Light Sensitivity in Myasthenia Gravis: Clinical Characteristics and Impact on Quality of Life.

IF 3.1 3区 医学 Q2 CLINICAL NEUROLOGY Muscle & Nerve Pub Date : 2025-06-01 Epub Date: 2025-03-05 DOI:10.1002/mus.28386
Eleonora Sabatelli, Luca Bonagura, Silvia Falso, Sofia Marini, Claudia Papi, Lucia Campetella, Michela Myriam De Maio, Raffaele Iorio
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Abstract

Introduction/aims: Light sensitivity is occasionally reported in myasthenia gravis patients, yet its prevalence, clinical characteristics, and impact on disease severity and quality of life remain insufficiently explored. This study aimed to evaluate the frequency, clinical characteristics, and the correlation of light sensitivity with myasthenia gravis severity and quality of life in patients.

Methods: Myasthenia gravis patients consecutively admitted to Fondazione Policlinico Universitario A. Gemelli in Rome between March and October 2023 were considered for the study. A demographically matched group of healthy controls was also included. Patients and controls completed the Visual Light Sensitivity Questionnaire-8 (VLSQ-8). The patient cohort additionally received the Quantitative Myasthenia Gravis (QMG) score, the Myasthenia Gravis Activities of Daily Living (MG-ADL) scale, and the Myasthenia Gravis Quality-of-Life-15 (MG-QoL-15) questionnaires.

Results: A total of 92 patients and 75 healthy controls participated. Light sensitivity was significantly more frequent among patients (36%, 33/92) than among controls (4%, 3/75). Patients with light sensitivity exhibited higher QMG (p < 0.0001), MG-ADL (p < 0.0001), and a decreased quality of life with higher MG-QoL-15 (p = 0.0003) scores than those without light sensitivity. Notably, light sensitivity severity positively correlated with diminished quality of life.

Discussion: These findings suggest that light sensitivity may be a feature of myasthenia gravis, with clinically relevant implications for patient well-being. This underscores the value of screening for and managing light sensitivity in routine myasthenia gravis care. Proactive identification and treatment strategies aimed at light sensitivity may help enhance overall quality of life.

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重症肌无力的光敏感:临床特征及对生活质量的影响。
简介/目的:重症肌无力患者偶有光敏感的报道,但其患病率、临床特征以及对疾病严重程度和生活质量的影响尚未得到充分探讨。本研究旨在评价重症肌无力患者光敏感的发生频率、临床特征及与重症肌无力严重程度和生活质量的相关性。方法:选取2023年3月至10月在罗马杰梅利大学基金会(Fondazione Policlinico Universitario A. Gemelli)连续收治的重症肌无力患者作为研究对象。还包括一组人口统计学匹配的健康对照。患者和对照组分别完成视觉光敏感性问卷-8 (VLSQ-8)。患者队列还接受了重症肌无力定量(QMG)评分、重症肌无力日常生活活动(MG-ADL)量表和重症肌无力生活质量15 (MG-QoL-15)问卷调查。结果:共有92例患者和75名健康对照者参与。患者的光敏感发生率(36%,33/92)明显高于对照组(4%,3/75)。讨论:这些发现提示,光敏性可能是重症肌无力的一个特征,对患者的健康有临床意义。这强调了在常规重症肌无力护理中筛查和管理光敏感性的价值。针对光敏感性的主动识别和治疗策略可能有助于提高整体生活质量。
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来源期刊
Muscle & Nerve
Muscle & Nerve 医学-临床神经学
CiteScore
6.40
自引率
5.90%
发文量
287
审稿时长
3-6 weeks
期刊介绍: Muscle & Nerve is an international and interdisciplinary publication of original contributions, in both health and disease, concerning studies of the muscle, the neuromuscular junction, the peripheral motor, sensory and autonomic neurons, and the central nervous system where the behavior of the peripheral nervous system is clarified. Appearing monthly, Muscle & Nerve publishes clinical studies and clinically relevant research reports in the fields of anatomy, biochemistry, cell biology, electrophysiology and electrodiagnosis, epidemiology, genetics, immunology, pathology, pharmacology, physiology, toxicology, and virology. The Journal welcomes articles and reports on basic clinical electrophysiology and electrodiagnosis. We expedite some papers dealing with timely topics to keep up with the fast-moving pace of science, based on the referees'' recommendation.
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