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本文引用的文献

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Impact on intracortical myelination trajectory of long acting injection versus oral risperidone in first-episode schizophrenia.长效注射利培酮与口服利培酮对首发精神分裂症患者皮质内髓鞘化轨迹的影响。
Schizophr Res. 2012 Sep;140(1-3):122-8. doi: 10.1016/j.schres.2012.06.036. Epub 2012 Jul 17.
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Oligodendrocyte genes, white matter tract integrity, and cognition in schizophrenia.少突胶质细胞基因、白质束完整性与精神分裂症认知。
Cereb Cortex. 2013 Sep;23(9):2044-57. doi: 10.1093/cercor/bhs188. Epub 2012 Jul 6.
3
Reduced myelin basic protein and actin-related gene expression in visual cortex in schizophrenia.精神分裂症患者视觉皮层髓鞘碱性蛋白和肌动蛋白相关基因表达减少。
PLoS One. 2012;7(6):e38211. doi: 10.1371/journal.pone.0038211. Epub 2012 Jun 1.
4
MTR abnormalities in subjects at ultra-high risk for schizophrenia and first-episode schizophrenic patients compared to healthy controls.与健康对照组相比,超高危精神分裂症患者和首发精神分裂症患者的 MTR 异常。
Schizophr Res. 2012 May;137(1-3):85-90. doi: 10.1016/j.schres.2012.01.020. Epub 2012 Feb 27.
5
Age-related changes in human and non-human primate white matter: from myelination disturbances to cognitive decline.人类和非人类灵长类动物白质的年龄相关变化:从髓鞘形成障碍到认知衰退。
Age (Dordr). 2012 Oct;34(5):1093-110. doi: 10.1007/s11357-011-9357-7. Epub 2011 Dec 28.
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Aberrations in the arcuate fasciculus are associated with auditory verbal hallucinations in psychotic and in non-psychotic individuals.弓状束的异常与精神病和非精神病个体的听觉言语幻觉有关。
Hum Brain Mapp. 2013 Mar;34(3):626-34. doi: 10.1002/hbm.21463. Epub 2011 Nov 23.
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Diffusion tensor imaging of cerebral white matter integrity in cognitive aging.认知衰老中脑白质完整性的扩散张量成像
Biochim Biophys Acta. 2012 Mar;1822(3):386-400. doi: 10.1016/j.bbadis.2011.08.003. Epub 2011 Aug 16.
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Neurocognitive predictors of work outcome in recent-onset schizophrenia.首发精神分裂症患者工作结局的神经认知预测因子。
Schizophr Bull. 2011 Sep;37 Suppl 2(Suppl 2):S33-40. doi: 10.1093/schbul/sbr084.
9
Mapping human cortical areas in vivo based on myelin content as revealed by T1- and T2-weighted MRI.基于 T1 加权和 T2 加权 MRI 显示的髓鞘含量对人体皮质区进行体内定位。
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10
Imputation techniques for the detection of microstructural changes in schizophrenia, with an application to magnetization transfer imaging.用于检测精神分裂症微观结构变化的推断技术,应用于磁化传递成像。
Schizophr Res. 2011 Oct;132(1):91-6. doi: 10.1016/j.schres.2011.07.023. Epub 2011 Aug 5.

联合白质成像提示精神分裂症视觉处理区域髓鞘形成缺陷。

Combined white matter imaging suggests myelination defects in visual processing regions in schizophrenia.

机构信息

Division of Psychiatry, Institute of Mental Health, University of Nottingham, Nottingham, UK.

出版信息

Neuropsychopharmacology. 2013 Aug;38(9):1808-15. doi: 10.1038/npp.2013.80. Epub 2013 Apr 4.

DOI:10.1038/npp.2013.80
PMID:23558741
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3712891/
Abstract

Diverse pathological changes occur in the white matter (WM) of patients with schizophrenia. Various microstructural alterations including a reduction in axonal number or diameter, reduced myelination, or poor coherence of fibers could account for these changes. Abnormal integrity of macromolecules such as myelin ('dysmyelination') can be studied by applying multiple modalities of WM imaging such as diffusion tensor imaging (DTI) and magnetization transfer imaging (MTI) in parallel. Using ultra-high field (7 Tesla) MTI in 17 clinically stable patients with schizophrenia and 20 controls, we evaluated the voxelwise distribution of macromolecular WM abnormalities. Patients had a significant reduction in magnetization transfer ratio (MTR) in WM adjacent to visual processing regions and inferior temporal cortex (Cohen's d=1.54). Among the regions showing MTR reduction, a concurrent reduction in fractional anisotropy (FA) occurs proximal to the lingual gyrus. Multiple regression analysis revealed that the degree of FA reduction in the putatively 'dysmyelinated' regions in patients predicted impaired processing speed (PS; β=0.74; P=0.003), a core cognitive dysfunction in schizophrenia. In controls, MTR/FA in the occipito-temporal regions were not associated with PS. Our findings suggest that dysmyelination in visual processing regions is present in patients with schizophrenia with greatest cognitive and functional impairment. Combined DTI/MTI deficits in the occipito-temporal region may be an important variable when considering potential treatment targets for improving cognitive function in schizophrenia.

摘要

精神分裂症患者的白质(WM)中会发生多种病理变化。各种微观结构改变,包括轴突数量或直径减少、髓鞘形成减少或纤维连贯性差,都可能导致这些变化。应用 WM 成像的多种模态,如弥散张量成像(DTI)和磁化传递成像(MTI),可以研究大分子如髓鞘的完整性异常(“脱髓鞘”)。我们在 17 名临床稳定的精神分裂症患者和 20 名对照中使用超高场(7 特斯拉)MTI,评估了大分子 WM 异常的体素分布。患者 WM 毗邻视觉处理区域和颞下回的磁化转移率(MTR)显著降低(Cohen's d=1.54)。在显示 MTR 降低的区域中,在舌回附近也出现了分数各向异性(FA)的同时降低。多元回归分析显示,患者中假定的“脱髓鞘”区域的 FA 降低程度与处理速度(PS)受损有关(β=0.74;P=0.003),PS 是精神分裂症的核心认知功能障碍。在对照组中,枕颞区域的 MTR/FA 与 PS 无关。我们的发现表明,精神分裂症患者的视觉处理区域存在脱髓鞘,与认知和功能障碍最严重的患者相关。枕颞区域的 DTI/MTI 联合缺陷可能是考虑改善精神分裂症认知功能的潜在治疗靶点的重要变量。