1Vanderbilt University School of Medicine,Neurology Department,Nashville,Tennessee.
2Clement J. Zablocki VA Medical Center,Mental Health Department,Milwaukee,Wisconsin.
J Int Neuropsychol Soc. 2018 Sep;24(8):864-875. doi: 10.1017/S1355617718000449. Epub 2018 Sep 7.
Obstructive sleep apnea (OSA) is associated with cognitive impairment but the relationships between specific biomarkers and neurocognitive domains remain unclear. The present study examined the influence of common health comorbidities on these relationships. Adults with suspected OSA (N=60; 53% male; M age=52 years; SD=14) underwent neuropsychological evaluation before baseline polysomnography (PSG). Apneic syndrome severity, hypoxic strain, and sleep architecture disturbance were assessed through PSG.
Depression (Center for Epidemiological Studies Depression Scale, CESD), pain, and medical comorbidity (Charlson Comorbidity Index) were measured via questionnaires. Processing speed, attention, vigilance, memory, executive functioning, and motor dexterity were evaluated with cognitive testing. A winnowing approach identified 9 potential moderation models comprised of a correlated PSG variable, comorbid health factor, and cognitive performance.
Regression analyses identified one significant moderation model: average blood oxygen saturation (AVO2) and depression predicting recall memory, accounting for 31% of the performance variance, p<.001. Depression was a significant predictor of recall memory, p<.001, but AVO2 was not a significant predictor. The interaction between depression and AVO2 was significant, accounting for an additional 10% of the variance, p<.001. The relationship between low AVO2 and low recall memory performance emerged when depression severity ratings approached a previously established clinical cutoff score (CESD=16).
This study examined sleep biomarkers with specific neurocognitive functions among individuals with suspected OSA. Findings revealed that depression burden uniquely influence this pathophysiological relationship, which may aid clinical management. (JINS, 2018, 28, 864-875).
阻塞性睡眠呼吸暂停(OSA)与认知障碍有关,但特定生物标志物与神经认知领域之间的关系尚不清楚。本研究探讨了常见健康合并症对这些关系的影响。怀疑患有 OSA 的成年人(N=60;53%为男性;M 年龄=52 岁;SD=14)在基线多导睡眠图(PSG)检查前接受神经心理评估。通过 PSG 评估呼吸暂停综合征严重程度、缺氧负荷和睡眠结构紊乱。
通过问卷测量抑郁(流行病学研究中心抑郁量表,CESD)、疼痛和医疗合并症(Charlson 合并症指数)。使用认知测试评估处理速度、注意力、警觉性、记忆、执行功能和运动灵巧度。一种筛选方法确定了 9 个潜在的调节模型,这些模型由一个相关的 PSG 变量、合并的健康因素和认知表现组成。
回归分析确定了一个显著的调节模型:平均血氧饱和度(AVO2)和抑郁预测回忆记忆,占表现方差的 31%,p<.001。抑郁是回忆记忆的显著预测因子,p<.001,但 AVO2 不是显著预测因子。抑郁和 AVO2 之间的相互作用是显著的,占方差的另外 10%,p<.001。当抑郁严重程度评分接近先前建立的临床临界评分(CESD=16)时,出现了低 AVO2 与低回忆记忆表现之间的关系。
本研究检查了疑似 OSA 个体的睡眠生物标志物与特定神经认知功能之间的关系。研究结果表明,抑郁负担会对这种病理生理关系产生独特的影响,这可能有助于临床管理。(JINS,2018,28,864-875)。