Cannabidiol is a component of marijuana that does not activate cannabinoid receptors, but moderately inhibits the degradation of the endocannabinoid anandamide. We previously reported that an elevation of anandamide levels in cerebrospinal fluid inversely correlated to psychotic symptoms. Furthermore, enhanced anandamide signaling let to a lower transition rate from initial prodromal states into frank psychosis as well as postponed transition. In our translational approach, we performed a double-blind, randomized clinical trial of cannabidiol vs amisulpride, a potent antipsychotic, in acute schizophrenia to evaluate the clinical relevance of our initial findings. Either treatment was safe and led to significant clinical improvement, but cannabidiol displayed a markedly superior side-effect profile. Moreover, cannabidiol treatment was accompanied by a significant increase in serum anandamide levels, which was significantly associated with clinical improvement. The results suggest that inhibition of anandamide deactivation may contribute to the antipsychotic effects of cannabidiol potentially representing a completely new mechanism in the treatment of schizophrenia.
The search for safe and effective drugs to treat schizophrenia is hindered by the complex nature of this disorder, which is known to involve multiple brain neurotransmitters.1 Among them are the endogenous cannabinoids, a family of lipid messengers that target the same cell surface receptors engaged by Δ9-tetrahydrocannabinol in marijuana.2 Because Δ9-tetrahydrocannabinol and other direct-acting cannabinoid agonists can induce psychotic symptoms both in healthy volunteers3, 4, 5 and schizophrenic patients,6, 7 it has been suggested that hyperactivity of the endocannabinoid system might contribute to psychotic states.8, 9 This idea has fueled two large-scale clinical trials with CB1-type cannabinoid receptor antagonists in schizophrenia, which yielded, however, negative results.10, 11 A diametrically opposite view — namely that certain components of the endocannabinoid system might have a protective role in schizophrenia — was suggested by studies with antipsychotic-naïve schizophrenic patients, in which it was found that the symptom intensity experienced by these subjects was negatively correlated with cerebrospinal levels of anandamide,12, 13 an endocannabinoid transmitter known to be involved in the regulation of pain, mood and cognition.14 Consistent with these clinical observations, animal experiments have shown that pharmacological blockade of anandamide degradation attenuates, rather than enhances, psychotic-like behaviors induced in rodents by amphetamine and phencyclidine.15, 16
Cannabidiol is a non-psychotropic component of marijuana that binds to CB1 receptors with only comparably very low affinity17, 18 and is devoid of overt cannabimimetic or pro-psychotic properties.17 Biochemical studies indicate that cannabidiol may enhance endogenous anandamide signaling indirectly, by inhibiting the intracellular degradation of anandamide catalyzed by the enzyme fatty acid amide hydrolase (FAAH).19 Furthermore, preliminary clinical case reports suggest that cannabidiol might exert antipsychotic effects in schizophrenic patients.20, 21, 22 In addition, experimental studies show that cannabidiol reduces psychosis-like effects of Δ9-tetrahydrocannabinol and synthetic analogs.22, 23
Materials and methods
Detection of fatty acid ethanolamides
FAAH activity was measured at 37 °C for 30 min in 0.5 ml of Tris buffer (50 mM, pH 7.5) containing fatty acid-free bovine serum albumin (0.05%, w/v), protein from tissue homogenates of the rat brain membranes (50 μg), cannabidiol (0.3 μM, 1 μM, 3 μM, 10 μM, 30 μM, 0.3 mM, 0.1 mM, and 1 mM) and (3H-ethanolamine) anandamide (10 000 d.p.m., specific activity 20 Ci mmol−1). For concentration response the drug CBD was dissolved in dimethyl sulfoxide and added to the samples at a final concentration of 1% dimethyl sulfoxide. The reactions were stopped with chloroform/methanol (1:1, 1 ml), and radioactivity was measured in the aqueous layers by liquid scintillation counting.
This study was a therapeutic-exploratory (phase II), double-blinded, monocenter, randomized, parallel-group, controlled clinical trial of cannabidiol vs amisulpride (CBD-CT1; ClinicalTrials.gov. Identifier: NCT00628290). The study protocol was approved by the Ethics Committee of the University of Cologne and the BfArM (Federal Institute for Drugs and Medical Products). Initially an independent psychiatrist assessed patients to confirm their ability to provide informed consent. Then, written informed consent was obtained from each patient following a detailed explanation of study procedures.
