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Published on: January 9, 2015
Obsessive-compulsive disorder, factor-analyzed symptom dimensions and serotonin transporter polymorphism
Se Joo Kim1, Hong Shick Lee, Chan-Hyung Kim
1Department of Psychiatry, Yonsei University College of Medicine, Seoul, Korea.
Abstract:
Recently, on the basis of the effects of serotonin (5-HT) reuptake inhibitors in obsessive-compulsive disorder (OCD) treatment, several candidate genes related to 5-HT regulation have been hypothesized to play an important role in the development of OCD. One of them is 5-HT transporter gene. Therefore, the aims of this study were to investigate the associations between 5-HT transporter polymorphism and OCD. One hundred and twenty-four OCD patients and 171 normal controls participated in this study. Genomic DNA was extracted from their blood. Comparison of the genotypes and allele frequencies of the SERTPR polymorphism between the OCD group and the control group was made. Using principal component analysis, we derived four factors from thirteen main contents of the Y-BOCS checklist and investigated the association between these four factors and the SERTPR polymorphism. In this case-control study, we could not find any associations between the SERTPR polymorphism and the development of OCD. In the OCD group, patients with the L genotype had higher scores for the religious/somatic factor than with the S genotype. In conclusion, the SERTPR polymorphism does not affect the development of OCD. But SERTPR polymorphisms affect certain factors of OC symptoms. Moreover, the factor analytic approach used in the present study has identified meaningful symptom dimensions to help guide future research.
Insights
The serotonin transporter gene (SERT PR) polymorphism is not linked to obsessive-compulsive disorder (OCD) development. However, SERT PR variations may influence specific obsessive-compulsive symptom dimensions, particularly religious/somatic factors.
Area of Science:
- Neuroscience
- Genetics
- Psychiatry
Background:
- Serotonin (5-HT) reuptake inhibitors are effective in treating obsessive-compulsive disorder (OCD).
- Candidate genes involved in 5-HT regulation, including the 5-HT transporter gene, are hypothesized to be implicated in OCD pathogenesis.
- The SERT PR polymorphism has been investigated as a potential genetic factor in OCD.
Purpose of the Study:
- To investigate the association between the 5-HT transporter gene (SERT PR) polymorphism and OCD.
- To explore the relationship between SERT PR polymorphism and specific symptom dimensions of OCD using factor analysis.
Main Methods:
- A case-control study involving 124 OCD patients and 171 healthy controls.
- Genomic DNA extraction and analysis of SERT PR polymorphism genotypes and allele frequencies.
- Principal component analysis of Yale-Brown Obsessive Compulsive Scale (Y-BOCS) checklist items to identify symptom factors.
Main Results:
- No significant association was found between SERT PR polymorphism and the overall development of OCD.
- In OCD patients, the L genotype of SERT PR was associated with higher scores on the religious/somatic symptom factor compared to the S genotype.
Conclusions:
- The SERT PR polymorphism does not appear to be a significant risk factor for the development of OCD.
- SERT PR polymorphism may influence specific symptom dimensions within OCD, such as religious and somatic concerns.
- Factor analysis can identify meaningful symptom dimensions that may be influenced by genetic factors in OCD.
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