Meta-analysis shows strong positive association of the neuregulin 1 ( NRG1 ) gene with schizophrenia
Open Access
- 10 May 2006
- journal article
- research article
- Published by Oxford University Press (OUP) in Human Molecular Genetics
- Vol. 15 (12) , 1995-2002
- https://doi.org/10.1093/hmg/ddl122
Abstract
Chromosome 8p22-p11 has been identified as a locus for schizophrenia in several genome-wide scans and confirmed by meta-analysis of published linkage data. Systematic fine mapping using extended Icelandic pedigrees identified an associated haplotype in the gene neuregulin 1 ( NRG1 ), also known as heuregulin, glial growth factor, NDF43 and ARIA. A 290 kb core at risk haplotype at the 5′ end of the gene (HAP ICE ), defined by five SNPs and two microsatellite polymorphisms was found to be associated with schizophrenia in the Icelandic and Scottish populations. A number of subsequent independent studies have attempted to replicate the association, and while some have been successful, the associated haplotype is not always HAP ICE . Furthermore, no obviously functional or pathogenic variants have been identified, and the relationship between the gene and schizophrenia has remained inconclusive. To reconcile these conflicting findings and to give a comprehensive picture of the genetic architecture of this important gene, we performed a meta-analysis of 13 published population-based and family-based association studies up to November 2005. We analysed data from the SNP markers SNP8NRG241930, SNP8NRG243177, SNP8NRG221132 and SNP8NRG221533, and the microsatellite markers 478B14-848, 420M9-1395. Across these studies, strong positive association was found for all six polymorphisms. The haplotype analysis also showed significant association in the pooled international populations (OR=1.22, 95% CI 1.15–1.3, P =8×10 −10 ). In Asian populations, the risk haplotype was focused around the two microsatellite markers, 478B14-848, 420M9-1395 (haplotype block B), and in Caucasian populations with the remaining four SNP markers (haplotype block A). This meta-analysis supports the involvement of NRG1 in the pathogenesis of schizophrenia, but with association between two different but adjacent haplotypes blocks in the Caucasian and Asian populations.Keywords
This publication has 47 references indexed in Scilit:
- Neuregulin 1-erbB signaling and the molecular/cellular basis of schizophreniaNature Neuroscience, 2004
- The genetics of schizophrenia: glutamate not dopamine?European Journal of Pharmacology, 2003
- Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part II: SchizophreniaAmerican Journal of Human Genetics, 2003
- Genes for schizophrenia? Recent findings and their pathophysiological implicationsThe Lancet, 2003
- Neuregulin 1 and Susceptibility to SchizophreniaAmerican Journal of Human Genetics, 2002
- Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophreniaMolecular Psychiatry, 2002
- Glutamatergic Mechanisms in SchizophreniaAnnual Review of Pharmacology and Toxicology, 2002
- Epidemiology of schizophrenia: the global burden of disease and disabilityArchiv Fur Psychiatrie Und Nervenkrankheiten, 2000
- The Genetic Epidemiology of Schizophrenia in a Finnish Twin CohortArchives of General Psychiatry, 1998
- Evidence for a schizophrenia vulnerability locus on chromosome 8p in the Irish Study of High-Density Schizophrenia FamiliesAmerican Journal of Psychiatry, 1996