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Novel CAG/CTG repeat expansion mutations do not contribute to the genetic risk for most cases of bipolar disorder or schizophrenia.

Authors :
Tsutsumi T
Holmes SE
McInnis MG
Sawa A
Callahan C
DePaulo JR
Ross CA
DeLisi LE
Margolis RL
Source :
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics [Am J Med Genet B Neuropsychiatr Genet] 2004 Jan 01; Vol. 124B (1), pp. 15-9.
Publication Year :
2004

Abstract

The possible presence of anticipation in bipolar affective disorder and schizophrenia has led to the hypothesis that repeat expansion mutations could contribute to the genetic etiology of these diseases. Using the repeat expansion detection (RED) assay, we have systematically examined genomic DNA from 100 unrelated probands with schizophrenia and 68 unrelated probands with bipolar affective disorder for the presence of CAG/CTG repeat expansions. Our results show that 28% of the probands with schizophrenia and 30% of probands with bipolar disorder have a CAG/CTG repeat in the expanded range, but that each expansion could be explained by one of three nonpathogenic repeat expansions known to exist in the general population. We conclude that novel CAG/CTG repeat expansions are not a common genetic risk factor for bipolar disorder or schizophrenia.<br /> (Copyright 2003 Wiley-Liss, Inc.)

Details

Language :
English
ISSN :
1552-4841
Volume :
124B
Issue :
1
Database :
MEDLINE
Journal :
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics
Publication Type :
Academic Journal
Accession number :
14681907
Full Text :
https://doi.org/10.1002/ajmg.b.20058