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1000 Titel
  • Eye movement biomarkers allow for the definition of phenotypes in Gaucher Disease
1000 Autor/in
  1. Donald, Aimee |
  2. Tan, Chong Y. |
  3. Chakrapani, Anupam |
  4. Hughes, Derralyn A. |
  5. Sharma, Reena |
  6. Cole, Duncan |
  7. Bardins, Stanislav |
  8. Gorges, Martin |
  9. Jones, Simon A. |
  10. Schneider, Erich |
1000 Erscheinungsjahr 2020
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2020-12-17
1000 Erschienen in
1000 Quellenangabe
  • 15(1):349
1000 Copyrightjahr
  • 2020
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1186/s13023-020-01637-9 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7745364/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Background!#!Neurological forms of Gaucher disease, the inherited disorder of β-Glucosylceramidase caused by bi-allelic variants in GBA1, is a progressive disorder which lacks a disease-modifying therapy. Systemic manifestations of disease are effectively treated with enzyme replacement therapy, however, molecules which cross the blood-brain barrier are still under investigation. Clinical trials of such therapeutics require robust, reproducible clinical endpoints to demonstrate efficacy and clear phenotypic definitions to identify suitable patients for inclusion in trials. The single consistent clinical feature in all patients with neuronopathic disease is the presence of a supranuclear saccadic gaze palsy, in the presence of Gaucher disease this finding serves as diagnostic of 'type 3' Gaucher disease.!##!Methods!#!We undertook a study to evaluate saccadic eye movements in Gaucher patients and to assess the role of the EyeSeeCam in measuring saccades. The EyeSeeCam is a video-oculography device which was used to run a protocol of saccade measures. We studied 39 patients with non-neurological Gaucher disease (type 1), 21 patients with type 3 (neurological) disease and a series of 35 healthy controls. Mean saccade parameters were compared across disease subgroups.!##!Results!#!We confirmed the saccadic abnormality in patients with type 3 Gaucher disease and identified an unexpected subgroup of patients with type 1 Gaucher disease who demonstrated significant saccade parameter abnormalities. These patients also showed subtle neurological findings and shared a GBA1 variant.!##!Conclusions!#!This striking novel finding of a potentially attenuated type 3 Gaucher phenotype associated with a specific GBA1 variant and detectable saccadic abnormality prompts review of current disease classification. Further, this finding highlights the broad spectrum of neuronopathic Gaucher phenotypes relevant when designing inclusion criteria for clinical trials.
1000 Sacherschließung
lokal Neuronopathic
lokal Eye Movements [MeSH]
lokal Rare disease
lokal Humans [MeSH]
lokal Neurodegenerative disease
lokal Ocular-motor
lokal Video-oculography
lokal Lysosomal storage diseases
lokal Gaucher Disease/diagnosis [MeSH]
lokal Gaucher Disease/genetics [MeSH]
lokal Eye tracker
lokal Saccades
lokal Glucosylceramidase/genetics [MeSH]
lokal Research
lokal Phenotype [MeSH]
lokal Biomarkers [MeSH]
1000 Liste der Beteiligten
  1. https://orcid.org/0000-0002-2623-5233|https://frl.publisso.de/adhoc/uri/VGFuLCBDaG9uZyBZLg==|https://frl.publisso.de/adhoc/uri/Q2hha3JhcGFuaSwgQW51cGFt|https://frl.publisso.de/adhoc/uri/SHVnaGVzLCBEZXJyYWx5biBBLg==|https://frl.publisso.de/adhoc/uri/U2hhcm1hLCBSZWVuYQ==|https://frl.publisso.de/adhoc/uri/Q29sZSwgRHVuY2Fu|https://frl.publisso.de/adhoc/uri/QmFyZGlucywgU3RhbmlzbGF2|https://frl.publisso.de/adhoc/uri/R29yZ2VzLCBNYXJ0aW4=|https://frl.publisso.de/adhoc/uri/Sm9uZXMsIFNpbW9uIEEu|https://frl.publisso.de/adhoc/uri/U2NobmVpZGVyLCBFcmljaA==
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1000 Erstellt am 2023-11-15T16:08:59.529+0100
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1000 Zuletzt bearbeitet Thu Nov 30 20:53:49 CET 2023
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