Department of Psychology, University of Southern California, Los Angeles, CA
Department of Physiology and Neuroscience, University of Southern California, Los Angeles, CA.
Diabetes Care. 2019 May;42(5):972-979. doi: 10.2337/dc18-1399. Epub 2019 Mar 4.
To investigate relationships among type 2 diabetes treatment, Alzheimer's disease(AD) biomarkers, and risk for dementia.
Participants were from the Alzheimer's Disease Neuroimaging Initiative ( = 1,289) and were dementia-free at baseline and underwent health assessment, cognitive testing, and MRI. A subset ( = 900) obtained a lumbar puncture to determine cerebrospinal fluid (CSF) phosphorylated tau (p-tau), total tau (t-tau), and β-amyloid 1-42 (Aβ1-42). Participants were grouped by fasting blood glucose and medication history: euglycemia (EU), prediabetes (PD), untreated diabetes (UD), and treated diabetes (TD). Relationships were investigated between treatment status and CSF biomarkers and risk for dementia.
The UD group displayed greater p-tau, t-tau, and p-tau/Aβ1-42 levels than the EU, PD, and TD groups ( values <0.05) and higher t-tau/Aβ1-42 than the EU and PD groups ( values <0.05). The UD group progressed to dementia at higher rates than the EU group (hazard ratio 1.602 [95% CI 1.057-2.429]; = 0.026).
Treatment status may alter the relationship between type 2 diabetes and both AD biomarker profile and risk for dementia. UD is associated with elevated tau pathology and risk for dementia, whereas TD is not. Although this study is observational and therefore causality cannot be inferred, findings support the potential importance of treatment status in AD risk associated with type 2 diabetes.
研究 2 型糖尿病治疗与阿尔茨海默病(AD)生物标志物及痴呆风险之间的关系。
参与者来自阿尔茨海默病神经影像学倡议(n = 1289),在基线时无痴呆,并接受了健康评估、认知测试和 MRI 检查。一部分参与者(n = 900)进行了腰椎穿刺,以确定脑脊液(CSF)中的磷酸化 tau(p-tau)、总 tau(t-tau)和 β-淀粉样蛋白 1-42(Aβ1-42)。参与者根据空腹血糖和用药史分为以下几组:血糖正常(EU)、糖尿病前期(PD)、未经治疗的糖尿病(UD)和经治疗的糖尿病(TD)。研究了治疗状况与 CSF 生物标志物和痴呆风险之间的关系。
与 EU、PD 和 TD 组相比,UD 组的 p-tau、t-tau 和 p-tau/Aβ1-42 水平更高(p 值均<0.05),t-tau/Aβ1-42 水平也高于 EU 和 PD 组(p 值均<0.05)。与 EU 组相比,UD 组进展为痴呆的比例更高(风险比 1.602[95%CI 1.057-2.429];p = 0.026)。
治疗状况可能改变 2 型糖尿病与 AD 生物标志物特征和痴呆风险之间的关系。UD 与 tau 病理学升高和痴呆风险增加相关,而 TD 则没有。尽管本研究为观察性研究,因此不能推断因果关系,但研究结果支持治疗状况在与 2 型糖尿病相关的 AD 风险中的重要性。