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Updated: Jun 15, 2026

Signal Attenuation as a Rat Model of Obsessive Compulsive Disorder
Published on: January 9, 2015
Genetics of early-onset obsessive-compulsive disorder
Susanne Walitza1, Jens R Wendland, Edna Gruenblatt
1Department of Child and Adolescent Psychiatry, University of Zurich, Zurich, Switzerland. susanne.walitza@kjpdzh.ch
Obsessive-compulsive disorder (OCD) affects 1-3% of the population, with early-onset cases being familial. Research is ongoing to identify genetic links, with the glutamate transporter gene SLC1A1 showing potential involvement.
Area of Science:
- Neuroscience
- Genetics
- Psychiatry
Background:
- Obsessive-compulsive disorder (OCD) involves intrusive thoughts and repetitive behaviors.
- OCD affects 1-3% of the general population, impacting children's development.
- Early-onset OCD often has a familial component.
Purpose of the Study:
- To investigate the genetic underpinnings of obsessive-compulsive disorder (OCD).
- To identify specific genes associated with OCD susceptibility.
- To explore the role of neurotransmitter systems in OCD etiology.
Main Methods:
- Analysis of candidate genes within linkage regions.
- Performance of three genome-wide linkage scans.
- Ongoing genome-wide association analyses.
Main Results:
- Most candidate gene analyses have not implicated specific genes in OCD.
- The glutamate transporter gene SLC1A1 on 9p24 has shown potential involvement.
- Further replication studies are needed for genome-wide association analyses.
Conclusions:
- Genetic factors play a role in obsessive-compulsive disorder (OCD).
- The glutamate transporter gene SLC1A1 is a potential candidate for OCD.
- Subtyping OCD by age of onset, symptoms, and comorbidities is crucial for future research.
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