Novel cerebrospinal fluid biomarkers of glucose transporter type 1 deficiency syndrome: Implications beyond the brain's energy deficit. Issue 1 (17th October 2022)

• Record Type: Journal Article
• Authors: Peters, Tessa M. A.; Merx, Jona; Kooijman, Pieter C.; Noga, Marek; de Boer, Siebolt; van Gemert, Loes A.; Salden, Guido; Engelke, Udo F. H.; Lefeber, Dirk J.; van Outersterp, Rianne E.; Berden, Giel; Boltje, Thomas J.; Artuch, Rafael; Pías‐Peleteiro, Leticia; García‐Cazorla, Ángeles; Barić, Ivo; Thöny, Beat; Oomens, Jos; Martens, Jonathan; Wevers, Ron A.; Verbeek, Marcel M.; Coene, Karlien L. M.; Willemsen, Michèl A. A. P.
• Is Part Of: Journal of inherited metabolic disease. Volume 46:Issue 1(2023)
• Page Start: 66
• Page End: 75
• Publication Date: 2022-10-17
• Subjects: next‐generation metabolic screening -- O‐glucosylation -- oligosaccharides -- SLC2A1 -- untargeted metabolomics; Metabolism, Inborn errors of -- Periodicals; Metabolism -- Disorders -- Periodicals; 616.39042
• DOI: 10.1002/jimd.12554
• Languages: English
• ISSNs: 0141-8955

Abstract

Abstract: We used next‐generation metabolic screening to identify new biomarkers for improved diagnosis and pathophysiological understanding of glucose transporter type 1 deficiency syndrome (GLUT1DS), comparing metabolic cerebrospinal fluid (CSF) profiles from 12 patients to those of 116 controls. This confirmed decreased CSF glucose and lactate levels in patients with GLUT1DS and increased glutamine at group level. We identified three novel biomarkers significantly decreased in patients, namely gluconic + galactonic acid, xylose‐α1‐3‐glucose, and xylose‐α1‐3‐xylose‐α1‐3‐glucose, of which the latter two have not previously been identified in body fluids. CSF concentrations of gluconic + galactonic acid may be reduced as these metabolites could serve as alternative substrates for the pentose phosphate pathway. Xylose‐α1‐3‐glucose and xylose‐α1‐3‐xylose‐α1‐3‐glucose may originate from glycosylated proteins; their decreased levels are hypothetically the consequence of insufficient glucose, one of two substrates for O ‐glucosylation. Since many proteins are O ‐glucosylated, this deficiency may affect cellular processes and thus contribute to GLUT1DS pathophysiology. The novel CSF biomarkers have the potential to improve the biochemical diagnosis of GLUT1DS. Our findings imply that brain glucose deficiency in GLUT1DS may cause disruptions at the cellular level that go beyond energy metabolism, underlining the importance of developing treatment strategies that directly target cerebral glucose uptake.