Expanded neurochemical profile in the early stage of Huntington disease using proton magnetic resonance spectroscopy

Isaac Mawusi Adanyeguh (1) , Marie-Lorraine Monin (1) , Daisy Rinaldi (1) , Leorah Freeman , Alexandra Durr (1) , Stéphane Lehéricy (1) , Pierre-Gilles Henry (2) , Fanny Mochel (1)

1 ICM - Institut du Cerveau et de la Moëlle Epinière = Brain and Spine Institute
2 UMN - University of Minnesota [Twin Cities]

The striatum is a well-known region affected in Huntington disease (HD). However, other regions, including the visual cortex, are implicated. We have identified previously an abnormal energy response in the visual cortex of patients at an early stage of HD using 31P magnetic resonance spectroscopy (31P MRS). We therefore sought to further characterize these metabolic alterations with 1H MRS using a well-validated semi-localized by adiabatic selective refocusing (semi-LASER) sequence that allows the measurement of an expanded number of neurometabolites. Ten early affected patients [Unified Huntington Disease Rating Scale (UHDRS), total motor score = 13.6 ± 10.8] and 10 healthy volunteers of similar age and body mass index (BMI) were recruited for the study. We performed 1H MRS in the striatum – the region that is primarily affected in HD – and the visual cortex. The protocol allowed a reliable quantification of 10 metabolites in the visual cortex and eight in the striatum, compared with three to five metabolites in previous 1H MRS studies performed in HD. We identified higher total creatine (p < 0.05) in the visual cortex and lower glutamate (p < 0.001) and total creatine (p < 0.05) in the striatum of patients with HD compared with controls. Less abundant neurometabolites [glutamine, γ-aminobutyric acid (GABA), glutathione, aspartate] showed similar concentrations in both groups. The protocol allowed the measurement of several additional metabolites compared with standard vendor protocols. Our study points to early changes in metabolites involved in energy metabolism in the visual cortex and striatum of patients with HD. Decreased striatal glutamate could reflect early neuronal dysfunction or impaired glutamatergic neurotransmission.

Domaines: Neurobiologie

Isaac Mawusi Adanyeguh, Marie-Lorraine Monin, Daisy Rinaldi, Leorah Freeman, Alexandra Durr, et al.. Expanded neurochemical profile in the early stage of Huntington disease using proton magnetic resonance spectroscopy. NMR in Biomedicine, In press, ⟨10.1002/nbm.3880⟩. ⟨hal-01688609⟩