Vlad Benjamin, Wang Yujie, Newsome Scott D, Balint Bettina
Department of Neurology, University Hospital Zurich, 8091 Zurich, Switzerland.
Department of Neurology, University of Washington, Seattle, WA 98195, USA.
Biomedicines. 2023 Sep 10;11(9):2500. doi: 10.3390/biomedicines11092500.
Stiff person spectrum disorders (SPSD) are paradigm autoimmune movement disorders characterized by stiffness, spasms and hyperekplexia. Though rare, SPSD represent a not-to-miss diagnosis because of the associated disease burden and treatment implications. After decades as an enigmatic orphan disease, major advances in our understanding of the evolving spectrum of diseases have been made along with the identification of multiple associated autoantibodies. However, the most important recent developments relate to the recognition of a wider affection, beyond the classic core motor symptoms, and to further insights into immunomodulatory and symptomatic therapies. In this review, we summarize the recent literature on the clinical and paraclinical spectrum, current pathophysiological understanding, as well as current and possibly future therapeutic strategies.
僵人谱系障碍(SPSD)是典型的自身免疫性运动障碍,其特征为僵硬、痉挛和惊吓反应亢进。尽管罕见,但由于相关的疾病负担和治疗意义,SPSD是一种不容错过的诊断。在作为一种神秘的罕见病存在数十年后,随着多种相关自身抗体的鉴定,我们对这一不断演变的疾病谱系的认识取得了重大进展。然而,最近最重要的进展涉及到认识到除了经典的核心运动症状外,还有更广泛的影响,并对免疫调节和对症治疗有了进一步的见解。在这篇综述中,我们总结了关于临床和副临床谱系、当前病理生理学认识以及当前和可能的未来治疗策略的最新文献。