles: 23 were heterozygous for N370S, 4 were heterozygous for 84GG, 3 were homozygous for N370S, and 1 was heterozygous for R496H. Among the 74 patients with Alzheimer's disease, 3 were identified as carriers of Gaucher's disease (4.1 percent; 95 percent confidence interval, 0.0 to 8.5 percent): 2 were heterozygous for N370S, and 1 was heterozygous for 84GG. Ninety-five carriers of Gaucher's disease were identified among the 1543 control subjects (6.2 percent; 95 percent confidence interval, 5.0 to 7.4 percent): 92 were heterozygous for N370S, and 3 were heterozygous for 84GG. Patients with Parkinson's disease had significantly greater odds of being carriers of Gaucher's disease than did patients with Alzheimer's disease (odds ratio, 10.8; 95 percent confidence interval, 3.0 to 46.6; P<0.001) or control subjects (odds ratio, 7.0; 95 percent confidence interval, 4.2 to 11.4; P<0.001). Among the patients with Parkinson's disease, patients who were carriers of Gaucher's disease were younger than those who were not carriers (mean [+/-SD] age at onset, 60.0+/-14.2 years vs. 64.2+/-11.7 years; P=0.04).Conclusions
Our results suggest that heterozygosity for a GBA mutation may predispose Ashkenazi Jews to Parkinson's disease.References
Articles referenced by this article (29)
A clinical genetic study of Parkinson's disease: evidence for dominant transmission.
Neurology, (3 Pt 1):499-506 1994
MED: 8145922
Genetic epidemiology of Parkinson's disease.
J Geriatr Psychiatry Neurol, (2):98-106 1998
MED: 9877530
The role of inheritance in sporadic Parkinson's disease: evidence from a longitudinal study of dopaminergic function in twins.
Ann Neurol, (5):577-582 1999
MED: 10319879
Mutation in the alpha-synuclein gene identified in families with Parkinson's disease.
Science, (5321):2045-2047 1997
MED: 9197268
Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism.
Nature, (6676):605-608 1998
MED: 9560156
Title not supplied
Parkinson's syndrome preceding clinical manifestation of Gaucher's disease.
Am J Hematol, (3):216-217 1999
MED: 10398575
Gaucher disease and parkinsonism: a phenotypic and genotypic characterization.
Mol Genet Metab, (4):313-321 2001
MED: 11509013
Gaucher disease associated with parkinsonism: four further case reports.
Am J Med Genet A, (4):348-351 2003
MED: 12522789
Show 10 more references (10 of 29)
Citations & impact
Impact metrics
Citations of article over time
Alternative metrics
Article citations
A PIKfyve modulator combined with an integrated stress response inhibitor to treat lysosomal storage diseases.
Proc Natl Acad Sci U S A, 121(34):e2320257121, 16 Aug 2024
Cited by: 1 article | PMID: 39150784
Lipids and α-Synuclein: adding further variables to the equation.
Front Mol Biosci, 11:1455817, 12 Aug 2024
Cited by: 0 articles | PMID: 39188788 | PMCID: PMC11345258
Review Free full text in Europe PMC
GBA1-Associated Parkinson's Disease Is a Distinct Entity.
Int J Mol Sci, 25(13):7102, 28 Jun 2024
Cited by: 0 articles | PMID: 39000225
Review
The annotation of <i>GBA1</i> has been concealed by its protein-coding pseudogene <i>GBAP1</i>.
Sci Adv, 10(26):eadk1296, 26 Jun 2024
Cited by: 3 articles | PMID: 38924406 | PMCID: PMC11204300
Prediction of motor and non-motor Parkinson's disease symptoms using serum lipidomics and machine learning: a 2-year study.
NPJ Parkinsons Dis, 10(1):123, 25 Jun 2024
Cited by: 0 articles | PMID: 38918434 | PMCID: PMC11199659
Go to all (358) article citations
Other citations
Data
Similar Articles
To arrive at the top five similar articles we use a word-weighted algorithm to compare words from the Title and Abstract of each citation.
Pilot association study of the beta-glucocerebrosidase N370S allele and Parkinson's disease in subjects of Jewish ethnicity.
Mov Disord, 20(1):100-103, 01 Jan 2005
Cited by: 62 articles | PMID: 15517591
Glucocerebrosidase activity in Parkinson's disease with and without GBA mutations.
Brain, 138(pt 9):2648-2658, 27 Jun 2015
Cited by: 206 articles | PMID: 26117366 | PMCID: PMC4564023
Prevalence of glucocerebrosidase mutations in the Israeli Ashkenazi Jewish population.
Hum Mutat, 12(4):240-244, 01 Jan 1998
Cited by: 56 articles | PMID: 9744474
Advances in GBA-associated Parkinson's disease--Pathology, presentation and therapies.
Neurochem Int, 93:6-25, 30 Dec 2015
Cited by: 34 articles | PMID: 26743617
Review