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Diagnostic value of MRS-quantified brain tissue lactate level in identifying children with mitochondrial disorders

OBJECTIVES: Magnetic resonance spectroscopy (MRS) of children with or without neurometabolic disease is used for the first time for quantitative assessment of brain tissue lactate signals, to elaborate on previous suggestions of MRS-detected lactate as a marker of mitochondrial disease. METHODS: Mul...

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Autores principales: Lunsing, Roelineke J., Strating, Kim, de Koning, Tom J., Sijens, Paul E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5306328/
https://www.ncbi.nlm.nih.gov/pubmed/27271921
http://dx.doi.org/10.1007/s00330-016-4454-8
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author Lunsing, Roelineke J.
Strating, Kim
de Koning, Tom J.
Sijens, Paul E.
author_facet Lunsing, Roelineke J.
Strating, Kim
de Koning, Tom J.
Sijens, Paul E.
author_sort Lunsing, Roelineke J.
collection PubMed
description OBJECTIVES: Magnetic resonance spectroscopy (MRS) of children with or without neurometabolic disease is used for the first time for quantitative assessment of brain tissue lactate signals, to elaborate on previous suggestions of MRS-detected lactate as a marker of mitochondrial disease. METHODS: Multivoxel MRS of a transverse plane of brain tissue cranial to the ventricles was performed in 88 children suspected of having neurometabolic disease, divided into ‘definite’ (n = 17, ≥1 major criteria), ‘probable’ (n = 10, ≥2 minor criteria), ‘possible’ (n = 17, 1 minor criterion) and ‘unlikely’ mitochondrial disease (n = 44, none of the criteria). Lactate levels, expressed in standardized arbitrary units or relative to creatine, were derived from summed signals from all voxels. Ten ‘unlikely’ children with a normal neurological exam served as the MRS reference subgroup. For 61 of 88 children, CSF lactate values were obtained. RESULTS: MRS lactate level (>12 arbitrary units) and the lactate-to-creatine ratio (L/Cr >0.22) differed significantly between the definite and the unlikely group (p = 0.015 and p = 0.001, respectively). MRS L/Cr also differentiated between the probable and the MRS reference subgroup (p = 0.03). No significant group differences were found for CSF lactate. CONCLUSION: MRS-quantified brain tissue lactate levels can serve as diagnostic marker for identifying mitochondrial disease in children. KEY POINTS: • MRS-detected brain tissue lactate levels can be quantified. • MRS lactate and lactate/Cr are increased in children with mitochondrial disease. • CSF lactate is less suitable as marker of mitochondrial disease.
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spelling pubmed-53063282017-02-27 Diagnostic value of MRS-quantified brain tissue lactate level in identifying children with mitochondrial disorders Lunsing, Roelineke J. Strating, Kim de Koning, Tom J. Sijens, Paul E. Eur Radiol Magnetic Resonance OBJECTIVES: Magnetic resonance spectroscopy (MRS) of children with or without neurometabolic disease is used for the first time for quantitative assessment of brain tissue lactate signals, to elaborate on previous suggestions of MRS-detected lactate as a marker of mitochondrial disease. METHODS: Multivoxel MRS of a transverse plane of brain tissue cranial to the ventricles was performed in 88 children suspected of having neurometabolic disease, divided into ‘definite’ (n = 17, ≥1 major criteria), ‘probable’ (n = 10, ≥2 minor criteria), ‘possible’ (n = 17, 1 minor criterion) and ‘unlikely’ mitochondrial disease (n = 44, none of the criteria). Lactate levels, expressed in standardized arbitrary units or relative to creatine, were derived from summed signals from all voxels. Ten ‘unlikely’ children with a normal neurological exam served as the MRS reference subgroup. For 61 of 88 children, CSF lactate values were obtained. RESULTS: MRS lactate level (>12 arbitrary units) and the lactate-to-creatine ratio (L/Cr >0.22) differed significantly between the definite and the unlikely group (p = 0.015 and p = 0.001, respectively). MRS L/Cr also differentiated between the probable and the MRS reference subgroup (p = 0.03). No significant group differences were found for CSF lactate. CONCLUSION: MRS-quantified brain tissue lactate levels can serve as diagnostic marker for identifying mitochondrial disease in children. KEY POINTS: • MRS-detected brain tissue lactate levels can be quantified. • MRS lactate and lactate/Cr are increased in children with mitochondrial disease. • CSF lactate is less suitable as marker of mitochondrial disease. Springer Berlin Heidelberg 2016-06-07 2017 /pmc/articles/PMC5306328/ /pubmed/27271921 http://dx.doi.org/10.1007/s00330-016-4454-8 Text en © The Author(s) 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Magnetic Resonance
Lunsing, Roelineke J.
Strating, Kim
de Koning, Tom J.
Sijens, Paul E.
Diagnostic value of MRS-quantified brain tissue lactate level in identifying children with mitochondrial disorders
title Diagnostic value of MRS-quantified brain tissue lactate level in identifying children with mitochondrial disorders
title_full Diagnostic value of MRS-quantified brain tissue lactate level in identifying children with mitochondrial disorders
title_fullStr Diagnostic value of MRS-quantified brain tissue lactate level in identifying children with mitochondrial disorders
title_full_unstemmed Diagnostic value of MRS-quantified brain tissue lactate level in identifying children with mitochondrial disorders
title_short Diagnostic value of MRS-quantified brain tissue lactate level in identifying children with mitochondrial disorders
title_sort diagnostic value of mrs-quantified brain tissue lactate level in identifying children with mitochondrial disorders
topic Magnetic Resonance
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5306328/
https://www.ncbi.nlm.nih.gov/pubmed/27271921
http://dx.doi.org/10.1007/s00330-016-4454-8
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