18F-FDG-PET correlates of cognitive impairment in ALS
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Abstract
Objective: To identify the metabolic signature of the various levels of cognitive deficits in amyotrophic lateral sclerosis (ALS) using 18F-2-fluoro-2-deoxy-d-glucose-PET (18F-FDG-PET).
Methods: A total of 170 ALS cases consecutively enrolled at the ALS Center of Turin underwent brain 18F-FDG-PET and were classified as displaying normal cognition (ALS-Cn; n = 94), full-blown frontotemporal dementia (ALS-FTD; n = 20), executive or nonexecutive cognitive impairment not fulfilling FTD criteria (ALS-Ci; n = 37), prevalent behavioral changes (n = 9), or nonclassifiable impairment (n = 10) according to neuropsychological testing. Group comparisons of 18F-FDG-PET pattern were carried out among the cognitive subgroups.
Results: We found a significantly reduced frontal and prefrontal metabolism in ALS-FTD as compared to ALS-Cn, while ALS-Ci showed an intermediate metabolic behavior in frontal cortex, being hypometabolic as compared to ALS-Cn, and relatively hypermetabolic as compared to ALS-FTD. Hypometabolism in frontal regions was associated in all comparisons to hypermetabolism in cerebellum, midbrain, and corticospinal tracts: the more severe the cognitive decline, the larger the size of the cluster and the statistical significance of 18F-FDG uptake differences.
Conclusions: This study demonstrated in a large cohort of patients with ALS a continuum of frontal lobe metabolic impairment reflecting the clinical and anatomic continuum ranging from pure ALS, through ALS with intermediate cognitive deficits, to ALS-FTD, and showing that patients with intermediate cognitive impairment display a characteristic metabolic pattern. Since 18F-FDG-PET allows us to estimate the cerebral lesion load in vivo in neurodegenerative diseases, it might be helpful to investigate in ALS its association with neuropsychological testing along the disease course to disclose the early metabolic signature of possible cognitive impairment.
GLOSSARY
- 18F-FDG-PET=
- 18F-2-fluoro-2-deoxy-d-glucose-PET;
- ALS=
- amyotrophic lateral sclerosis;
- ALS-Bi=
- amyotrophic lateral sclerosis with behavioral impairment;
- ALS-Ci=
- amyotrophic lateral sclerosis with cognitive impairment;
- ALS-Cn=
- amyotrophic lateral sclerosis with normal cognition;
- ALS-Nc=
- amyotrophic lateral sclerosis with nonclassifiable cognitive impairment;
- ALSFRS-R=
- Amyotrophic Lateral Sclerosis Functional Rating Scale–revised;
- DSM-IV-TR=
- Diagnostic and Statistical Manual of Mental Disorders, 4th edition, text revision;
- FTD=
- frontotemporal dementia;
- FTLD=
- frontotemporal lobar degeneration;
- pTDP-43=
- phosphorylated TDP-43
Footnotes
↵* These authors contributed equally to this work.
Go to Neurology.org for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.
- Received June 23, 2015.
- Accepted in final form August 28, 2015.
- © 2015 American Academy of Neurology
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Letters: Rapid online correspondence
- Response to dr. Abe
- Adriano Chio, Professor of Neurology, University of Turin, Italyachio@usa.net
- Marco Pagani, Rome, Italy; Antonio Canosa, Turin, Italy
Submitted January 14, 2016 - ALS with cognitive dysfunction
- Kazuo Abe, Professor, Hyogo College of Medicineabe_neurology@mac.com
Submitted January 11, 2016
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