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The impact of antidepressants and genetic polymorphisms on emotion.

Impact of Escitalopram and Serotonin Transporter Polymorphisms on Emotion Processing and Regulation In Healthy Participants: A Randomised Controlled Trial

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12611000719932
Acronym
None
Enrollment
50
Registered
2011-07-11
Start date
2011-07-19
Completion date
Unknown
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Selective serotonin reuptake inhibitors (SSRIs) are a type of medication and are a first line treatment for major depression and anxiety. While recent studies have shown that neuroimaging and genetics may be used to predict response to SSRI treatment, (see Kemp, Gordon, Rush, & Willams, 2008 for review) basic experimental research is needed to determine exactly how the effects of SSRIs improve symptoms of depression and anxiety. Acute administration of SSRIs may increase processing of positive emotional information, providing a foundation for subsequent changes in thoughts and behaviour (see Harmer, 2008). In order to examine this further, a number of critical issues remain to be addressed. One such issue is the serotonin transporter (5­HTT) gene. The different forms of this gene (5­HTT polymorphisms; l/l, l/s, or s/s alleles) have been reported to moderate the impact of SSRIs on emotion perception (Hinkelmann et al., 2010). However, researchers are yet to examine the interacting roles of SSRIs and the 5­HTT polymorphisms on emotional processing in real­time. A second issue is that researchers are yet to account for the different types of emotional processing and emotion regulation strategies under different conditions. Aims: The aims of this study are to examine the impact of acute administration of an SSRI (escitalopram oxalate) and 5­HTT polymorphisms on covert and overt emotion processing and strategies to regulate this processing. Participants: 50 students will be recruited from first year Psychology students, genotyped and scanned under placebo and escitalopram conditions using a randomised controlled design. Given 5­HTT polymorphisms frequencies of 30% (l/l), 50% (l/s), and 20% (s/s) it is expected that a minimum of 15 participants homozygous for the L ­allele and 35 participants with at least one copy of the S ­allele will be recruited. Treatment: Administration of escitalopram oxalate (20mg) or placebo (saccharin, an artificial sweetener). Participants will complete experimental tasks once peak absorption has been reached. One week later (for compete elimination of drug), participants will be administered the alternate treatment and complete the experimental tasks once again. Tasks: Data will be collected using functional magnetic resonance imaging (fMRI) during rest, covert and overt emotion processing of different images from the International Affective Picture System. Participants will be asked to either passively view or reappraise emotions evoked by the presented stimuli. Questionnaires: Depression, Anxiety and Stress Scales; Patient Health Questionnaire; GAD­7 anxiety questionnaire; Early life stress; Ratings of emotional images Experimental Design: 2 Group (5­HTT s­allele, l­allele) X 2 (escitalopram oxalate, placebo) within­-subject design.

Interventions

Escitalopram (single oral dose, 20mg) crossed over with Placebo (saccharin, single oral dose) with a washout period of 7 days.

Sponsors

The University of Sydney
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Crossover
Primary purpose
Treatment
Masking
Blinded (masking used)

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

Female Aged 18-50 Caucasian (if recruitment is slow, we will remove this criterion) Fluent in English

Exclusion criteria

Not on any medication (minimum 1 month drug-free; with the exception of the contraceptive pill) or illicit drugs. Pregnancy (which will be tested at each visit) Breastfeeding Drug or alcohol addiction A history of brain injury, loss of consciousness, stroke, psychiatric, neurological disorder or other serious medical conditions (e.g., cardiovascular disease and diabetes).

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026