Abstract

IntroductionPhenotypic variants of progressive supranuclear palsy (PSP) are all characterized by the combination of motor symptoms of parkinsonism with a number of neuropsychiatric and cognitive disorders. Despite the strong effort in characterizing these features in PSP, alexithymia and anhedonia have not been investigated at present. Here, we aimed at investigating the qualitative and quantitative differences of alexithymia and anhedonia in the two more frequent variants of PSP, Richardson's syndrome (PSP‐RS) and PSP with predominant parkinsonism (PSP‐P) compared to Parkinson's disease (PD) patients recruited within 24 months after the onset of motor symptoms.MethodsOne hundred fifty‐five PD, 11 PSP‐P, and 14 PSP‐RS patients underwent clinical, neuropsychiatric, and neuropsychological evaluations. Alexithymia was assessed using the Toronto Alexithymia Scale‐20 item (TAS‐20), and hedonic tone was measured by the Snaith–Hamilton Pleasure Scale (SHAPS).ResultsIn PSP‐P and PSP‐RS patients, the frequency of alexithymia diagnosis was higher than in PD. On the TAS‐20 scores, PSP‐RS performed worse in the total score and in F2 sub‐scale when compared to PD. Among patients with diagnosis of depression, PSP‐RS showed higher scores in TAS‐20 total and TAS‐20 F2 than PD. No significant differences in TAS‐20 scores were found in nondepressed patients. Finally, we did not find significant differences among PD, PSP‐P, and PSP‐RS groups in the SHAPS scores.ConclusionsAlexithymia is identifiable very early in PSP‐P and PSP‐RS patients. Alexithymic symptoms differentiate PSP‐RS group from PD group but not between the two subtypes of PSP. Further, alexithymia in PSP seems to be predicted by the presence of depression. Altered emotional capability could be related to specific neurophysiological dysfunction occurring precociously in PSP; therefore, its identification could orient the diagnosis toward PSP cases.

Highlights

  • Phenotypic variants of progressive supranuclear palsy (PSP) are all characterized by the combination of motor symptoms of parkinsonism with a number of neuropsychiatric and cognitive disorders

  • Alexithymia and anhedonia have been reported frequently in patients suffering from Parkinson's disease (PD); it is still not clear whether they are a secondary phenomenon linked to depression and apathy sever‐ ity (Assogna, Cravello, Caltagirone, & Spalletta, 2011; Assogna et al, 2016) or a disease primary characteristic (Assogna et al, 2011, 2016; Spalletta et al, 2013) linked to frontal lobe dysregulation

  • On the bases of this background, the aim of the study was to analyze qualitative and quantitative differences of alexithymia and anhedonia in PSP‐RS and PSP with predominant parkinsonism (PSP‐P) compared to PD patients, early in the disease course

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Summary

Introduction

Phenotypic variants of progressive supranuclear palsy (PSP) are all characterized by the combination of motor symptoms of parkinsonism with a number of neuropsychiatric and cognitive disorders. We aimed at investigating the qualitative and quantitative differences of alexithymia and anhedonia in the two more frequent variants of PSP, Richardson's syndrome (PSP‐RS) and PSP with predominant parkinsonism (PSP‐P) compared to Parkinson's disease (PD) patients recruited within 24 months after the onset of motor symptoms. Richardson's syndrome (PSP‐RS) and PSP with pre‐ dominant parkinsonism (PSP‐P) are the most frequent phenotypes (Hoglinger et al, 2017) of PSP. Despite the strong effort in characterizing the neuropsychiatric and neuropsychological features of the different variants of PSP, alexithymia and anhedonia have not been investigated at present. Alexithymia and anhedonia have been reported frequently in patients suffering from Parkinson's disease (PD); it is still not clear whether they are a secondary phenomenon linked to depression and apathy sever‐ ity (Assogna, Cravello, Caltagirone, & Spalletta, 2011; Assogna et al, 2016) or a disease primary characteristic (Assogna et al, 2011, 2016; Spalletta et al, 2013) linked to frontal lobe dysregulation

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