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本文引用的文献

1
Accelerated white matter aging in schizophrenia: role of white matter blood perfusion.精神分裂症中白质加速老化:白质血流灌注的作用
Neurobiol Aging. 2014 Oct;35(10):2411-2418. doi: 10.1016/j.neurobiolaging.2014.02.016. Epub 2014 Feb 28.
2
Permeability-diffusivity modeling vs. fractional anisotropy on white matter integrity assessment and application in schizophrenia.基于弥散-渗透建模与各向异性分数对白质完整性评估及其在精神分裂症中的应用。
Neuroimage Clin. 2013 Jul 11;3:18-26. doi: 10.1016/j.nicl.2013.06.019. eCollection 2013.
3
Accelerated brain aging in schizophrenia and beyond: a neuroanatomical marker of psychiatric disorders.精神分裂症及其他疾病中的脑加速老化:精神疾病的神经解剖学标志物
Schizophr Bull. 2014 Sep;40(5):1140-53. doi: 10.1093/schbul/sbt142. Epub 2013 Oct 13.
4
Diving deep into white matter to improve our understanding of the pathophysiology of schizophrenia.深入研究白质以增进我们对精神分裂症病理生理学的理解。
Biol Psychiatry. 2013 Sep 15;74(6):396-7. doi: 10.1016/j.biopsych.2013.07.007.
5
White matter hyperintensities on MRI in high-altitude U-2 pilots.MRI 上的高空 U-2 飞行员的脑白质高信号。
Neurology. 2013 Aug 20;81(8):729-35. doi: 10.1212/WNL.0b013e3182a1ab12.
6
Mechanisms of sporadic cerebral small vessel disease: insights from neuroimaging.散发性脑小血管病的发病机制:神经影像学的启示。
Lancet Neurol. 2013 May;12(5):483-97. doi: 10.1016/S1474-4422(13)70060-7.
7
Alterations of superficial white matter in schizophrenia and relationship to cognitive performance.精神分裂症患者脑白质表层改变及其与认知表现的关系。
Neuropsychopharmacology. 2013 Sep;38(10):1954-62. doi: 10.1038/npp.2013.93. Epub 2013 Apr 16.
8
Myelin and axon abnormalities in schizophrenia measured with magnetic resonance imaging techniques.磁共振成像技术测量精神分裂症的髓鞘和轴突异常。
Biol Psychiatry. 2013 Sep 15;74(6):451-7. doi: 10.1016/j.biopsych.2013.03.003. Epub 2013 Apr 6.
9
What does anisotropy measure? Insights from increased and decreased anisotropy in selective fiber tracts in schizophrenia.各向异性测量什么?精神分裂症选择性纤维束各向异性增加和减少的见解。
Front Integr Neurosci. 2013 Mar 11;7:9. doi: 10.3389/fnint.2013.00009. eCollection 2013.
10
Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.五种主要精神疾病具有共同影响的风险基因座的鉴定:全基因组分析。
Lancet. 2013 Apr 20;381(9875):1371-1379. doi: 10.1016/S0140-6736(12)62129-1. Epub 2013 Feb 28.

多模态白质成像研究精神分裂症中分数各向异性降低及其与年龄相关的下降情况。

Multimodal white matter imaging to investigate reduced fractional anisotropy and its age-related decline in schizophrenia.

作者信息

Kochunov Peter, Chiappelli Joshua, Wright Susan N, Rowland Laura M, Patel Beenish, Wijtenburg S Andrea, Nugent Katie, McMahon Robert P, Carpenter William T, Muellerklein Florian, Sampath Hemalatha, Hong L Elliot

机构信息

Maryland Psychiatric Research Center, Department of Psychiatry, University of Maryland School of Medicine, Baltimore, MD 21228, USA; Department of Physics, University of Maryland Baltimore County, Baltimore, MD 21250, USA.

Maryland Psychiatric Research Center, Department of Psychiatry, University of Maryland School of Medicine, Baltimore, MD 21228, USA.

出版信息

Psychiatry Res. 2014 Aug 30;223(2):148-56. doi: 10.1016/j.pscychresns.2014.05.004. Epub 2014 May 21.

DOI:10.1016/j.pscychresns.2014.05.004
PMID:24909602
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4100065/
Abstract

We hypothesized that reduced fractional anisotropy (FA) of water diffusion and its elevated aging-related decline in schizophrenia patients may be caused by elevated hyperintensive white matter (HWM) lesions, by reduced permeability-diffusivity index (PDI), or both. We tested this hypothesis in 40/30 control/patient participants. FA values for the corpus callosum were calculated from high angular resolution diffusion tensor imaging (DTI). Whole-brain volume of HWM lesions was quantified by 3D-T2w-fluid-attenuated inversion recovery (FLAIR) imaging. PDI for corpus callosum was ascertained using multi b-value diffusion imaging (15 b-shells with 30 directions per shell). Patients had significantly lower corpus callosum FA values, and there was a significant age-by-diagnosis interaction. Patients also had significantly reduced PDI but no difference in HWM volume. PDI and HWM volume were significant predictors of FA and captured the diagnosis-related variance. Separately, PDI robustly explained FA variance in schizophrenia patients, but not in controls. Conversely, HWM volume made equally significant contributions to variability in FA in both groups. The diagnosis-by-age effect of FA was explained by a PDI-by-diagnosis interaction. Post hoc testing showed a similar trend for PDI of gray mater. Our study demonstrated that reduced FA and its accelerated decline with age in schizophrenia were explained by pathophysiology indexed by PDI, rather than HWM volume.

摘要

我们推测,精神分裂症患者水扩散分数各向异性(FA)降低及其与衰老相关的升高的下降可能是由高血压性白质(HWM)病变增加、通透性-扩散指数(PDI)降低或两者共同导致的。我们在40名对照/30名患者参与者中验证了这一假设。胼胝体的FA值通过高角分辨率扩散张量成像(DTI)计算得出。HWM病变的全脑体积通过三维T2加权液体衰减反转恢复(FLAIR)成像进行量化。胼胝体的PDI通过多b值扩散成像(15个b壳层,每个壳层30个方向)确定。患者的胼胝体FA值显著较低,且存在显著的年龄与诊断交互作用。患者的PDI也显著降低,但HWM体积无差异。PDI和HWM体积是FA的显著预测因子,并捕捉到了与诊断相关的差异。单独来看,PDI有力地解释了精神分裂症患者的FA差异,但在对照组中则不然。相反,HWM体积对两组FA的变异性贡献相当。FA的诊断与年龄效应由PDI与诊断的交互作用解释。事后检验显示灰质PDI有类似趋势。我们的研究表明,精神分裂症患者FA降低及其随年龄加速下降是由PDI所指示的病理生理学解释的,而非HWM体积。