A study of voice and non-voice processing in Prader-Willi syndrome

Abstract Background Prader-Willi syndrome (PWS) is a rare and complex neurodevelopmental disorder of genetic origin. It manifests itself in endocrine and cognitive problems, including highly pronounced hyperphagia and severe obesity. In many cases, impaired acquisition of social and communication sk...

Full description

Bibliographic Details
Main Authors: Kuzma Strenilkov, Jimmy Debladis, Juliette Salles, Marion Valette, Carine Mantoulan, Denise Thuilleaux, Virginie Laurier, Catherine Molinas, Pascal Barone, Maïthé Tauber
Format: Article
Language:English
Published: BMC 2020-01-01
Series:Orphanet Journal of Rare Diseases
Subjects:
Online Access:https://doi.org/10.1186/s13023-020-1298-8
id doaj-1f3b3d235f8d4386a0fa41da577da8a7
record_format Article
spelling doaj-1f3b3d235f8d4386a0fa41da577da8a72021-01-24T12:09:50ZengBMCOrphanet Journal of Rare Diseases1750-11722020-01-0115111210.1186/s13023-020-1298-8A study of voice and non-voice processing in Prader-Willi syndromeKuzma Strenilkov0Jimmy Debladis1Juliette Salles2Marion Valette3Carine Mantoulan4Denise Thuilleaux5Virginie Laurier6Catherine Molinas7Pascal Barone8Maïthé Tauber9Brain & Cognition Research Center (CerCo), University of Toulouse Paul SabatierBrain & Cognition Research Center (CerCo), University of Toulouse Paul SabatierBrain & Cognition Research Center (CerCo), University of Toulouse Paul SabatierPrader-Willi Syndrome Reference Center, Children’s Hospital-INSERM-University of Toulouse Paul SabatierPrader-Willi Syndrome Reference Center, Children’s Hospital-INSERM-University of Toulouse Paul SabatierMarine HospitalMarine HospitalPrader-Willi Syndrome Reference Center, Children’s Hospital-INSERM-University of Toulouse Paul SabatierBrain & Cognition Research Center (CerCo), University of Toulouse Paul SabatierPrader-Willi Syndrome Reference Center, Children’s Hospital-INSERM-University of Toulouse Paul SabatierAbstract Background Prader-Willi syndrome (PWS) is a rare and complex neurodevelopmental disorder of genetic origin. It manifests itself in endocrine and cognitive problems, including highly pronounced hyperphagia and severe obesity. In many cases, impaired acquisition of social and communication skills leads to autism spectrum features, and individuals with this syndrome are occasionally diagnosed with autism spectrum disorder (ASD) using specific scales. Given that communicational skills are largely based on vocal communication, it is important to study human voice processing in PWS. We were able to examine a large number of participants with PWS (N = 61) recruited from France’s national reference center for PWS and other hospitals. We tested their voice and nonvoice recognition abilities, as well as their ability to distinguish between voices and nonvoices in a free choice task. We applied the hierarchical drift diffusion model (HDDM) with Bayesian estimation to compare decision-making in participants with PWS and controls. Results We found that PWS participants were impaired on both voice and nonvoice processing, but displayed a compensatory ability to perceive voices. Participants with uniparental disomy had poorer voice and nonvoice perception than participants with a deletion on chromosome 15. The HDDM allowed us to demonstrate that participants with PWS need to accumulate more information in order to make a decision, are slower at decision-making, and are predisposed to voice perception, albeit to a lesser extent than controls. Conclusions The categorization of voices and nonvoices is generally preserved in participants with PWS, though this may not be the case for the lowest IQ.https://doi.org/10.1186/s13023-020-1298-8Prader-Willi syndromeVoice processingSocial interactionsAutism spectrum disorder
collection DOAJ
language English
format Article
sources DOAJ
author Kuzma Strenilkov
Jimmy Debladis
Juliette Salles
Marion Valette
Carine Mantoulan
Denise Thuilleaux
Virginie Laurier
Catherine Molinas
Pascal Barone
Maïthé Tauber
spellingShingle Kuzma Strenilkov
Jimmy Debladis
Juliette Salles
Marion Valette
Carine Mantoulan
Denise Thuilleaux
Virginie Laurier
Catherine Molinas
Pascal Barone
Maïthé Tauber
A study of voice and non-voice processing in Prader-Willi syndrome
