陈立婷,彭德昌,李健,李海军,叶成龙,余宏辉,辛会珍,龚洪翰.阻塞性睡眠呼吸暂停患者默认网络功能连接及拓扑属性异常[J].中国医学影像技术,2018,34(8):1153~1158 |
阻塞性睡眠呼吸暂停患者默认网络功能连接及拓扑属性异常 |
Abnormality of functional connectivity and topological properties of default mode network in patients with obstructive sleep apnea |
投稿时间:2017-10-19 修订日期:2018-04-16 |
DOI:10.13929/j.1003-3289.201710073 |
中文关键词: 睡眠呼吸暂停,阻塞性 默认网络 功能连接 静息态 磁共振成像 图论 |
英文关键词:Sleep apnea, obstructive Default mode network Functional connectivity Resting-state Magnetic resonance imaging Graph theory |
基金项目:国家自然科学基金(81560285)、江西省创新课题自然基金(YC2016-S100)、江西省教育厅基金(700544006)、江西省自然科学基金(20171BAB205070)。 |
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中文摘要: |
目的 观察阻塞性睡眠呼吸暂停(OSA)患者脑默认网络(DMN)内部各亚区的功能连接(FC)及拓扑属性的异常改变。方法 采集40例男性重度OSA患者(OSA组)和43名睡眠正常的男性志愿者(对照组)的静息态fMRI数据,以20个DMN亚区为种子点构建DMN的FC网络,获得OSA患者DMN各亚区间FC异常的脑区。计算拓扑属性参数小世界指数(σ)、网络全局效率(Eglob)和网络局部效率(Eloc),并评估与临床资料的相关性。结果 OSA组和对照组DMN均存在小世界属性。与对照组比较,OSA组前—后DMN、后DMN内部FC减低(P均<0.05),Eloc减低(P=0.02)。OSA组DMN异常的FC与Eglob值(r=-0.736,P<0.001)、蒙特利尔认知(MoCA)量表评分(r=-0.453,P=0.006)呈负相关。结论 OSA患者DMN内部各亚区功能连接受损,且DMN拓扑属性异常改变,可能是其认知、记忆等功能障碍的神经影像学机制。 |
英文摘要: |
Objective To explore the disrupted functional connectivity (FC) of the sub-regions and topological reorganization of the default mode network (DMN) in patients with obstructive sleep apnea (OSA). Methods Resting-state fMRI data were obtained from 40 male patients with severe OSA (OSA group) and 43 male healthy controls (control group). Twenty sub-regions of DMN were specifically selected as ROIs, and functional connectivity (FC) of DMN architecture was constructed. Then the abnormal FC of sub-regions in patients with OSA was observed. The topological properties of DMN were characterized. The topological attribute parameters, such as small-world index (σ), network global efficiency (Eglob) and network local efficiency (Eloc) were calculated, and their relationship with clinical data were evaluated. Results DMN exhibited small-world topology in both OSA and control groups. Compared with control group, OSA group showed significantly decreased FC in the anterior-posterior DMN and posterior DMN (all P<0.05), and decreased Eloc (P=0.02). Abnormal DMN FC was negatively correlated to Eglob (r=-0.736, P<0.001) and MoCA scores (r=-0.453, P=0.006) in OSA group. Conclusion OSA patients showed disrupted FC within DMN sub-regions and topological properties of DMN, which might be the neuroimaging mechanism of cognitive function and memory deficits in patients with OSA. |
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