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Signal Attenuation as a Rat Model of Obsessive Compulsive Disorder
Published on: January 9, 2015
Predicting genetic loading from symptom patterns in obsessive- compulsive disorder: a latent variable analysis
Carmi Schooler1, Andrew J Revell, Kiara R Timpano
1Section on Socio-Environmental Studies, Intramural Research Program, National Institute of Mental Health, Bethesda, Maryland 20892-8408, USA. carmi.schooler@nih.gov
Researchers identified two distinct obsessive-compulsive disorder (OCD) subpopulations using latent variable mixture modeling. One group exhibited more familial OCD, earlier onset, and greater severity, aiding genetic studies.
Area of Science:
- Psychiatry
- Genetics
- Computational Biology
Background:
- Familial and genetic factors influence some obsessive-compulsive disorder (OCD) symptom dimensions.
- Previous studies relied on exploratory analyses of symptom categories, not individual symptoms.
Purpose of the Study:
- To identify meaningful patient subgroupings in obsessive-compulsive disorder (OCD).
- To utilize a novel latent variable mixture model for subgroup identification.
Main Methods:
- Confirmatory factor analysis of a 65-item OCD symptom inventory from 398 probands.
- Latent variable mixture model analysis using five symptom factors to identify OCD subpopulations.
Main Results:
- Two statistically separate OCD subpopulations were identified.
- One subpopulation showed a significantly higher proportion of affected relatives and earlier onset.
- This group also presented with more severe OCD symptoms, psychiatric comorbidity, and impairment.
Conclusions:
- This research paradigm identified characteristics of individuals with familial OCD.
- Findings may aid genome-wide linkage and association studies for OCD.
- The approach may serve as a model for other symptom-based medical disorder studies.
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