Show simple item record

dc.contributor.authorBenito-León, J.
dc.contributor.authorElan D., Louis
dc.contributor.authorMato-Abad, Virginia
dc.contributor.authorDydak, Ulrike
dc.contributor.authorÁlvarez-Linera, Juan
dc.contributor.authorHernández-Tamames, Juan Antonio
dc.contributor.authorMolina-Arjona, José Antonio
dc.contributor.authorMalpica, Norberto
dc.contributor.authorMatarazzo, Michele
dc.contributor.authorRomero Muñoz, Juan Pablo 
dc.contributor.authorSánchez-Ferro, Álvaro
dc.date.accessioned2016-10-19T11:18:00Z
dc.date.available2016-10-19T11:18:00Z
dc.date.issued2016
dc.identifier.issn1536-5964
dc.identifier.urihttp://hdl.handle.net/10641/1241
dc.description.abstractThe pathogenesis of orthostatic tremor (OT) remains unclear, although some evidence points to dysfunction in the brainstem or cerebellum. We used single voxel proton magnetic resonance spectroscopy (1H-MRS) (3 T) to investigate whether neurochemical changes underlie abnormal cerebellar or cortical function in OT. Fourteen OT patients and 14 healthy controls underwent 1H-MRS studies with voxels placed in midparietal gray matter and cerebellum (vermis and central white matter). Spectral analysis was analyzed using the software package LCModel (version 6.3). The absolute metabolite concentrations and ratios of total N-acetylaspartate+N-acetylaspartyl glutamate (NAA), choline-containing compounds, myoinositol, and glutamate+glutamine to creatine were calculated. In midparietal gray matter spectra, we found a significant decrease in the absolute concentration of NAA in OT patients versus healthy controls (7.76±0.25 vs 8.11±0.45, P=0.017). A similar decrease in NAA was seen in the cerebellar vermis (7.33±0.61 vs 8.55±1.54, P=0.014) and cerebellar white matter (8.54±0.79 vs 9.95±1.57, P=0.010). No differences in the other metabolites or their ratios were observed. Reductions in both cerebral cortical and cerebellar NAA suggest that there is neuronal damage or loss in OT, raising the intriguing question as to whether OT is a neurodegenerative disease. Along with clinical history and electrophysio0logical examination, 1H-MRS could serve as a useful diagnostic aid for OT.spa
dc.language.isoengspa
dc.publisherMedicinespa
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 España*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/*
dc.subjectCase–control studyspa
dc.subjectCerebellumspa
dc.subjectMagnetic resonance imagingspa
dc.subjectOrthostatic tremorspa
dc.subjectPathophysiologyspa
dc.subjectProton magneticspa
dc.subjectResonance spectroscopyspa
dc.titleIn vivo neurometabolic profiling in orthostatic tremorspa
dc.typearticlespa
dc.description.versionpost-printspa
dc.rights.accessRightsopenAccessspa
dc.description.extent338 KBspa


Files in this item

FilesSizeFormatView
In_vivo_neurometabolic_profilingJP ...337.4KbPDFView/Open

This item appears in the following Collection(s)

Show simple item record

Atribución-NoComercial-SinDerivadas 3.0 España
Except where otherwise noted, this item's license is described as Atribución-NoComercial-SinDerivadas 3.0 España