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精神分裂症中的神经炎症与白质病理学:系统综述

Neuroinflammation and white matter pathology in schizophrenia: systematic review.

作者信息

Najjar Souhel, Pearlman Daniel M

机构信息

Neuroinflammation Research Group, Epilepsy Center Division, Department of Neurology, NYU School of Medicine, New York, New York, United States.

Neuroinflammation Research Group, Epilepsy Center Division, Department of Neurology, NYU School of Medicine, New York, New York, United States; The Dartmouth Institute of Health Policy and Clinical Practice, Audrey and Theodor Geisel School of Medicine at Dartmouth, Hanover, New Hampshire, United States.

出版信息

Schizophr Res. 2015 Jan;161(1):102-12. doi: 10.1016/j.schres.2014.04.041. Epub 2014 Jun 16.

Abstract

BACKGROUND

Neuroinflammation and white matter pathology have each been independently associated with schizophrenia, and experimental studies have revealed mechanisms by which the two can interact in vitro, but whether these abnormalities simultaneously co-occur in people with schizophrenia remains unclear.

METHOD

We searched MEDLINE, EMBASE, PsycINFO and Web of Science from inception through 12 January 2014 for studies reporting human data on the relationship between microglial or astroglial activation, or cytokines and white matter pathology in schizophrenia.

RESULTS

Fifteen studies totaling 792 subjects (350 with schizophrenia, 346 controls, 49 with bipolar disorder, 37 with major depressive disorder and 10 with Alzheimer's disease) met all eligibility criteria. Five neuropathological and two neuroimaging studies collectively yielded consistent evidence of an association between schizophrenia and microglial activation, particularly in white rather than gray matter regions. Ultrastructural analysis revealed activated microglia near dystrophic and apoptotic oligodendroglia, demyelinating and dysmyelinating axons and swollen and vacuolated astroglia in subjects with schizophrenia but not controls. Two neuroimaging studies found an association between carrier status for a functional single nucleotide polymorphism in the interleukin-1β gene and abnormal white as well as gray matter volumes in schizophrenia but not controls. A neuropathological study found that orbitofrontal white matter neuronal density was increased in schizophrenia cases exhibiting high transcription levels of pro-inflammatory cytokines relative to those exhibiting low transcription levels and to controls. Schizophrenia was associated with decreased astroglial density specifically in subgenual cingulate white matter and anterior corpus callosum, but not other gray or white matter areas. Astrogliosis was consistently absent. Data on astroglial gene expression, mRNA expression and protein concentration were inconsistent.

CONCLUSION

Neuroinflammation is associated with white matter pathology in people with schizophrenia, and may contribute to structural and functional disconnectivity, even at the first episode of psychosis.

摘要

背景

神经炎症和白质病变均已分别独立地与精神分裂症相关联,并且实验研究已经揭示了二者在体外可能相互作用的机制,但这些异常是否同时出现在精神分裂症患者中仍不清楚。

方法

我们检索了MEDLINE、EMBASE、PsycINFO和Web of Science数据库,涵盖从建库至2014年1月12日期间报告有关精神分裂症中微胶质细胞或星形胶质细胞激活、细胞因子与白质病变之间关系的人类数据的研究。

结果

共有15项研究符合所有纳入标准,涉及792名受试者(350名精神分裂症患者、346名对照、49名双相情感障碍患者、37名重度抑郁症患者和10名阿尔茨海默病患者)。五项神经病理学研究和两项神经影像学研究共同提供了一致的证据,表明精神分裂症与微胶质细胞激活相关,尤其是在白质而非灰质区域。超微结构分析显示,在精神分裂症患者而非对照组中,营养不良和凋亡的少突胶质细胞、脱髓鞘和髓鞘形成异常的轴突附近存在激活的微胶质细胞,以及肿胀和空泡化的星形胶质细胞。两项神经影像学研究发现,白细胞介素-1β基因功能性单核苷酸多态性的携带者状态与精神分裂症患者而非对照组的白质和灰质体积异常有关。一项神经病理学研究发现,与低转录水平的精神分裂症患者及对照组相比,表现出促炎细胞因子高转录水平的精神分裂症患者眶额白质神经元密度增加。精神分裂症与星形胶质细胞密度降低相关,特别是在膝下扣带回白质和胼胝体前部,但在其他灰质或白质区域则不然。星形胶质细胞增生始终不存在。关于星形胶质细胞基因表达、mRNA表达和蛋白质浓度的数据并不一致。

结论

神经炎症与精神分裂症患者的白质病变相关,并且可能导致结构和功能连接障碍,即使在精神病发作的首发阶段也是如此。

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