Association study of the dystrobrevin-binding gene with schizophrenia in Australian and Indian samples

Holliday, Elizabeth G., Handoko, Herlina Y., James, Michael R., McGrath, John J., Nertney, Deborah A., Tirupati, Sujit, Thara, Rangaswamy, Levinson, Douglas F., Hayward, Nicholas K., Mowry, Bryan J., & Nyholt, Dale R. (2006) Association study of the dystrobrevin-binding gene with schizophrenia in Australian and Indian samples. Twin Research and Human Genetics, 9(4), pp. 531-539.

View at publisher

Abstract

Numerous studies have reported association between variants in the dystrobrevin binding protein 1 (dysbindin) gene (DTNBP1) and schizophrenia. However, the pattern of results is complex and to date, no specific risk marker or haplotype has been consistently identified. The number of single nucleotide polymorphisms (SNPs) tested in these studies has ranged from 5 to 20. We attempted to replicate previous findings by testing 16 SNPs in samples of 41 Australian pedigrees, 194 Australian cases and 180 controls, and 197 Indian pedigrees. No globally significant evidence for association was observed in any sample, despite power calculations indicating sufficient power to replicate several previous findings. Possible explanations for our results include sample differences in background linkage disequilibrium and/or risk allele effect size, the presence of multiple risk alleles upon different haplotypes, or the presence of a single risk allele upon multiple haplotypes. Some previous associations may also represent false positives. Examination of Caucasian HapMap phase II genotype data spanning the DTNBP1 region indicates upwards of 40 SNPs are required to satisfactorily assess all nonredundant variation within DTNBP1 and its potential regulatory regions for association with schizophrenia. More comprehensive studies in multiple samples will be required to determine whether specific DTNBP1 variants function as risk factors for schizophrenia.

Impact and interest:

19 citations in Scopus
Search Google Scholar™
16 citations in Web of Science®

Citation counts are sourced monthly from Scopus and Web of Science® citation databases.

These databases contain citations from different subsets of available publications and different time periods and thus the citation count from each is usually different. Some works are not in either database and no count is displayed. Scopus includes citations from articles published in 1996 onwards, and Web of Science® generally from 1980 onwards.

Citations counts from the Google Scholar™ indexing service can be viewed at the linked Google Scholar™ search.

ID Code: 92157
Item Type: Journal Article
Refereed: Yes
Keywords: *Alleles, Australia, Carrier Proteins/*genetics, Case-Control Studies, European Continental Ancestry Group, Female, *Genetic Predisposition to Disease, Haplotypes, Humans, India, *Linkage Disequilibrium, Male, *Polymorphism, Single Nucleotide, Risk Factors, Schizophrenia/*genetics
DOI: 10.1375/183242706778025035
ISSN: 1832-4274
Divisions: Current > QUT Faculties and Divisions > Faculty of Health
Current > Institutes > Institute of Health and Biomedical Innovation
Deposited On: 28 Jan 2016 00:27
Last Modified: 28 Jan 2016 00:27

Export: EndNote | Dublin Core | BibTeX

Repository Staff Only: item control page