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* Obsessive-Compulsive Disorder
* Genetics
Am J Psychiatry 157:1160-1161, July 2000
© 2000 American Psychiatric Association


Brief Report

Is the 5-HT1Dß Receptor Gene Implicated in the Pathogenesis of Obsessive-Compulsive Disorder?

Emanuela Mundo, , M.D., Margaret A. Richter, , M.D., Fariba Sam, , B.Sc., Fabio Macciardi, , M.D., Ph.D., and James L. Kennedy, , M.D.

OBJECTIVE: Obsessive-compulsive disorder (OCD) is a psychiatric condition for which strong evidence of a genetic component and serotonergic system involvement exists. Recent studies have shown that sumatriptan, a selective ligand of the serotonin (5-HT)1Dß autoreceptor, modifies OCD symptoms. The aim of this study was to investigate the presence of linkage disequilibrium between the 5-HT1Dß receptor gene, which has a variant caused by a silent G to C substitution at nucleotide 861 of the coding region, and OCD.METHOD: DNA was collected from 67 probands who met DSM-IV criteria for OCD and from their living parents or siblings. Transmission Disequilibrium Test/sib-Transmission Disequilibrium Test analyses were then conducted with the DNA data.RESULTS: Thirty-two families were informative for the analysis, which showed a preferential transmission of the G allele to the affected subjects.CONCLUSIONS: If the results are confirmed, there may be important implications for the 5-HT1Dß receptor gene in the pathogenesis and treatment of OCD.




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