Narjes Ahmadian, Mark Gosselink, Sigrid A. Otto, Dimitri Welting, Kiki Tesselaar, Tom J. Snijders, Pieter van Eijsden, Jeanine J. Prompers, Dennis W. J. Klomp, Evita Wiegers
Abstract Objective This study investigates the dynamic metabolic characteristics of glioblastoma (GBM) using Deuterium Metabolic Imaging (DMI) at 7 T, aiming to dynamically characterize the Warburg effect in vivo. Material and methods Five newly diagnosed GBM patients underwent dynamic DMI prior to any treatment. 3D 2 H free-induction-decay (FID)-Magnetic resonance spectroscopy imaging (MRSI) measurements (11:44 min per scan) were performed at 7 T during ~ 100 min following [6,6’- 2 H 2 ]glucose consumption. Venous plasma glucose and plasma 2 H-Glc atom percent enrichment (APE) levels were measured during the scan. Brain 2 H-glucose ( 2 H-Glc), 2 H-Glutamate/Glutamine ( 2 H-Glx), 2 H-Lactate ( 2 H-Lac), 2 H-Lac/ 2 H-Glx were analyzed with a two-level (time and tissue type) Linear Mixed Model. Results Brain 2 H-Glc levels were similar across tissue types. 2 H-Glx was significantly lower in tumors compared to normal appearing brain tissue (NABT) ( p < 0.01). 2 H-Lac was significantly higher in tumors compared to NABT ( P < 0.01). The 2 H-Lac/ 2 H-Glx ratio provided tumor-specific contrast, starting 40-50 min post [6,6’- 2 H 2 ]glucose consumption. Venous plasma glucose and 2 H-Glc APE increased within 50 min and venous 2 H-Glc APE stabilized at ~ 60%. Discussion Dynamic DMI at 7 T reveals metabolic alterations in GBM, particularly through the 2 H-Lac/ 2 H-Glx ratio. This contrast was primarily driven by decreased 2 H-Glx rather than profoundly increased 2 H-Lac. These findings support the utility of DMI in assessing metabolic reprogramming in brain tumors.