Analysis of Globotriaosylceramide (Gb) in Liquid Urine: A Straightforward Assay Using Tandem Mass Spectrometry.

Curr Protoc

Division of Medical Genetics, Department of Laboratory Medicine, CIUSSS de l'Estrie-CHUS, Sherbrooke, Quebec, Canada.

Published: June 2024

AI Article Synopsis

  • Fabry disease (FD) is caused by mutations in the GLA gene, leading to the buildup of a fatty substance called globotriaosylceramide (Gb), which can cause serious health issues like heart problems, kidney failure, and strokes.
  • A new methodology involves analyzing urine samples for Gb and creatinine using ultra-high performance liquid chromatography coupled to tandem mass spectrometry (UHPLC-MS/MS) to provide accurate results for diagnosing and monitoring FD.
  • The protocol has been fully validated, showing high stability for sample conditions and providing age-specific Gb/creatinine reference limits for effective patient evaluation.

Article Abstract

Fabry disease (FD) is a lysosomal storage disorder caused by variants in the GLA gene encoding α-galactosidase A, an enzyme required for catabolism of globotriaosylceramide (Gb). Accumulation of Gb in patients' cells, tissues, and biological fluids causes clinical manifestations including ventricular hypertrophy, renal insufficiency, and strokes. This protocol describes a methodology to analyze urinary Gb and creatinine. Samples are diluted with an internal standard solution containing Gb(C17:0) and creatinine-D, centrifuged, and directly analyzed by ultra-high performance liquid chromatography coupled to tandem mass spectrometry (UHPLC-MS/MS) using an 8.7-min method. Eight Gb isoforms [C16:0, C18:0, C20:0, C22:1, C22:0, C24:1, C24:0, and (C24:0)OH] are analyzed and the total is normalized to creatinine. Confirmation ions are monitored to detect potential interferences. The Gb limit of quantification is 0.023 µg/ml. Its interday coefficients of variation (3 concentrations measured) are ≤15.4%. This method minimizes matrix effects (≤6.5%) and prevents adsorption or precipitation of Gb. Urine samples are stable (bias <15%) for 2 days at 21°C, 7 days at 4°C, and 4 freeze/thaw cycles, whereas prepared samples are stable for 5 days at 21°C, and 14 days at 4°C. The Gb/creatinine age-related upper reference limits (mean + 2 standard deviations) are 29 mg/mol creatinine (<7 years) and 14 mg/mol creatinine (≥7 years). This simple, robust protocol has been fully validated (ISO 15189) and provides a valuable tool for diagnosis and monitoring of FD patients. © 2024 The Authors. Current Protocols published by Wiley Periodicals LLC. Basic Protocol: Analysis of urinary globotriaosylceramide (Gb) and creatinine by UHPLC-MS/MS Support Protocol 1: Preparation of the urinary quality controls Support Protocol 2: Preparation of the urine matrix used for the Gb calibration curve Support Protocol 3: Preparation of the Gb calibrators Support Protocol 4: Preparation of the working solution containing the internal standards Support Protocol 5: Preparation of the creatinine calibrators Support Protocol 6: Preparation of the UHPLC solutions and mobile phases.

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http://dx.doi.org/10.1002/cpz1.1087DOI Listing

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