Evidence map›Paper›PMID 42138778›Full record

ReviewActa neurologica Belgica2026

Therapeutic effects of cannabinoids on Parkinson's disease: an updated systematic review and meta-analysis of randomized controlled trials.

Mark Messak, Ahmed Abdelmageed, Ahmed Noureldeen Abbas, Youssef Mandour, Ahmed Talkhan, Mahmoud Fadel Eltohami, Dua'a Kanaan, Fawaz K Alfahmi, Habiba Tariq Saeed, Lara Hamzeh Hamzeh and 2 more

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In one paragraph

Review in Acta neurologica Belgica, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Mark MessakFaculty of Medicine, Helwan University, Helwan, Egypt. markwael2003@gmail.com.ORCID http://orcid.org/0009-0001-2571-3934
Ahmed AbdelmageedFaculty of Medicine, Mansoura University, Mansoura, Egypt.ORCID http://orcid.org/0009-0002-7902-690X
Ahmed Noureldeen AbbasFaculty of Medicine, Minia University, Minia, Egypt.
Youssef Mandour *Faculty of Medicine, Mansoura University, Mansoura, Egypt.ORCID http://orcid.org/0009-0006-1019-2925
Ahmed Talkhan *Faculty of Medicine, Mansoura University, Mansoura, Egypt.ORCID http://orcid.org/0009-0009-7975-6479
Mahmoud Fadel EltohamiMedical Institute of Tambov State University Named After G.R. Derzhavin, Tambov, Russia.
Dua'a Kanaan *School of Medicine, The University of Jordan, Amman, Jordan.
Fawaz K Alfahmi *College of Medicine, Taif University, Taif, Saudi Arabia.ORCID http://orcid.org/0009-0008-4779-4166
Habiba Tariq Saeed *Faculty of Medicine, Tanta University, Tanta, Egypt.ORCID http://orcid.org/0009-0009-8515-8723
Lara Hamzeh Hamzeh *Faculty of Medicine, Caucasus International University, Tbilisi, Georgia.ORCID http://orcid.org/0009-0003-4170-7619
Lamees TamanFaculty of Medicine, Tanta University, Tanta, Egypt.ORCID http://orcid.org/0009-0005-8594-4063
Ahmed NegidaDepartment of Neurology, Virginia Commonwealth University, Richmond, VA, USA.ORCID http://orcid.org/0000-0001-5363-6369

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeCurrent treatments for Parkinson's disease (PD) are primarily symptomatic and may lead to motor fluctuations and levodopa-induced dyskinesia over time, highlighting the need to repurpose other medications. Cannabinoids have gained attention as potential repurposed treatments. This systematic review and meta-analysis evaluated their efficacy in PD while addressing limitations of previous reviews, including low statistical power and inclusion of cannabinoid antagonists in pooled analyses.

methodsA literature search was conducted through PubMed, Scopus, and Web of Science, identifying randomized controlled trials (RCTs) evaluating the use of cannabinoids in PD. Quality assessment was done via RoB-2. A random-effects meta-analysis was performed using the meta and metafor packages in R, with mean differences (MD) or standardized mean differences (SMD; Hedges' g) reported with 95% confidence interval (CI). A sensitivity analysis was carried out to assess the robustness of our findings. In crossover trials, effect sizes and standard errors were extrapolated from the reported CIs, considering the paired design.

resultsEleven RCTs were identified, six of which were eligible for meta-analysis due to the absence of poolable outcomes in the remainder. Cannabinoids did not significantly improve PD severity (SMD = 0.16, 95% CI[-0.13 to 0.44], p = 0.27, I²=0%), motor examination (SMD=-0.08, 95% CI[-0.35 to 0.20], p = 0.57, I²=0%), motor experiences of daily living (SMD=-0.08, 95% CI[-0.49 to 0.33], p = 0.71, I²=0%), non-motor symptoms (SMD= -0.03, 95% CI[-0.72 to 0.67], p = 0.94, I²= 64.3%). Sensitivity analysis excluding Peball et al. showed that the pooled estimate of non-motor symptoms was largely driven by nabilone (SMD = 0.34, 95%CI [-0.19 to 0.88], p = 0.21, I²=0%), suggesting a drug-specific benefit signal.

conclusionCannabinoids have not shown significant benefit in PD; however, our findings should be interpreted with caution. The nabilone benefit signal for non-motor symptoms represents a distinct question warranting dedicated trials. Future studies should use standardized, pharmacologically stratified protocols.

Indexed as

CannabidiolCannabinoid receptor 1Cannabinoid receptor 2Delta-9-tetrahydrocannabinolParkinson's disease

Identifiers

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.