Relative frequency of primary headaches in patients with neuromyelitis optica spectrum disorder: A cross-sectional study.

IF 0.5 Q4 CLINICAL NEUROLOGY
Mohammadreza Etemadifar, Masoud Etemadifar, Seyyed Ali Alaei, Mahdi Norouzi
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Abstract

Background: Neuromyelitis optica spectrum disorder (NMOSD) is a rare autoimmune inflammatory disease predominantly affecting the central nervous system (CNS). Headaches, although common in patients with multiple sclerosis (MS), have been less studied in NMOSD. This study aimed to investigate the prevalence, characteristics, and associated symptoms of headaches in patients with NMOSD. Methods: This cross-sectional study included 120 patients with NMOSD recruited from MS clinics in Isfahan City, Iran, between 2023 and 2024. Patients were assessed for headache prevalence and characteristics. An expert neurologist conducted examinations to exclude secondary causes of headaches and classified headache types according to the International Classification of Headache Disorders (ICHD-3). Results: Eighteen patients (15%) reported headaches, all of whom were women. The average age of these patients was 41.27 ± 11.33 years, and the average onset age of NMOSD was 34.60 ± 12.12 years. Of the 18 patients, 14 were diagnosed with migraine and 4 with tension headaches. Patients with migraine reported more severe pain (severity score: 6.00 ± 1.42) than those with tension headaches (4.20 ± 1.35). Headache onset was equally likely to occur before or after an NMOSD diagnosis. Significant associated symptoms included photophobia, phonophobia, and nausea in patients with migraine, with a substantial impact on occupational disability reported by 57% of migraine sufferers and 50% of tension headache sufferers. Conclusion: Headaches, particularly migraines, are prevalent in patients with NMOSD and significantly impact their quality of life (QOL) and occupational functioning. These findings emphasize the need for clinicians to recognize headache patterns in NMOSD for accurate diagnosis and effective management. Further longitudinal studies are warranted to explore causal mechanisms and develop targeted interventions.

视神经脊髓炎谱系障碍患者原发性头痛的相对频率:一项横断面研究。
背景:视神经脊髓炎谱系障碍(NMOSD)是一种罕见的自身免疫性炎症性疾病,主要影响中枢神经系统(CNS)。头痛虽然在多发性硬化症(MS)患者中很常见,但对NMOSD的研究较少。本研究旨在调查NMOSD患者头痛的患病率、特征和相关症状。方法:这项横断面研究包括2023年至2024年间从伊朗伊斯法罕市多发性硬化症诊所招募的120例NMOSD患者。评估患者头痛的患病率和特征。一位神经科专家进行了检查,以排除头痛的继发性原因,并根据国际头痛疾病分类(ICHD-3)对头痛类型进行了分类。结果:18例患者(15%)报告头痛,均为女性。患者平均年龄41.27±11.33岁,NMOSD平均发病年龄34.60±12.12岁。在这18名患者中,14人被诊断为偏头痛,4人被诊断为紧张性头痛。偏头痛患者报告的疼痛严重程度(严重程度评分:6.00±1.42)高于紧张性头痛患者(4.20±1.35)。在诊断为NMOSD之前或之后,头痛发作的可能性是一样的。显著的相关症状包括偏头痛患者的畏光、恐音和恶心,57%的偏头痛患者和50%的紧张性头痛患者报告了对职业残疾的重大影响。结论:头痛,特别是偏头痛,在NMOSD患者中普遍存在,并显著影响其生活质量(QOL)和职业功能。这些发现强调临床医生需要认识NMOSD的头痛模式,以便准确诊断和有效治疗。进一步的纵向研究是必要的,以探索因果机制和制定有针对性的干预措施。
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来源期刊
Current Journal of Neurology
Current Journal of Neurology CLINICAL NEUROLOGY-
CiteScore
0.80
自引率
14.30%
发文量
30
审稿时长
12 weeks
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