Literature DB >> 32298718

Convergent brain microstructure across multiple genetic models of schizophrenia and autism spectrum disorder: A feasibility study.

Brian R Barnett1, Cameron P Casey1, Maribel Torres-Velázquez2, Paul A Rowley3, John-Paul J Yu4.   

Abstract

Neuroimaging studies of psychiatric illness have revealed a broad spectrum of structural and functional perturbations that have been attributed in part to the complex genetic heterogeneity underpinning these disorders. These perturbations have been identified in both preclinical genetic models and in patients when compared to control populations, but recent work has also demonstrated strong evidence for genetic, molecular, and structural convergence of several psychiatric diseases. We explored potential similarities in neural microstructure in preclinical genetic models of ASD (Fmr1, Nrxn1, Pten) and schizophrenia (Disc1 svΔ2) and in age- and sex-matched control animals with diffusion tensor imaging (DTI) and neurite orientation dispersion and density imaging (NODDI). Our findings demonstrate a convergence in brain microstructure across these four genetic models with both tract-based and region-of-interest based analyses, which continues to buttress an emerging understanding of converging neural microstructure in psychiatric disease.
Copyright © 2020 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  DTI; Disc1; Fmr1; NODDI; Nrxn1; Pten

Mesh:

Year:  2020        PMID: 32298718      PMCID: PMC7685399          DOI: 10.1016/j.mri.2020.04.002

Source DB:  PubMed          Journal:  Magn Reson Imaging        ISSN: 0730-725X            Impact factor:   2.546


  47 in total

1.  Haploinsufficiency of MeCP2-interacting transcriptional co-repressor SIN3A causes mild intellectual disability by affecting the development of cortical integrity.

Authors:  Josefine S Witteveen; Marjolein H Willemsen; Thaís C D Dombroski; Nick H M van Bakel; Willy M Nillesen; Josephus A van Hulten; Eric J R Jansen; Dave Verkaik; Hermine E Veenstra-Knol; Conny M A van Ravenswaaij-Arts; Jolien S Klein Wassink-Ruiter; Marie Vincent; Albert David; Cedric Le Caignec; Jolanda Schieving; Christian Gilissen; Nicola Foulds; Patrick Rump; Tim Strom; Kirsten Cremer; Alexander M Zink; Hartmut Engels; Sonja A de Munnik; Jasper E Visser; Han G Brunner; Gerard J M Martens; Rolph Pfundt; Tjitske Kleefstra; Sharon M Kolk
Journal:  Nat Genet       Date:  2016-07-11       Impact factor: 38.330

Review 2.  Autoimmunity, Autoantibodies, and Autism Spectrum Disorder.

Authors:  Elizabeth Edmiston; Paul Ashwood; Judy Van de Water
Journal:  Biol Psychiatry       Date:  2016-09-01       Impact factor: 13.382

3.  Disrupted in Schizophrenia 1 Interactome: evidence for the close connectivity of risk genes and a potential synaptic basis for schizophrenia.

Authors:  L M Camargo; V Collura; J-C Rain; K Mizuguchi; H Hermjakob; S Kerrien; T P Bonnert; P J Whiting; N J Brandon
Journal:  Mol Psychiatry       Date:  2006-10-17       Impact factor: 15.992

4.  Convergent microstructural brain changes across genetic models of autism spectrum disorder-A pilot study.

Authors:  Paul A Rowley; Jose Guerrero-Gonzalez; Andrew L Alexander; John-Paul J Yu
Journal:  Psychiatry Res Neuroimaging       Date:  2018-12-08       Impact factor: 2.376

5.  Variation in DISC1 affects hippocampal structure and function and increases risk for schizophrenia.

Authors:  Joseph H Callicott; Richard E Straub; Lukas Pezawas; Michael F Egan; Venkata S Mattay; Ahmad R Hariri; Beth A Verchinski; Andreas Meyer-Lindenberg; Rishi Balkissoon; Bhaskar Kolachana; Terry E Goldberg; Daniel R Weinberger
Journal:  Proc Natl Acad Sci U S A       Date:  2005-06-06       Impact factor: 11.205

6.  Disrupted in schizophrenia 1 (DISC1): association with schizophrenia, schizoaffective disorder, and bipolar disorder.

Authors:  Colin A Hodgkinson; David Goldman; Judith Jaeger; Shalini Persaud; John M Kane; Robert H Lipsky; Anil K Malhotra
Journal:  Am J Hum Genet       Date:  2004-09-22       Impact factor: 11.025

Review 7.  Monogenic mouse models of autism spectrum disorders: Common mechanisms and missing links.

Authors:  S W Hulbert; Y-H Jiang
Journal:  Neuroscience       Date:  2015-12-28       Impact factor: 3.590

8.  Integrated analysis of whole-exome sequencing and transcriptome profiling in males with autism spectrum disorders.

Authors:  Marta Codina-Solà; Benjamín Rodríguez-Santiago; Aïda Homs; Javier Santoyo; Maria Rigau; Gemma Aznar-Laín; Miguel Del Campo; Blanca Gener; Elisabeth Gabau; María Pilar Botella; Armand Gutiérrez-Arumí; Guillermo Antiñolo; Luis Alberto Pérez-Jurado; Ivon Cuscó
Journal:  Mol Autism       Date:  2015-04-15       Impact factor: 7.509

9.  A developmental, longitudinal investigation of autism phenotypic profiles in fragile X syndrome.

Authors:  Michelle Lee; Gary E Martin; Elizabeth Berry-Kravis; Molly Losh
Journal:  J Neurodev Disord       Date:  2016-12-30       Impact factor: 4.025

10.  Profiles of aberrant white matter microstructure in fragile X syndrome.

Authors:  Scott S Hall; Robert F Dougherty; Allan L Reiss
Journal:  Neuroimage Clin       Date:  2016-01-14       Impact factor: 4.881

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.