Bubu Omonigho M, Umasabor-Bubu Ogie Q, Turner Arlener D, Parekh Ankit, Mullins Anna E, Kam Korey, Birckbichler Madeline K, Mukhtar Fahad, Mbah Alfred K, Williams Natasha J, Rapoport David M, de Leon Mony, Jean-Louis Girardin, Ayappa Indu, Varga Andrew W, Osorio Ricardo S
Center for Sleep and Brain Health, Department of Psychiatry, NYU Grossman School of Medicine, New York, New York, USA.
Center for Healthful Behavior Change, Department of Population Health, New York Grossman School of Medicine, New York, USA.
Alzheimers Dement. 2020 Oct 8. doi: 10.1002/alz.12184.
Obstructive sleep apnea (OSA) is associated with Alzheimer's disease (AD) biomarkers in cognitively normal (CN) and mild cognitive impaired (MCI) participants. However, independent and combined effects of OSA, amyloid beta (Aβ) and tau-accumulation on AD time-dependent progression risk is unclear.
Study participants grouped by biomarker profile, as described by the A/T/N scheme, where "A" refers to aggregated Aβ, "T" aggregated tau, and "N" to neurodegeneration, included 258 CN (OSA-positive [OSA+] [A+TN+ n = 10, A+/TN- n = 6, A-/TN+ n = 10, A-/TN- n = 6 and OSA-negative [OSA-] [A+TN+ n = 84, A+/TN- n = 11, A-/TN+ n = 96, A-/TN- n = 36]) and 785 MCI (OSA+ [A+TN+ n = 35, A+/TN- n = 15, A-/TN+ n = 25, A-/TN- n = 16] and OSA- [A+TN+ n = 388, A+/TN- n = 28, A-/TN+ n = 164, A-/TN- n = 114]) older-adults from the Alzheimer's Disease Neuroimaging Initiative cohort. Cox proportional hazards regression models estimated the relative hazard of progression from CN-to-MCI and MCI-to-AD, among baseline OSA CN and MCI patients, respectively. Multi-level logistic mixed-effects models with random intercept and slope investigated the synergistic associations of self-reported OSA, Aβ, and tau burden with prospective cognitive decline.
Independent of TN-status (CN and MCI), OSA+/Aβ+ participants were approximately two to four times more likely to progress to MCI/AD (P < .001) and progressed 6 to 18 months earlier (P < .001), compared to other participants combined (ie, OSA+/Aβ-, OSA-/Aβ+, and OSA-/Aβ-). Notably, OSA+/Aβ- versus OSA-/Aβ- (CN and MCI) and OSA+/TN- versus OSA-/TN- (CN) participants showed no difference in the risk and time-to-MCI/AD progression. Mixed effects models demonstrated OSA synergism with Aβ (CN and MCI [β = 1.13, 95% confidence interval (CI), 0.74 to 1.52, and β = 1.18, 95%CI, 0.82 to 1.54]) respectively, and with tau (MCI [β = 1.31, 95% CI, 0.87 to 1.47]), P < .001 for all.
OSA acts in synergism with Aβ and with tau, and all three acting together result in synergistic neurodegenerative mechanisms especially as Aβ and tau accumulation becomes increasingly abnormal, thus leading to shorter progression time to MCI/AD in CN and MCI-OSA patients, respectively.
在认知正常(CN)和轻度认知障碍(MCI)参与者中,阻塞性睡眠呼吸暂停(OSA)与阿尔茨海默病(AD)生物标志物相关。然而,OSA、淀粉样β蛋白(Aβ)和tau蛋白积累对AD时间依赖性进展风险的独立及联合影响尚不清楚。
研究参与者按照A/T/N方案所描述的生物标志物特征分组,其中“A”指聚集的Aβ,“T”指聚集的tau蛋白,“N”指神经退行性变。该分组包括来自阿尔茨海默病神经影像学倡议队列的258名CN患者(OSA阳性[OSA+][A+TN+ n = 10,A+/TN- n = 6,A-/TN+ n = 10,A-/TN- n = 6]和OSA阴性[OSA-][A+TN+ n = 84,A+/TN- n = 11,A-/TN+ n = 96,A-/TN- n = 36])和785名MCI患者(OSA+[A+TN+ n = 35,A+/TN- n = 15,A-/TN+ n = 25,A-/TN- n = 16]和OSA-[A+TN+ n = 388,A+/TN- n = 28,A-/TN+ n = 164,A-/TN- n = 114])。Cox比例风险回归模型分别估计了基线时OSA CN和MCI患者从CN进展为MCI以及从MCI进展为AD的相对风险。具有随机截距和斜率的多级逻辑混合效应模型研究了自我报告的OSA、Aβ和tau蛋白负担与前瞻性认知衰退的协同关联。
与其他参与者组合(即OSA+/Aβ-、OSA-/Aβ+和OSA-/Aβ-)相比,无论TN状态(CN和MCI)如何,OSA+/Aβ+参与者进展为MCI/AD的可能性大约高两到四倍(P <.001),且进展时间提前6至18个月(P <.001)。值得注意的是,OSA+/Aβ-与OSA-/Aβ-(CN和MCI)以及OSA+/TN-与OSA-/TN-(CN)参与者在进展为MCI/AD的风险和时间上没有差异。混合效应模型分别显示OSA与Aβ(CN和MCI[β = 1.13,95%置信区间(CI),0.74至1.52,以及β = 1.18,95%CI,0.82至1.54])以及与tau蛋白(MCI[β = 1.31,95%CI,0.87至1.47])存在协同作用,所有P值均<.001。
OSA与Aβ以及与tau蛋白存在协同作用,三者共同作用会导致协同的神经退行性机制,尤其是随着Aβ和tau蛋白积累变得越来越异常,从而分别导致CN和MCI-OSA患者进展为MCI/AD的时间缩短。