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Tako-Tsubo Syndrome in Amyotrophic Lateral Sclerosis: Single-Center Case Series and Brief Literature Review.
Napoli, Giovanni; Rubin, Martina; Cutillo, Gianni; Schito, Paride; Russo, Tommaso; Quattrini, Angelo; Filippi, Massimo; Riva, Nilo.
Afiliação
  • Napoli G; Neurorehabilitation, Neurology Unit and Neurophysiology Unit, San Raffaele Scientific Institute, 20132 Milan, Italy.
  • Rubin M; Neurorehabilitation, Neurology Unit and Neurophysiology Unit, San Raffaele Scientific Institute, 20132 Milan, Italy.
  • Cutillo G; Neuroimaging Research Unit, Institute of Experimental Neurology, Division of Neuroscience, San Raffaele Scientific Institute, 20132 Milan, Italy.
  • Schito P; Neurorehabilitation, Neurology Unit and Neurophysiology Unit, San Raffaele Scientific Institute, 20132 Milan, Italy.
  • Russo T; Neurorehabilitation, Neurology Unit and Neurophysiology Unit, San Raffaele Scientific Institute, 20132 Milan, Italy.
  • Quattrini A; Experimental Neuropathology Unit, Institute of Experimental Neurology (INSPE), Division of Neuroscience, San Raffaele Scientific Institute, 20132 Milan, Italy.
  • Filippi M; Neurorehabilitation, Neurology Unit and Neurophysiology Unit, San Raffaele Scientific Institute, 20132 Milan, Italy.
  • Riva N; Experimental Neuropathology Unit, Institute of Experimental Neurology (INSPE), Division of Neuroscience, San Raffaele Scientific Institute, 20132 Milan, Italy.
Int J Mol Sci ; 24(15)2023 Jul 28.
Article em En | MEDLINE | ID: mdl-37569475
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease with variable phenotypic expressions which has been associated with autonomic dysfunction. The cardiovascular system seems to be affected especially in the context of bulbar involvement. We describe four new cases of Tako-Tsubo syndrome (TTS) in ALS patients with an appraisal of the literature. We present a late-stage ALS patient with prominent bulbar involvement that presented TTS during hospitalization. We then retrospectively identify three additional ALS-TTS cases reporting relevant clinical findings. TTS cardiomyopathy has been observed in different acute neurological conditions, and the co-occurrence of ALS and TTS has already been reported. Cardiovascular autonomic dysfunctions have been described in ALS, especially in the context of an advanced diseases and with bulbar involvement. Noradrenergic hyperfunction linked to sympathetic denervation and ventilatory deficits coupled in different instances with a trigger event could play a synergistic role in the development of TTS in ALS. Sympathetic hyperfunctioning and ventilatory deficits in conjunction with cardiac autonomic nerves impairment may play a role in the development of TTS in a context of ALS.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Neurodegenerativas / Cardiomiopatia de Takotsubo / Disautonomias Primárias / Esclerose Lateral Amiotrófica Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Int J Mol Sci Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Neurodegenerativas / Cardiomiopatia de Takotsubo / Disautonomias Primárias / Esclerose Lateral Amiotrófica Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Int J Mol Sci Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Itália