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Psychopathological and cognitive effects of therapeutic cannabinoids in multiple sclerosis: a double-blind, placebo controlled, crossover study.

Massimiliano Aragona, Emanuela Onesti, Valentina Tomassini, Antonella Conte, Shiva Gupta, Francesca Gilio, Patrizia Pantano, Carlo Pozzilli, Maurizio Inghilleri

Clinical Neuropharmacology 2009 DOI: 10.1097/wnf.0b013e3181633497 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Randomized, double-blind, placebo-controlled, parallel group crossover trial Peer reviewed
Sample size 17
Population Cannabis-naïve patients with multiple sclerosis
Dose free-dose
Duration 8 weeks (3 weeks per phase)
Measures Symptom Checklist-90 Revised, Self-rating Anxiety Scale, Multiple Sclerosis Functional Composite, Paced Auditory Serial Addition Test, Visual Analogue Scale on health-related quality of life, Multiple Sclerosis Impact Scale-29, Fatigue Severity Scale
Key findings Cannabinoid treatment did not induce psychopathology or impair cognition in cannabis-naïve patients with MS, with no significant differences between cannabis and placebo phases on any measure. However, Delta-9-tetrahydrocannabinol blood levels correlated positively with General Symptomatic Index and interpersonal sensitivity, aggressive behaviour, and paranoiac tendencies subscale scores, suggesting that at doses higher than therapeutic levels these features might arise, though the authors state greater statistical power is needed to confirm this.

Abstract

To study possible psychopathological symptoms and cognitive deficits, abuse induction, as well as general tolerability and effects on quality of life, fatigue and motor function in cannabis-naïve patients with multiple sclerosis (MS) treated with a free-dose cannabis plant extract (Sativex). In an 8-week, randomized, double-blind, placebo-controlled, parallel group crossover trial, 17 cannabis-naïve patients with MS were assessed at baseline and at the end of the cannabis and placebo phases of the trial (each of 3 weeks) by means of Symptom Checklist-90 Revised, Self-rating Anxiety Scale, Multiple Sclerosis Functional Composite (of which 1 dimension is the Paced Auditory Serial Additional Test that was used to evaluate cognition), Visual Analogue Scale on health-related quality of life, Multiple Sclerosis Impact Scale-29, and Fatigue Severity Scale. Postplacebo versus postcannabinoid scores showed that no significant differences could be detected on all the variables under study. A significant positive correlation was found between Delta-9-tetrahydrocannabinol blood levels and scores at the General Symptomatic Index and at the "interpersonal sensitivity," "aggressive behaviour," and "paranoiac tendencies" subscales of the Symptom Checklist-90 Revised. No serious adverse events, abuse tendencies, or direct withdrawal symptoms were reported. Increased desire for Sativex with secondary depression was reported in 1 subject. Cannabinoid treatment did not induce psychopathology and did not impair cognition in cannabis-naïve patients with MS. However, the positive correlation between blood levels of Delta-9-tetrahydrocannabinol and psychopathological scores suggests that at dosages higher than those used in therapeutic settings, interpersonal sensitivity, aggressiveness, and paranoiac features might arise, although greater statistical power would be necessary to confirm this finding.

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