Guy, Carol, Bowen, Timothy ![]() ![]() ![]() ![]() |
Abstract
OBJECTIVE: The purpose of this study was to identify the specific expanded CAG/CTG trinucleotide repeat associated with bipolar disorder. METHOD: The study employed an efficient multistage approach for using a genomic CAG/CTG screening set. RESULTS: The authors found no evidence of expanded repeats at 43 polymorphic autosomal loci and seven X chromosomal loci. Secondary screening was pursued at the only locus that contained a large allele (37 repeats) in the primary screening. No association was found between allele size and diagnostic status. CONCLUSIONS: It is highly unlikely that expansions in repeat size at any of the 50 candidate trinucleotide repeat loci examined are responsible for the association between expanded CAG/ CTG repeats and bipolar disorder. However, although the authors prioritized the repeats that were a priori most likely to be involved, the study does not reject the more general hypothesis that expanded CAG/CTG repeats are implicated in the pathogenesis of bipolar disorder.
Item Type: | Article |
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Date Type: | Publication |
Status: | Published |
Schools: | Medicine MRC Centre for Neuropsychiatric Genetics and Genomics (CNGG) Neuroscience and Mental Health Research Institute (NMHRI) |
Subjects: | R Medicine > R Medicine (General) |
Uncontrolled Keywords: | Alleles,Bipolar Disorder/etiology,Bipolar Disorder/genetics*,DNA/genetics,Genetic Markers,Genotype,Humans,Models, Genetic,Polymerase Chain Reaction,Polymorphism, Genetic,Trinucleotide Repeats/genetics*,X Chromosome Substances Genetic Markers,DNA |
Additional Information: | Publication Types Research Support, Non-U.S. Gov't Full Text Sources Silverchair Information Systems Ovid Technologies, Inc. ProQuest Other Literature Sources COS Scholar Universe Medical Bipolar Disorder - MedlinePlus Health Information |
Publisher: | American Psychiatric Publishing |
ISSN: | 0002-953X |
Last Modified: | 12 Dec 2022 08:55 |
URI: | https://orca.cardiff.ac.uk/id/eprint/57981 |
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