Weber Isaac, Zagona-Prizio Caterina, Sivesind Torunn E, Adelman Madeline, Szeto Mindy D, Liu Ying, Sillau Stefan H, Bainbridge Jacquelyn, Klawitter Jost, Sempio Cristina, Dunnick Cory A, Leehey Maureen A, Dellavalle Robert P
Mercy Hopsital St. Louis, St. Louis, MO, United States.
Department of Dermatology, University of Colorado School of Medicine, Aurora, CO, United States.
JMIR Dermatol. 2024 Mar 11;7:e49965. doi: 10.2196/49965.
Seborrheic dermatitis (SD) affects 18.6%-59% of persons with Parkinson disease (PD), and recent studies provide evidence that oral cannabidiol (CBD) therapy could reduce sebum production in addition to improving motor and psychiatric symptoms in PD. Therefore, oral CBD could be useful for improving symptoms of both commonly co-occurring conditions.
This study investigates whether oral CBD therapy is associated with a decrease in SD severity in PD.
Facial photographs were collected as a component of a randomized (1:1 CBD vs placebo), parallel, double-blind, placebo-controlled trial assessing the efficacy of a short-term 2.5 mg per kg per day oral sesame solution CBD-rich cannabis extract (formulated to 100 mg/mL CBD and 3.3 mg/mL THC) for reducing motor symptoms in PD. Participants took 1.25 mg per kg per day each morning for 4 ±1 days and then twice daily for 10 ±4 days. Reviewers analyzed the photographs independently and provided a severity ranking based on the Seborrheic Dermatitis Area and Severity Index (SEDASI) scale. Baseline demographic and disease characteristics, as well as posttreatment SEDASI averages and the presence of SD, were analyzed with 2-tailed t tests and Pearson χ tests. SEDASI was analyzed with longitudinal regression, and SD was analyzed with generalized estimating equations.
A total of 27 participants received a placebo and 26 received CBD for 16 days. SD severity was low in both groups at baseline, and there was no treatment effect. The risk ratio for patients receiving CBD, post versus pre, was 0.69 (95% CI 0.41-1.18; P=.15), compared to 1.20 (95% CI 0.88-1.65; P=.26) for the patients receiving the placebo. The within-group pre-post change was not statistically significant for either group, but they differed from each other (P=.07) because there was an estimated improvement for the CBD group and an estimated worsening for the placebo group.
This study does not provide solid evidence that oral CBD therapy reduces the presence of SD among patients with PD. While this study was sufficiently powered to detect the primary outcome (efficacy of CBD on PD motor symptoms), it was underpowered for the secondary outcomes of detecting changes in the presence and severity of SD. Multiple mechanisms exist through which CBD can exert beneficial effects on SD pathogenesis. Larger studies, including participants with increased disease severity and longer treatment periods, may better elucidate treatment effects and are needed to determine CBD's true efficacy for affecting SD severity.
ClinicalTrials.gov NCT03582137; https://clinicaltrials.gov/ct2/show/NCT03582137.
脂溢性皮炎(SD)影响18.6%-59%的帕金森病(PD)患者,最近的研究提供证据表明,口服大麻二酚(CBD)疗法除了可改善PD患者的运动和精神症状外,还能减少皮脂分泌。因此,口服CBD可能有助于改善这两种常见共病的症状。
本研究调查口服CBD疗法是否与PD患者SD严重程度降低相关。
作为一项随机(1:1 CBD与安慰剂对照)、平行、双盲、安慰剂对照试验的一部分,收集面部照片,该试验评估每日每千克2.5毫克口服芝麻溶液富含CBD的大麻提取物(配制为100毫克/毫升CBD和3.3毫克/毫升四氢大麻酚)用于减轻PD患者运动症状的疗效。参与者每天早晨服用1.25毫克/千克,持续4±1天,然后每天服用两次,持续10±4天。评审人员独立分析照片,并根据脂溢性皮炎面积和严重程度指数(SEDASI)量表提供严重程度排名。使用双尾t检验和Pearson χ检验分析基线人口统计学和疾病特征,以及治疗后SEDASI平均值和SD的存在情况。对SEDASI进行纵向回归分析,对SD进行广义估计方程分析。
共有27名参与者接受安慰剂,26名接受CBD治疗16天。两组在基线时SD严重程度均较低,且无治疗效果。接受CBD治疗的患者治疗后与治疗前的风险比为0.69(95%CI 0.41-1.18;P=0.15),而接受安慰剂治疗的患者为1.20(95%CI 0.88-1.65;P=0.26)。两组组内治疗前后的变化均无统计学意义,但二者存在差异(P=0.07),因为CBD组估计有改善,而安慰剂组估计有恶化。
本研究未提供确凿证据表明口服CBD疗法可降低PD患者中SD的发生率。虽然本研究有足够的效力检测主要结局(CBD对PD运动症状的疗效),但检测SD发生率和严重程度变化的次要结局效力不足。CBD可通过多种机制对SD发病机制产生有益影响。需要开展更大规模的研究,纳入疾病严重程度更高的参与者和更长的治疗期,以更好地阐明治疗效果,并确定CBD对影响SD严重程度的真正疗效。
ClinicalTrials.gov NCT03582137;https://clinicaltrials.gov/ct2/show/NCT03582137