Men and women age 18–50 years who had a diagnosis of schizophrenia or schizophreniform psychosis according to the DSM-IV criteria were eligible for the study. All patients were hospitalized at baseline and through day 28 after random assignment to treatment. A total number of 42 inpatients of the Department of Psychiatry and Psychotherapy of the University of Cologne participated in the study. In all, 37 patients were suffering from acute paranoid schizophrenia (DSM-IV 295.30). Another 5 patients were initially diagnosed as suffering from schizophreniform psychosis (DSM-IV 295.40) based on the duration of illness, but were followed-up and diagnosed with paranoid schizophrenia after completing the study. Only acutely psychotic patients with a total Brief Psychiatric Rating Scale (BPRS) score 36 and a BPRS THOT factor (thought disorders) score 12 were eligible to participate. Patients with a positive urine drug screening for illicit drugs in general and cannabinoids in particular were not allowed to participate to avoid an interaction of currently bioactive cannabinoids (including cannabidiol) with treatment. Further exclusion criteria were relevant psychiatric disorders including substance use disorders, previous treatment with a depot antipsychotic within 3 months before the participation in the study, a history of treatment resistance, defined by the persistence of severe symptoms despite adequate treatment with at least two antipsychotics or prior treatment with clozapine, a relevant and/or unstable medical condition and an insufficient contraception, pregnancy or breast-feeding in female patients.
We enrolled 42 acutely exacerbated schizophrenic patients who had met the DSM-IV criteria. In all, 39 patients were evaluated according to modified intention-to-treat (Table 1), 33 were observed and treated per protocol and all 42 were valid for safety evaluation (Figure 1). After a screening period of up to 7 days and a minimum period of 3 antipsychotic-free days patients were randomized (1:1) to receive either cannabidiol or amisulpride starting with 200 mg per day each and increased stepwise by 200 mg per day to a daily dose of 200 mg four times daily (total 800 mg per day) each within the first week. The hospital pharmacy provided individual medication kits according to a randomization sequence prepared by a person otherwise not involved in the study (drawing paper lots out of a bowl). The respective treatment was maintained for another 3 weeks. A reduction of each treatment to 600 mg per day was allowed for clinical reasons, such as unwanted side effects after week 2, which was the case for three patients in the cannabidiol and five patients in the amisulpride treatment group. In addition, lorazepam co-medication was allowed with up to 7.5 mg per day during the entire study.
The end points of the clinical trials are generally accepted and recommended by the European Medicines Agency for the measurement of clinically observed changes in patients with an acute schizophrenic and schizophreniform psychosis. The BPRS and the Positive and Negative Syndrome Scale (PANSS) were both used as primary outcome measures for the assessment of psychotic symptoms at baseline, day 14 and day 28 of the treatment period of the trial. The BPRS was implemented in the trial to establish a fast to assess safety parameter in case of a relevant worsening of symptoms in single patients and was assessed on day 7 and day 21 if clinically relevant by investigator's decision. Side effects were evaluated using the Extrapyramidal Symptom Scale (EPS) and included the measurement of serum prolactin (μg l−1) and body weight (kg). Safety measures included repeated electrocardiograms as well as routine blood parameters.
Hypotheses and statistical analysis
The primary study objective was to determine whether cannabidiol given for 28 days was non-inferior to amisulpride in the treatment of patients with schizophrenia as measured by the PANSS and the BPRS. Side effects were evaluated using the Extrapyramidal Symptom Scale and included the measurement of serum prolactin (μg l−1) and body weight (kg). Safety measures included repeated electrocardiograms as well as routine blood values. These end points are generally accepted and recommended by the European Medicines Agency for the measurement of clinically observed changes in patients with an acute schizophrenic and schizophreniform psychosis.
We planned to randomly assign 35 patients to each treatment group which would have provided 82% power to detect an effect size of 0.7 (≈9/13=Δ/σ) in the change-from-baseline PANSS/BPRS total score at a two-sided 5% significance level using an unadjusted two-sample t-test.26 Unfortunately, enrolment was significantly affected by the exclusion of cannabinoid-positive patients in urine drug screening (Figure 1), which led to a termination of the study due to expiration of funding.
