Duffy Shantel L, Lagopoulos Jim, Terpening Zoe, Lewis Simon J G, Grunstein Ron, Mowszowski Loren, Cross Nathan, Hermens Daniel F, Hickie Ian B, Naismith Sharon L
Healthy Brain Ageing Program, The University of Sydney, Camperdown, Australia.
Clinical Research Unit, Brain and Mind Centre, The University of Sydney, Camperdown, Australia.
Sleep. 2016 Apr 1;39(4):899-906. doi: 10.5665/sleep.5650.
Sleep disordered breathing (SDB) is common in older adults and is strongly associated with cognitive decline, with increasing evidence suggesting that it may represent a risk factor for dementia. Given that SDB is characterized by intermittent episodes of hypoxemia during sleep, it is possible that cognitive impairment may relate to cerebral oxidative stress. This study aimed to examine the relationship between nocturnal markers of hypoxemia and proton magnetic resonance spectroscopy ((1)H-MRS) markers of oxidative stress within the anterior cingulate cortex (ACC) of the brain.
Twenty-four older adults (mean age = 67.9 y) at-risk for dementia were recruited from our Healthy Brain Ageing Research Clinic. At-risk was defined as participants seeking help for assessment and/or intervention for cognitive decline, including those with subjective and/or objective cognitive complaints. This could occur in the context of prior depression or risk factors (e.g., vascular) for dementia. All participants underwent psychiatric, medical and neuropsychological assessment followed by overnight polysomnography. In addition, participants underwent (1)H-MRS to derive levels of ACC metabolite glutathione (GSH) reported as a ratio to creatine (GSH/Cr).
Increased levels of GSH/Cr were associated with lower oxygen desaturation (r = -0.54, P = 0.007) and more severe apnea-hypopnea index scores during rapid eye movement sleep (r = 0.42, P = 0.050). In addition, ACC GSH/Cr correlated with poorer executive functioning (i.e., response inhibition: r = -0.49, P = 0.015; set shifting: r = -0.43, P = 0.037).
Markers of nocturnal hypoxemia and SDB are associated with cerebral oxidative stress in older people at-risk for dementia, suggesting a potential mechanism by which SDB may contribute to brain degeneration, cognitive decline, and dementia. Further work focused on utilizing this biomarker for the early identification and treatment of this possible modifiable risk factor in older persons is now warranted.
睡眠呼吸紊乱(SDB)在老年人中很常见,且与认知能力下降密切相关,越来越多的证据表明它可能是痴呆症的一个风险因素。鉴于SDB的特征是睡眠期间间歇性低氧血症发作,认知障碍可能与脑氧化应激有关。本研究旨在探讨夜间低氧血症标志物与大脑前扣带回皮质(ACC)氧化应激的质子磁共振波谱((1)H-MRS)标志物之间的关系。
从我们的健康脑老化研究诊所招募了24名有痴呆症风险的老年人(平均年龄=67.9岁)。有风险被定义为寻求认知能力下降评估和/或干预帮助的参与者,包括有主观和/或客观认知主诉的人。这可能发生在既往有抑郁症或痴呆症风险因素(如血管因素)的情况下。所有参与者都接受了精神、医学和神经心理学评估,随后进行了整夜多导睡眠图检查。此外,参与者接受了(1)H-MRS检查以得出ACC代谢物谷胱甘肽(GSH)的水平,以与肌酸的比率(GSH/Cr)报告。
GSH/Cr水平升高与较低的氧饱和度下降相关(r=-0.54,P=0.007),并且与快速眼动睡眠期间更严重的呼吸暂停低通气指数评分相关(r=0.42,P=0.050)。此外,ACC的GSH/Cr与较差的执行功能相关(即反应抑制:r=-0.49,P=0.015;定势转换:r=-0.43,P=0.037)。
夜间低氧血症和SDB的标志物与有痴呆症风险的老年人的脑氧化应激相关,这表明SDB可能导致脑退化、认知能力下降和痴呆症的一种潜在机制。现在有必要进一步开展工作,重点利用这种生物标志物对老年人中这种可能可改变的风险因素进行早期识别和治疗。