Clinical course and biomarkers in patients with type 1 Gaucher disease and Parkinson's disease: A retrospective cohort study

Introduction Pathogenic variants in GBA1 , the gene encoding beta-glucocerebrosidase, are significant genetic risk factors for Parkinson's disease (PD). Patients with type 1 Gaucher disease (GD1), caused by biallelic GBA1 variants, have approximately six-fold higher lifetime risk for PD compared to the general population. However, few studies have described the clinical presentation of GD-associated PD (GD-PD) in GD1 patients. We describe the variable presentation of PD and evaluate clinical characteristics and biomarkers in a cohort of patients with concurrent diagnoses of GD-PD. Methods Retrospective case-control analysis of GD1 patients within a single academic clinic from 2010 to 2020 comparing against age- and sex-matched controls. Results Among eleven patients diagnosed with GD-PD, the median age of GD1 diagnosis was 33 years (interquartile range/IQR 28–54 years), and all were on treatment with enzyme replacement therapy ( n = 8, 72.7%) or substrate reduction therapy ( n = 3, 27.3%) at follow-up. The average age of onset of PD symptoms was 54.6 years old with a median age of onset of 53 years old (IQR 47–59) and four patients developing symptoms before the age of 50. The majority ( n = 9, 81.8%) were treated with levodopa/carbidopa with or without deep brain stimulation. Within this limited cohort, neither clinical phenotype nor systemic GD biomarkers distinguished GD-PD cases from controls. Conclusions Data from this single-center cohort demonstrate considerable variability in GD-PD among GD1 individuals and suggest that GD1 patients may have increased risk of GD-PD before the age of 50. Routine screening for PD in GD1 patients starting at age 40 may aid early diagnosis and close monitoring for initiation of PD-directed treatment.

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Journal
Molecular Genetics and Metabolism Reports
Published
2026-09-16
DOI
https://doi.org/10.1016/j.ymgmr.2026.101358
Primary Topic
Lysosomal Storage Disorders Research
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article
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0.00

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article

Clinical course and biomarkers in patients with type 1 Gaucher disease and Parkinson's disease: A retrospective cohort study

Hetanshi Naik, Manisha Balwani, Roy N. Alcalay, Chanan Stauffer et al.
Molecular Genetics and Metabolism Reports
Lysosomal Storage Disorders Research
article

Clinical course and biomarkers in patients with type 1 Gaucher disease and Parkinson's disease: A retrospective cohort study

Hetanshi Naik, Manisha Balwani, Roy N. Alcalay, Chanan Stauffer, Luca Fierro, Ayuko Iverson, Drew B. Sinha
article en

Abstract

Introduction Pathogenic variants in GBA1 , the gene encoding beta-glucocerebrosidase, are significant genetic risk factors for Parkinson's disease (PD). Patients with type 1 Gaucher disease (GD1), caused by biallelic GBA1 variants, have approximately six-fold higher lifetime risk for PD compared to the general population. However, few studies have described the clinical presentation of GD-associated PD (GD-PD) in GD1 patients. We describe the variable presentation of PD and evaluate clinical characteristics and biomarkers in a cohort of patients with concurrent diagnoses of GD-PD. Methods Retrospective case-control analysis of GD1 patients within a single academic clinic from 2010 to 2020 comparing against age- and sex-matched controls. Results Among eleven patients diagnosed with GD-PD, the median age of GD1 diagnosis was 33 years (interquartile range/IQR 28–54 years), and all were on treatment with enzyme replacement therapy ( n = 8, 72.7%) or substrate reduction therapy ( n = 3, 27.3%) at follow-up. The average age of onset of PD symptoms was 54.6 years old with a median age of onset of 53 years old (IQR 47–59) and four patients developing symptoms before the age of 50. The majority ( n = 9, 81.8%) were treated with levodopa/carbidopa with or without deep brain stimulation. Within this limited cohort, neither clinical phenotype nor systemic GD biomarkers distinguished GD-PD cases from controls. Conclusions Data from this single-center cohort demonstrate considerable variability in GD-PD among GD1 individuals and suggest that GD1 patients may have increased risk of GD-PD before the age of 50. Routine screening for PD in GD1 patients starting at age 40 may aid early diagnosis and close monitoring for initiation of PD-directed treatment.

Molecular Genetics and Metabolism ReportsVol. 49
Columbia University Irving Medical Center (US), Icahn School of Medicine at Mount Sinai (US)
Icahn School of Medicine at Mount Sinai
Good health and well-being
Openalex Percentile: Top 12%
Lysosomal Storage Disorders Research
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