The Complement Control-Related Genes CSMD1 and CSMD2 Associate to Schizophrenia

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; Vidar M Steen

doi:10.1016/j.biopsych.2011.01.030

The Complement Control-Related Genes CSMD1 and CSMD2 Associate to Schizophrenia

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 AndreassenSven Cichon, Vidar M Steen

113 Citationer (Scopus)

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.

Originalsprog	Engelsk
Tidsskrift	Biological Psychiatry
Vol/bind	70
Udgave nummer	1
Sider (fra-til)	35-42
Antal sider	8
ISSN	0006-3223
DOI	https://doi.org/10.1016/j.biopsych.2011.01.030
Status	Udgivet - 1 jul. 2011

Adgang til dokumentet

10.1016/j.biopsych.2011.01.030

Citationsformater

Håvik, B., Le Hellard, S., Rietschel, M., Lybæk, H., Djurovic, S., Mattheisen, M., Mühleisen, T. W., Degenhardt, F., Priebe, L., Maier, W., Breuer, R., Schulze, T. G., Agartz, I., Melle, I., Hansen, T., Bramham, C. R., Nöthen, M. M., Stevens, B., Werge, T., ... Steen, V. M. (2011). The Complement Control-Related Genes CSMD1 and CSMD2 Associate to Schizophrenia. Biological Psychiatry, 70(1), 35-42. https://doi.org/10.1016/j.biopsych.2011.01.030

Håvik, B, Le Hellard, S, Rietschel, M, Lybæk, H, Djurovic, S, Mattheisen, M, Mühleisen, TW, Degenhardt, F, Priebe, L, Maier, W, Breuer, R, Schulze, TG, Agartz, I, Melle, I, Hansen, T, Bramham, CR, Nöthen, MM, Stevens, B, Werge, T, Andreassen, OA, Cichon, S & Steen, VM 2011, 'The Complement Control-Related Genes CSMD1 and CSMD2 Associate to Schizophrenia', Biological Psychiatry, bind 70, nr. 1, s. 35-42. https://doi.org/10.1016/j.biopsych.2011.01.030

@article{4abaafd893e44d50a9101bdf5863ace5,

title = "The Complement Control-Related Genes CSMD1 and CSMD2 Associate to Schizophrenia",

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.",

author = "Bjarte H{\aa}vik and {Le Hellard}, Stephanie and Marcella Rietschel and Helle Lyb{\ae}k and Srdjan Djurovic and Manuel Mattheisen and M{\"u}hleisen, {Thomas W} and Franziska Degenhardt and Lutz Priebe and Wolfgang Maier and Rene Breuer and Schulze, {Thomas G} and Ingrid Agartz and Ingrid Melle and Thomas Hansen and Bramham, {Clive R} and N{\"o}then, {Markus M} and Beth Stevens and Thomas Werge and Andreassen, {Ole A} and Sven Cichon and Steen, {Vidar M}",

year = "2011",

month = jul,

day = "1",

doi = "10.1016/j.biopsych.2011.01.030",

language = "English",

volume = "70",

pages = "35--42",

journal = "Biological Psychiatry",

issn = "0006-3223",

publisher = "Elsevier",

number = "1",

}

TY - JOUR

T1 - The Complement Control-Related Genes CSMD1 and CSMD2 Associate to Schizophrenia

AU - Håvik, Bjarte

AU - Le Hellard, Stephanie

AU - Rietschel, Marcella

AU - Lybæk, Helle

AU - Djurovic, Srdjan

AU - Mattheisen, Manuel

AU - Mühleisen, Thomas W

AU - Degenhardt, Franziska

AU - Priebe, Lutz

AU - Maier, Wolfgang

AU - Breuer, Rene

AU - Schulze, Thomas G

AU - Agartz, Ingrid

AU - Melle, Ingrid

AU - Hansen, Thomas

AU - Bramham, Clive R

AU - Nöthen, Markus M

AU - Stevens, Beth

AU - Werge, Thomas

AU - Andreassen, Ole A

AU - Cichon, Sven

AU - Steen, Vidar M

PY - 2011/7/1

Y1 - 2011/7/1

N2 - 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.

AB - 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.

U2 - 10.1016/j.biopsych.2011.01.030

DO - 10.1016/j.biopsych.2011.01.030

M3 - Journal article

C2 - 21439553

SN - 0006-3223

VL - 70

SP - 35

EP - 42

JO - Biological Psychiatry

JF - Biological Psychiatry

IS - 1

ER -

The Complement Control-Related Genes CSMD1 and CSMD2 Associate to Schizophrenia

Abstract

Adgang til dokumentet

Fingeraftryk

Citationsformater