Evidence map›Paper›PMID 31743601›Full record

ArticleBrain and behavior2019

Alexithymia and anhedonia in early Richardson's syndrome and progressive supranuclear palsy with predominant parkinsonism.

Francesca Assogna, Clelia Pellicano, Luca Cravello, Cinzia Savini, Lucia Macchiusi, Mariangela Pierantozzi, Alessandro Stefani, Bruno Mercuri, Carlo Caltagirone, Francesco E Pontieri and 1 more

Open access · goldAbstract read
In one paragraph

Article in Brain and behavior, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 24% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Alexithymia in Alzheimer's Disease.Journal of clinical medicine · 2020
    Article
  4. Article
  5. Article
  6. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 6 institutions in 1 country.

Francesca AssognaFondazione Santa Lucia, IRCCS, Roma, Italy.ORCID 0000-0003-4315-7879
Clelia PellicanoFondazione Santa Lucia, IRCCS, Roma, Italy.ORCID 0000-0002-3272-1094
Luca CravelloCentro Alzheimer, ASST Rhodense, Rho, Italy.
Cinzia SaviniFondazione Santa Lucia, IRCCS, Roma, Italy.
Lucia MacchiusiFondazione Santa Lucia, IRCCS, Roma, Italy.
Mariangela PierantozziDipartimento di Medicina dei Sistemi, Università "Tor Vergata", Roma, Italy.
Alessandro StefaniDipartimento di Medicina dei Sistemi, Università "Tor Vergata", Roma, Italy.
Bruno MercuriUOC Neurologia, Azienda Ospedaliera "San Giovanni Addolorata", Roma, Italy.
Carlo CaltagironeFondazione Santa Lucia, IRCCS, Roma, Italy.
Francesco E PontieriDipartimento di Neuroscienze, Salute Mentale e Organi di Senso, "Sapienza" Università di Roma, Roma, Italy.
Gianfranco SpallettaFondazione Santa Lucia, IRCCS, Roma, Italy.ORCID 0000-0002-7432-4249
Fondazione Santa Lucia · ITUniversity of Rome Tor Vergata · ITAzienda Ospedaliera San Giovanni Addolorata · ITAziende Socio Sanitaria Territoriale RhodenseOspedale di Belcolle · ITSapienza University of Rome · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Affective SymptomsAgedAnhedoniaFemaleHumansMaleMiddle AgedNeuropsychological TestsParkinsonian DisordersSupranuclear Palsy, Progressivealexithymiaanhedonianonmotor symptomsParkinson's diseaseprogressive supranuclear palsy

Identifiers

PMID31743601
PMCPMC6908877
OpenAlexW2991220992

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

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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.