Center for MR Research, University of Illinois, Chicago, IL, USA; Department of Radiology, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, China.
Department of Biobehavioral Health Science, University of Illinois, Chicago, IL, USA; Center for Sleep and Health, College of Nursing, University of Illinois, Chicago, IL, USA.
Sleep Med. 2019 Jan;53:51-59. doi: 10.1016/j.sleep.2018.09.011. Epub 2018 Sep 29.
To investigate factors associated with residual sleepiness in patients who were highly adherent to continuous positive airway pressure (CPAP). Nocturnal inactivity, comorbidities, concomitant medications, and, in particular, white matter (WM) differences using diffusion magnetic resonance imaging (MRI) were explored using a continuous-time random-walk (CTRW) model.
Twenty-seven male patients (30-55 years of age) with obstructive sleep apnea (OSA) received CPAP as the only treatment (CPAP ≥ 6 h/night) for at least 30 days. Based on the Psychomotor Vigilance Task (PVT) results, participants were divided into a non-sleepy group (lapses ≤ 5; n = 18) and a sleepy group (lapses > 5; n = 9). Mean nocturnal inactivity (sleep proxy) was measured using actigraphy for one week. Diffusion-weighted imaging (DWI) with high b-values, as well as diffusion tensor imaging (DTI), was performed on a 3 T MRI scanner. The DWI dataset was analyzed using the CTRW model that yielded three parameters: temporal diffusion heterogeneity α, spatial diffusion heterogeneity β, and an anomalous diffusion coefficient D. The differences in α, β, and D between the two groups were investigated by a whole-brain analysis using tract-based spatial statistics (TBSS), followed by a regional analysis on individual fiber tracts using a standard parcellation template. Results from the CTRW model were compared with those obtained from DTI. The three CTRW parameters were also correlated with the clinical assessment scores, Epworth Sleepiness Scale (ESS), PVT lapses, and PVT mean reaction time (MRT) in specific fiber tracts.
There were no differences between groups in mean sleep duration, comorbidities, and the number or type of medications, including alerting and sedating medications. In the whole-brain DWI analysis, the sleepy group showed higher α (17.27% of the WM voxels) and D (17.14%) when compared to the non-sleepy group (P < 0.05), whereas no significant difference in β was observed. In the regional fiber analysis, the sleepy and non-sleepy groups showed significant differences in α, β, or their combinations in a total of 12 fiber tracts; whereas similar differences were not observed in DTI parameters, when age was used as a covariate. Additionally, moderate to strong correlations between the CTRW parameters (α, β, or D) and the sleepiness assessment scores (ESS, PVT lapses, or PVT MRT) were observed in specific fiber tracts (|R| = 0.448-0.654, P = 0.0003-0.019).
The observed differences in the CTRW parameters between the two groups indicate that WM alterations can be a possible mechanism to explain reversible versus residual sleepiness observed in OSA patients with identical high level of CPAP use. The moderate to strong correlations between the CTRW parameters and the clinical scores suggest the possibility of developing objective and quantitative imaging markers to complement clinical assessment of OSA patients.
使用扩散磁共振成像(dMRI)中的连续时间随机游走(CTRW)模型,研究与高度依从持续气道正压通气(CPAP)的患者残余嗜睡相关的因素。探索了夜间不活动、合并症、伴随药物治疗,特别是使用弥散磁共振成像(dMRI)测量的脑白质(WM)差异。
27 名患有阻塞性睡眠呼吸暂停(OSA)的男性患者(30-55 岁)接受 CPAP 治疗(每晚≥6 小时)至少 30 天。根据精神运动警觉任务(PVT)的结果,参与者被分为非嗜睡组(失误≤5;n=18)和嗜睡组(失误>5;n=9)。一周内使用活动记录仪测量夜间平均不活动(睡眠代理)。在 3T MRI 扫描仪上进行高 b 值弥散加权成像(DWI)和弥散张量成像(DTI)。DWI 数据集使用 CTRW 模型进行分析,该模型产生了三个参数:时间扩散异质性α、空间扩散异质性β和异常扩散系数 D。使用基于纤维束的空间统计学(TBSS)对两组之间的α、β和 D 进行全脑分析,然后使用标准分割模板对个体纤维束进行区域分析。使用 CTRW 模型比较 DTI 结果。还将三个 CTRW 参数与临床评估评分、Epworth 嗜睡量表(ESS)、PVT 失误和特定纤维束中的 PVT 平均反应时间(MRT)相关联。
两组在平均睡眠时间、合并症和药物数量或类型方面无差异,包括觉醒和镇静药物。在全脑 DWI 分析中,与非嗜睡组相比,嗜睡组的α(WM 体素的 17.27%)和 D(17.14%)更高(P<0.05),而β无显著差异。在区域纤维分析中,嗜睡组和非嗜睡组在总共 12 条纤维束中α、β或它们的组合存在显著差异;而在 DTI 参数中,当使用年龄作为协变量时,没有观察到相似的差异。此外,在特定纤维束中观察到 CTRW 参数(α、β或 D)与嗜睡评估评分(ESS、PVT 失误或 PVT MRT)之间存在中度至强相关性(|R|=0.448-0.654,P=0.0003-0.019)。
两组之间 CTRW 参数的差异表明,WM 改变可能是解释 OSA 患者在使用相同高水平 CPAP 治疗时出现可逆性与残余嗜睡的可能机制。CTRW 参数与临床评分之间的中度至强相关性表明,有可能开发客观和定量的成像标志物来补充 OSA 患者的临床评估。