Orphanet Journal of Rare Diseases
Prader-Willi syndrome
Voice processing
Social interactions
Autism spectrum disorder
author_facet Kuzma Strenilkov
Jimmy Debladis
Juliette Salles
Marion Valette
Carine Mantoulan
Denise Thuilleaux
Virginie Laurier
Catherine Molinas
Pascal Barone
Maïthé Tauber
author_sort Kuzma Strenilkov
title A study of voice and non-voice processing in Prader-Willi syndrome
title_short A study of voice and non-voice processing in Prader-Willi syndrome
title_full A study of voice and non-voice processing in Prader-Willi syndrome
title_fullStr A study of voice and non-voice processing in Prader-Willi syndrome
title_full_unstemmed A study of voice and non-voice processing in Prader-Willi syndrome
title_sort study of voice and non-voice processing in prader-willi syndrome
publisher BMC
series Orphanet Journal of Rare Diseases
issn 1750-1172
publishDate 2020-01-01
description Abstract Background Prader-Willi syndrome (PWS) is a rare and complex neurodevelopmental disorder of genetic origin. It manifests itself in endocrine and cognitive problems, including highly pronounced hyperphagia and severe obesity. In many cases, impaired acquisition of social and communication skills leads to autism spectrum features, and individuals with this syndrome are occasionally diagnosed with autism spectrum disorder (ASD) using specific scales. Given that communicational skills are largely based on vocal communication, it is important to study human voice processing in PWS. We were able to examine a large number of participants with PWS (N = 61) recruited from France’s national reference center for PWS and other hospitals. We tested their voice and nonvoice recognition abilities, as well as their ability to distinguish between voices and nonvoices in a free choice task. We applied the hierarchical drift diffusion model (HDDM) with Bayesian estimation to compare decision-making in participants with PWS and controls. Results We found that PWS participants were impaired on both voice and nonvoice processing, but displayed a compensatory ability to perceive voices. Participants with uniparental disomy had poorer voice and nonvoice perception than participants with a deletion on chromosome 15. The HDDM allowed us to demonstrate that participants with PWS need to accumulate more information in order to make a decision, are slower at decision-making, and are predisposed to voice perception, albeit to a lesser extent than controls. Conclusions The categorization of voices and nonvoices is generally preserved in participants with PWS, though this may not be the case for the lowest IQ.
topic Prader-Willi syndrome
Voice processing
Social interactions
Autism spectrum disorder
url https://doi.org/10.1186/s13023-020-1298-8
work_keys_str_mv AT kuzmastrenilkov astudyofvoiceandnonvoiceprocessinginpraderwillisyndrome
AT jimmydebladis astudyofvoiceandnonvoiceprocessinginpraderwillisyndrome
AT juliettesalles astudyofvoiceandnonvoiceprocessinginpraderwillisyndrome
AT marionvalette astudyofvoiceandnonvoiceprocessinginpraderwillisyndrome
AT carinemantoulan astudyofvoiceandnonvoiceprocessinginpraderwillisyndrome
AT denisethuilleaux astudyofvoiceandnonvoiceprocessinginpraderwillisyndrome
AT virginielaurier astudyofvoiceandnonvoiceprocessinginpraderwillisyndrome
AT catherinemolinas astudyofvoiceandnonvoiceprocessinginpraderwillisyndrome
AT pascalbarone astudyofvoiceandnonvoiceprocessinginpraderwillisyndrome
AT maithetauber astudyofvoiceandnonvoiceprocessinginpraderwillisyndrome
AT kuzmastrenilkov studyofvoiceandnonvoiceprocessinginpraderwillisyndrome
AT jimmydebladis studyofvoiceandnonvoiceprocessinginpraderwillisyndrome
AT juliettesalles studyofvoiceandnonvoiceprocessinginpraderwillisyndrome
AT marionvalette studyofvoiceandnonvoiceprocessinginpraderwillisyndrome
AT carinemantoulan studyofvoiceandnonvoiceprocessinginpraderwillisyndrome
AT denisethuilleaux studyofvoiceandnonvoiceprocessinginpraderwillisyndrome
AT virginielaurier studyofvoiceandnonvoiceprocessinginpraderwillisyndrome
AT catherinemolinas studyofvoiceandnonvoiceprocessinginpraderwillisyndrome
AT pascalbarone studyofvoiceandnonvoiceprocessinginpraderwillisyndrome
AT maithetauber studyofvoiceandnonvoiceprocessinginpraderwillisyndrome
_version_ 1724326269913399296