Investigating the Effect of a Single-dose of Levetiracetam on Brain Function, Chemistry and Cognitive Performance in Psychosis Risk
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 69
- 试验地点
- 2
- 主要终点
- Magnetic resonance Imaging (MRI) measure of rCBF using arterial spin labelling (ASL) in the hippocampus.
研究概览
简要总结
Background
Psychosis is a mental health condition that affects around 3 in 100 people in their lifetime. Most treatments for psychosis target a brain chemical called dopamine but they don't work for everyone and don't address many of the symptoms.
People with psychosis and people at risk of developing psychosis show differences in a part of the brain called the hippocampus, such as smaller size and increased activity. This hyperactivity may be associated with cognitive difficulties (thinking and memory).
The basis of this hippocampal hyperactivity is thought to be a deficit in excitation and inhibition of brain cells. Excitation causes brain cells to send signals more frequently, and inhibition causes cells to send signals less frequently. A balance between these signals is important for the brain, including the hippocampus, to function properly.
Approach
Levetiracetam is a medication that is widely used to treat epilepsy and which helps balance excitation-inhibition in the brain. We will use brain imaging, using Magnetic Resonance Imaging (MRI), to test if levetiracetam can help reduce hippocampal hyperactivity, alter connectivity and change levels of brain chemicals in people who are at risk of developing psychosis.
Participants (18-40 years), identified as at risk of psychosis through the Outreach and Support in South London (OASIS) teams, will attend an initial visit at the Institute of Psychiatry, Psychology & Neuroscience. This will involve questions about experiences and feelings, assessment of thinking and memory, and a blood test. They will then attend two scanning visits at the Centre for Neuroimaging Sciences, during which they will take capsules of either levetiracetam or placebo (in a randomised order) before having a 60 mins MRI scan. The MRI scan will look at blood flow to the hippocampus, resting activity, activity during a cognitive task and levels of brain chemicals.
A case-control sample of 33 healthy individuals aged 18-40 will be recruited from Greater London. We will recruit a healthy control (HC) sample to establish the presence of hippocampal dysfunction in our CHR-P group by comparing the MRI data for CHR-P under the placebo condition with that of the HC sample. The HC individuals will attend the screening visit and one scanning visit. They will not receive any medication.
Funded by the Wellcome Trust and conducted by King's College London researchers, the study spans 2-3 months per participant.
Impact
Our study will provide important evidence about how levetiracetam affects brain function, and how this relates to cognition. This knowledge may lead to innovative approaches for understanding and treating psychosis early.
详细描述
Can the acute administration of levetiracetam modulate hippocampal rCBF, resting-state fMRI connectivity, cognitive performance and cortical glutamatergic levels in CHR individuals?
Study Design:
Investigators will address the above research question using a randomised, double-blind, placebo-paired, within-subject crossover design on 36 participants at CHR for psychosis. The study will enrich the CHR sample and reduce heterogeneity by selecting patients who present with positive symptoms (score 3-5 on Clinical Assessment of At Risk Mental State (CAARMS) unusual thought content or non-bizarre ideas subscales), as known proxy measures of hippocampal dysfunction (Allen et al., 2018a; Modinos et al., 2018; Tregellas et al., 2014).
Previous rCBF studies including our own (Allen et al., 2016, 2018a; Percie du Sert et al., 2023) have robustly demonstrated hippocampal hyperactivity in CHR individuals compared to healthy controls. Nevertheless, the presence of hippocampal dysfunction in our CHR group will be established by comparing the MRI data for CHR under placebo condition with that of 33 healthy controls recruited from the Greater London area.
Sample:
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 主要目的
- Other
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
盲法说明
Participants and investigators will be blinded to the randomised order of administration of levetiracetam and placebo.
Once screening procedures have confirmed the subject's eligibility to enter the study, a random list (i.e., of A B B A A A B B) will be created using an automated online random generator. A researcher that is not involved in the study will be responsible for randomisation and documentation. This information will then be given to the South London and Maudsley NHS Foundation Trust Pharmacy where the levetiracetam / placebo capsules will be dispensed from in visually identical capsules for blinding to the A's or B's. Only the SLaM Pharmacy contact will know what capsules were allocated to A's or B's and will keep the enrolment log blinded from the enrolment log kept by the study researcher.
