Evidence map›Paper›PMID 38954274›Full record

ArticleNeurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology2024

Emotional awareness in patients with amyotrophic lateral sclerosis.

Veronica Faltracco, Barbara Poletti, Edoardo Nicolò Aiello, Alessandra Telesca, Eleonora Dalla Bella, Enrica Bersano, Vincenzo Silani, Nicola Ticozzi, Giuseppe Lauria, Monica Consonni

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Article in Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Veronica FaltraccoThird Neurology Unit and Motor Neuron Disease Centre, Fondazione IRCCS Istituto Neurologico Carlo Besta, Via Luigi Celoria 11, 20133, Milan, Italy.
Barbara Poletti *Department of Neurology and Laboratory of Neuroscience, IRCCS Istituto Auxologico Italiano, Milan, Italy.
Edoardo Nicolò Aiello *Department of Neurology and Laboratory of Neuroscience, IRCCS Istituto Auxologico Italiano, Milan, Italy.
Alessandra TelescaSchool of Medicine and Surgery, PhD Program in Neuroscience, University of Milano-Bicocca, Monza, Italy.
Eleonora Dalla BellaThird Neurology Unit and Motor Neuron Disease Centre, Fondazione IRCCS Istituto Neurologico Carlo Besta, Via Luigi Celoria 11, 20133, Milan, Italy.
Enrica BersanoThird Neurology Unit and Motor Neuron Disease Centre, Fondazione IRCCS Istituto Neurologico Carlo Besta, Via Luigi Celoria 11, 20133, Milan, Italy.
Vincenzo SilaniDepartment of Neurology and Laboratory of Neuroscience, IRCCS Istituto Auxologico Italiano, Milan, Italy.
Nicola TicozziDepartment of Neurology and Laboratory of Neuroscience, IRCCS Istituto Auxologico Italiano, Milan, Italy.
Giuseppe LauriaThird Neurology Unit and Motor Neuron Disease Centre, Fondazione IRCCS Istituto Neurologico Carlo Besta, Via Luigi Celoria 11, 20133, Milan, Italy.
Monica ConsonniThird Neurology Unit and Motor Neuron Disease Centre, Fondazione IRCCS Istituto Neurologico Carlo Besta, Via Luigi Celoria 11, 20133, Milan, Italy. monica.consonni@istituto-besta.it.ORCID http://orcid.org/0000-0002-0479-2290

Funding

Fondazione Regionale per la Ricerca Biomedica, Regione Lombardia 2015-0023Fondo Europeo di Sviluppo Regionale, Regione Lombardia (POR FESR 2014-2020) 1157625Ministero della Salute RRC
6 · The paper itself

Abstract

introductionIt has been recently acknowledged that deficits in experiencing and processing one's own emotions, also termed alexithymia, may possibly feature the frontotemporal-spectrum disorders. This study aims to determine whether alexithymia could be included within the frontotemporal syndromes of amyotrophic lateral sclerosis (ALS).

methodsAlexithymic traits were estimated in a cohort of 68 non-demented ALS patients with the 20-item Toronto Alexithymia Scale (TAS-20). Patients were assessed for the identification of motor-phenotypes and frontotemporal syndromes based on current classification criteria. Spearman's coefficients explored the correlates of TAS-20 measures with motor-functional profiles, global cognitive, social-cognitive (emotion recognition and empathy) and behavioral status.

resultsAbnormal TAS-20 scores were found in 13% of patients, and their distribution did not vary within motor and frontotemporal phenotypes. Significant associations were detected between TAS-20 and executive (p ≤ .011), memory (p = .006), state-anxiety (p ≤ .013) and depression measures (p ≤ .010). By contrast, TAS-20 scores were unrelated to social-cognitive performances, dysexecutive and apathetic profiles. Disease duration was the only motor-functional feature being related to the TAS-20 (p ≤ .008).

conclusionsAlexithymia of potential clinical relevance occur in a minority of ALS patients, and its neuropsychological correlates mostly resemble those featuring the general population. Hence, it is unlikely that alexithymia is a specific feature of frontotemporal-spectrum characterizing ALS, rather it could be an expression of psychogenic factors as a reaction to the disease.

Indexed as

Affective SymptomsAmyotrophic Lateral SclerosisAgedAwarenessCohort StudiesEmotionsFemaleHumansMaleMiddle AgedNeuropsychological TestsAlexithymiaAmyotrophic lateral sclerosisFrontotemporal degenerationNeuropsychologySocial cognition

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.