Add-on MEmaNtine to Dopamine Antagonism to Improve Negative Symptoms at First Psychosis

  • STATUS
    Recruiting
  • End date
    Dec 31, 2024
  • participants needed
    46
  • sponsor
    Bjorn H. Ebdrup
Updated on 5 September 2021
dopamine
amisulpride
psychiatric disorder
antipsychotics
psychotic episode
schizophrenia
hallucinations
a 12
schizoaffective disorder
delusions
delusional disorder

Summary

Antipsychotics affects the brain's dopamine system, and the drugs reduce delusions, hallucinations, and disorganized thinking, which are cardinal symptoms of psychotic disorders. However, negative symptoms e.g. anhedonia, avolition, and social withdrawal, as well as cognitive deficits, are not sufficiently treated.

Memantine is used to treat Alzheimer's disease and affects the brain's glutamate system. AMEND is a 12-week, double-blind, placebo-controlled, randomized clinical trial (RCT) testing effects of add-on memantine to initial antipsychotic treatment in never-treated patients with first-episode psychosis.

The main aim is to reduce negative symptoms. Secondary outcomes are cognition, psychotic symptoms, side effects. Glutamate levels in the brain will be measured before and after 12 weeks using an ultra-high field strength (7 Tesla) magnetic resonance scanner.

AMEND will apply rational drug repurposing to optimize treatment of patients experiencing their first psychotic episode.

Description

BACKGROUND Scientific basis/Rationale Antipsychotic medication is efficacious in treating positive psychotic symptoms such as delusions, hallucinations, and disorganized thinking, which are cardinal symptoms of schizophrenia spectrum disorders. However, antipsychotic treatment does not ameliorate the accompanying negative symptoms (e.g. anhedonia, avolition, and social withdrawal), and cognitive deficits, which are highly disabling and predictive of patients' long-term prognosis. Importantly, shortening the interval between onset of psychosis and initiation of an efficient intervention lead to better long-term outcome.

The pathophysiology of psychosis is complex and involves multiple neurotransmitters, e.g. serotoninergic-, GABAergic, and glutamatergic systems, but modulation (particularly antagonism) of striatal dopamine D2 receptors (D2R) remain the key common denominator of all licensed antipsychotics. Nevertheless, around one third of patients with psychosis display inadequate response to antidopaminergic treatment, and persistent negative symptoms is a critical predictor for future treatment resistance.

Glutamate hypothesis of psychosis Mounting evidence from post-mortem-, brain imaging-, genetic-, and pharmacologic challenge studies indicate glutamatergic dysregulation, specifically of the N-methyl-D-aspartate receptor (NMDAR), as part of the pathophysiology of psychosis and schizophrenia. Through excitotoxicity, glutamate dysregulation may underlie structural degeneration, e.g. in hippocampus, which is a key finding in schizophrenia spectrum patients. Nevertheless, cross-sectional 3T MRS glutamate levels between first-episode patients and HC have shown equivocal results, e.g. likely reflecting differences in glutamate levels across brain regions and in variable previous antipsychotic exposure of included patients. Using 3T MRS, investigator recently reported increased thalamic glutamate levels in antipsychotic-nave patients with first-episode psychosis compared to HC. Importantly, high thalamic levels predicted poor treatment response. Other studies have also associated glutamate levels with outcome. Investigator have shown that aberrations in the thalamic glutamate levels are heritable, related to psychosis, and extend to individuals at ultra-high risk for psychosis (UHR). Investigator have found that thalamic and ACC levels of glutamate are associated with symptomology and cognition, specifically spatial working memory, set-shifting, and attention both in UHR and first episode psychosis. Cutting-edge 7T MRS can non-invasively determine brain metabolite levels of e.g. -aminobutyric acid (GABA), N-acetylaspartate, N-acetylaspartyl, and importantly, 7T allows to discriminate glutamate concentrations from glutathione and glutamine. Moreover, multiple voxels/brain regions can be investigated with 7T. In the context of glutamate and psychosis, the thalamus, anterior cingulate cortex (ACC), hippocampus, dorsolateral prefrontal cortex (DLPFC), and basal ganglia are of particular interest.

Regarding brain structure, application of structural 7T sequences allows for increased sensitivity to quantify neurodegeneration e.g. hippocampal subfield segmentation. Finally, high resolution quantification of tissue parameters such as iron deposition using quantitative susceptibility mapping allow characterization of subtle changes in the 'dopaminergic regions' of the basal ganglia, including striatum, pallidum, and substantia nigra.