入排标准
- 年龄范围
- 18 Years 至 40 Years(Adult)
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •CHR-P inclusion criteria
- •Age range 18-40 years
- •Capacity to consent to participation in the study
- •Inclusion into attenuated psychosis group as assessed by the CAARMS
- •Scores 3-5 on CAARMS unusual thought content or non-bizarre ideas subscales
排除标准
- •Past episode of psychosis
- •Current exposure to drugs with strong GABAergic or glutamatergic effects (benzodiazepines, anticonvulsants, mood stabilisers, zopiclone, zolpidem, ketamine, opiates, atomoxetine, memantine)
- •Current/recent exposure to any antipsychotic medication
- •Diagnosis of any neurological disorder, including epilepsy
- •Current pregnancy/breastfeeding
- •Severe renal impairment
- •Known allergy to levetiracetam
- •Contraindication to MRI scanning
- •IQ<70 as determined with WAIS-III
- •CHR-P individuals are not deemed to have a full-blown mental health disorder. However, in the event that a CHR-P individual is acutely ill and lacking capacity to consent, they will not be approached to take part in this study.
- •HC inclusion criteria
- •Age range 18-40 years
- •Capacity to consent to participation in the study
- •HC exclusion criteria:
- •Personal history of mental health conditions
- •Any first-degree relative with a psychotic disorder
- •Diagnosis of any neurological disorder, including epilepsy
- •Currently pregnant, breastfeeding, or trying to conceive
- •Current exposure to drugs with strong GABAergic or glutamatergic effects (benzodiazepines, anticonvulsants, mood stabilisers, zopiclone, zolpidem, ketamine, opiates, atomoxetine, memantine)
- •Current/recent exposure to any antipsychotic medication
- •Contraindication to MRI scanning
- •IQ<70 as determined with WAIS-III
研究组 & 干预措施
Levetiracetam, then Placebo
Participants will receive two levetiracetam 250mg capsules on the first scanning visit. On the second scanning visit they will receive two 37.5mg capsules of ascorbic acid.
干预措施: Levetiracetam (Drug)
Levetiracetam, then Placebo
Participants will receive two levetiracetam 250mg capsules on the first scanning visit. On the second scanning visit they will receive two 37.5mg capsules of ascorbic acid.
干预措施: Placebo (Drug)
Placebo, then Levetiracetam
Participants will receive two 37.5mg capsules of ascorbic acid on the first scanning visit. On the second scanning visit they will receive two levetiracetam 250mg capsules.
干预措施: Placebo (Drug)
Placebo, then Levetiracetam
Participants will receive two 37.5mg capsules of ascorbic acid on the first scanning visit. On the second scanning visit they will receive two levetiracetam 250mg capsules.
干预措施: Levetiracetam (Drug)
结局指标
主要结局
Magnetic resonance Imaging (MRI) measure of rCBF using arterial spin labelling (ASL) in the hippocampus.
时间窗: 1 hour after single dose levetiracetam vs placebo
3D pseudo-Continuous Arterial Spin Labelling (3D-pCASL) sequence will be used to measure rCBF.
次要结局
- Brain functional resting-state fMRI measures (including Amplitude of Low-Frequency Fluctuation (ALFF))(1 hour after single dose levetiracetam vs placebo)
- Brain functional MRI activation during a scene processing task.(1 hour after single dose levetiracetam vs placebo)
- Levels of GABAergic and glutamatergic metabolites in the anterior cingulate cortex (ACC) as measured by proton magnetic resonance spectroscopy (1H-MRS).(1 hour after single dose levetiracetam vs placebo)
- Emotion recognition performance(30 mins after single dose of levetiracetam vs placebo and at screening visit)
- Spatial Span working memory performance(30 mins after administration of levetiracetam/placebo and at screening visit for CHR participants)
