Mass Spectrometry Evaluation of Biomarkers in the Vitreous Fluid in Gaucher Disease Type 3 with Disease Progression Despite Long-Term Treatment
Autor: | Jeff Barnes, Leanne Zimmer, Frank A. Stockl, Donald R. Duerksen, Cheryl Rockman-Greenberg, Christiane Auray-Blais, Aizeddin A. Mhanni, Janine L. Johnston, Michel Boutin |
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Jazyk: | angličtina |
Rok vydání: | 2020 |
Předmět: |
medicine.medical_specialty
congenital hereditary and neonatal diseases and abnormalities Visual acuity genetic structures medicine.medical_treatment Clinical Biochemistry Vitrectomy Disease Gastroenterology Article vitreous 03 medical and health sciences 0302 clinical medicine Internal medicine glucosylceramide medicine Substrate reduction therapy gaucher 030304 developmental biology 0303 health sciences lcsh:R5-920 Vitreous Fluid business.industry Disease progression Metabolic disorder Enzyme replacement therapy medicine.disease eye diseases lsd 030221 ophthalmology & optometry medicine.symptom business lcsh:Medicine (General) uplc-ms/ms |
Zdroj: | Diagnostics, Vol 10, Iss 2, p 69 (2020) Diagnostics Volume 10 Issue 2 |
ISSN: | 2075-4418 |
Popis: | Intraocular lesions have been infrequently reported in patients with Gaucher disease type 3 (GD3). We previously reported siblings with GD3 who responded well to the combination of enzyme replacement therapy (ERT) and substrate reduction therapy (SRT). Here we report progressive bilateral vitreous and preretinal deposits with declining visual acuity requiring bilateral vitrectomies in one of these siblings. These ocular manifestations had progressed despite combined ERT and SRT with improvement in visual acuity after vitrectomies. Vitrectomy fluid analysis performed for the first time by ultra-performance liquid chromatography&ndash tandem mass spectrometry (UPLC-MS/MS) identified a high concentration of glucosylceramide (GluCer) in the patient (262.842 nM) compared to a sample (0.428 nM from a patient without a lysosomal storage or known hereditary metabolic disorder). The GluCer detected in our patient was resolved into 12 different isoforms including two methylated ones. No evidence of galactosylceramide (GalCer) was detected. The development of these intraocular manifestations and their characterization by UPLC-MS/MS indicate a need for ongoing ophthalmologic evaluation of all GD patients and for new therapies that can cross the blood&ndash retinal and blood&ndash brain barriers for patients with GD and other neuropathic lysosomal storage disorders. |
Databáze: | OpenAIRE |
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