Cytochrome P450-2D6 Screening Among Elderly Using Antidepressants (CYSCE)

Phase 4

Completed

• Conditions: Depression; Depressive Disorder; Ultrarapid Metabolizer Due to Cytochrome P450 CYP2D6 Variant; Poor Metabolizer Due to Cytochrome P450 CYP2D6 Variant; Intermediate Metabolizer Due to Cytochrome P450 CYP2D6 Variant
• Interventions: Other: Genotype information accompanied by a drug dosing advice

• Registration Number: NCT01778907
• Lead Sponsor: University of Groningen

Brief Summary

Depression is common among elderly with an estimated prevalence of 5%. Due to ageing the national burden will double in the coming decade. Antidepressants as TCAs and SSRIs are effective in reducing symptoms, especially in people with severe depression. To optimize treatment efficacy and reduce side effects, the Pharmacogenetics Working Group of the Royal Dutch Pharmacists Association developed guidelines for dose-adaptation, for instance for antidepressants such as nortriptyline and venlafaxine based on their main relevant genotype (CYP2D6) accompanied by Therapeutic Drug Monitoring. Such personalized drug dosing based on pharmacogenetic information at the start of therapy can speed up the titration phase of antidepressants to establish an adequate maintenance dose. However, pharmacogenetic screening programs are expensive and evidence on effects and costs of such a program among elderly antidepressant starters from randomized controlled studies is lacking. The investigators will conduct a pragmatic randomized controlled trial to determine the effects and costs of pharmacogenetic screening information to optimize drug dosing in depressed elderly patients who start with nortriptyline or venlafaxine.

Objective: The primary objective is to determine the effects of pharmacogenetic screening for CYP2D6 on the time to reach adequate blood levels as an accepted proxy for adequate treatment. Secondary objectives include adverse drug reactions and cost-effectiveness

Study design: pragmatic randomized controlled intervention study

Detailed Description

This study is a multicenter randomized controlled trial in which psychiatric elderly care centers participate in the Netherlands. Deviating genotypes are expected to be found in \~30% of the population, therefore the study consist out of two parts. First a basic study in which \~750 patients, starting with nortriptyline or venlafaxine will be genotyped to identify patients with deviating genotypes (Poor, Intermediate or Ultrarapid Metabolizers). Second in the main study 150 patients with a deviating genotype are randomly allocated to two study arms one with and one without information on the genotype. From the extensive metabolizers('normal'genotype) 75 patients are allocated to a third arm as an external control.

Study Timeline

• Study First Submitted: 2013-01-22
• Study First Submitted QC: 2013-01-25
• Study First Posted: 2013-01-29
• Study Start: 2013-02
• Primary Completion: 2017-05
• Study Completion: 2017-06
• Status Verified: 2017-08
• Last Update Submitted: 2017-08-15
• Last Update Posted: 2017-08-18

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 202

Inclusion Criteria

• Major depression according to DSM-IV (296.2x, 296.3x) criteria for which the treating psychiatrist decided to start drug treatment with either nortriptyline or venlafaxine.
• Competent to understand the informed consent procedure

Exclusion Criteria

• Use of clinically relevant CYP2D6 inhibitors
• Use of clinically relevant CYP2D6 inducers
• Use of other drugs that affect plasma levels as co-medication
• Serious hepatic failure
• Patients for which drug treatment with venlafaxine is started and a GFR < 30 ml/min.
• Patients with the very rare genotype: Intermediate Metabolizer with duplications (IMDUP).

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Deviating genotype (DG-I)	Genotype information accompanied by a drug dosing advice	In the intervention group, genotype information accompanied by a drug dosing advice will be given to the treating physician. Blood level of the drug will be communicated by a dedicated research team to the treating physician according to daily practice.

Primary Outcome Measures

Name	Time	Method
Serum drug levels of nortriptyline or venlafaxine	After 2, 4 and 6 weeks treatment started, after the 6th week sampling continues every 2 weeks untill adequate serum drug level is reached with an expected average of 8 weeks	Serum drug levels will be assessed by 'dried blood spot' analysis, blood will be obtained by a fingerprick.; Adequate serum drug levels is defined as: serum drug levels within the therapeutic window (for nortriptyline 50-150 µg/L, for venlafaxine 200-400 µg/L in combination with stable drug dosing for at least 3 weeks.

Secondary Outcome Measures

Name	Time	Method
Quality of life questionnaire	After 2, 4 and 6 weeks treatment started and if adequate serum drug levels are not reached in 6 weeks, every 2 weeks, untill adequate serum drug levels are reached with an expected average of 8 weeks	Quality of life will be assessed by the EQ5D questionnaire. This information will also be used for a cost-effectiveness analysis.
Adverse drug events Questionnaire	At start of treatment and from that moment on, every 2 weeks untill adequate drug serum levels are reached with an expected average of 8 weeks	Adverse drug events will be assessed by a self-reported questionnaire (ASEC). Two different questionnaires will be used, one for the side-effects of venlafaxine and another one for nortriptyline. Both are based one the ASEC questionnaire.
Self reported Severity of depression Questionnaire	After 2, 4 and 6 weeks treatment started and if adequate serum drug levels are not reached in 6 weeks, every 2 weeks, untill adequate serum drug levels are reached with an expected average of 8 weeks	Severity of depression by means of the QIDS-SR.
Productivity Questionnaire	After 2, 4 and 6 weeks treatment started and if adequate serum drug levels are not reached in 6 weeks, every 2 weeks, untill adequate serum drug levels are reached with an expected average of 8 weeks	Effects on productivity by means of the Short Form-Health and Labour Questionnaire, part Labour. This information will also be used for a cost-effectiveness analysis.
Drug use	At inclusion, after 2, 4 and 6 weeks after inclusion and if adequate serum drug levels are not reached in 6 weeks, every 2 weeks, untill adequate serum drug level is reached with an expected average of 8 weeks	Drug use, including exact dosing and duration of prescription will be assessed by self reported drug use by the patient. This information will also be used for a cost-effectiveness analysis.
Data on health care associated resource use	After 2, 4 and 6 weeks treatment started and if adequate serum drug levels are not reached in 6 weeks, every 2 weeks, untill adequate serum drug levels are reached with an expected average of 8 weeks	Data on health care associated resource use (e.g. visits to the specific specialists including diagnoses; drug use including exact dosing and durations of prescriptions; hospitalizations, inclusive exact intensities of care; and lab values if relevant). This information will also be used for a cost-effectiveness analysis.

Trial Locations

Locations (11)

GGZ WNB; 🇳🇱 Halsteren, Brabant, Netherlands

Reinier van Arkel groep; 🇳🇱 's-Hertogenbosch, Netherlands

Jeroen Bosch Ziekenhuis; 🇳🇱 's-Hertogenbosch, Netherlands

GGZ Centraal; 🇳🇱 Ermelo, Netherlands

GGz inGeest; 🇳🇱 Amsterdam, Netherlands

Parnassia; 🇳🇱 Den Haag, Netherlands

Lentis; 🇳🇱 Groningen, Netherlands

University Medical Centre Groningen; 🇳🇱 Groningen, Netherlands

GGZ-NHN; 🇳🇱 Heiloo, Netherlands

GGZ Friesland; 🇳🇱 Leeuwarden, Netherlands

Isala Klinieken; 🇳🇱 Zwolle, Netherlands