Unlocking the Mechanisms of Hidradenitis Suppurativa: Inflammation and miRNA Insights.

IF 1.9 4区 医学 Q3 DERMATOLOGY Clinical, Cosmetic and Investigational Dermatology Pub Date : 2024-12-11 eCollection Date: 2024-01-01 DOI:10.2147/CCID.S483871
Emily Ames, Maggie Sanders, Marley Jacobs, Thomas A Vida
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Abstract

Inflammatory skin diseases impose a significant burden on patients and healthcare systems worldwide. Among these, hidradenitis suppurativa (HS) is particularly notable for its chronic and recurrent nature. Recurrent nodules, abscesses, and scarring in apocrine gland-rich areas characterize the disease, including the groin, axillae, and perianal regions. Despite its considerable physical and psychological impact, the precise mechanisms driving HS remain elusive. Recent advancements in understanding the inflammatory processes involved in HS have highlighted the TNF-alpha, IL-1β, and IL-17/IL-23 pathways, which play crucial roles in initiating and perpetuating the disease. Moreover, specific microRNAs (miRNAs), such as miR-24-1-5p, miR146a-5p, mirR-26a-5p, miR-206, miR-338-3p, and miR-338-5p, are involved in these inflammatory processes. Dysregulation of these miRNAs contributes to aberrant cytokine expression and persistent inflammation, foreseeably exacerbating HS disease progression. This narrative review hypothesizes that miRNA dysregulation triggers aberrant expression in specific inflammatory pathways, contributing to HS's clinical manifestations and progression. We explore the implicated miRNAs' potential as biomarkers for earlier disease detection and as novel therapeutic targets. Identifying miRNA dysregulation offers new opportunities for earlier and more accurate diagnosis, potentially allowing clinicians to intervene before severe disease manifestations occur. Furthermore, therapeutic strategies to modulate miRNA expression could target the inflammatory pathways driving HS, leading to more personalized and effective treatments. This review also discusses future research directions to enhance the clinical management of HS. A better understanding of miRNA involvement in HS offers new avenues for research and management, ultimately improving patient outcomes and quality of life.

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炎症性皮肤病给全世界的患者和医疗系统带来了沉重的负担。其中,化脓性扁桃体炎(HS)因其慢性和复发性而尤为突出。在腹股沟、腋窝和肛周等腺体分泌丰富的部位反复出现结节、脓肿和瘢痕是该病的特征。尽管 HS 对患者的生理和心理造成了巨大的影响,但其确切的发病机制仍然难以捉摸。最近在了解 HS 所涉及的炎症过程方面取得的进展突显了 TNF-α、IL-1β 和 IL-17/IL-23 通路,这些通路在疾病的诱发和延续中发挥着至关重要的作用。此外,特定的微小核糖核酸(miRNA),如 miR-24-1-5p、miR146a-5p、mirR-26a-5p、miR-206、miR-338-3p 和 miR-338-5p 也参与了这些炎症过程。这些 miRNA 的失调会导致细胞因子表达异常和炎症持续存在,从而可预见地加剧 HS 的病情发展。本综述假设,miRNA 失调会引发特定炎症通路的异常表达,从而导致 HS 的临床表现和进展。我们探讨了受影响的 miRNA 作为生物标记物的潜力,以便更早地发现疾病并作为新的治疗靶点。识别 miRNA 失调为更早和更准确的诊断提供了新的机会,有可能让临床医生在出现严重疾病表现之前进行干预。此外,调控 miRNA 表达的治疗策略可以靶向驱动 HS 的炎症通路,从而实现更个性化、更有效的治疗。本综述还讨论了加强 HS 临床治疗的未来研究方向。更好地了解 miRNA 在 HS 中的参与为研究和管理提供了新途径,最终可改善患者的预后和生活质量。
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来源期刊
CiteScore
2.80
自引率
4.30%
发文量
353
审稿时长
16 weeks
期刊介绍: Clinical, Cosmetic and Investigational Dermatology is an international, peer-reviewed, open access journal that focuses on the latest clinical and experimental research in all aspects of skin disease and cosmetic interventions. Normal and pathological processes in skin development and aging, their modification and treatment, as well as basic research into histology of dermal and dermal structures that provide clinical insights and potential treatment options are key topics for the journal. Patient satisfaction, preference, quality of life, compliance, persistence and their role in developing new management options to optimize outcomes for target conditions constitute major areas of interest. The journal is characterized by the rapid reporting of clinical studies, reviews and original research in skin research and skin care. All areas of dermatology will be covered; contributions will be welcomed from all clinicians and basic science researchers globally.
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