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Status: Bibliographieeintrag

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Verfasst von:Håvik, Bjarte [VerfasserIn]   i
 Le Hellard, Stephanie [VerfasserIn]   i
 Rietschel, Marcella [VerfasserIn]   i
 Lybæk, Helle [VerfasserIn]   i
 Djurovic, Srdjan [VerfasserIn]   i
 Mattheisen, Manuel [VerfasserIn]   i
 Mühleisen, Thomas W. [VerfasserIn]   i
 Degenhardt, Franziska [VerfasserIn]   i
 Priebe, Lutz [VerfasserIn]   i
 Maier, Wolfgang [VerfasserIn]   i
 Breuer, René [VerfasserIn]   i
 Schulze, Thomas Gerd [VerfasserIn]   i
 Agartz, Ingrid [VerfasserIn]   i
 Melle, Ingrid [VerfasserIn]   i
 Hansen, Thomas [VerfasserIn]   i
 Bramham, Clive R. [VerfasserIn]   i
 Nöthen, Markus M. [VerfasserIn]   i
 Stevens, Beth [VerfasserIn]   i
 Werge, Thomas [VerfasserIn]   i
 Andreassen, Ole A. [VerfasserIn]   i
 Cichon, Sven [VerfasserIn]   i
 Steen, Vidar M. [VerfasserIn]   i
Titel:The complement control-related genes CSMD1 and CSMD2 associate to schizophrenia
Verf.angabe:Bjarte Håvik, Stephanie Le Hellard, Marcella Rietschel, Helle Lybæk, Srdjan Djurovic, Manuel Mattheisen, Thomas W. Mühleisen, Franziska Degenhardt, Lutz Priebe, Wolfgang Maier, Rene Breuer, Thomas G. Schulze, Ingrid Agartz, Ingrid Melle, Thomas Hansen, Clive R. Bramham, Markus M. Nöthen, Beth Stevens, Thomas Werge, Ole A. Andreassen, Sven Cichon, and Vidar M. Steen
E-Jahr:2011
Jahr:[1 July 2011]
Umfang:8 S.
Illustrationen:Diagramme
Fussnoten:Gesehen am 23.09.2022
Titel Quelle:Enthalten in: Biological psychiatry
Ort Quelle:Amsterdam [u.a.] : Elsevier Science, 1985
Jahr Quelle:2011
Band/Heft Quelle:70(2011), 1 vom: Juli, Seite 35-42
ISSN Quelle:1873-2402
Abstract:Background - Patients with schizophrenia often suffer from cognitive dysfunction, including impaired learning and memory. We recently demonstrated that long-term potentiation in rat hippocampus, a mechanistic model of learning and memory, is linked to gene expression changes in immunity-related processes involved in complement activity and antigen presentation. We therefore aimed to examine whether key regulators of these processes are genetic susceptibility factors in schizophrenia. - Methods - Analysis of genetic association was based on data mining of genotypes from a German genome-wide association study and a multiplex GoldenGate tag single nucleotide polymorphism (SNP)-based assay of Norwegian and Danish case-control samples (Scandinavian Collaboration on Psychiatric Etiology), including 1133 patients with schizophrenia and 2444 healthy control subjects. - Results - Allelic associations were found across all three samples for eight common SNPs in the complement control-related gene CSMD2 (CUB and Sushi Multiple Domains 2) on chromosome 1p35.1-34.3, of which rs911213 reached a statistical significance comparable to that of a genome wide threshold (p value = 4.0 × 10−8; odd ratio = .73, 95% confidence interval = .65-.82). The second most significant gene was CSMD1 on chromosome 8p23.2, a homologue to CSMD2. In addition, we observed replicated associations in the complement surface receptor CD46 as well as the major histocompatibility complex genes HLA-DMB and HLA-DOA. - Conclusions - These data demonstrate a significant role of complement control-related genes in the etiology of schizophrenia and support disease mechanisms that involve the activity of immunity-related pathways in the brain.
DOI:doi:10.1016/j.biopsych.2011.01.030
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: https://doi.org/10.1016/j.biopsych.2011.01.030
 Volltext: https://www.sciencedirect.com/science/article/pii/S0006322311001223
 DOI: https://doi.org/10.1016/j.biopsych.2011.01.030
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:Complement cascade
 csmd1
 csmd2
 human leukocyte antigen (HLA)
 immunity
 schizophrenia
K10plus-PPN:1817357476
Verknüpfungen:→ Zeitschrift

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