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首页> 外文期刊>Journal of sleep research >Narcolepsy with cataplexy and comorbid immunopathological diseases
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Narcolepsy with cataplexy and comorbid immunopathological diseases

机译:发作性睡病伴瘫痪症和合并免疫病理疾病

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Evidence suggests that autoimmune diseases tend to co-occur so that patients with an autoimmune disorder are at higher risk of a second autoimmune disease. The association between allergic and autoimmune diseases is also of considerable interest. There are no reports on the association between sporadic or familial narcolepsy with cataplexy and other non-neurological immune-mediated diseases. This study reported on the comorbid immunopathological diseases associated with narcolepsy. One-hundred and fifty six narcoleptic patients with a mean age at diagnosis of 39.1 +/- 17.8 years (range, 6-70 years) were assessed using the clinical history, physical and neurological examinations, sleep questionnaires, neuroimaging and human leucocyte antigen typing. Diagnosis was confirmed by polysomnography followed by a multiple sleep latency test or by measuring hypocretin-1 levels. Patients with immunopathological diseases were matched for gender and age at the onset of narcoleptic symptoms with narcoleptic patients without immunopathological diseases. Twenty-six patients (16.6%; 50% women; one familial, 25 sporadic) had one or more immunopathological diseases associated: autoimmune diseases, such as idiopathic thrombocytopenic purpura, multiple sclerosis, systemic lupus erythematosus, psoriasis, Crohn's disease, ulcerative colitis, autoimmune thyroid disease, Peyronie's disease and idiopathic recurrent facial palsy; other immunopathological diseases, like atopic dermatitis, allergic asthma and allergic rhinitis. Although not significant, the age at diagnosis of narcolepsy was 9.3 years earlier in patients with narcolepsy + immunopathological diseases. The results demonstrate that the prevalence of comorbid immunopathological diseases is high in narcolepsy, and cataplexy is significantly more severe in patients with narcolepsy + immunopathological diseases.
机译:有证据表明,自身免疫性疾病倾向于同时发生,因此患有自身免疫性疾病的患者罹患第二种自身免疫性疾病的风险更高。过敏性疾病和自身免疫性疾病之间的关联也引起了广泛关注。没有关于散发性或家族性发作性睡病与瘫痪和其他非神经性免疫介导疾病之间的关联的报道。这项研究报告了与发作性睡病相关的合并免疫病理疾病。使用临床病史,体格和神经系统检查,睡眠调查表,神经影像学和人类白细胞抗原分型评估了156例平均诊断年龄为39.1 +/- 17.8岁(范围为6-70岁)的麻醉性患者。 。通过多导睡眠监测,随后的多次睡眠潜伏期测试或通过测量hypocretin-1水平来确诊。具有发作性症状的免疫病理性疾病患者的性别和年龄与没有免疫病理性疾病的发作性疾病患者相匹配。 26名患者(16.6%; 50%妇女; 1名家庭成员,25名散发性)患有一种或多种相关的免疫病理疾病:自身免疫性疾病,例如特发性血小板减少性紫癜,多发性硬化症,系统性红斑狼疮,牛皮癣,克罗恩病,溃疡性结肠炎,自身免疫性甲状腺疾病,佩罗尼氏病和特发性复发性面神经麻痹;其他免疫病理疾病,如特应性皮炎,过敏性哮喘和过敏性鼻炎。发作性睡病+免疫病理疾病患者的发作性睡病诊断年龄虽然不显着,但要早9.3岁。结果表明,发作性睡病合并症的免疫病理疾病患病率较高,发作性睡病+免疫病理性疾病患者的瘫痪病严重得多。

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