Failure to confirm allelic and haplotypic association between markers at the chromosome 6p22.3 dystrobrevin-binding protein 1 (DTNBP1) locus and schizophrenia

<p>Abstract</p> <p>Background</p> <p>Previous linkage and association studies may have implicated the Dystrobrevin-binding protein 1 (DTNBP1) gene locus or a gene in linkage disequilibrium with DTNBP1 on chromosome 6p22.3 in genetic susceptibility to schizophrenia.</...

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Main Authors: Kirwin Simon, Kandasami Gomathinayagam, Punukollu Bhaskar, Morgan Jenny, Moorey Helen, Lamb Graham, Bass Nicholas, Pimm Jonathan, Thirumalai Srinivasa, Lawrence Jacob, Choudhury Khalid, Puri Vinay, McQuillin Andrew, Datta Susmita R, Sule Akeem, Quested Digby, Curtis David, Gurling Hugh MD
Format: Article
Language:English
Published: BMC 2007-09-01
Series:Behavioral and Brain Functions
Online Access:http://www.behavioralandbrainfunctions.com/content/3/1/50
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spelling doaj-ad0484af40af4e70b9dff38d9c6cd6f92020-11-24T21:08:02ZengBMCBehavioral and Brain Functions1744-90812007-09-01315010.1186/1744-9081-3-50Failure to confirm allelic and haplotypic association between markers at the chromosome 6p22.3 dystrobrevin-binding protein 1 (DTNBP1) locus and schizophreniaKirwin SimonKandasami GomathinayagamPunukollu BhaskarMorgan JennyMoorey HelenLamb GrahamBass NicholasPimm JonathanThirumalai SrinivasaLawrence JacobChoudhury KhalidPuri VinayMcQuillin AndrewDatta Susmita RSule AkeemQuested DigbyCurtis DavidGurling Hugh MD<p>Abstract</p> <p>Background</p> <p>Previous linkage and association studies may have implicated the Dystrobrevin-binding protein 1 (DTNBP1) gene locus or a gene in linkage disequilibrium with DTNBP1 on chromosome 6p22.3 in genetic susceptibility to schizophrenia.</p> <p>Methods</p> <p>We used the case control design to test for of allelic and haplotypic association with schizophrenia in a sample of four hundred and fifty research subjects with schizophrenia and four hundred and fifty ancestrally matched supernormal controls. We genotyped the SNP markers previously found to be significantly associated with schizophrenia in the original study and also other markers found to be positive in subsequent studies.</p> <p>Results</p> <p>We could find no evidence of allelic, genotypic or haplotypic association with schizophrenia in our UK sample.</p> <p>Conclusion</p> <p>The results suggest that the DTNBP1 gene contribution to schizophrenia must be rare or absent in our sample. The discrepant allelic association results in previous studies of association between DTNBP1 and schizophrenia could be due population admixture. However, even positive studies of European populations do not show any consistent DTNBP1 alleles or haplotypes associated with schizophrenia. Further research is needed to resolve these issues. The possible confounding of linkage with association in family samples already showing linkage at 6p22.3 might be revealed by testing genes closely linked to DTNBP1 for allelic association and by restricting family based tests of association to only one case per family.</p> http://www.behavioralandbrainfunctions.com/content/3/1/50
collection DOAJ
language English
format Article
sources DOAJ
author Kirwin Simon
Kandasami Gomathinayagam
Punukollu Bhaskar
Morgan Jenny
Moorey Helen
Lamb Graham
Bass Nicholas
Pimm Jonathan
Thirumalai Srinivasa
Lawrence Jacob
Choudhury Khalid
Puri Vinay
McQuillin Andrew
Datta Susmita R
Sule Akeem
Quested Digby
Curtis David
Gurling Hugh MD
spellingShingle Kirwin Simon
Kandasami Gomathinayagam
Punukollu Bhaskar
Morgan Jenny
Moorey Helen
Lamb Graham
Bass Nicholas
Pimm Jonathan
Thirumalai Srinivasa
Lawrence Jacob
Choudhury Khalid
Puri Vinay
McQuillin Andrew
Datta Susmita R
Sule Akeem
Quested Digby
Curtis David
Gurling Hugh MD
Failure to confirm allelic and haplotypic association between markers at the chromosome 6p22.3 dystrobrevin-binding protein 1 (DTNBP1) locus and schizophrenia
Behavioral and Brain Functions
author_facet Kirwin Simon
Kandasami Gomathinayagam
Punukollu Bhaskar
Morgan Jenny
Moorey Helen
Lamb Graham
Bass Nicholas
Pimm Jonathan
Thirumalai Srinivasa
Lawrence Jacob
Choudhury Khalid
Puri Vinay
McQuillin Andrew
Datta Susmita R
Sule Akeem
Quested Digby
Curtis David
Gurling Hugh MD
author_sort Kirwin Simon
title Failure to confirm allelic and haplotypic association between markers at the chromosome 6p22.3 dystrobrevin-binding protein 1 (DTNBP1) locus and schizophrenia
title_short Failure to confirm allelic and haplotypic association between markers at the chromosome 6p22.3 dystrobrevin-binding protein 1 (DTNBP1) locus and schizophrenia
title_full Failure to confirm allelic and haplotypic association between markers at the chromosome 6p22.3 dystrobrevin-binding protein 1 (DTNBP1) locus and schizophrenia
title_fullStr Failure to confirm allelic and haplotypic association between markers at the chromosome 6p22.3 dystrobrevin-binding protein 1 (DTNBP1) locus and schizophrenia
title_full_unstemmed Failure to confirm allelic and haplotypic association between markers at the chromosome 6p22.3 dystrobrevin-binding protein 1 (DTNBP1) locus and schizophrenia
title_sort failure to confirm allelic and haplotypic association between markers at the chromosome 6p22.3 dystrobrevin-binding protein 1 (dtnbp1) locus and schizophrenia
publisher BMC
series Behavioral and Brain Functions
issn 1744-9081
publishDate 2007-09-01
description <p>Abstract</p> <p>Background</p> <p>Previous linkage and association studies may have implicated the Dystrobrevin-binding protein 1 (DTNBP1) gene locus or a gene in linkage disequilibrium with DTNBP1 on chromosome 6p22.3 in genetic susceptibility to schizophrenia.</p> <p>Methods</p> <p>We used the case control design to test for of allelic and haplotypic association with schizophrenia in a sample of four hundred and fifty research subjects with schizophrenia and four hundred and fifty ancestrally matched supernormal controls. We genotyped the SNP markers previously found to be significantly associated with schizophrenia in the original study and also other markers found to be positive in subsequent studies.</p> <p>Results</p> <p>We could find no evidence of allelic, genotypic or haplotypic association with schizophrenia in our UK sample.</p> <p>Conclusion</p> <p>The results suggest that the DTNBP1 gene contribution to schizophrenia must be rare or absent in our sample. The discrepant allelic association results in previous studies of association between DTNBP1 and schizophrenia could be due population admixture. However, even positive studies of European populations do not show any consistent DTNBP1 alleles or haplotypes associated with schizophrenia. Further research is needed to resolve these issues. The possible confounding of linkage with association in family samples already showing linkage at 6p22.3 might be revealed by testing genes closely linked to DTNBP1 for allelic association and by restricting family based tests of association to only one case per family.</p>
url http://www.behavioralandbrainfunctions.com/content/3/1/50
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