Evidence map›Paper›PMID 37240189›Full record

ArticleInternational journal of molecular sciences2023

The Spectrum of Neurological and Sensory Abnormalities in Gaucher Disease Patients: A Multidisciplinary Study (SENOPRO).

Maria Giulia Tullo, Emanuele Cerulli Irelli, Francesca Caramia, Gianmarco Tessari, Carlo Di Bonaventura, Rosaria Turchetta, Anna Teresa Giallonardo, Giovanna Palumbo, Simona Bianchi, Francesca Atturo and 4 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

8 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Observational
  3. Article
  4. Fucosidosis: A Review of a Rare Disease.International journal of molecular sciences · 2025
    Review
  5. Review
  6. Review
  7. Article
  8. Review
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

14 authors at 3 institutions in 1 country.

Maria Giulia TulloDepartment of Translational and Precision Medicine, "La Sapienza" University of Rome, 00161 Rome, Italy.
Emanuele Cerulli IrelliDepartment of Human Neuroscience, "La Sapienza" University of Rome, 00185 Rome, Italy.
Francesca CaramiaDepartment of Human Neuroscience, "La Sapienza" University of Rome, 00185 Rome, Italy.ORCID 0000-0002-8396-1282
Gianmarco TessariDepartment of Psychology, "La Sapienza" University of Rome, 00185 Rome, Italy.
Carlo Di BonaventuraDepartment of Human Neuroscience, "La Sapienza" University of Rome, 00185 Rome, Italy.
Rosaria TurchettaDepartment of Sense Organs, "La Sapienza" University of Rome, 00185 Rome, Italy.
Anna Teresa GiallonardoDepartment of Human Neuroscience, "La Sapienza" University of Rome, 00185 Rome, Italy.
Giovanna PalumboDepartment of Translational and Precision Medicine, "La Sapienza" University of Rome, 00161 Rome, Italy.
Simona BianchiDepartment of Translational and Precision Medicine, "La Sapienza" University of Rome, 00161 Rome, Italy.
Francesca AtturoDepartment of Sense Organs, "La Sapienza" University of Rome, 00185 Rome, Italy.ORCID 0000-0002-4423-2271
Marcella NebbiosoDepartment of Sense Organs, "La Sapienza" University of Rome, 00185 Rome, Italy.ORCID 0000-0002-5512-0849
Patrizia ManciniDepartment of Sense Organs, "La Sapienza" University of Rome, 00185 Rome, Italy.ORCID 0000-0003-0556-2056
Cecilia GuarigliaDepartment of Psychology, "La Sapienza" University of Rome, 00185 Rome, Italy.
Fiorina GionaDepartment of Translational and Precision Medicine, "La Sapienza" University of Rome, 00161 Rome, Italy.ORCID 0000-0001-8054-6158
Sapienza University of Rome · ITFondazione Santa Lucia · ITUniversity of Chieti-Pescara · IT

Funding

Sanofi 000106_19_CTN
6 · The paper itself

Abstract

Gaucher disease (GD) has been increasingly recognized as a continuum of phenotypes with variable neurological and sensory involvement. No study has yet specifically explored the spectrum of neuropsychiatric and sensory abnormalities in GD patients through a multidisciplinary approach. Abnormalities involving the nervous system, including sensory abnormalities, cognitive disturbances, and psychiatric comorbidities, have been identified in GD1 and GD3 patients. In this prospective study, named SENOPRO, we performed neurological, neuroradiological, neuropsychological, ophthalmological, and hearing assessments in 22 GD patients: 19 GD1 and 3 GD3. First, we highlighted a high rate of parkinsonian motor and non-motor symptoms (including high rates of excessive daytime sleepiness), especially in GD1 patients harboring severe glucocerebrosidase variants. Secondly, neuropsychological evaluations revealed a high prevalence of cognitive impairment and psychiatric disturbances, both in patients initially classified as GD1 and GD3. Thirdly, hippocampal brain volume reduction was associated with impaired short- and long-term performance in an episodic memory test. Fourthly, audiometric assessment showed an impaired speech perception in noise in the majority of patients, indicative of an impaired central processing of hearing, associated with high rates of slight hearing loss both in GD1 and GD3 patients. Finally, relevant structural and functional abnormalities along the visual system were found both in GD1 and GD3 patients by means of visual evoked potentials and optical coherence tomography. Overall, our findings support the concept of GD as a spectrum of disease subtypes, and support the importance of in-depth periodic monitoring of cognitive and motor performances, mood, sleep patterns, and sensory abnormalities in all patients with GD, independently from the patient's initial classification.

Indexed as

Gaucher DiseaseEvoked Potentials, VisualGlucosylceramidaseHumansProspective StudiesGlucosylceramidaseaudiometriccognitiveevoked potentialsGaucher diseasehearing lossParkinson’s diseasepsychiatricsleep

Identifiers

PMID37240189
PMCPMC10218502
OpenAlexW4377041722

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.