The primary efficacy variable was the intra-individual difference of PANSS and BPRS at baseline (days −8 to −1) and day 28, that is, PANSS/BPRS (baseline) minus PANSS/BPRS (day 28). The primary hypothesis to be tested confirmatory with the parametric Sasabuchi test, (α=2.5%, one-sided) was relevant inferiority of cannabidiol vs amisulpride, that is, H0: μCannabidiol−θ·μAmisulpride≤0 vs H1: μCannabidiol−θ·μAmisulpride>0 with θ=80% (μ denotes the expected value).27 Equivalently, a 95% confidence interval for the ratio μCannabidiol/μAmisulpride was calculated (according to Fieller). The non-inferiority parameter θ=80% was chosen because in the literature PANSS/BPRS changes of 20–50% are discussed as ‘response to therapy’.28 Thus, changes up to 20% can be deemed clinically irrelevant (especially because of the large intra-individual variance; compare CPMP/EWP, 1998).29
Patients with missing post baseline measures were excluded from the efficacy analysis. Thus, the ‘modified intention-to-treat’ set encompassed all patients who had been randomized, had received any study medication and had provided a valid PANSS/BPRS at day 14 or 28. A missing PANSS/BPRS at day 28 was imputed by the last valid preceding value ‘last observation carried forward’, LOCF. The ‘per protocol’ set encompassed all patients who had been treated, and observed according to protocol.
A mixed effects repeated measures model (unstructured covariance matrix) for the change-from-baseline included baseline as a covariate with treatment, visit and treatment-by-visit interaction as fixed effects (missing values were not imputed). The same analysis model was chosen for secondary outcomes and side effects. Specific contrasts were evaluated (between groups at specific visits, between visits within groups).
The ‘valid for safety’ set encompassed all patients who were randomized and received any study medication. On the basis of this the treatment-emergent adverse events were compared among treatment groups using Fisher's exact test. Owing to the exploratory nature of the study, all analyses were performed without adjustment for multiplicity. Statistical analyses were done using IBM SPSS Statistics 19 (Somers, NY, USA) and R 2.12.1 (Vienna, Austria; Sasabuchi test, Fieller's confidence interval).
The basic hypothesis for our translational approach was that enhancement of anandamide signaling by administration of cannabidiol should result in an improvement of psychotic symptoms. To put this hypothesis to test, we performed a 4-week double-blind, parallel-group, randomized, active-controlled clinical trial of cannabidiol vs the dopamine D2/D3-receptor antagonist amisulpride—one of the most effective drugs currently in use for the treatment of schizophrenia.30 Patients undergoing either cannabidiol or amisulpride treatment showed significant clinical improvement, assessed by the reduction in PANSS total score (P<0.001, day 28 vs day 0, Figure 2a) as well as for all subcategories of symptoms of schizophrenia (Figures 2b–d, Table 2). Comparison (modified intention-to-treat) of the clinical effects of amisulpride and cannabidiol revealed no relevant difference between the two treatments (1.0, 95% confidence interval −12.6 to 14.6, P=0.884; Table 2); the confirmatory test of non-inferiority with 80% retention bound yielded a ratio of means 0.94 (CBD/AMI) with 95% confidence interval 0.55–1.59. Thus non-inferiority seems highly plausible, but could not be demonstrated, P=0.27 (one-sided). Results were very similar using the per protocol set and/or the BPRS (Table 2). We found no difference in the proportion of responders (20% improvement in PANSS total score) to each treatment (CBD 15/20, AMI 14/19, P=1.000). Furthermore, lorazepam co-medication did not significantly influence our results (Supplementary Figure 1). These results suggest that cannabidiol is as effective at improving psychotic symptoms as the standard antipsychotic amisulpride.
The use of antipsychotic drugs is associated with frequent side effects, which markedly influence acute compliance and long-term treatment adherence. These include motor disturbances (so-called extrapyramidal symptoms), weight gain and sexual dysfunction. Compared with amisulpride, we found that treatment with cannabidiol was associated with significantly fewer extrapyramidal symptoms (P=0.006; Figure 3a), less weight gain (P=0.010; Figure 3b), and lower prolactin increase—a predictor of galactorrhoea and sexual dysfunction (P<0.001; Figure 3c). Furthermore, cannabidiol was well-tolerated (Supplementary Table 3) and did not significantly affect hepatic or cardiac functions.
