Kumar Rajesh, Pham Tiffany T, Macey Paul M, Woo Mary A, Yan-Go Frisca L, Harper Ronald M
Department of Anesthesiology ; Department of Radiological Sciences ; The Brain Research Institute, University of California at Los Angeles, Los Angeles, CA.
Department of Neurobiology, David Geffen School of Medicine at UCLA, Los Angeles, CA.
Sleep. 2014 Apr 1;37(4):723-32. doi: 10.5665/sleep.3578.
Patients with obstructive sleep apnea (OSA) show significant white matter injury; whether that injury represents myelin or axonal damage is unclear. The objective was to examine myelin and axonal changes in patients with newly diagnosed OSA over control subjects.
Cross-sectional study.
University-based medical center.
Twenty-three newly-diagnosed, treatment-naïve OSA and 23 age- and sex-matched control subjects.
None.
Radial and axial diffusivity maps, calculated from diffusion tensor imaging data (3.0 Tesla MRI scanner), indicating diffusion perpendicular (myelin status) or parallel (axonal status) to fibers, respectively, were normalized, smoothed, and compared between groups (analysis of covariance; covariate: age). Global brain radial and axial diffusivity values, and global brain volume with myelin and axonal changes were determined, and region-of-interest analyses performed in areas of significant differences between groups based on voxel-based procedures. Global radial and axial diffusivity values were significantly reduced in OSA versus control subjects (radial, P = 0.004; axial, P = 0.019), with radial (myelin) diffusivity reduced more than axial (axonal), and more left-sided reduction for both measures. Localized declines for myelin and axonal measures appeared in the dorsal and ventral medulla, cerebellar cortex and deep nuclei, basal ganglia, hippocampus, amygdala, corpus callosum, insula, cingulate and medial frontal cortices, and other cortical areas (P < 0.005), all regions mediating functions affected in OSA.
Fiber injury appears in critical medullary respiratory regulatory sites, as well as cognitive and autonomic control areas. Myelin is more affected in newly diagnosed OSA than axons, and primarily on the left side, possibly from the increased myelin sensitivity to hypoxia and asymmetric perfusion.
阻塞性睡眠呼吸暂停(OSA)患者存在明显的白质损伤;但这种损伤是髓鞘还是轴突损伤尚不清楚。本研究旨在对比新诊断的OSA患者与对照者的髓鞘和轴突变化。
横断面研究。
大学附属医院。
23名新诊断的、未接受过治疗的OSA患者以及23名年龄和性别匹配的对照者。
无。
从扩散张量成像数据(3.0特斯拉磁共振成像扫描仪)计算得出径向和轴向扩散率图,分别表示与纤维垂直(髓鞘状态)或平行(轴突状态)方向的扩散,经标准化、平滑处理后在两组间进行比较(协方差分析;协变量:年龄)。确定全脑的径向和轴向扩散率值以及有髓鞘和轴突变化的全脑体积,并基于体素程序在两组间有显著差异的区域进行感兴趣区分析。与对照者相比,OSA患者的全脑径向和轴向扩散率值显著降低(径向,P = 0.004;轴向,P = 0.019),其中径向(髓鞘)扩散率降低幅度大于轴向(轴突),且两种测量结果在左侧的降低更为明显。髓鞘和轴突测量值的局部下降出现在延髓背侧和腹侧、小脑皮质和深部核团、基底神经节、海马体、杏仁核、胼胝体、岛叶、扣带回和内侧额叶皮质以及其他皮质区域(P < 0.005),所有这些区域均参与OSA中受影响的功能调节。
纤维损伤出现在关键的髓质呼吸调节部位以及认知和自主控制区域中。新诊断的OSA患者中髓鞘比轴突受影响更大,且主要在左侧,这可能是由于髓鞘对缺氧和不对称灌注的敏感性增加所致。