Dermatomyositis: Practical Guidance and Unmet Needs.

IF 6.2 Q1 IMMUNOLOGY
ImmunoTargets and Therapy Pub Date : 2024-03-06 eCollection Date: 2024-01-01 DOI:10.2147/ITT.S381472
Lydia Cassard, Noelle Seraly, Maureen Riegert, Aditi Patel, Anthony P Fernandez
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引用次数: 0

Abstract

Dermatomyositis is a heterogeneous idiopathic inflammatory myopathy associated with various cutaneous manifestations and variable presence of myositis, interstitial lung disease, and other visceral organ involvement. An accurate diagnosis of dermatomyositis requires correlating clinical examination findings with serological and histological findings. Familiarity with pathognomonic and common cutaneous manifestations of dermatomyositis, which are highlighted here, can be especially helpful in making an accurate diagnosis. Additionally, evaluating patients for presence of myositis-specific autoantibodies can further support or refute a dermatomyositis diagnosis. When present, myositis-specific autoantibodies can also help guide workups for various dermatomyositis-associated manifestations, as each is associated with relatively distinct clinical characteristics. Evaluating patients for various systemic manifestations often relies on expert opinion recommendations; however, societal guideline statements concerning the evaluation of some manifestations have recently been described. Although malignancy-associated dermatomyositis is a well-accepted subtype, there is limited evidence to support extensive malignancy screening has a favorable benefit-risk ratio in most dermatomyositis patients. However, recent research has uncovered novel associations between dermatomyositis and malignancy, suggesting the possibility of identifying high-risk subsets of dermatomyositis patients in whom malignancy screening may have a high value. Treatment for dermatomyositis has remained largely unchanged over the past several decades. Although many dermatomyositis patients can be effectively treated with current options, either as monotherapy or with combination regimens, there is a need for more targeted and effective DM therapies, in general, and for MDA5(+) dermatomyositis-associated rapidly progressive interstitial lung disease. Fortunately, significant current and emerging research activities evaluating various novel medications for dermatomyositis provide hope for exciting future advances in patients with this intriguing immune-mediated disease.

皮肌炎:实用指南和未满足的需求。
皮肌炎是一种异质性的特发性炎症性肌病,伴有各种皮肤表现和不同程度的肌炎、间质性肺病及其他内脏器官受累。要准确诊断皮肌炎,需要将临床检查结果与血清学和组织学检查结果联系起来。熟悉皮肌炎的病理特征和常见皮肤表现(在此重点介绍)尤其有助于做出准确诊断。此外,评估患者是否存在肌炎特异性自身抗体可进一步支持或反驳皮肌炎诊断。如果存在肌炎特异性自身抗体,还有助于指导各种皮肌炎相关表现的检查,因为每种表现都有相对不同的临床特征。对患者各种系统性表现的评估通常依赖于专家的意见建议;不过,最近也出现了一些关于评估某些表现的社会指南声明。虽然恶性肿瘤相关皮肌炎是一种公认的亚型,但目前支持广泛的恶性肿瘤筛查对大多数皮肌炎患者具有有利的收益风险比的证据有限。不过,最近的研究发现了皮肌炎与恶性肿瘤之间的新关联,这表明有可能识别出皮肌炎患者中的高风险亚群,对这些患者进行恶性肿瘤筛查可能具有很高的价值。过去几十年来,皮肌炎的治疗方法基本没有变化。尽管许多皮肌炎患者可以通过目前的单药治疗或联合治疗方案得到有效治疗,但总体而言,仍需要更具针对性和更有效的皮肌炎疗法,以及针对与MDA5(+)皮肌炎相关的快速进展性间质性肺病的疗法。幸运的是,目前对皮肌炎的各种新型药物进行评估的重要研究活动和新兴研究活动为这一引人关注的免疫介导疾病患者的治疗带来了令人振奋的希望。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
16.50
自引率
0.00%
发文量
7
审稿时长
16 weeks
期刊介绍: Immuno Targets and Therapy is an international, peer-reviewed open access journal focusing on the immunological basis of diseases, potential targets for immune based therapy and treatment protocols employed to improve patient management. Basic immunology and physiology of the immune system in health, and disease will be also covered.In addition, the journal will focus on the impact of management programs and new therapeutic agents and protocols on patient perspectives such as quality of life, adherence and satisfaction.
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