Kumawat Vijay, Tripathi Parmatma Prasad, M Netravathi, Mahadevan Anita, Vittal Anchan Vidyashree
Transfusion Medicine and Haematology, National Institute of Mental Health and Neurosciences, Bengaluru, India.
Transfusion Medicine and Haematology, National Institute of Mental Health and Neurosciences, Bengaluru, India.
Hematol Transfus Cell Ther. 2024 Oct-Dec;46(4):443-449. doi: 10.1016/j.htct.2023.11.014. Epub 2024 Feb 1.
The stiff person syndrome (SPS) is a rare and disabling neurological disorder characterized by muscle stiffness, painful spasms and rigidity involving the proximal and axial limb muscles, with an estimated incidence of 1 case per million per year. The first line of treatment for symptomatic management includes gamma-aminobutyric acid (GABA)ergic agonists, benzodiazepines and baclofen. The therapeutic plasma exchange (TPE), alone or as an adjuvant to other forms of immunomodulation, has been used as a therapeutic option, particularly in refractory cases.
An observational study was performed to review SPS patient symptoms, comorbidities, electromyography (EMG) studies and treatment, identifying autoantibodies, therapeutic plasma exchange (TPE) procedural details and clinical response.
Five patients (4 male and one female) were treated with TPE during the study period as adjuvant therapy. The average age was 47 years (range 34 - 61 years), and anti-glutamic acid decarboxylase 65-kilodalton isoform (anti-GAD65) antibodies were positive in 80 % (4/5) of the patient population. All patients received immunosuppressive drugs along with TPE. Four patients received TPE during the first admission and one received it during the third hospital admission. All patients showed good improvement immediately after TPE, but it was not a sustainable effect.
TPE may be helpful as adjuvant therapy for SPS patients to provide relief from clinical symptoms.
僵人综合征(SPS)是一种罕见的致残性神经系统疾病,其特征为肌肉僵硬、疼痛性痉挛以及近端和躯干肢体肌肉的强直,估计年发病率为百万分之一。症状管理的一线治疗包括γ-氨基丁酸(GABA)能激动剂、苯二氮䓬类药物和巴氯芬。治疗性血浆置换(TPE)单独使用或作为其他免疫调节形式的辅助手段,已被用作一种治疗选择,尤其是在难治性病例中。
进行了一项观察性研究,以回顾SPS患者的症状、合并症、肌电图(EMG)检查及治疗情况,确定自身抗体、治疗性血浆置换(TPE)的操作细节及临床反应。
在研究期间,5例患者(4例男性和1例女性)接受了TPE辅助治疗。平均年龄为47岁(范围34 - 61岁),80%(4/5)的患者抗谷氨酸脱羧酶65千道尔顿亚型(抗GAD65)抗体呈阳性。所有患者在接受TPE的同时还接受了免疫抑制药物治疗。4例患者在首次入院时接受了TPE,1例在第三次住院时接受了TPE。所有患者在TPE后立即显示出良好的改善,但效果并不持久。
TPE作为SPS患者的辅助治疗可能有助于缓解临床症状。