INTRODUCTION
Atopic dermatitis (AD) is a chronic, multifactorial skin disorder characterized by dry skin and pruritus. In AD patients, pruritus can range from mildly irritating and distressful to completely disabling, resulting in a negative impact on patients’ quality of life.1 Application of topical emollients to help restore the skin barrier has been a cornerstone of treatment, but often results in limited clinical benefits.2 While topical corticosteroids are effective, adverse effects such as skin atrophy and dyspigmentation are associated with prolonged application, which limits their use.3 Recently, the role of the nervous system has become recognized in the pathogenesis of AD.4 Specifically, dysregulation of neuro-cutaneous physiology, at the skin-nerve interface level appears to be central in the pathogenesis of itch.3
Studies on atopic skin lesions have demonstrated an increase in nerve density and an upregulation of inflammatory neuropeptides such as substance P.5 The understanding of this mechanism has led to the use of off-label neuromodulators such as topical capsaicin and naltrexone. Both these therapies have shown to improve itch in AD patients.6
Another class of neuromodulators that has been explored is palmitoylethanolamide (PEA), which is considered an endocannabinoid.7 Several studies3,8-11 have demonstrated efficacy of PEA in the treatment of various dermatologic disorders including AD. In a study by Eberlein et al, it was demonstrated that emollient containing PEA reduced pruritus, erythema, and excoriation by 58.6%.12 Similar to endocannabinoids,
Studies on atopic skin lesions have demonstrated an increase in nerve density and an upregulation of inflammatory neuropeptides such as substance P.5 The understanding of this mechanism has led to the use of off-label neuromodulators such as topical capsaicin and naltrexone. Both these therapies have shown to improve itch in AD patients.6
Another class of neuromodulators that has been explored is palmitoylethanolamide (PEA), which is considered an endocannabinoid.7 Several studies3,8-11 have demonstrated efficacy of PEA in the treatment of various dermatologic disorders including AD. In a study by Eberlein et al, it was demonstrated that emollient containing PEA reduced pruritus, erythema, and excoriation by 58.6%.12 Similar to endocannabinoids,