Glutamate antagonist treatment Against this background, modulation of glutamatergic NMDAR has been investigated as a potential treatment target in patients with psychosis and schizophrenia. Memantine is a non-competitive NMDAR antagonist used for treatment of Alzheimer's disease. Two recent meta-analyses and one systematic review have concluded that adjunctive memantine to antipsychotics is safe and significantly improves negative symptoms in chronic medicated patients with schizophrenia. One of the meta-analyses also indicated a potential effect on global levels of cognition. Memantine has been theorized to ameliorate progression of negative symptoms by counteracting excitotoxicity correlated to high glutamate levels in early stages of psychosis, but this has not been investigated in initially antipsychotic-nave patients. Finally, the intriguing fact that pharmacologically similar antagonists of NMDARs (e.g. memantine and ketamine) exert almost paradoxical effects in humans highlights the importance of understanding the pathophysiology of NMDAR modulation in psychosis.

Study medication Amisulpride All patients will be treated with amisulpride, as the standard of care treatment.

Tablet amisulpride (100-800 mg/day) is a second-generation antipsychotic and a first-line, generic drug against psychosis and schizophrenia in Denmark. Amisulpride primarily binds to D2 and D3 receptors, but also has affinity for serotonin 5-HT7 receptors. In AMEND, amisulpride is chosen because it is the most selective licensed antidopaminergic compound to treat psychosis. Side effects include sedation, weight gain, hyperprolactinemia, and extrapyramidal symptoms. Investigator have previously used amisulpride in a similar cohort of antipsychotic-nave patients and have gained extensive insights regarding its clinical effects and relation to striatal dopamine receptor activity, reward system, brain structure, weight gain, and sexual side effects. Of note, amisulpride has been approved for treatment of negative symptoms in schizophrenia, however, in investigators previous cohort negative symptoms did not improve.

Memantine Tablet memantine (10-20 mg/day) is an generic drug approved for treatment of Alzheimer's Disease(AD) showing benefits on the main domains of AD i.e. cognition, function, behavior, and clinical global change. Memantine acts through uncompetitive, open-channel NMDAR antagonism, and has minimal activity for GABAergic, dopaminergic, adrenergic, histaminergic, and glycinergic receptors. There are no known interactions between memantine and antipsychotics. Side effects include fatigue, dizziness, constipation, anxiety, headache, diarrhoea, and nausea. In previous memantine add-on RCTs in schizophrenia patients, the reported side effects did not differ from placebo. Memantine has no abuse potential.

Placebo Placebo tablets will be coated to match memantine 10 or 20 mg.

Study population Antipsychotic-nave, first-episode schizophrenia spectrum patients with first-episode psychosis.

Patients will be recruited from psychiatric hospitals and outpatients psychiatric centers in the capital region (Copenhagen area), where doctors or nursing staff will inform relevant patients about the project and contact the doctor or nurse from the AMEND team, if the patients accept and might fulfil the inclusion criteria. A diagnostic interview, Present State Examination(PSE), will be performed before inclusion to assess if the patients fulfil the inclusion criteria. In addition, to fulfilling the diagnostic criteria, it should be medically assessed that the patient would benefit from antipsychotic treatment. Furthermore, somatic and neurological examination, as well as screening of pregnancy and substance abuse, will be performed before inclusion.

Aim of study/ outstanding research questions to be answered in our study? Summary of concept By rational combination of two licensed, off-patent drugs, amisulpride and memantine, AMEND aims to optimize treatment of psychosis alongside with unravelling the signature of memantine response. If successful, AMEND will provide pivotal neurobiological evidence for future stratification of patients with first-episode psychosis before initial antipsychotic treatment.

Hypotheses

Investigator hypothesize that add-on of memantine to amisulpride:

  • Will be superior to reduce negative symptoms and that this effect will correlate with reduced glutamate levels in thalamus after 12 weeks.
  • Will exert the most pronounced effect in patients, who display higher baseline thalamic glutamate levels than HC, and this subgroup of patients will also experience better total symptom control.
  • Will improve domains of cognition, and specifically that effects on working memory, set-shifting, and attention will be predicted by initial glutamate levels in thalamus and anterior cingulate cortex (ACC).

