• Birte Schmitz, Xin Wang, Peter B Barker, Ulrich Pilatus, Paul Bronzlik, Mete Dadak, Kai G Kahl, Heinrich Lanfermann, and Xiao-Qi Ding.
• Institute of Diagnostic and Interventional Neuroradiology, Hannover Medical School, Germany.
• J Neuroimaging. 2018 Jul 1; 28 (4): 416-421.

Background And PurposeTo investigate accumulative aging effects on neurometabolism in human brain and to collect a reference dataset.MethodsFifty-four healthy volunteers aged evenly between 22 and 73 years were studied using whole-brain 1 H-MR spectroscopic imaging in combination with 31 P-MRS at 3T. Global metabolite concentrations of brain N-acetylaspartate (NAA), total choline (tCho), and total creatine (tCr), as well as phosphocreatine (PCr), adenosine-5'-triphosphate (ATP), phosphomonoesters (PME), phosphodiesters (PDE), and inorganic phosphate (Pi) were determined. Fractional volumes of brain gray matter (FVGM), white matter (FVWM), and total tissue (FVTB, GM+WM) were also estimated.ResultsWith age, NAA, ATP, and PME, as well as FVTB and FVGM decreased and tCho and FVWM increased linearly. Positive correlations were found between FVGM and global concentrations of NAA, ATP, PME, and Pi.ConclusionAge-related accumulative metabolic changes in aging human brain correlated with reduced neuronal metabolic activity and density, reflected by decreased NAA, reduced mitochondrial activity by decreased ATP, and reduced membrane synthesis by decreased PME. These changes are associated with age-related decrease of neuronal volume. Global NAA and ATP might be used as surrogate biomarker for monitoring aging in human brain.Copyright © 2018 by the American Society of Neuroimaging.

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