Mitochondrial Dysfunctions in Patients with Migraine

R. Alloush, M. Haroun, A. Shalash, H. El-Fawal, M. Hamdy
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引用次数: 1

Abstract

Study Objectives: Migraine is a complex neurovascular disease and is believed to be due to a mixture of genetic and environmental factors. Study design: This was a cross-sectional observational prospective hospital based study conducted on 100 participants. They were divided into two groups; Group A: 50 migrainous patients according to the criteria of the International Classification of Headache Disorders and Group B: 50 healthy subjects both groups were age and sex matched. All subjects underwent a full neurological and psychiatric examination. Full headache evaluation sheet used in headache outpatient clinic in Ain Shams University Hospitals and HIT-6? Headache Impact Test was used. Assay of serum level of N-acetyl-aspartate (NAA) as mitochondrial function marker was done. Results: There was no significant difference between both groups regarding gender, age or age group, marital state, education, residence and special habits. However, there was a statistical significant difference as regards family history of migraine more in patient group. In this study, serum NAA levels in migraine patients were significantly lower than in healthy controls. Decreased NAA level is generally believed to be a sign of reduced neuronal and glial mitochondrial function. Also, migraine with aura patients showed lower NAA levels when compared to migraine without aura subtypes. However, there was no significant correlation was found between NAA serum levels, and gender, age at onset, age group, type of aura, duration of the illness, type of onset of pain, frequent site of pain, time to max severity, severity of attack, and daily functions (social life, work, psychological wellbeing, sleep and cognition). Conclusions: Findings of this study indicate that NAA in serum may be a marker for neuronal dysfunction predisposing to migraine, probably related to the reduced mitochondria function.
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偏头痛患者的线粒体功能障碍
研究目的:偏头痛是一种复杂的神经血管疾病,被认为是遗传和环境因素共同作用的结果。研究设计:这是一项以医院为基础的横断面观察性前瞻性研究,共有100名参与者。他们被分为两组;A组:50例符合国际头痛疾病分类标准的偏头痛患者;B组:50例年龄、性别匹配的健康受试者。所有受试者都接受了全面的神经和精神检查。在艾因沙姆斯大学附属医院头痛门诊使用的完整头痛评估表和HIT-6?采用头痛冲击试验。测定线粒体功能标志物n -乙酰-天冬氨酸(NAA)的血清水平。结果:两组在性别、年龄或年龄组、婚姻状况、教育程度、居住地、特殊习惯等方面无显著差异。然而,在偏头痛家族史方面,患者组有统计学意义的差异。在这项研究中,偏头痛患者的血清NAA水平明显低于健康对照组。NAA水平降低通常被认为是神经元和胶质线粒体功能降低的标志。此外,与无先兆偏头痛亚型相比,有先兆偏头痛患者的NAA水平较低。然而,NAA血清水平与性别、发病年龄、年龄组、先兆类型、病程、疼痛发作类型、疼痛频繁部位、最大发作时间、发作严重程度和日常功能(社会生活、工作、心理健康、睡眠和认知)之间无显著相关性。结论:本研究结果提示血清NAA可能是偏头痛神经功能障碍的标志物,可能与线粒体功能降低有关。
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