Primary and secondary endpoints Primary Endpoints Primary endpoint will be reduction in negative symptoms as measured with Positive and Negative Syndrome Scale (PANSS) negative symptoms after 12 weeks of treatment [PANSS negative baseline - PANSS negative at week 12]. Assessments will be supplemented by Brief Negative Symptom Scale (BNSS) scores.

Secondary endpoints Secondary endpoints include changes in cognition (in particular working memory, set-shifting, and attention), PANSS positive and total other clinical measures, level of functioning, side effects, and glutamate levels in five a priori selected regions: thalamus, anterior cingulate cortex (ACC), hippocampus, dorsolateral prefrontal cortex (DLPFC), and basal ganglia.

Exploratory endpoints include associations between clinical data, quality of life, brain metabolites in other regions, e.g. ACC, and structural measures (e.g. hippocampus subfields), and basal ganglia quantification. Interactions between baseline brain metabolite levels and brain structure in patients and HC will also be investigated.

Material and methods Study design This investigator-initiated, double blinded randomized controlled trial, will establish a cohort of 46 antipsychotic- nave first episode psychosis patients aged 18-45. Patients will be recruited from psychiatric out- and inpatient clinics in the Capital Region of Copenhagen.

Patients will be allocated to 12 weeks treatment with [amisulpride plus memantine] OR [amisulpride plus placebo]. Randomisation will be stratified by PANSS negative sub score categorizing patients in a "Low PANSS baseline<20" and "High PANSS baseline>=20".

The randomisation will use permuted blocs in sizes of 4,6 and 8, to ensure an even distribution among the two groups since the number of patients in the two groups will not be restricted.

The pharmacy (Region Hovedstadens apotek) will manage the randomisation. Twenty healthy controls matched on age, gender and parental socio-economic status will be recruited by advertisement and undergo baseline- and 12-week examinations.

Trial design Double blinded randomized controlled trial.

Study phase Phase I, known medicine (memantine) tested for new indication (psychosis).

Timeline Estimated study duration To increase power of secondary analyses, enrolment will continue until 18 participants in each arm have completed examinations. Moreover, AMEND will be extended to 12 weeks based on the median trial duration in the meta-analysis of add-on memantine (12 weeks (mean 11.5 weeks)).

Based on our center's 20 years of experience with recruitment and treatment of antipsychotic-nave patents, we expect an inclusion rate of 2 patients per month and an attrition rate of 25%. Thus, recruitment of 46 patients will take 2 years.

The project will take place from 1st of May 2021 until 31st December 2024.

Details
Condition Negative Symptoms With Primary Psychotic Disorder, psychotic disorders, Psychosis, psychotic, psychotic disorder
Treatment Placebo, memantine
Clinical Study IdentifierNCT04789915
SponsorBjorn H. Ebdrup
Last Modified on5 September 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Patients
Antipsychotic-nave, first episode psychosis
Fulfilling the diagnostic criteria of schizophrenia, persistent delusional disorder, acute and transient psychotic disorders, schizoaffective disorder, other non-organic psychotic disorders and unspecified non-organic disorders (ICD-10: F20.x; F22.x; F23.x; F24.x; F25.x; F28; F29); verified by PSE interview
Age: 18-45 years
Legally competent (In Danish: 'myndige og habile i retslig forstand')
Healthy controls
No first-degree relative with known major psychiatric disorder (ICD-10: F1x; F2x; F3x)
Age 18-45 years
Legally competent (In Danish: 'myndige og habile i retslig forstand')

Exclusion Criteria

Patients
Prior use of antipsychotic medication
Treatment with antidepressant medication the last 7 days
Current substance dependence ICD-10 (F1x.2) or substance abuse in any period up to 3 months prior to referral (exception: tobacco/nicotine, F17.2)
Head injury with more than 5 minutes of unconsciousness, lifetime
Any coercive measure
Metal implanted by operation
Head or neck tattoos
Pacemaker
Pregnancy (assessed by urine HCG)
Female patients: Unwillingness to use safe contraception (Intra Uterine Device/System or hormonal contraceptives) during the study period
Severe physical illness
Allergies to any of the ingredients in the amisulpride tablets or memantine tablets
Healthy controls
Lifetime substance abuse/dependence ICD-10 (F1x.1/F1x.2) (exception: tobacco/nicotine, F17.1/F17.2)
Lifetime treatment with antidepressants
Head injury with more than 5 minutes of unconsciousness
Metal implanted by operation
Head or neck tattoos
Pacemaker
Pregnancy (assessed by urine HCG)
Severe physical illness
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