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使用 ACD-A 抗凝剂采集时,血液生物标志物可区分脑淀粉样蛋白状态和认知诊断。

Blood Biomarkers Discriminate Cerebral Amyloid Status and Cognitive Diagnosis when Collected with ACD-A Anticoagulant.

机构信息

Alzheimer's Disease Research Center, University of Kansas, Kansas City, KS, 66160, United States.

Department of Neurology, University of Kansas Medical Center, Kansas City, KS, 66160, United States.

出版信息

Curr Alzheimer Res. 2023;20(8):557-566. doi: 10.2174/0115672050271523231111192725.

Abstract

BACKGROUND

The development of biomarkers that are easy to collect, process, and store is a major goal of research on current Alzheimer's Disease (AD) and underlies the growing interest in plasma biomarkers. Biomarkers with these qualities will improve diagnosis and allow for better monitoring of therapeutic interventions. However, blood collection strategies have historically differed between studies. We examined the ability of various ultrasensitive plasma biomarkers to predict cerebral amyloid status in cognitively unimpaired individuals when collected using acid citrate dextrose (ACD). We then examined the ability of these biomarkers to predict cognitive impairment independent of amyloid status.

METHODS

Using a cross-sectional study design, we measured amyloid beta 42/40 ratio, pTau-181, neurofilament-light, and glial fibrillary acidic protein using the Quanterix Simoa® HD-X platform. To evaluate the discriminative accuracy of these biomarkers in determining cerebral amyloid status, we used both banked plasma and 18F-AV45 PET cerebral amyloid neuroimaging data from 140 cognitively unimpaired participants. We further examined their ability to discriminate cognitive status by leveraging data from 42 cognitively impaired older adults. This study is the first, as per our knowledge, to examine these specific tests using plasma collected using acid citrate dextrose (ACD), as well as the relationship with amyloid PET status.

RESULTS

Plasma AB42/40 had the highest AUC (0.833, 95% C.I. 0.767-0.899) at a cut-point of 0.0706 for discriminating between the two cerebral amyloid groups (sensitivity 76%, specificity 78.5%). Plasma NFL at a cut-point of 20.58pg/mL had the highest AUC (0.908, 95% CI 0.851- 0.966) for discriminating cognitive impairment (sensitivity 84.8%, specificity 89.9%). The addition of age and apolipoprotein e4 status did not improve the discriminative accuracy of these biomarkers.

CONCLUSION

Our results suggest that the Aβ42/40 ratio is useful in discriminating clinician-rated elevated cerebral amyloid status and that NFL is useful for discriminating cognitive impairment status. These findings reinforce the growing body of evidence regarding the general utility of these biomarkers and extend their utility to plasma collected in a non-traditional anticoagulant.

摘要

背景

开发易于采集、处理和存储的生物标志物是当前阿尔茨海默病 (AD) 研究的主要目标,这也是对血浆生物标志物日益关注的基础。具有这些特性的生物标志物将改善诊断,并能够更好地监测治疗干预措施。然而,历史上,血液采集策略在不同的研究中存在差异。我们检查了在使用柠檬酸葡萄糖酸 (ACD) 采集时,各种超灵敏血浆生物标志物预测认知正常个体脑淀粉样状态的能力。然后,我们检查了这些生物标志物预测认知障碍的能力,而与淀粉样蛋白状态无关。

方法

使用横断面研究设计,我们使用 Quanterix Simoa® HD-X 平台测量了淀粉样β 42/40 比值、pTau-181、神经丝轻链和神经胶质纤维酸性蛋白。为了评估这些生物标志物在确定脑淀粉样状态方面的判别准确性,我们使用了来自 140 名认知正常个体的储备血浆和 18F-AV45 PET 脑淀粉样神经影像学数据。我们进一步利用来自 42 名认知障碍老年人的数据检查了它们区分认知状态的能力。据我们所知,这是首次使用柠檬酸葡萄糖酸 (ACD) 采集的血浆检查这些特定测试,以及与淀粉样蛋白 PET 状态的关系。

结果

血浆 AB42/40 在区分两种脑淀粉样蛋白组时,截断值为 0.0706,具有最高的 AUC(0.833,95%置信区间为 0.767-0.899)(灵敏度 76%,特异性 78.5%)。血浆 NFL 在截断值为 20.58pg/mL 时,具有最高的 AUC(0.908,95%置信区间为 0.851-0.966),用于区分认知障碍(灵敏度 84.8%,特异性 89.9%)。年龄和载脂蛋白 E4 状态的增加并没有提高这些生物标志物的判别准确性。

结论

我们的结果表明,Aβ42/40 比值可用于区分临床医生评估的升高脑淀粉样状态,而 NFL 可用于区分认知障碍状态。这些发现强化了这些生物标志物的一般适用性的大量证据,并将其适用性扩展到以非传统抗凝剂采集的血浆。

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