School of Life and Health Sciences, Aston Brain Centre, Aston University, Birmingham, UK.
Regional Neuromuscular Clinic, Queen Elizabeth Hospital, University Hospitals of Birmingham, Birmingham, UK.
Eur J Neurol. 2018 Jan;25(1):135-141. doi: 10.1111/ene.13459. Epub 2017 Oct 19.
The frequency of pain and cramps is uncertain in anti-myelin associated glycoprotein antibody (anti-MAG) neuropathy. Whether these symptoms may affect function/quality of life is unknown.
A cross-sectional study of the prevalence, correlates and impact of pain, pain subtypes and cramps, their severity, frequency and anatomical distribution was performed for 55 clinically stable patients with anti-MAG neuropathy.
Pain of any type was reported by 80% of subjects. The most common subtype was paraesthesiae and dysaesthesiae (70%). Cramps were reported by >60% of patients, with lower limb cramps in all and upper limb cramps in about 20%. Cramps affected daily activities in >30% of these subjects, sleep in 60%, ability to exercise in >30%. Total pain score correlated with several Short Form 36 health-related quality of life (SF-36 HR-QoL) measures (P < 0.05), with Inflammatory Rasch-built Overall Disability Scale (I-RODS) (P = 0.006) and 10-m timed walk (P = 0.019). An independent association was ascertained with I-RODS (P = 0.002). Different pain subtypes showed multiple associations with SF-36 HR-QoL measures and/or functional scales. Upper limb cramps had multiple SF-36 HR-QoL functional correlates, with an independent association with the Overall Neuropathy Limitation Score (ONLS) (P = 0.004). Cramp severity correlated with ONLS (P = 0.04) and I-RODS (P = 0.028) and inversely with level of physiotherapy input (P = 0.009). Cramp frequency was associated with tremor score (P = 0.004) and multiple SF-36 HR-QoL subsections.
Neuropathic pain and cramps may affect function and quality of life in anti-MAG neuropathy. Optimizing treatments of these symptoms, including by adequate levels of physiotherapy, may be beneficial in affected patients and requires further research.
抗髓鞘相关糖蛋白抗体(anti-MAG)神经病患者的疼痛和痉挛频率不确定。这些症状是否会影响功能/生活质量尚不清楚。
对 55 例临床稳定的抗 MAG 神经病患者进行了疼痛、疼痛亚型和痉挛的患病率、相关性和影响,以及疼痛严重程度、频率和解剖分布的横断面研究。
80%的患者报告有任何类型的疼痛。最常见的亚型是感觉异常和感觉异常(70%)。超过 60%的患者报告有痉挛,所有患者均有下肢痉挛,约 20%的患者有上肢痉挛。超过 30%的这些患者的日常活动受到痉挛的影响,60%的患者受到睡眠的影响,超过 30%的患者受到运动能力的影响。总疼痛评分与多个健康相关生活质量(SF-36 HR-QoL)量表(P<0.05)相关,与炎症 Rasch 构建整体残疾量表(I-RODS)(P=0.006)和 10 米定时行走(P=0.019)相关。与 I-RODS 也有独立关联(P=0.002)。不同的疼痛亚型与 SF-36 HR-QoL 量表和/或功能量表有多种关联。上肢痉挛与多个 SF-36 HR-QoL 功能相关,与总体神经病变限制评分(ONLS)(P=0.004)有独立关联。痉挛严重程度与 ONLS(P=0.04)和 I-RODS(P=0.028)相关,与物理治疗投入水平呈负相关(P=0.009)。痉挛频率与震颤评分(P=0.004)和多个 SF-36 HR-QoL 亚量表相关。
抗 MAG 神经病患者的神经病理性疼痛和痉挛可能会影响功能和生活质量。优化这些症状的治疗,包括通过足够水平的物理治疗,可能对受影响的患者有益,需要进一步的研究。