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Diurnal variability of glucose tetrasaccharide (Glc(4)) excretion in patients with glycogen storage disease type III

AIM: The urinary glucose tetrasaccharide, Glcα1‐6Glcα1‐4Glcα1‐4Glc (Glc(4)), is a glycogen limit dextrin that is elevated in patients with glycogen storage disease (GSD) type III. We evaluated the potential of uncooked cornstarch therapy to interfere with Glc(4) monitoring, by measuring the diurnal...

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Detalles Bibliográficos
Autores principales: Young, Sarah P., Khan, Aleena, Stefanescu, Ela, Seifts, Andrea M., Hijazi, Ghada, Austin, Stephanie, Kishnani, Priya S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7932871/
https://www.ncbi.nlm.nih.gov/pubmed/33728245
http://dx.doi.org/10.1002/jmd2.12181
Descripción
Sumario:AIM: The urinary glucose tetrasaccharide, Glcα1‐6Glcα1‐4Glcα1‐4Glc (Glc(4)), is a glycogen limit dextrin that is elevated in patients with glycogen storage disease (GSD) type III. We evaluated the potential of uncooked cornstarch therapy to interfere with Glc(4) monitoring, by measuring the diurnal variability of Glc(4) excretion in patients with GSD III. METHODS: Voids were collected at home over 24 hours, stored at 4°C and frozen within 48 hours. Glc(4) was analyzed using liquid chromatography‐tandem mass spectrometry and normalized to creatinine. RESULTS: Subjects with GSD III (median age: 13.5 years, range: 3.7‐62; n = 18) completed one or more 24‐hour urine collection, and 28/36 collections were accepted for analysis. Glc(4) was elevated in 16/18 subjects (median: 13 mmol/mol creatinine, range: 2‐75, reference range: <3). In collections with elevated Glc(4) (23/28), two‐thirds (15/23) had low diurnal variability in Glc(4) excretion (coefficient of variation [CV%] <25). The diurnal variability was significantly correlated with the Glc(4) concentration (Pearson R = .644, P < .05), but not with the dose of uncooked cornstarch. High intraday variability (>25%) was not consistently observed in repeat collections by the same subject. CONCLUSIONS: The extent and variability of Glc(4) excretion relative to creatinine was not correlated with cornstarch dose. A majority of collections showed low variability over 24 hours. These findings support the use of single time‐point collections to evaluate Glc(4) in patients with GSD III treated with cornstarch. However, repeat sampling over short time‐periods will provide the most accurate assessment of Glc(4) excretion, as intraday variability may be increased in patients with high Glc(4) excretion.