Department of Medicine, College of Medicine, Kyung Hee University, Seoul 02447, Republic of Korea.
KM Science Research Division, Korea Institute of Oriental Medicine, Daejeon 34054, Republic of Korea.
Int J Mol Sci. 2023 Jul 20;24(14):11711. doi: 10.3390/ijms241411711.
Alopecia areata (AA) is an autoimmune dermatological disease with multifactorial etiology and is characterized by reversible hair loss in patches. AA may be closely related to emotional stress and influenced by psychological factors as part of its pathophysiology; however, its etiology remains predominantly unknown. This review aimed to elucidate the association between AA occurrence and the neuropeptide substance P (SP) and corticotropin-releasing hormone (CRH), which are secreted during emotional stress, and have been understood to initiate and advance the etiopathogenesis of AA. Therefore, this review aimed to explain how SP and CRH initiate and contribute to the etiopathogenesis of AA. To assess the etiopathogenesis of AA, we conducted a literature search on PubMed and ClinicalTrials.gov. Overall, several authors described interactions between the hair follicles (HFs) and the stress-associated signaling substances, including SP and CRH, in the etiology of AA; this was attributed to the understanding in that AA can occur without the loss of HFs, similar to that observed in hereditary hair loss with age. Most studies demonstrated that the collapse of "immune privilege" plays a crucial role in the development and exacerbation of the AA; nonetheless, a few studies indicated that substances unrelated to autoimmunity may also cause apoptosis in keratocytes, leading to the development of AA. We investigated both the autoimmune and apoptotic pathways within the etiology of AA and assessed the potential interactions between the key substances of both pathways to evaluate potential therapeutic targets for the treatment of AA. Clinical trials of marketed/unreviewed intervention drugs for AA were also reviewed to determine their corresponding target pathways.
斑秃(AA)是一种具有多因素病因的自身免疫性皮肤病,其特征是斑块状可逆性脱发。AA 可能与情绪压力密切相关,并受心理因素的影响,这是其病理生理学的一部分;然而,其病因主要仍不清楚。本综述旨在阐明 AA 发病与神经肽 P 物质(SP)和促肾上腺皮质释放激素(CRH)之间的关系,这两种物质在情绪压力下分泌,被认为是 AA 发病机制的启动和进展的原因。因此,本综述旨在解释 SP 和 CRH 如何引发和促进 AA 的发病机制。为了评估 AA 的发病机制,我们在 PubMed 和 ClinicalTrials.gov 上进行了文献检索。总的来说,几位作者描述了毛囊(HFs)与包括 SP 和 CRH 在内的与应激相关的信号物质之间的相互作用在 AA 的发病机制中的作用;这归因于这样一种理解,即 AA 可以在不失去 HFs 的情况下发生,类似于遗传性脱发随年龄增长而发生的情况。大多数研究表明,“免疫豁免”的崩溃在 AA 的发展和恶化中起着关键作用;尽管如此,一些研究表明,与自身免疫无关的物质也可能导致角朊细胞凋亡,导致 AA 的发生。我们研究了 AA 发病机制中的自身免疫和凋亡途径,并评估了两条途径的关键物质之间的潜在相互作用,以评估治疗 AA 的潜在治疗靶点。还回顾了 AA 的市售/未审查干预药物的临床试验,以确定其相应的靶途径。