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视神经脊髓炎和视神经脊髓炎谱系障碍:自然史与长期预后,来自印度的经验

Neuromyelitis optica and neuromyelitis optica spectrum disorder: Natural history and long-term outcome, an Indian experience.

作者信息

Jagtap Sujit Abajirao, Mandliya Alok, Sarada C, Nair M D

机构信息

Department of Neurology, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Trivandrum, Kerala, India.

出版信息

J Neurosci Rural Pract. 2015 Jul-Sep;6(3):331-5. doi: 10.4103/0976-3147.158755.

Abstract

BACKGROUND

Neuromyelitis optica (NMO) has evolved from devic's classical description to a broader disease spectrum, from monophasic illness to a polyphasic illness with multiple recurrences, disease confined to optic nerve and spinal cord to now brain stem, cerebrum and even endocrinopathy due to hypothalamic involvement.

OBJECTIVES

To report, the epidemiological characteristics, clinical presentations, recurrence rate, treatment and response to therapy in 26 patients with NMO and NMO spectrum disorder among the Indian population.

METHODS

We performed observational, retrospective analysis of our prospectively maintained data base of patients with NMO, longitudinally extensive transverse myelitis during the period of January 2003-December 2012 who satisfied the national multiple sclerosis society (NMSS) task force criteria for diagnosis of NMO and NMO spectrum disorder.

RESULTS

There were 26 patients (female: male, 21:5), the mean age of onset of symptom was 27 years (range 9-58, standard deviation = 12). Twenty-one patients (80%) fulfilled NMSS criteria for NMO while rest 5 patients (20%) were considered as NMO spectrum disorder. Seven patients (27%) had a monophasic illness, 19 patients (73%) had a polyphasic illness with recurrences. The Median recurrence rate was 4/patient in the polyphasic group. 13 (50%) patient were tested for aquaporin 4 antibody, 8 (61%) were positive while 5 patients (39%) were negative. All patients received intravenous methyl prednisolone, 9 patients (35%) required further treatment for acute illness in view of unresponsiveness to steroids. Thirteen patients (50%) received disease-modifying agents for recurrences. Mean duration of follow-up was 5 years. All patients had a good outcome (modified Rankin scale, <3) except one who had poor visual recovery.

CONCLUSION

Neuromyelitis optica/NMO spectrum disorder is demyelinating disorder with female predominance, polyphasic course, myelitis being most common event although brain stem involvement is not uncommon with NMO antibody positivity in 60% patients, confirms the literature data.

摘要

背景

视神经脊髓炎(NMO)已从德维克的经典描述发展为更广泛的疾病谱,从单相疾病发展为具有多次复发的多相疾病,疾病范围从局限于视神经和脊髓扩展到现在的脑干、大脑,甚至因下丘脑受累而出现内分泌病。

目的

报告26例印度人群中视神经脊髓炎及视神经脊髓炎谱系障碍患者的流行病学特征、临床表现、复发率、治疗及治疗反应。

方法

我们对2003年1月至2012年12月期间前瞻性维护的视神经脊髓炎患者数据库进行了观察性回顾分析,这些患者患有纵向广泛横贯性脊髓炎,符合美国国家多发性硬化症协会(NMSS)工作组对视神经脊髓炎及视神经脊髓炎谱系障碍的诊断标准。

结果

共有26例患者(女性∶男性为21∶5),症状出现的平均年龄为27岁(范围9 - 58岁,标准差 = 12)。21例患者(80%)符合NMSS的视神经脊髓炎标准,其余5例患者(20%)被视为视神经脊髓炎谱系障碍。7例患者(27%)为单相疾病,19例患者(73%)为有复发的多相疾病。多相组患者的中位复发率为每人4次。13例(50%)患者检测了水通道蛋白4抗体,8例(61%)为阳性,5例(39%)为阴性。所有患者均接受了静脉注射甲泼尼龙治疗,9例(35%)患者因对类固醇无反应而需要针对急性疾病进行进一步治疗。13例(50%)患者因复发接受了疾病修正治疗。平均随访时间为5年。除1例视力恢复不佳外,所有患者预后良好(改良Rankin量表评分<3)。

结论

视神经脊髓炎/视神经脊髓炎谱系障碍是一种脱髓鞘疾病,以女性为主,呈多相病程,脊髓炎是最常见的事件,尽管脑干受累并不少见,60%的患者NMO抗体呈阳性,这证实了文献数据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b1a/4481785/f64ecf64f892/JNRP-6-331-g003.jpg

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