Borson Soo, Scanlan James, Friedman Seth, Zuhr Elizabeth, Fields Julie, Aylward Elizabeth, Mahurin Rodney, Richards Todd, Anzai Yoshimi, Yukawa Michi, Yeh Shingshing
Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle,WA, USA.
Int J Chron Obstruct Pulmon Dis. 2008;3(3):429-34. doi: 10.2147/copd.s2066.
Previous studies have shown that COPD adversely affects distant organs and body systems, including the brain. This pilot study aims to model the relationships between respiratory insufficiency and domains related to brain function, including low mood, subtly impaired cognition, systemic inflammation, and brain structural and neurochemical abnormalities. Nine healthy controls were compared with 18 age- and education-matched medically stable-COPD patients, half of whom were oxygen-dependent. Measures included depression, anxiety, cognition, health status, spirometry, oximetry at rest and during 6-minute walk, and resting plasma cytokines and soluble receptors, brain MRI, and MR spectroscopy in regions relevant to mood and cognition. ANOVA was used to compare controls with patients and with COPD subgroups (oxygen users [n = 9] and nonusers [n = 9]), and only variables showing group differences at p < or = 0.05 were included in multiple regressions controlling for age, gender, and education to develop the final model. Controls and COPD patients differed significantly in global cognition and memory, mood, and soluble TNFR1 levels but not brain structural or neurochemical measures. Multiple regressions identified pathways linking disease severity with impaired performance on sensitive cognitive processing measures, mediated through oxygen dependence, and with systemic inflammation (TNFR1), related through poor 6-minute walk performance. Oxygen desaturation with activity was related to indicators of brain tissue damage (increased frontal choline, which in turn was associated with subcortical white matter attenuation). This empirically derived model provides a conceptual framework for future studies of clinical interventions to protect the brain in patients with COPD, such as earlier oxygen supplementation for patients with desaturation during everyday activities.
先前的研究表明,慢性阻塞性肺疾病(COPD)会对包括大脑在内的远处器官和身体系统产生不利影响。这项初步研究旨在建立呼吸功能不全与大脑功能相关领域之间的关系模型,这些领域包括情绪低落、轻微认知障碍、全身炎症以及大脑结构和神经化学异常。将9名健康对照者与18名年龄和教育程度匹配的病情稳定的COPD患者进行比较,其中一半患者依赖氧气。测量指标包括抑郁、焦虑、认知、健康状况、肺活量测定、静息和6分钟步行期间的血氧饱和度测定、静息血浆细胞因子和可溶性受体、脑部MRI以及与情绪和认知相关区域的磁共振波谱分析。采用方差分析比较对照者与患者以及COPD亚组(吸氧者[n = 9]和未吸氧者[n = 9]),在多重回归分析中仅纳入p≤0.05时显示出组间差异的变量,并对年龄、性别和教育程度进行控制,以建立最终模型。对照者和COPD患者在整体认知和记忆、情绪以及可溶性肿瘤坏死因子受体1(TNFR1)水平上存在显著差异,但在大脑结构或神经化学测量方面无差异。多重回归分析确定了疾病严重程度与敏感认知加工测量指标受损之间的联系途径,这种联系通过氧气依赖介导,还确定了与全身炎症(TNFR1)的联系,这种联系通过6分钟步行表现不佳相关。活动时的氧饱和度下降与脑组织损伤指标(额叶胆碱增加,进而与皮质下白质衰减相关)有关。这个基于经验得出的模型为未来研究保护COPD患者大脑的临床干预措施提供了一个概念框架,例如对日常活动中出现氧饱和度下降的患者更早地进行氧疗。