Literature DB >> 22377578

Preliminary structure and predictive value of attenuated negative symptoms in 22q11.2 deletion syndrome.

Maude Schneider1, Martial Van der Linden, Bronwyn Glaser, Eleonora Rizzi, Sophie P Dahoun, Christine Hinard, Lucia Bartoloni, Stylianos E Antonarakis, Martin Debbané, Stephan Eliez.   

Abstract

Current research in schizophrenia suggests that negative symptoms cannot be considered a unitary construct and should be divided in two dimensions: lack of motivation and impoverishment of expression. In addition, negative symptoms are particularly related to decreased daily-life functioning. In the present study, we aimed to replicate these results in a sample of participants with 22q11.2 deletion syndrome (22q11DS), a neurogenetic condition associated with high risk of developing schizophrenia. We also expected to observe an association between the COMT Val/Met polymorphism and negative symptoms. We examined the factorial structure of negative symptoms in a sample of 47 individuals with 22q11DS using the Structured Interview for Prodromal Symptoms (SIPS) and the Positive and Negative Syndrome Scale (PANSS). We also performed stepwise regression analyses to investigate the associations between negative symptoms, adaptive skills and the COMT Val/Met polymorphism. Negative symptoms were explained by a two-factor solution, namely the "amotivation and social withdrawal" and the "emotional withdrawal and expression" dimensions. The motivational dimension was significantly associated with daily-life functioning. Met carriers were rated as experiencing significantly more symptoms of amotivation. The results are interpreted in the light of existing cognitive models in the field of motivation and schizophrenia.
Copyright © 2012 Elsevier Ltd. All rights reserved.

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Year:  2012        PMID: 22377578     DOI: 10.1016/j.psychres.2011.08.017

Source DB:  PubMed          Journal:  Psychiatry Res        ISSN: 0165-1781            Impact factor:   3.222


  28 in total

1.  Persistent gating deficit and increased sensitivity to NMDA receptor antagonism after puberty in a new mouse model of the human 22q11.2 microdeletion syndrome: a study in male mice.

Authors:  Michael Didriksen; Kim Fejgin; Simon R O Nilsson; Michelle R Birknow; Hannah M Grayton; Peter H Larsen; Jes B Lauridsen; Vibeke Nielsen; Pau Celada; Noemi Santana; Pekka Kallunki; Kenneth V Christensen; Thomas M Werge; Tine B Stensbøl; Jan Egebjerg; Francois Gastambide; Francesc Artigas; Jesper F Bastlund; Jacob Nielsen
Journal:  J Psychiatry Neurosci       Date:  2017-01       Impact factor: 6.186

2.  Subthreshold psychotic symptoms in 22q11.2 deletion syndrome.

Authors:  Sunny X Tang; James J Yi; Tyler M Moore; Monica E Calkins; Christian G Kohler; Daneen A Whinna; Margaret C Souders; Elaine H Zackai; Donna M McDonald-McGinn; Beverly S Emanuel; Warren B Bilker; Ruben C Gur; Raquel E Gur
Journal:  J Am Acad Child Adolesc Psychiatry       Date:  2014-06-19       Impact factor: 8.829

3.  Negative subthreshold psychotic symptoms distinguish 22q11.2 deletion syndrome from other neurodevelopmental disorders: A two-site study.

Authors:  Ehud Mekori-Domachevsky; Yael Guri; James Yi; Omri Weisman; Monica E Calkins; Sunny X Tang; Raz Gross; Donna M McDonald-McGinn; Beverly S Emanuel; Elaine H Zackai; Gil Zalsman; Abraham Weizman; Ruben C Gur; Raquel E Gur; Doron Gothelf
Journal:  Schizophr Res       Date:  2016-12-29       Impact factor: 4.939

4.  Facial emotion perception by intensity in children and adolescents with 22q11.2 deletion syndrome.

Authors:  Arnaud Leleu; Guillaume Saucourt; Caroline Rigard; Gabrielle Chesnoy; Jean-Yves Baudouin; Massimiliano Rossi; Patrick Edery; Nicolas Franck; Caroline Demily
Journal:  Eur Child Adolesc Psychiatry       Date:  2015-07-07       Impact factor: 4.785

Review 5.  Neurobiological background of negative symptoms.

Authors:  Silvana Galderisi; Eleonora Merlotti; Armida Mucci
Journal:  Eur Arch Psychiatry Clin Neurosci       Date:  2015-03-24       Impact factor: 5.270

6.  Mother-Child Interaction as a Window to a Unique Social Phenotype in 22q11.2 Deletion Syndrome and in Williams Syndrome.

Authors:  Omri Weisman; Ruth Feldman; Merav Burg-Malki; Miri Keren; Ronny Geva; Gil Diesendruck; Doron Gothelf
Journal:  J Autism Dev Disord       Date:  2015-08

7.  Multimodal investigation of triple network connectivity in patients with 22q11DS and association with executive functions.

Authors:  Maria C Padula; Marie Schaer; Elisa Scariati; Johanna Maeder; Maude Schneider; Stephan Eliez
Journal:  Hum Brain Mapp       Date:  2017-01-24       Impact factor: 5.038

8.  Performance on a computerized neurocognitive battery in 22q11.2 deletion syndrome: A comparison between US and Israeli cohorts.

Authors:  James J Yi; Ronnie Weinberger; Tyler M Moore; Monica E Calkins; Yael Guri; Donna M McDonald-McGinn; Elaine H Zackai; Beverly S Emanuel; Raquel E Gur; Doron Gothelf; Ruben C Gur
Journal:  Brain Cogn       Date:  2016-05-17       Impact factor: 2.310

Review 9.  Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders.

Authors:  N Hiroi; T Takahashi; A Hishimoto; T Izumi; S Boku; T Hiramoto
Journal:  Mol Psychiatry       Date:  2013-08-06       Impact factor: 15.992

10.  Education and employment trajectories from childhood to adulthood in individuals with 22q11.2 deletion syndrome.

Authors:  Mariela Mosheva; Virginie Pouillard; Yael Fishman; Lydia Dubourg; Dafna Sofrin-Frumer; Yaffa Serur; Abraham Weizman; Stephan Eliez; Doron Gothelf; Maude Schneider
Journal:  Eur Child Adolesc Psychiatry       Date:  2018-06-22       Impact factor: 4.785

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