How well do plasma Alzheimer's disease biomarkers reflect the CSF amyloid status?

IF 8.7 1区 医学 Q1 CLINICAL NEUROLOGY Journal of Neurology, Neurosurgery, and Psychiatry Pub Date : 2024-12-18 DOI:10.1136/jnnp-2024-334122
Jemma Hazan, Emily Abel, Miguel Rosa Grilo, Deborah Alawode, Ines Laranjinha, Amanda J Heslegrave, Kathy Y Liu, Jonathan M Schott, Robert Howard, Henrik Zetterberg, Nick C Fox
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Abstract

Background: Can plasma biomarkers as well as cerebrospinal fluid (CSF) perform in the separation of amyloid-beta-positive (Aβ+) vs amyloid-beta-negative (Aβ-) groups across an age range seen in an NHS cognitive disorder clinic?

Methods: As part of the routine diagnostic investigation of 111 clinic patients who had contemporaneous blood and CSF samples taken, patients were categorised into Aβ+ and Aβ- groups based on their CSF in an Aβ42/40 ratio. We then evaluated four single molecule array (Simoa) Quanterix assays, quantifying single plasma analytes and ratios (p-tau217, p-tau217/Aβ42 ratio, p-tau181, p-tau181/Aβ42 ratio and Aβ42/40 ratio) in their ability to distinguish between these groups and the effect of age.

Results: The median (range) age of participants was 66 (55-79) years with 48 females (43.2%). The areas under the curve (AUC), not accounting for age, for the ability to discriminate Aβ+ from Aβ- groups were plasma p-tau217 AUC=0.94, Aβ42/40 AUC=0.78 and p-tau181 AUC=0.77. Combining p-tau217/Aβ42 increased the AUC to 0.97. The difference between the groups was influenced by age with less separation in older individuals: a significant negative interaction term between age and group for plasma p-tau217 concentrations (-0.037, p=0.013) and p-tau217/Aβ42 ratio (-0.007, p=0.008).

Conclusions: There was variable performance of plasma biomarkers to recapitulate the CSF assay. Both p-tau217 and p-tau217/Aβ42 showed excellent promise as surrogates of CSF amyloid status, although with slightly reduced performance in older individuals. There was poorer discriminatory ability for p-tau181 and Aβ42/40. Further research is needed to address potential age-related confounds.

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血浆阿尔茨海默病生物标志物反映脑脊液淀粉样蛋白状态的效果如何?
背景:血浆生物标志物和脑脊液(CSF)是否可以在NHS认知障碍诊所中观察到的跨年龄范围的淀粉样蛋白- β阳性(Aβ+)和淀粉样蛋白- β阴性(Aβ-)组的分离?方法:对111例同期采血的临床患者进行常规诊断调查,根据Aβ42/40的脑脊液比例将患者分为Aβ+组和Aβ-组。然后,我们评估了四种单分子阵列(Simoa) Quanterix测定方法,定量了单个血浆分析物和比率(p-tau217、p-tau217/ a - β42比率、p-tau181、p-tau181/ a - β42比率和a - β42/40比率)区分这些组的能力和年龄的影响。结果:参与者的年龄中位数(范围)为66(55-79)岁,其中48名女性(43.2%)。血浆p-tau217 AUC=0.94, a - β42/40 AUC=0.78, p-tau181 AUC=0.77,曲线下面积(AUC)与年龄无关。p-tau217/ a - β42组合使AUC提高到0.97。组间差异受年龄影响,老年人分离较少:血浆p-tau217浓度(-0.037,p=0.013)和p-tau217/ a - β42比值(-0.007,p=0.008)在年龄和组间呈显著负交互作用项。结论:血浆生物标志物表现不一,可以概括脑脊液检测。p-tau217和p-tau217/ a - β42作为脑脊液淀粉样蛋白状态的替代物显示出良好的前景,尽管在老年人中的表现略有下降。p-tau181和a - β42/40的区分能力较差。需要进一步的研究来解决潜在的与年龄相关的混淆。
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来源期刊
CiteScore
15.70
自引率
1.80%
发文量
888
审稿时长
6 months
期刊介绍: The Journal of Neurology, Neurosurgery & Psychiatry (JNNP) aspires to publish groundbreaking and cutting-edge research worldwide. Covering the entire spectrum of neurological sciences, the journal focuses on common disorders like stroke, multiple sclerosis, Parkinson’s disease, epilepsy, peripheral neuropathy, subarachnoid haemorrhage, and neuropsychiatry, while also addressing complex challenges such as ALS. With early online publication, regular podcasts, and an extensive archive collection boasting the longest half-life in clinical neuroscience journals, JNNP aims to be a trailblazer in the field.
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