Combining structural and metabolic markers in a quantitative MRI study of motor neuron diseases

Abstract Objective To assess the performance of a combination of three quantitative MRI markers (iron deposition, basal neuronal metabolism, and regional atrophy) for differential diagnosis between amyotrophic lateral sclerosis (ALS) and primary lateral sclerosis (PLS). Methods In total, 33 ALS, 12...

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Autores principales: Antonietta Canna, Francesca Trojsi, Federica Di Nardo, Giuseppina Caiazzo, Gioacchino Tedeschi, Mario Cirillo, Fabrizio Esposito
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Publicado: Wiley 2021
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spelling oai:doaj.org-article:8bf52f1e28ca4c1cafda87f3953e494d2021-11-19T13:55:31ZCombining structural and metabolic markers in a quantitative MRI study of motor neuron diseases2328-950310.1002/acn3.51418https://doaj.org/article/8bf52f1e28ca4c1cafda87f3953e494d2021-09-01T00:00:00Zhttps://doi.org/10.1002/acn3.51418https://doaj.org/toc/2328-9503Abstract Objective To assess the performance of a combination of three quantitative MRI markers (iron deposition, basal neuronal metabolism, and regional atrophy) for differential diagnosis between amyotrophic lateral sclerosis (ALS) and primary lateral sclerosis (PLS). Methods In total, 33 ALS, 12 PLS, and 28 healthy control (HC) subjects underwent a 3T MRI study including single‐ and multi‐echo sequences for gray matter (GM) volumetry and quantitative susceptibility mapping (QSM) and a pseudo‐continuous arterial spin labeling (ASL) sequence for cerebral blood flow (CBF) measurement. Mean values of QSM, CBF, and GM volumes were extracted in the motor cortex, basal ganglia, thalamus, amygdala, and hippocampus. A generalized linear model was applied to the three measures to binary discriminate between groups. The diagnostic performances were evaluated via receiver operating characteristic analyses. Results A significant discrimination was obtained: between ALS and HCs in the left and right motor cortex, where QSM increases were respectively associated with disability scores and disease duration; between PLS and ALS in the left motor cortex, where PLS patients resulted significantly more atrophic; between ALS and HC in the right motor cortex, where GM volumes were associated with upper motor neuron scores. Significant discrimination between ALS and HC was achieved in subcortical structures only combining all three parameters. Interpretation While increased QSM values in the motor cortex of ALS patients is a consolidated finding, combining QSM, CBF, and GM volumetry shows higher diagnostic potential for differentiating ALS patients from HC subjects and, in the motor cortex, between ALS and PLS.Antonietta CannaFrancesca TrojsiFederica Di NardoGiuseppina CaiazzoGioacchino TedeschiMario CirilloFabrizio EspositoWileyarticleNeurosciences. Biological psychiatry. NeuropsychiatryRC321-571Neurology. Diseases of the nervous systemRC346-429ENAnnals of Clinical and Translational Neurology, Vol 8, Iss 9, Pp 1774-1785 (2021)
institution DOAJ
collection DOAJ
language EN
topic Neurosciences. Biological psychiatry. Neuropsychiatry
RC321-571
Neurology. Diseases of the nervous system
RC346-429
spellingShingle Neurosciences. Biological psychiatry. Neuropsychiatry
RC321-571
Neurology. Diseases of the nervous system
RC346-429
Antonietta Canna
Francesca Trojsi
Federica Di Nardo
Giuseppina Caiazzo
Gioacchino Tedeschi
Mario Cirillo
Fabrizio Esposito
Combining structural and metabolic markers in a quantitative MRI study of motor neuron diseases
description Abstract Objective To assess the performance of a combination of three quantitative MRI markers (iron deposition, basal neuronal metabolism, and regional atrophy) for differential diagnosis between amyotrophic lateral sclerosis (ALS) and primary lateral sclerosis (PLS). Methods In total, 33 ALS, 12 PLS, and 28 healthy control (HC) subjects underwent a 3T MRI study including single‐ and multi‐echo sequences for gray matter (GM) volumetry and quantitative susceptibility mapping (QSM) and a pseudo‐continuous arterial spin labeling (ASL) sequence for cerebral blood flow (CBF) measurement. Mean values of QSM, CBF, and GM volumes were extracted in the motor cortex, basal ganglia, thalamus, amygdala, and hippocampus. A generalized linear model was applied to the three measures to binary discriminate between groups. The diagnostic performances were evaluated via receiver operating characteristic analyses. Results A significant discrimination was obtained: between ALS and HCs in the left and right motor cortex, where QSM increases were respectively associated with disability scores and disease duration; between PLS and ALS in the left motor cortex, where PLS patients resulted significantly more atrophic; between ALS and HC in the right motor cortex, where GM volumes were associated with upper motor neuron scores. Significant discrimination between ALS and HC was achieved in subcortical structures only combining all three parameters. Interpretation While increased QSM values in the motor cortex of ALS patients is a consolidated finding, combining QSM, CBF, and GM volumetry shows higher diagnostic potential for differentiating ALS patients from HC subjects and, in the motor cortex, between ALS and PLS.
format article
author Antonietta Canna
Francesca Trojsi
Federica Di Nardo
Giuseppina Caiazzo
Gioacchino Tedeschi
Mario Cirillo
Fabrizio Esposito
author_facet Antonietta Canna
Francesca Trojsi
Federica Di Nardo
Giuseppina Caiazzo
Gioacchino Tedeschi
Mario Cirillo
Fabrizio Esposito
author_sort Antonietta Canna
title Combining structural and metabolic markers in a quantitative MRI study of motor neuron diseases
title_short Combining structural and metabolic markers in a quantitative MRI study of motor neuron diseases
title_full Combining structural and metabolic markers in a quantitative MRI study of motor neuron diseases
title_fullStr Combining structural and metabolic markers in a quantitative MRI study of motor neuron diseases
title_full_unstemmed Combining structural and metabolic markers in a quantitative MRI study of motor neuron diseases
title_sort combining structural and metabolic markers in a quantitative mri study of motor neuron diseases
publisher Wiley
publishDate 2021
url https://doaj.org/article/8bf52f1e28ca4c1cafda87f3953e494d
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