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C9orf72 hexanucleotide repeat expansions are not a common cause of obsessive-compulsive disorder.

Authors :
Arthur KC
Rivera AM
Samuels J
Wang Y
Grados M
Goes FS
Maher B
Nestadt G
Traynor BJ
Source :
Journal of the neurological sciences [J Neurol Sci] 2017 Apr 15; Vol. 375, pp. 71-72. Date of Electronic Publication: 2017 Jan 12.
Publication Year :
2017

Abstract

Obsessive-compulsive disorder (OCD) is a polygenic neuropsychiatric disorder characterized by repetitive thoughts and behaviors that cause distress. The pathogenic repeat expansion [GGGGCC] <subscript>n</subscript> found at the C9orf72 locus is the most common cause of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD), and has also been documented in patients with psychosis and schizophrenia. Furthermore, obsessions and compulsions have been identified in patients diagnosed with ALS and/or FTD and carrying the pathogenic repeat expansion. Here, we performed genetic screening for the C9orf72 repeat expansion on 573 patients diagnosed with OCD. None of the patients were found to carry the expansion. The results show that patients with OCD do not commonly carry the pathogenic repeat expansion and therefore should not be routinely screened. OCD and psychotic patients who do test positive for the C9orf72, however, should be closely observed for the later development of FTD and ALS.<br /> (Published by Elsevier B.V.)

Details

Language :
English
ISSN :
1878-5883
Volume :
375
Database :
MEDLINE
Journal :
Journal of the neurological sciences
Publication Type :
Academic Journal
Accession number :
28320191
Full Text :
https://doi.org/10.1016/j.jns.2017.01.040