Neuropsychiatric Systemic Lupus Erythematosus: Pathogenesis, Clinical Aspects and Treatment
暫譯: 神經精神系統性紅斑狼瘡:病因學、臨床面貌與治療
Hirohata, Shunsei
- 出版商: Springer
- 出版日期: 2018-12-28
- 售價: $6,930
- 貴賓價: 9.5 折 $6,584
- 語言: 英文
- 頁數: 200
- 裝訂: Quality Paper - also called trade paper
- ISBN: 3030095037
- ISBN-13: 9783030095031
海外代購書籍(需單獨結帳)
商品描述
Neuropsychiatric manifestation in systemic lupus erythematosus (NPSLE) is one of the most recalcitrant complications of the disease. According to the 1999 ACR nomenclature and case definitions, diffuse psychiatric/neuropsychological syndromes in NPSLE (anxiety disorder, acute confusional state, cognitive dysfunction, mood disorder, psychosis) (diffuse NPSLE) present psychiatric manifestations unlike neurologic syndromes (focal NPSLE) originating from focal CNS lesions, such as cerebrovascular disease, demyelinating syndrome, headache, aseptic meningitis, chorea, seizures and myelopathy. A number of studies have reported that diffuse NPSLE is usually associated with the presence of autoantibodies against neuronal cells in serum as well as in cerebrospinal fluid (CSF). Moreover, IL-6 has been shown to be elevated in CSF of patients with diffuse NPSLE.
Recently, it has been demonstrated that the severity of blood-brain barrier damages plays a crucial role in the development of acute confusional state, the severest form of diffuse NPSLE through the accelerated entry of larger amounts of autoantibodies to NMDA receptor subunit NR2 into the CNS. Since the importance of autoantibodies in the NPSLE has been now evident, such an aggressive treatment, especially B cell depleting therapy, would make sense in that it would reduce the levels of pathogenic autoantibodies, leading to a better prognosis of NPSLE.
As far as we know, no single book specifically dedicated to NPSLE alone has been published as yet. As mentioned above, NPSLE constitutes a vastly expanding field of research with increasing numbers of papers published annually. Therefore, we believe that an effort to collect and critically review these publications is invaluable. Such an effort will provide an important contribution to basic researchers as well as clinicians working in the field of neurology, rheumatology, psychiatry and internal medicine fields.商品描述(中文翻譯)
神經精神表現於系統性紅斑狼瘡(NPSLE)是該疾病最難治療的併發症之一。根據1999年美國風濕病學會(ACR)的命名法和病例定義,NPSLE中的擴散性精神病/神經心理綜合症(如焦慮症、急性混亂狀態、認知功能障礙、情緒障礙、精神病)(擴散性NPSLE)呈現出與源自於局部中樞神經系統病變的神經綜合症(局部NPSLE)不同的精神表現,後者包括腦血管疾病、脫髓鞘綜合症、頭痛、無菌性腦膜炎、舞蹈症、癲癇和脊髓病。許多研究報告指出,擴散性NPSLE通常與血清及腦脊髓液(CSF)中對神經元細胞的自體抗體存在有關。此外,IL-6在擴散性NPSLE患者的CSF中顯示出升高。
最近的研究顯示,血腦屏障損傷的嚴重程度在急性混亂狀態的發展中扮演著關鍵角色,這是擴散性NPSLE最嚴重的形式,因為它加速了大量自體抗體進入中樞神經系統,特別是針對NMDA受體亞基NR2的自體抗體。由於自體抗體在NPSLE中的重要性已經顯而易見,因此這種積極的治療,特別是B細胞耗竭療法,將是合理的,因為它可以降低致病性自體抗體的水平,從而改善NPSLE的預後。
據我們所知,目前尚未出版專門針對NPSLE的單一書籍。如上所述,NPSLE構成了一個不斷擴大的研究領域,每年發表的論文數量不斷增加。因此,我們相信,收集並批判性地回顧這些出版物的努力是非常寶貴的。這樣的努力將為從事神經學、風濕病學、精神病學和內科領域的基礎研究人員和臨床醫生提供重要的貢獻。
作者簡介
Shunsei Hirohata - Shunsei Hirohata graduated from The University of Tokyo School of Medicine in 1980. After the 2-year residency, he joined the Department of Medicine & Physical Therapy, The University of Tokyo. He moved to Teikyo University School of Medicine in 1992 (Associated professor), to Kitasato University School of Medicine in 2006 (Professor), and to Nobuhara Hospital in 2017 (Vice Director). His research topics include neuro-Behcet's disease, neuropsychiatric SLE and bone marrow abnormalities in rheumatoid arthritis. He also works as a visiting professor in Kitasato University School of Medicine.
作者簡介(中文翻譯)
廣畑俊生 - 廣畑俊生於1980年畢業於東京大學醫學院。經過兩年的住院醫師訓練後,他加入東京大學醫學與物理治療系。1992年,他轉至帝京大學醫學院擔任副教授,2006年轉至北里大學醫學院擔任教授,2017年轉至信原醫院擔任副院長。他的研究主題包括神經性貝赫切特病、神經精神性系統性紅斑狼瘡及類風濕性關節炎的骨髓異常。他同時也擔任北里大學醫學院的客座教授。