Literature DB >> 27524298

Neurocognitive profile in psychotic versus nonpsychotic individuals with 22q11.2 deletion syndrome.

Ronnie Weinberger1, James Yi2, Monica Calkins3, Yael Guri1, Donna M McDonald-McGinn4, Beverly S Emanuel4, Elaine H Zackai4, Kosha Ruparel3, Miri Carmel5, Elena Michaelovsky5, Abraham Weizman6, Ruben C Gur2, Raquel E Gur2, Doron Gothelf7.   

Abstract

The 22q11.2 deletion syndrome (22q11DS) is associated with increased rates of psychotic disorders and cognitive deficits, but large scale studies are needed to elucidate their interaction. The objective of this two-center study was to identify the neurocognitive phenotype of individuals with 22q11DS and psychotic disorders. We hypothesized that psychotic 22q11DS individuals compared to nonpsychotic deleted individuals would have more severe neurocognitive deficits, especially in executive function and social cognition. These deficits would be present when compared to IQ- matched individuals with Williams Syndrome (WS). Three groups were ascertained from the Tel Aviv and Philadelphia centers: 22q11DS individuals with a psychotic disorder (n=31), nonpsychotic 22q11DS (n=86) and typically-developing controls (TD, n=828). In Tel Aviv a group of individuals with WS (n=18) matched in IQ to the 22q11DS psychotic group was also included. The Penn Computerized Neurocognitive Battery (CNB) was used to assess a wide-range of cognitive functions and all patients underwent structured psychiatric evaluations. 22q11DS individuals performed poorly on all CNB domains compared to TD. Participants with 22q11DS and psychosis, compared to nonpsychotic 22q11DS, had more severe deficits in global neurocognitive performance (GNP), executive function, social cognition and episodic memory domains. The primary deficits were also significant when comparing the Tel Aviv 22q11DS psychotic group to IQ-matched individuals with WS. In conclusion, 22q11DS individuals with a psychotic disorder have specific neurocognitive deficits that are reliably identified cross nationality using the CNB. These cognitive dysfunctions should be further studied as potential endophenotypes of psychosis in 22q11DS and as targets for intervention.
Copyright © 2016 Elsevier B.V. and ECNP. All rights reserved.

Entities:  

Keywords:  22q11.2 deletion syndrome; Neurocognition; Penn computerized neurocognitive battery; Psychosis; Schizophrenia

Mesh:

Year:  2016        PMID: 27524298     DOI: 10.1016/j.euroneuro.2016.08.003

Source DB:  PubMed          Journal:  Eur Neuropsychopharmacol        ISSN: 0924-977X            Impact factor:   4.600


  15 in total

1.  Psychiatric and cognitive characteristics of individuals with Danon disease (LAMP2 gene mutation).

Authors:  Maya Yardeni; Omri Weisman; Hanna Mandel; Ronnie Weinberger; Giovanni Quarta; Joel Salazar-Mendiguchía; Pablo Garcia-Pavia; Maria José Lobato-Rodríguez; Lourdes Fajardo Simon; Freimark Dov; Michael Arad; Doron Gothelf
Journal:  Am J Med Genet A       Date:  2017-06-19       Impact factor: 2.802

2.  Structural Connectivity and Emotion Recognition Impairment in Children and Adolescents with Chromosome 22q11.2 Deletion Syndrome.

Authors:  Ashley F P Sanders; Diana A Hobbs; Tracey A Knaus; Elliott A Beaton
Journal:  J Autism Dev Disord       Date:  2022-08-02

3.  Comparing the broad socio-cognitive profile of youth with Williams syndrome and 22q11.2 deletion syndrome.

Authors:  O Weisman; R Feldman; M Burg-Malki; M Keren; R Geva; G Diesendruck; D Gothelf
Journal:  J Intellect Disabil Res       Date:  2017-10-08

4.  Childhood Executive Functioning Predicts Young Adult Outcomes in 22q11.2 Deletion Syndrome.

Authors:  Avery B Albert; Tamara Abu-Ramadan; Wendy R Kates; Wanda Fremont; Kevin M Antshel
Journal:  J Int Neuropsychol Soc       Date:  2018-10       Impact factor: 2.892

Review 5.  Pathways to understanding psychosis through rare - 22q11.2DS - and common variants.

Authors:  Raquel E Gur; David R Roalf; Aaron Alexander-Bloch; Donna M McDonald-McGinn; Ruben C Gur
Journal:  Curr Opin Genet Dev       Date:  2021-02-08       Impact factor: 5.578

Review 6.  A cross-comparison of cognitive ability across 8 genomic disorders.

Authors:  Michael Mortillo; Jennifer G Mulle
Journal:  Curr Opin Genet Dev       Date:  2021-05-31       Impact factor: 4.665

7.  An implicit and reliable neural measure quantifying impaired visual coding of facial expression: evidence from the 22q11.2 deletion syndrome.

Authors:  Arnaud Leleu; Emilie Favre; Alexandre Yailian; Hugo Fumat; Juliette Klamm; Isabelle Amado; Jean-Yves Baudouin; Nicolas Franck; Caroline Demily
Journal:  Transl Psychiatry       Date:  2019-02-04       Impact factor: 6.222

8.  Lower [18F]fallypride binding to dopamine D2/3 receptors in frontal brain areas in adults with 22q11.2 deletion syndrome: a positron emission tomography study.

Authors:  Esther D A van Duin; Jenny Ceccarini; Jan Booij; Zuzana Kasanova; Claudia Vingerhoets; Jytte van Huijstee; Alexander Heinzel; Siamak Mohammadkhani-Shali; Oliver Winz; Felix Mottaghy; Inez Myin-Germeys; Thérèse van Amelsvoort
Journal:  Psychol Med       Date:  2019-04-02       Impact factor: 7.723

Review 9.  Functional Anatomy of the Inferior Longitudinal Fasciculus: From Historical Reports to Current Hypotheses.

Authors:  Guillaume Herbet; Ilyess Zemmoura; Hugues Duffau
Journal:  Front Neuroanat       Date:  2018-09-19       Impact factor: 3.856

10.  Cognitive deficits in childhood, adolescence and adulthood in 22q11.2 deletion syndrome and association with psychopathology.

Authors:  Sinead Morrison; Samuel J R A Chawner; Therese A M J van Amelsvoort; Ann Swillen; Claudia Vingerhoets; Elfi Vergaelen; David E J Linden; Stefanie Linden; Michael J Owen; Marianne B M van den Bree
Journal:  Transl Psychiatry       Date:  2020-02-03       Impact factor: 7.989

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