Almuntashiri Nawaf, El Sharazly Basma M, Carter Wayne G
Clinical Toxicology Research Group, School of Medicine, University of Nottingham, Royal Derby Hospital Centre, Derby DE22 3DT, UK.
Forensic Toxicology Services Administration, Ministry of Health, P.O. Box 290, Makkah 25315, Saudi Arabia.
Biomolecules. 2025 Jun 4;15(6):816. doi: 10.3390/biom15060816.
Neuropathic pain is a chronic disorder that arises from damaged or malfunctioning nerves. Hypersensitivity to stimuli, also known as hyperalgesia, can cause a person to experience pain from non-painful stimuli, termed allodynia. Cannabis-based medicines (CBMs) may provide new treatment options to manage neuropathic pain. A review of the relevant studies was conducted to evaluate the effectiveness of CBMs in treating neuropathic pain. Scientific literature was systematically searched from January 2003 to December 2024 using the Web of Science Core Collection, PubMed, and MEDLINE. A total of 22 randomized controlled trials (RCTs) were identified that considered the use of 1',1'-dimethylheptyl-Δ-tetrahydrocannabinol-11-oic acid (CT-3), Δ-tetrahydrocannabinol (Δ-THC), cannabidiol (CBD), combinations of Δ-THC with CBD, and cannabidivarin for treatment of neuropathic pain. Significant reductions in pain were reported in 15 studies focused on the treatment of multiple sclerosis, spinal cord injuries, diabetic neuropathy, postherpetic neuralgia, HIV-associated sensory neuropathy, peripheral neuropathic pain, complex regional pain syndrome, chronic radicular neuropathic pain, and peripheral neuropathy of the lower extremities. These positive outcomes often adopted personalized and adjusted dosing strategies. By contrast, seven RCTs observed no significant pain relief compared to placebo, although some had minor improvements in secondary outcomes, such as mood and sleep. Collectively, CBM treatments may improve pain scores, but study limitations such as small sample sizes and study durations, high placebo response rates, and trial unblinding because of the psychoactive effects of cannabinoids all hinder data interpretation and the extrapolation to chronic pain conditions. Hence, future RCTs will need to have larger numbers and be more extended studies that explore optimal dosing and delivery methods and identify patient subgroups that are most likely to benefit. While CBMs show potential, their current use balances modest benefits against possible adverse effects and variable outcomes.
神经性疼痛是一种由神经受损或功能失调引起的慢性疾病。对刺激的超敏反应,也称为痛觉过敏,可导致人对非疼痛性刺激产生疼痛,即痛觉异常。基于大麻的药物(CBMs)可能为管理神经性疼痛提供新的治疗选择。对相关研究进行了综述,以评估CBMs治疗神经性疼痛的有效性。使用科学网核心合集、PubMed和MEDLINE从2003年1月至2024年12月对科学文献进行了系统检索。共确定了22项随机对照试验(RCT),这些试验考虑使用1',1'-二甲基庚基-Δ-四氢大麻酚-11-酸(CT-3)、Δ-四氢大麻酚(Δ-THC)、大麻二酚(CBD)、Δ-THC与CBD的组合以及大麻二萜酚治疗神经性疼痛。15项针对多发性硬化症、脊髓损伤、糖尿病性神经病变、带状疱疹后神经痛、HIV相关感觉神经病变、周围神经性疼痛、复杂性区域疼痛综合征、慢性神经根性神经病变以及下肢周围神经病变治疗的研究报告疼痛有显著减轻。这些积极结果通常采用个性化和调整剂量的策略。相比之下,7项RCT与安慰剂相比未观察到显著的疼痛缓解,尽管有些试验在次要结局如情绪和睡眠方面有轻微改善。总体而言,CBMs治疗可能会改善疼痛评分,但研究局限性如样本量小和研究持续时间短、高安慰剂反应率以及由于大麻素的精神活性作用导致的试验非盲法等都阻碍了数据解释以及向慢性疼痛状况的外推。因此,未来的RCT需要有更大的样本量并且是更长期的研究,以探索最佳剂量和给药方法,并确定最可能受益的患者亚组。虽然CBMs显示出潜力,但它们目前应用时在适度益处与可能的不良反应及可变结果之间进行权衡。