Study register · detail
Harm
GRADE
Moderate
611 citations
Samplen = 13 Pat.
Duration3 days
ControlPlacebo
EndpointPANSS
Blindingdoppelblind
DesignRCT (3-day, double-blind, placebo-controlled)
Cannabinoidthc
Max. dose5.0 mg
Routeinhalativ
Key finding
Δ9-THC transiently exacerbated core cognitive and psychotic symptoms in schizophrenia patients.
Summary
n=13 stable antipsychotically treated schizophrenia patients, i.v. Δ9-THC 0/2,5/5 mg, double-blind, placebo-controlled; THC transiently increased positive, negative and general symptoms (PANSS), learning/memory deficits, perceptual disturbances, akathisia as well as prolactin and cortisol. Schizophrenia patients responded more vulnerably to cognitive THC effects than healthy control subjects.
P
PopulationStable, antipsychotically treated schizophrenia patients, n=13
I
InterventionIntravenous Δ9-THC 2,5 mg and 5 mg, 3-day crossover design
C
ControlPlacebo (0 mg i.v. Δ9-THC)
O
OutcomeΔ9-THC transiently increased learning/memory deficits, positive/negative/general schizophrenia symptoms, perceptual alterations, motor side effects and prolactin/cortisol; schizophrenia patients showed increased vulnerability to cognitive effects compared to healthy controls
Confidence in the evidence
Moderate
The third of four GRADE levels, the effect estimate is probably reliable.
Downgraded for
Imprecision
Quality profile
Sample size
★★★★★
Blinding
Double-blind
Effect size
Harm
Citations / year
★★★★★
Authors
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Abstract
<h4>Background</h4>Recent advances in the neurobiology of cannabinoids have renewed interest in the association between cannabis and psychotic disorders.<h4>Methods</h4>In a 3-day, double-blind, randomized, placebo-controlled study, the behavioral, cognitive, motor, and endocrine effects of 0 mg, 2.5 mg, and 5 mg intravenous Delta-9-tetrahydrocannabinol (Delta-9-THC) were characterized in 13 stable, antipsychotic-treated schizophrenia patients. These data were compared with effects in healthy subjects reported elsewhere.<h4>Results</h4>Delta-9-tetrahydrocannabinol transiently increased 1) learning and recall deficits; 2) positive, negative, and general schizophrenia symptoms; 3) perceptual alterations; 4) akathisia, rigidity, and dyskinesia; 5) deficits in vigilance; and 6) plasma prolactin and cortisol. Schizophrenia patients were more vulnerable to Delta-9-THC effects on recall relative to control subjects. There were no serious short- or long-term adverse events associated with study participation.<h4>Conclusions</h4>Delta-9-tetrahydrocannabinol is associated with transient exacerbation in core psychotic and cognitive deficits in schizophrenia. These data do not provide a reason to explain why schizophrenia patients use or misuse cannabis. Furthermore, Delta-9-THC might differentially affect schizophrenia patients relative to control subjects. Finally, the enhanced sensitivity to the cognitive effects of Delta-9-THC warrants further study into whether brain cannabinoid receptor dysfunction contributes to the pathophysiology of the cognitive deficits associated with schizophrenia.
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