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Acta Neurologica Belgica· 2026Q2· Review

Ambroxol in Gaucher disease and GBA1-related Parkinson disease: an updated systematic review

Patryk Lipiński, Aleksandra Jezela-Stanek, Anna Tylki‐Szymańska

Short summary

Ambroxol (ABX) shows potential biochemical and neurological improvements in Gaucher disease (GD) and GBA1-related Parkinson disease (GBA1-PD), but evidence is limited by small, uncontrolled studies and variable outcome definitions.

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Key points

  • Ambroxol (ABX) has been investigated for Gaucher disease (GD) and GBA1-related Parkinson disease (GBA1-PD) due to its ability to increase glucocerebrosidase activity.
  • Evidence for ABX in GD consists mainly of small, uncontrolled reports describing biochemical and neurological improvements, but with varied outcome definitions.
  • Conclusions for GBA1-PD are provisional, with a key study only available as a non-peer-reviewed preprint and no clear disease modification shown.
  • Safety data for chronic high-dose ABX treatment is limited.
  • Biomarker changes alone are insufficient to establish clinical efficacy for ABX in these conditions.

AI-generated from the title and abstract; the full text is not read.

Abstract

Abstract Background Ambroxol (ABX) is a central nervous system (CNS)-penetrant compound that can increase glucocerebrosidase activity and has been investigated in Gaucher disease (GD) and GBA1 -related Parkinson disease ( GBA1 -PD). Methods This PRISMA 2020 systematic review and narrative synthesis searched PubMed/MEDLINE, Europe PMC, SSRN and ClinicalTrials.gov through 19 August 2026, with an additional Web of Science Core Collection search performed during revision on 14 September 2026, without restrictions on date, language or publication status. Two reviewers independently selected studies, extracted data and assessed risk of bias using design-specific tools. Substantial clinical and methodological heterogeneity precluded meta-analysis Results Of 149 records in the original searches, 137 were screened, 41 full texts were assessed and 20 clinical outcome reports were included. The additional Web of Science search retrieved 50 records and did not identify further clinical outcome reports. Evidence in GD consisted mainly of small, uncontrolled and sometimes overlapping reports. Biochemical and neurological improvements were described in selected patients, but outcome definitions and functional responses varied. In GBA1-PD, conclusions remain provisional because the AMBITIOUS results are available only as a non-peer-reviewed preprint and did not show disease modification. Evidence on the safety of chronic high-dose treatment is limited. Conclusions Biomarker changes alone do not establish clinical efficacy. ABX remains an off-label, investigational treatment in GD and GBA1-PD, and no GBA1 genotype or functional assay currently defines a validated indication.

The authors' abstract, as published at the source. Acta Neurologica Belgica, 2026 · DOI ↗

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Field: Physiology

PhysiologyMedicine