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Pharmacokinetic and Pharmacodynamic Effects of Escitalopram Depending on Genetic Polymorphisms of the ABCB1-gene

Blood-brain-barrier Permeability of Escitalopram Depending on Genetic Polymorphisms of the ABCB1-gene: Effect on Sleep and Procedural Learning

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00550485
Enrollment
79
Registered
2007-10-30
Start date
2007-10-31
Completion date
2018-07-06
Last updated
2019-03-27

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

Conditions

Pharmacokinetics

Brief summary

The ABCB1-gene product P-glycoprotein is an integral membrane protein that actively transports substrates out of the intracellular compartment. One of the major sites of its action is the blood-brain-barrier. It is highly expressed in brain capillary endothelial cells and involved in limiting the access of substrates such as antidepressants to the central nervous system. A single nucleotide polymorphism (SNP) of the ABCB1-gene was recently identified showing a different treatment response to antidepressant drugs depending on the genotype. Therefore, it is assumed that healthy subjects with different genotypes of that SNP will be associated with significantly different brain levels of the antidepressant escitalopram after 6 days of intake. Sleep recordings are a useful bio-marker for effects of antidepressants on the CNS. Selective serotonin reuptake inhibitors (e.g. escitalopram) cause a suppression of REM sleep and a stronger fragmentation of sleep compared to untreated subjects. Higher plasma levels of antidepressants affected the sleep to a greater extent than lower levels. In line with this finding, we suppose that sleep EEG recordings of healthy subjects with different genotypes of the above mentioned SNP will be differently affected after taking 6 days escitalopram. In addition, effects of drug intake on the gene expression in lymphocytes and metabolic changes will be assessed.

Interventions

DRUGescitalopram

escitalopram 4 mg

Sponsors

Max-Planck-Institute of Psychiatry
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
20 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

* healthy males 20-30 years

Exclusion criteria

* any medication

Design outcomes

Primary

MeasureTime frameDescription
Time spent in rapid-eye-movement (REM) sleep assessed by polysomnography.after 6 days of intake of escitalopramTime spent in rapid-eye-movement (REM) sleep assessed by polysomnography.

Secondary

MeasureTime frameDescription
Sleep stagesafter 6 days of intake of escitalopramSleep stages beside REM sleep (wake, NonREM sleep) assessed by polysomnography
Sleep continuityafter 6 days of intake of escitalopramSleep continuity measures assessed by polysomnography
ABCB1 gene expressionbaseline and after 6 days of intake of escitaloprammessenger ribonucleic acid (mRNA) expression of the target gene ABCB1
Metabolic changesbaseline and after 6 days of intake of escitalopramSmall molecule metabolic changes in blood serum

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026