<sup>18</sup> F FDG-PET correlates of motor neuron disease motor variants

F-fluorodeoxyglucose positron emission tomography (FDG-PET) is an established biomarker in amyotrophic lateral sclerosis (ALS), the metabolic correlates of motor neuron disease (MND) motor variants remain poorly defined. This is why we investigated patterns of cerebral glucose metabolism across the spectrum of MNDs, including progressive muscular atrophy (PMA), primary lateral sclerosis (PLS), and ALS. We retrospectively included 18 PMA, 25 PLS, and 43 matched non-hereditary ALS patients according to most recent diagnostic criteria. FDG-PET imaging revealed similar widespread hypometabolism in PMA, as in ALS, whereas PLS showed a more focal motor cortical pattern of hypometabolism. Despite clinical differences between MND subtypes, PMA and ALS showed similar FDG-PET metabolic patterns, whereas PLS exhibited a more restricted cortical signature in this retrospective study.

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Publication Details

Journal
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
Published
2026-06-09
DOI
https://doi.org/10.1080/21678421.2026.2682820
Primary Topic
Amyotrophic Lateral Sclerosis Research
Type
article
Field-Weighted Citation Impact
0.00

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article

18 F FDG-PET correlates of motor neuron disease motor variants

Fouke Ombelet, Nikita Lamaire, Frederik Hobin, Boris Deleu et al.
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
Amyotrophic Lateral Sclerosis Research
article

18 F FDG-PET correlates of motor neuron disease motor variants

Fouke Ombelet, Nikita Lamaire, Frederik Hobin, Boris Deleu, Kato Bracaval, Koen Van Laere, Joke De Vocht, Philip Van Damme, Patrick Dupont
article en

Abstract

F-fluorodeoxyglucose positron emission tomography (FDG-PET) is an established biomarker in amyotrophic lateral sclerosis (ALS), the metabolic correlates of motor neuron disease (MND) motor variants remain poorly defined. This is why we investigated patterns of cerebral glucose metabolism across the spectrum of MNDs, including progressive muscular atrophy (PMA), primary lateral sclerosis (PLS), and ALS. We retrospectively included 18 PMA, 25 PLS, and 43 matched non-hereditary ALS patients according to most recent diagnostic criteria. FDG-PET imaging revealed similar widespread hypometabolism in PMA, as in ALS, whereas PLS showed a more focal motor cortical pattern of hypometabolism. Despite clinical differences between MND subtypes, PMA and ALS showed similar FDG-PET metabolic patterns, whereas PLS exhibited a more restricted cortical signature in this retrospective study.

Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
Allen Institute for Brain Science (US), Laboratoire de Neurosciences Cognitives (FR), Institut des Sciences Cognitives Marc Jeannerod (FR), Cognitive Research (United States) (US), Institute of Neurobiology (BG), KU Leuven (BE)
Target ALS, KU Leuven
Good health and well-being
Openalex Percentile: Top 10%
Amyotrophic Lateral Sclerosis Research
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