Ding Xiuhua, Kryscio Richard J, Turner Joshua, Jicha Gregory A, Cooper Gregory, Caban-Holt Allison, Schmitt Frederick A, Abner Erin L
College of Public Health, University of Kentucky, Lexington, Kentucky.
Sanders-Brown Center on Aging, University of Kentucky, Lexington, Kentucky.
J Am Geriatr Soc. 2016 Dec;64(12):2472-2478. doi: 10.1111/jgs.14393. Epub 2016 Nov 1.
To investigate the association between baseline sleep apnea and risk of incident dementia in the Prevention of Alzheimer's Disease with Vitamin E and Selenium (PREADViSE) study and to explore whether the association depends on apolipoprotein E (APOE) ɛ4 allele status.
Secondary analysis based on data collected during PREADViSE.
Participants were assessed at 128 local clinical study sites during the clinical trial phase and later were followed by telephone from a centralized location.
Men enrolled in PREADViSE (without dementia or other active neurological conditions that affect cognition such as major psychiatric disorders, including depression; N = 7,547).
Participants were interviewed at baseline for sleep apnea. The Memory Impairment Screen (MIS) was administered to each participant annually. Subjects who failed this initial screen were tested with secondary screening tests. Medical history and medication use were determined, and the AD8 dementia screening instrument was used.
The effect of self-reported sleep apnea on dementia risk depended on APOE ɛ4 status. When the allele was absent, baseline self-reported sleep apnea was associated with a 66% higher risk of developing dementia (95% confidence interval = 2-170%), whereas self-reported sleep apnea conferred no additional risk for participants with an ɛ4 allele.
Sleep apnea may increase risk of dementia in the absence of APOE ɛ4. This may help inform prevention strategies for dementia or AD in older men with sleep apnea. Registration: PREADViSE is registered at ClinicalTrials.gov: NCT00040378.
在维生素E和硒预防阿尔茨海默病(PREADViSE)研究中,调查基线睡眠呼吸暂停与痴呆症发病风险之间的关联,并探讨这种关联是否取决于载脂蛋白E(APOE)ε4等位基因状态。
基于PREADViSE期间收集的数据进行二次分析。
在临床试验阶段,在128个当地临床研究地点对参与者进行评估,随后从一个集中地点通过电话进行随访。
参与PREADViSE的男性(无痴呆症或其他影响认知的活动性神经疾病,如包括抑郁症在内的主要精神疾病;N = 7547)。
在基线时对参与者进行睡眠呼吸暂停访谈。每年对每位参与者进行记忆障碍筛查(MIS)。初次筛查未通过的受试者接受二次筛查测试。确定病史和用药情况,并使用AD8痴呆筛查工具。
自我报告的睡眠呼吸暂停对痴呆风险的影响取决于APOE ε4状态。当不存在该等位基因时,基线自我报告的睡眠呼吸暂停与痴呆症发病风险高66%相关(95%置信区间 = 2 - 170%),而自我报告的睡眠呼吸暂停对携带ε4等位基因的参与者没有额外风险。
在没有APOE ε4的情况下,睡眠呼吸暂停可能会增加患痴呆症的风险。这可能有助于为患有睡眠呼吸暂停的老年男性制定痴呆症或阿尔茨海默病的预防策略提供信息。注册情况:PREADViSE在ClinicalTrials.gov注册:NCT00040378。