4.1 Article

Effects of Cannabinoid Administration for Pain: A Meta-Analysis and Meta-Regression

Journal

EXPERIMENTAL AND CLINICAL PSYCHOPHARMACOLOGY
Volume 27, Issue 4, Pages 370-382

Publisher

AMER PSYCHOLOGICAL ASSOC
DOI: 10.1037/pha0000281

Keywords

cannabis; cannabinoid; marijuana; pain; meta-analysis

Funding

  1. National Institute on Drug Abuse [F31 DA044013, U01 DA041156, R01 DA041353, R01 DA033156, R01 DA040537, K01 DA037819]
  2. National Institute of Mental Health [K01 MH115272]
  3. National Institute on Minority Health and Health Disparities [U54 MD012393, 5378]
  4. National Institute of Allergy and Infectious Diseases [R01 AI107655]
  5. National Science Foundation [CNS-1532061, BCS-1805645]

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Chronic pain states have resulted in an overreliance on opioid pain relievers, which can carry significant risks when used long term. As such, alternative pain treatments are increasingly desired. Although emerging research suggests that cannabinoids have therapeutic potential regarding pain, results from studies across pain populations have been inconsistent. To provide meta-analytic clarification regarding cannabis's impact on subjective pain, we identified studies that assessed drug-induced pain modulations under cannabinoid and corresponding placebo conditions. A literature search yielded 25 peer-reviewed records that underwent data extraction. Baseline and end-point data were used to compute standardized effect size estimates (Cohen's d) across cannabinoid administrations (k = 39) and placebo administrations (k = 26). Standardized effects were inverse-variance weighted and pooled across studies for meta-analytic comparison. Results revealed that cannabinoid administration produced a medium-to-large effect across included studies, Cohen's d = -0.58, 95% confidence interval (CI) [-0.74, -0.43], while placebo administration produced a small-to-medium effect, Cohen's d = -0.39, 95% CI [-0.52, -0.26]. Meta-regression revealed that cannabinoids, beta = -0.43, 95% CI [-0.62, -0.24], p < .05, synthetic cannabinoids, beta = -0.39, 95% CI [-0.65, -0.14], p < .05, and sample size, beta = 0.01, 95% CI [0.00, 0.01], p < .05, were associated with marked pain reduction. These outcomes suggest that cannabinoid-based pharmacotherapies may serve as effective replacement/adjunctive options regarding pain, however, additional research is warranted. Additionally, given demonstrated neurocognitive side effects associated with some constituent cannabinoids (i.e., THC), subsequent work may consider developing novel therapeutic agents that capitalize on cannabis's analgesic properties without producing adverse effects. Public Health Significance Chronic pain states are an ever-growing concern in the United States, costing an estimated $600 billion annually in lost labor and health care expenses. These, and other, conditions have resulted in an overreliance on opioid-based pharmacotherapies. Results from the current meta-analysis provide some support that cannabinoids might mitigate subjective pain among patients with pain-related clinical conditions.

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