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Patients with psoriasis have a higher risk of schizophrenia: A systematic review and meta-analysis of observational studies.银屑病患者患精神分裂症的风险更高:一项观察性研究的系统评价和荟萃分析。
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本文引用的文献

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Alterations in Cerebrospinal Fluid in Patients with Bipolar Syndromes.双相综合征患者脑脊液的改变。
Front Psychiatry. 2016 Dec 8;7:194. doi: 10.3389/fpsyt.2016.00194. eCollection 2016.
2
Prevalence and clinical characteristics of serum neuronal cell surface antibodies in first-episode psychosis: a case-control study.首发精神病血清神经元细胞表面抗体的患病率及临床特征:一项病例对照研究
Lancet Psychiatry. 2017 Jan;4(1):42-48. doi: 10.1016/S2215-0366(16)30375-3. Epub 2016 Dec 8.
3
How neuroinflammation contributes to neurodegeneration.神经炎症如何导致神经退行性变。
Science. 2016 Aug 19;353(6301):777-83. doi: 10.1126/science.aag2590.
4
Maternal immune activation: Implications for neuropsychiatric disorders.母体免疫激活:对神经精神疾病的影响。
Science. 2016 Aug 19;353(6301):772-7. doi: 10.1126/science.aag3194.
5
Celecoxib Adjunctive Treatment to Antipsychotics in Schizophrenia: A Review of Randomized Clinical Add-On Trials.塞来昔布辅助抗精神病药物治疗精神分裂症:随机临床附加试验综述
Mediators Inflamm. 2016;2016:3476240. doi: 10.1155/2016/3476240. Epub 2016 Jul 25.
6
All naturally occurring autoantibodies against the NMDA receptor subunit NR1 have pathogenic potential irrespective of epitope and immunoglobulin class.所有针对 NMDA 受体亚单位 NR1 的天然自身抗体无论表位和免疫球蛋白类别如何都具有致病潜力。
Mol Psychiatry. 2017 Dec;22(12):1776-1784. doi: 10.1038/mp.2016.125. Epub 2016 Aug 9.
7
Slowly progressive LGI1 encephalitis with isolated late-onset cognitive dysfunction: a treatable mimic of Alzheimer's disease.伴有孤立性迟发性认知功能障碍的缓慢进展性LGI1脑炎:一种可治疗的阿尔茨海默病模仿症。
Eur J Neurol. 2016 May;23(5):e28-9. doi: 10.1111/ene.12939.
8
Evidence of cerebrospinal fluid abnormalities in patients with depressive syndromes.抑郁综合征患者脑脊液异常的证据。
J Affect Disord. 2016 Jul 1;198:178-84. doi: 10.1016/j.jad.2016.03.030. Epub 2016 Mar 10.
9
An open-label, pilot trial of adjunctive tocilizumab in schizophrenia.一项关于托珠单抗辅助治疗精神分裂症的开放标签试点试验。
J Clin Psychiatry. 2016 Feb;77(2):275-6. doi: 10.4088/JCP.15l09920.
10
The effect of antipsychotic drugs on nonspecific inflammation markers in the first episode of schizophrenia.抗精神病药物对精神分裂症首发患者非特异性炎症标志物的影响。
Vojnosanit Pregl. 2015 Dec;72(12):1085-92. doi: 10.2298/vsp140526016s.

精神分裂症轻度脑炎假说的伦理意义

Ethical Implications of the Mild Encephalitis Hypothesis of Schizophrenia.

作者信息

Riedmüller Rita, Müller Sabine

机构信息

Mind and Brain Research, Department of Psychiatry and Psychotherapy, CCM, Charité - Universitätsmedizin Berlin , Berlin , Germany.

出版信息

Front Psychiatry. 2017 Mar 13;8:38. doi: 10.3389/fpsyt.2017.00038. eCollection 2017.

DOI:10.3389/fpsyt.2017.00038
PMID:28348532
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5346578/
Abstract

Schizophrenia is a serious mental disease with a high mortality rate and severe social consequences. Due to insufficient knowledge about its etiopathogenesis, curative treatments are not available. One of the most promising new research concepts is the mild encephalitis hypothesis of schizophrenia, developed mainly by Karl Bechter and Norbert Müller. According to this hypothesis, a significant subgroup of schizophrenia patients suffer from a mild, but chronic, form of encephalitis with markedly different etiologies ranging from viral infections, traumas to autoimmune diseases. This inflammatory process is thought to occur in the beginning or during the course of the disease. In this article, we investigate the consequences of the mild encephalitis hypothesis of schizophrenia for the scientific community, and evaluate these consequences ethically. The mild encephalitis hypothesis implies that schizophrenia would no longer be considered an incurable psychiatric disorder. Instead, it would be considered a chronic, but treatable, neurological disease. This paradigm shift would doubtlessly have significant consequences: (1) major reforms would be necessary in the theoretical conceptualization of schizophrenia, which would challenge the psychiatric diagnostic systems, Diagnostic and Statistical Manual of Mental Disorders version 5 and ICD-10. (2) Psychotic patients should be treated in interdisciplinary teams, optimally in neuropsychiatric units; additionally, specialists for endocrinology, diabetology, and cardiology should be consulted for the frequently occuring somatic comorbidities. (3) Current diagnostic procedures and (4) therapies would have to be modified significantly. (5) There might be repercussions for the pharmaceutical industry as well: first, because old drugs with expired patent protection could partly replace expensive drugs and, second, because there would be a demand for the development of new anti-inflammatory drugs. (6) Legal evaluation of compulsory treatment orders might have to be reconsidered in light of causal therapies; leading to increased legal approval and reduced need for compulsory treatment orders due to better patient compliance. (7) The social inclusion of patients might improve, if treatment became more effective regarding cognitive and social functioning. (8) The stigmatization of patients and their relatives might decrease.

摘要

精神分裂症是一种严重的精神疾病,死亡率高且会造成严重的社会后果。由于对其病因发病机制的了解不足,目前尚无治愈性治疗方法。最有前景的新研究概念之一是精神分裂症的轻度脑炎假说,主要由卡尔·贝希特和诺伯特·米勒提出。根据这一假说,相当一部分精神分裂症患者患有轻度但慢性的脑炎,其病因明显不同,包括病毒感染、创伤和自身免疫性疾病。这种炎症过程被认为发生在疾病的初期或病程中。在本文中,我们研究了精神分裂症轻度脑炎假说对科学界的影响,并从伦理角度对这些影响进行了评估。轻度脑炎假说意味着精神分裂症将不再被视为一种无法治愈的精神障碍。相反,它将被视为一种慢性但可治疗的神经疾病。这种范式转变无疑会产生重大影响:(1)精神分裂症的理论概念化需要进行重大改革,这将挑战精神疾病诊断系统《精神疾病诊断与统计手册》第5版和ICD - 10。(2)精神病患者应由跨学科团队治疗,最好是在神经精神科病房;此外,对于频繁出现的躯体合并症,应咨询内分泌科、糖尿病科和心脏病科专家。(3)当前的诊断程序和(4)治疗方法必须进行重大修改。(5)这可能也会对制药行业产生影响:首先,因为专利保护过期的旧药可能会部分取代昂贵的药物;其次,因为会有开发新抗炎药物的需求。(6)鉴于因果疗法,可能需要重新考虑强制治疗令的法律评估;由于患者依从性提高,导致强制治疗令的法律批准增加,需求减少。(7)如果治疗在认知和社会功能方面变得更有效,患者的社会融入可能会改善。(8)患者及其亲属的污名化可能会减少。