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Pharmacogenetic evaluation of a DISP1 gene variant in antidepressant treatment of obsessive–compulsive disorder.

Authors :
Lisoway, Amanda J.
Zai, Gwyneth
Tiwari, Arun K.
Zai, Clement C.
Wigg, Karen
Goncalves, Vanessa
Zhang, Danning
Freeman, Natalie
Müller, Daniel J.
Kennedy, James L.
Richter, Margaret A.
Source :
Human Psychopharmacology: Clinical & Experimental; Jul2018, Vol. 33 Issue 4, p1-1, 6p
Publication Year :
2018

Abstract

Abstract: Objectives: A recent genome‐wide association study (GWAS) in obsessive–compulsive disorder (OCD) reported a significant marker in the dispatched homolog 1 (Drosophila) gene (DISP1 gene) associated with serotonin reuptake inhibitor (SRI) antidepressant response (Qin et al., ). DISP1 has never been examined before in terms of association with SRI response until this GWAS. We attempt to replicate the GWAS finding by investigating the association of the DISP1 rs17162912 polymorphism with SRI response in our sample of 112 European Caucasian OCD patients. Methods: Patients were previously treated naturalistically with up to 6 different SRIs sequentially, including 5 selective SRIs (fluoxetine, fluvoxamine, sertraline, paroxetine, and citalopram) and 1 SRI (clomipramine). Each medication trial was evaluated retrospectively for response and was rated categorically as either responder or nonresponder using the Clinical Global Impression–Improvement scale. Fisher's exact test was used to investigate the relationship between the DISP1 rs17162912 genotype distribution and SRI response. Results: We did not observe a significant association between rs17162912 and SRI response (p = .32). Conclusion: This replication study did not support the role of DISP1 in predicting SRI response in OCD; however, methodological differences between the original GWAS and our study, as well as limited power and low minor allele frequency, may have hindered replication. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
08856222
Volume :
33
Issue :
4
Database :
Complementary Index
Journal :
Human Psychopharmacology: Clinical & Experimental
Publication Type :
Academic Journal
Accession number :
130628584
Full Text :
https://doi.org/10.1002/hup.2659