The relation between dietary polysaccharide intake and urinary excretion of tetraglucoside

• Published in: Journal of inherited metabolic disease 2025-01, Vol.48 (1), p.e12801
• Main Authors: Gross-Valle, Candelas, Jacobs, Tessa C, Dijck-Brouwer, Janneke D A, Lubberts, Janniek, Bakker, Barbara M, Bakker, Stephan J L, van der Veen, Yvonne, Schreuder, Andrea B, Derks, Terry G J, van der Krogt, Jennifer, Groen, Joost, Heiner-Fokkema, M Rebecca
• Format: Article
• Language: English
• Subjects: Adult; Biomarkers - urine; Female; Glucans - administration & dosage; Glucans - urine; Glycogen Storage Disease - urine; Humans; Kidney Transplantation; Male; Middle Aged; Original; Polysaccharides - administration & dosage; Polysaccharides - urine; Tandem Mass Spectrometry
• ISSN: 0141-8955; 1573-2665; 1573-2665
• DOI: 10.1002/jimd.12801

The urinary metabolite tetraglucoside (Glc4) is a potential biomarker for hepatic glycogen storage diseases (GSDs). Glc4 is believed to reflect body glycogen content and/or turnover. However, dietary polysaccharide intake may influence Glc4 excretion, potentially limiting the utility of Glc4 as a monitoring biomarker in hepatic GSDs. We aimed to investigate the association of dietary polysaccharide intake with Glc4 excretion. Urinary Glc4 excretion (mmol/mmol creatinine and mmol/24 h) was analyzed using a validated LC-MS/MS method. Data was analyzed from 65 kidney transplant recipients and 58 healthy kidney donors in the TransplantLines cohort study. Spearman's correlation and multivariable linear regression analyses were performed. In the multivariable analysis, dry lean body mass (DLBM), dietary polysaccharide intake, transplantation status, age, sex, and glycated hemoglobin (HbA1c) served as independent variables. Daily variation was examined in 21 healthy individuals of urinary Glc4 excretion in 2-h collections over a 24-h period. Mixed generalized additive models were built to study the association of prior polysaccharide intake with Glc4 excretion. No (univariate) associations were found between polysaccharide intake and Glc4 excretion. However, a significant interaction between DLBM and polysaccharide on 24 h Glc4 excretion was observed in the multivariate analysis. Glc4 excretion throughout the day exhibited no relationship to prior polysaccharide intake. Our findings suggest an indirect effect of polysaccharide intake on Glc4 excretion, potentially due to changes in muscle glycogen content and/or turnover. We have found no evidence that dietary polysaccharides under normal intakes increase urinary Glc4 directly.