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Interplay between spinal cord and cerebral cortex metabolism in amyotrophic lateral sclerosis

We recently reported the potential of Hough transform in delineating spinal cord metabolism by (18)F-fluorodeoxyglucose PET/CT scanning in amyotrophic lateral sclerosis. The present study aimed to verify the relationship between spinal cord and brain metabolism in 44 prospectively recruited patients...

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Detalles Bibliográficos
Autores principales: Marini, Cecilia, Morbelli, Silvia, Cistaro, Angelina, Campi, Cristina, Caponnetto, Claudia, Bauckneht, Matteo, Bellini, Alessandro, Buschiazzo, Ambra, Calamia, Iolanda, Beltrametti, Mauro C, Margotti, Simone, Fania, Piercarlo, Poggi, Ilaria, Cabona, Corrado, Capitanio, Selene, Piva, Roberta, Calvo, Andrea, Moglia, Cristina, Canosa, Antonio, Massone, AnnaMaria, Nobili, Flavio, Mancardi, Gianluigi, Chiò, Adriano, Piana, Michele, Sambuceti, Gianmario
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6061793/
https://www.ncbi.nlm.nih.gov/pubmed/30730551
http://dx.doi.org/10.1093/brain/awy152
Descripción
Sumario:We recently reported the potential of Hough transform in delineating spinal cord metabolism by (18)F-fluorodeoxyglucose PET/CT scanning in amyotrophic lateral sclerosis. The present study aimed to verify the relationship between spinal cord and brain metabolism in 44 prospectively recruited patients affected by amyotrophic lateral sclerosis submitted to (18)F-fluorodeoxyglucose brain and whole-body PET/CT. Patients were studied to highlight the presence of brain hypo- or hypermetabolism with respect to healthy controls, and multiple regression analysis was performed to evaluate the correlation between spinal cord and brain metabolism. Our results confirmed higher (18)F-fluorodeoxyglucose uptake in both cervical and dorsal spinal cord in patients with amyotrophic lateral sclerosis with respect to controls. This finding was paralleled by the opposite pattern in the brain cortex that showed a generalized reduction in tracer uptake. This hypometabolism was particularly evident in wide regions of the frontal-dorsolateral cortex while it did not involve the midbrain. Bulbar and spinal disease onset was associated with similar degree of metabolic activation in the spinal cord. However, among spinal onset patients, upper limb presentation was associated with a more pronounced metabolic activation of cervical segment. Obtained data suggest a differential neuro-pathological state or temporal sequence in disease progression.