Previous work has suggested that cannabidiol may protect anandamide from deactivation by interfering with FAAH activity 15. We confirmed this result showing that cannabidiol inhibits FAAH in rat brain membranes with a median effective concentration of 8.6±0.2 μM (n=12). We further found that cannabidiol, at a concentration that reduces FAAH activity by ∼50% (10 μM), does not significantly interact with a broad panel of neurotransmitter receptors that are relevant to schizophrenia, including dopamine, glutamate and serotonine. To determine whether treatment with cannabidiol reduces FAAH activity in our study subjects, we measured anandamide concentrations in serum before and after exposure to cannabidiol or amisulpride. Anandamide levels were higher in subjects exposed to cannabidiol than in those exposed to amisulpride (Figure 4a). Importantly, the serum levels of two additional FAAH substrates—the non-cannabimimetic lipid mediators palmitoylethanolamide (Figure 4b) and oleoylethanolamide (Figure 4c)—were also elevated in schizophrenic patients treated with cannabidiol, compared with those treated with amisulpride.
Next, to assess whether the ability to impair FAAH activity might contribute to the antipsychotic effects of cannabidiol, we investigated the relationship between changes in serum anandamide levels and psychotic symptoms (median slope analysis). We found a statistically significant association between increase in anandamide levels and decrease in psychotic symptoms in patients treated with cannabidiol (P=0.0012). In contrast, no such association was found in patients treated with amisulpride (P=0.64) (Figure 5). Moreover, no such relationship was apparent for serum oleoylethanolamide (median slopes: cannabidiol −0.05 1/(pmol ml−1), P=1.00, amisulpride 5.91 1/(pmol ml−1), P=0.30) or serum palmitoylethanolamide (median slopes: cannabidiol −3.8 1/(pmol ml−1), P=0.091, amisulpride −5.6 1/(pmol ml−1), P=0.19). These findings suggest the existence of a functional link between the antipsychotic effects of cannabidiol and its ability to inhibit anandamide degradation, though further research is needed to determine whether this link represents cause and effect.
Our results provide evidence that the non-cannabimimetic constituent of marijuana, cannabidiol, exerts clinically relevant antipsychotic effects that are associated with marked tolerability and safety, when compared with current medications. Although a plethora of pharmacological mechanisms have recently been suggested relevant for the antipsychotic effect of cannabidiol31 the primary pharmacological mechanism through which cannabidiol exerts this antipsychotic effect in humans is unclear at present. However, the significant association observed in cannabidiol-treated patients between improvement of clinical symptoms and serum anandamide levels suggests that the ability of cannabidiol to inhibit the FAAH activity and enhance intrinsic anandamide signaling might be a functionally relevant component of its antipsychotic properties. Although only serum levels of anandamide were assessed in this study in comparison with cerebrospinal fluid samples,13, 32 the systemic effect of cannabidiol on FAAH inhibition is highly likely to be reflected in this compartment. In addition, while serum values of endocannabinoids have been found less useful in early stages of schizophrenia, they have been reported valuable in more chronic cases.33, 34 Our interpretation is supported by two sets of clinical data. First, in a relatively large cohort of antipsychotic-naïve schizophrenic patients (n=47), cerebrospinal anandamide levels were found to be inversely correlated with psychotic symptoms.13 Second, high-risk subjects for psychosis35 who exhibited lower cerebrospinal levels of anandamide also showed a higher risk for transiting to frank psychosis.32 As is often the case in this type of study, we cannot exclude that cannabidiol may reduce psychotic symptoms through complementary or even alternative mechanisms to FAAH inhibition, including interactions with serotonin 5-HT1A receptors,36 GPR55 receptors37 and transient receptor potential vanilloid-1 receptors.19 Nevertheless, our results do provide a rationale for additional clinical testing of selective FAAH inhibitors in schizophrenia.
This study was supported by grants from the Stanley Medical Research Institute (FML) and the National Institute on Drug Abuse (DP). The funding sources had no influence on the design of the study or the analysis and interpretation of the results. We acknowledge the contribution of Drs Frauke Schultze-Lutter and Stephan Ruhrmann to the protocol and design and of Drs Christian Mauss, Brit M Nolden, Tobias Buzello, Miriam A Neatby and Anita Haensel to the execution of the clinical part of this study. We are also grateful to Prof Andrea Giuffrida for his fruitful input during the course of this study.
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Supplementary Information accompanies the paper on the Translational Psychiatry website (http://www.nature.com/tp)