Literature DB >> 27517838

Association between prematurity and the evolution of psychotic disorders in 22q11.2 deletion syndrome.

Yael Midbari Kufert1, Ariela Nachmani2,3, Einat Nativ4, Abraham Weizman5,6,7, Doron Gothelf8,9.   

Abstract

In this study, we report the developmental, physical and psychiatric manifestations of 22q11.2 deletion syndrome (22q11.2DS) in a large Israeli cohort, and search for a possible association between preterm birth and the risk for psychotic disorders. The study population consisted of 128 individuals with 22q11.2DS (77 male, 51 female), aged 1-55 years (mean ± SD 12.9 ± 11.0). All subjects underwent a comprehensive medical evaluation. All subjects older than 5 years (n = 104) were also evaluated psychiatrically. Overall, we found rates of physical manifestations similar to those previously reported in the literature. Psychiatric disorders were very common among our study population, with psychotic disorders occurring in 16.3 % of the psychiatrically evaluated population. We found an association between the presence of psychotic disorders and preterm birth. Our results replicate and extend the findings of a previous work and suggest that the evolution of psychosis in 22q11.2DS is a neurodevelopmental process with early obstetric and medical precursors.

Entities:  

Keywords:  Gestational age; Prematurity; Psychosis; Schizophrenia; Velocardiofacial syndrome

Mesh:

Year:  2016        PMID: 27517838     DOI: 10.1007/s00702-016-1607-5

Source DB:  PubMed          Journal:  J Neural Transm (Vienna)        ISSN: 0300-9564            Impact factor:   3.575


  28 in total

1.  Preterm birth and psychiatric disorders in young adult life.

Authors:  Chiara Nosarti; Abraham Reichenberg; Robin M Murray; Sven Cnattingius; Mats P Lambe; Li Yin; James MacCabe; Larry Rifkin; Christina M Hultman
Journal:  Arch Gen Psychiatry       Date:  2012-06

Review 2.  Preterm birth and neurodevelopmental outcome: a review.

Authors:  Carla Arpino; Eliana Compagnone; Maria L Montanaro; Denise Cacciatore; Angela De Luca; Angelica Cerulli; Stefano Di Girolamo; Paolo Curatolo
Journal:  Childs Nerv Syst       Date:  2010-03-27       Impact factor: 1.475

Review 3.  Neurodevelopmental outcome of the late preterm infant.

Authors:  Ira Adams-Chapman
Journal:  Clin Perinatol       Date:  2006-12       Impact factor: 3.430

4.  Hypoparathyroidism and autoimmunity in the 22q11.2 deletion syndrome.

Authors:  Kari Lima; Tore G Abrahamsen; Anette Bøe Wolff; Eystein Husebye; Mohammad Alimohammadi; Olle Kämpe; Ivar Følling
Journal:  Eur J Endocrinol       Date:  2011-05-23       Impact factor: 6.664

Review 5.  Velo-cardio-facial syndrome: a distinctive behavioral phenotype.

Authors:  R J Shprintzen
Journal:  Ment Retard Dev Disabil Res Rev       Date:  2000

Review 6.  Developmental trajectories in 22q11.2 deletion.

Authors:  Ann Swillen; Donna McDonald-McGinn
Journal:  Am J Med Genet C Semin Med Genet       Date:  2015-05-18       Impact factor: 3.908

7.  Schizophrenia-like neurophysiological abnormalities in 22q11.2 deletion syndrome and their association to COMT and PRODH genotypes.

Authors:  Omer Zarchi; Miri Carmel; Chen Avni; Josef Attias; Amos Frisch; Elena Michaelovsky; Miriam Patya; Tamar Green; Ronnie Weinberger; Abraham Weizman; Doron Gothelf
Journal:  J Psychiatr Res       Date:  2013-08-01       Impact factor: 4.791

8.  Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.

Authors:  A K Ryan; J A Goodship; D I Wilson; N Philip; A Levy; H Seidel; S Schuffenhauer; H Oechsler; B Belohradsky; M Prieur; A Aurias; F L Raymond; J Clayton-Smith; E Hatchwell; C McKeown; F A Beemer; B Dallapiccola; G Novelli; J A Hurst; J Ignatius; A J Green; R M Winter; L Brueton; K Brøndum-Nielsen; P J Scambler
Journal:  J Med Genet       Date:  1997-10       Impact factor: 6.318

9.  Genotype-phenotype correlation in 22q11.2 deletion syndrome.

Authors:  Elena Michaelovsky; Amos Frisch; Miri Carmel; Miriam Patya; Omer Zarchi; Tamar Green; Lina Basel-Vanagaite; Abraham Weizman; Doron Gothelf
Journal:  BMC Med Genet       Date:  2012-12-17       Impact factor: 2.103

10.  Prevalence of hypocalcaemia and its associated features in 22q11·2 deletion syndrome.

Authors:  Evelyn Ning Man Cheung; Susan R George; Gary A Costain; Danielle M Andrade; Eva W C Chow; Candice K Silversides; Anne S Bassett
Journal:  Clin Endocrinol (Oxf)       Date:  2014-05-27       Impact factor: 3.478

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  4 in total

1.  Neuropsychiatric aspects of 22q11.2 deletion syndrome: considerations in the prenatal setting.

Authors:  Anne S Bassett; Gregory Costain; Christian R Marshall
Journal:  Prenat Diagn       Date:  2016-11-14       Impact factor: 3.050

Review 2.  A Mini Review on the Contribution of the Anterior Cingulate Cortex in the Risk of Psychosis in 22q11.2 Deletion Syndrome.

Authors:  Maria C Padula; Elisa Scariati; Marie Schaer; Stephan Eliez
Journal:  Front Psychiatry       Date:  2018-08-17       Impact factor: 4.157

3.  Identifying neurodevelopmental anomalies of white matter microstructure associated with high risk for psychosis in 22q11.2DS.

Authors:  Joëlle Bagautdinova; Maria C Padula; Daniela Zöller; Corrado Sandini; Maude Schneider; Marie Schaer; Stephan Eliez
Journal:  Transl Psychiatry       Date:  2020-11-24       Impact factor: 6.222

4.  Ocular findings in 22q11.2 deletion syndrome: A systematic literature review and results of a Dutch multicenter study.

Authors:  Emma N M M von Scheibler; Emy S van der Valk Bouman; Myrthe A Nuijts; Noël J C Bauer; Tos T J M Berendschot; Pit Vermeltfoort; Levinus A Bok; Agnies M van Eeghen; Michiel L Houben; Thérèse A M J van Amelsvoort; Erik Boot; Michelle B van Egmond-Ebbeling
Journal:  Am J Med Genet A       Date:  2021-11-12       Impact factor: 2.578

  4 in total

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