Study register · detail
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187 citations
SampleNarrative Review
ControlMS patients without neuropathic pain, also…
Blindingn.a.
DesignNarrative Review
Cannabinoidkombination
THC:CBD1:1
Max. dose43.6 mg
Routeoromukosal
Key finding
Narrative review presents theoretical foundations and existing evidence for clinical endocannabinoid deficiency in migraine, fibromyalgia and irritable bowel syndrome; no primary empirical data on intervention effects reported.
Summary
Russo's theory of clinical endocannabinoid deficiency: migraine, fibromyalgia and irritable bowel syndrome as prototype conditions with hypothetical ECS dysfunction. Mechanistic hypothesis with indirect clinical relevance, no systematic data extraction.
P
PopulationMultiple sclerosis patients with central neuropathic pain, n=20 (10 with pain, 10 without pain as control group), EDSS ≤3.5, DN4 ≥4
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InterventionSativex (THC/CBD oromucosal spray, 2,7 mg THC + 2,5 mg CBD per spray), average of 8 sprays daily over 4 weeks
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ControlMS patients without neuropathic pain, also treated with Sativex (comparison group, no placebo control)
O
OutcomeSignificant pain reduction on VAS and improved quality of life after 4 weeks; neurophysiologically increased fronto-central gamma-band oscillation and enhanced pain-motor integration (measured via LEP and TMS)
Quality profile
Sample size
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Blinding
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Citations / year
★★★★★
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Abstract
Medicine continues to struggle in its approaches to numerous common subjective pain syndromes that lack objective signs and remain treatment resistant. Foremost among these are migraine, fibromyalgia, and irritable bowel syndrome, disorders that may overlap in their affected populations and whose sufferers have all endured the stigma of a psychosomatic label, as well as the failure of endless pharmacotherapeutic interventions with substandard benefit. The commonality in symptomatology in these conditions displaying hyperalgesia and central sensitization with possible common underlying pathophysiology suggests that a clinical endocannabinoid deficiency might characterize their origin. Its base hypothesis is that all humans have an underlying endocannabinoid tone that is a reflection of levels of the endocannabinoids, anandamide (arachidonylethanolamide), and 2-arachidonoylglycerol, their production, metabolism, and the relative abundance and state of cannabinoid receptors. Its theory is that in certain conditions, whether congenital or acquired, endocannabinoid tone becomes deficient and productive of pathophysiological syndromes. When first proposed in 2001 and subsequently, this theory was based on genetic overlap and comorbidity, patterns of symptomatology that could be mediated by the endocannabinoid system (ECS), and the fact that exogenous cannabinoid treatment frequently provided symptomatic benefit. However, objective proof and formal clinical trial data were lacking. Currently, however, statistically significant differences in cerebrospinal fluid anandamide levels have been documented in migraineurs, and advanced imaging studies have demonstrated ECS hypofunction in post-traumatic stress disorder. Additional studies have provided a firmer foundation for the theory, while clinical data have also produced evidence for decreased pain, improved sleep, and other benefits to cannabinoid treatment and adjunctive lifestyle approaches affecting the ECS.
The impediment to action advances action.