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  • The International Journal of Neuropsychopharmacology, Volume 4, Issue 3
  • September 2001, pp. 269-272

Association study of the serotonin transporter gene polymorphism in obsessive–compulsive disorder

  • Beatriz Camarena (a1), Gina Rinetti (a1), Carlos Cruz (a1), Sandra Hernández (a1), Juan Ramón de la Fuente (a2) and Humberto Nicolini (a1)
  • DOI: http://dx.doi.org/10.1017/S1461145701002516
  • Published online: 01 September 2001
Abstract

The hypothesis implicating the serotonergic system in the pathophysiology of obsessive–compulsive disorder (OCD) is supported by the therapeutic efficacy of selective serotonin reuptake inhibitors (SSRIs). Since SSRIs act on the serotonin transporter (5-HTT), it has been suggested that the 5-HTT gene (SCL6A4) could be a good candidate for OCD. The SCL6A4 gene has a 44-bp insertion/deletion polymorphism in its promoter region (5-HTTLPR). Previous studies have revealed an association between OCD and the l allele. We analysed the 5-HTTLPR polymorphic system in 115 Mexican OCD patients and 136 controls. No significant association was found between l allele and OCD (χ2 = 1·54, d.f. = 1, p = 0·21). Furthermore, we assessed alternative methods that employ family-based designs in a sample of 43 trios. Haplotype-based haplotype relative risk and transmission disequilibrium analysis did not show a preferential transmission of l allele to OCD probands. Our results indicate the need to analyse larger samples using family-based methods.

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Corresponding author
Address for correspondence: H. Nicolini, Departamento de Genética Psiquiátrica, Instituto Nacional de Psiquiatría Ramón de la Fuente Muñiz, Mexico D.F., 14370, México. Tel.: (525)573-2437 Fax: (525) 513-3722 E-mail: nicolini_humberto@yahoo.com
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The International Journal of Neuropsychopharmacology
  • ISSN: 1461-1457
  • EISSN: 1469-5111
  • URL: /core/journals/the-international-journal-of-neuropsychopharmacology
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