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Am J Med Genet B Neuropsychiatr Genet. 2008 Sep 5;147B(6):850-8. doi: 10.1002/ajmg.b.30699.

Association of the serotonin transporter polymorphism and obsessive-compulsive disorder: systematic review.

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  • 1Yale Child Study Center, Yale University School of Medicine, New Haven, Connecticut 06520, USA. michael.bloch@yale.edu <michael.bloch@yale.edu>

Abstract

We investigated the association between the long (l) and short (s) alleles of the serotonin transporter polymorphism (5-HTTLPR) in the promoter region of the SLC6A4 gene and obsessive-compulsive disorder (OCD) using meta-analysis to combine all published data from case-control and family based association studies (2,283 cases). In stratified meta-analysis we investigated whether age of sample (child and adult), ethnicity (Caucasian and Asian) and study design (case-control and family-based association studies) moderated any association. In the overall meta-analysis we found no evidence of association between genetic variation at the 5-HTTLPR locus and OCD. We did find significant heterogeneity between studies. In the stratified meta-analyses, we demonstrated a significant association between the l-allele and OCD in family-based association studies and in studies involving children and Caucasians. Our meta-analysis suggests the possibility that the l-allele may be associated with OCD in specific OCD subgroups such as childhood-onset OCD and in Caucasians. Further meta-analyses based on individual patient data would be helpful in determining whether age of OCD onset, gender and the presence of comorbid illness (e.g., tics) moderates the relationship between 5-HTTLPR and OCD.

2008 Wiley-Liss, Inc.

PMID:
18186076
[PubMed - indexed for MEDLINE]
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