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Volume 61, Issue 6, Pages 734-742 (15 March 2007)


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Analysis of Association Between the Serotonin Transporter and Antidepressant Response in a Large Clinical Sample

Jeffrey B. Krafta, Eric J. Petersa, Susan L. Slagerb, Greg D. Jenkinsb, Megan S. Reinaldab, Patrick J. McGrathc, Steven P. HamiltonaCorresponding Author Informationemail address

Received 13 October 2005; received in revised form 26 April 2006; accepted 6 July 2006. published online 24 November 2006.

Background

SLC6A4 encodes the serotonin transporter, the protein primarily responsible for the termination of serotonin neurotransmission. Because many antidepressants inhibit the transporter, it has been the focus of intense pharmacogenetic analysis. We sought to replicate our previous findings that SLC6A4 is associated with response to a selective serotonin reuptake inhibitor (SSRI) in a large case–control study.

Methods

Genotypes at the SLC6A4 locus were obtained for 1,914 subjects in the Sequenced Treatment Alternatives to Relieve Depression (STAR*D) study and then tested for association to treatment response of the SSRI citalopram.

Results

Nine tagging single nucleotide polymorphisms and two variants previously associated with antidepressant response, including a promoter repeat polymorphism, were genotyped. Single marker and haplotypic analyses failed to detect association with antidepressant response in the largest clinical sample studied to date.

Conclusions

The lack of association between response to an SSRI and variation at the SLC6A4 locus in this large sample, carefully characterized for response to citalopram, strongly suggests that SSRI response in major depression is not determined by DNA variation at this locus. These findings do not replicate findings of a number of studies with considerably smaller sample sizes. Other genetic determinants of SSRI response in depression should be sought.

a Department of Psychiatry and Center for Human Genetics, University of California, San Francisco, California

b Division of Biostatistics, Mayo Clinic College of Medicine, Rochester, Minnesota

c New York State Psychiatric Institute and Columbia University, New York, New York.

Corresponding Author InformationAddress reprint requests to Steven P. Hamilton, M.D., Ph.D., Department of Psychiatry, University of California, San Francisco, 401 Parnassus Avenue, Box NGL, San Francisco, CA 94143-0984

PII: S0006-3223(06)00941-3

doi:10.1016/j.biopsych.2006.07.017


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