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脑脊液中可溶性 TREM2 升高的生物学相关性。

Biological correlates of elevated soluble TREM2 in cerebrospinal fluid.

机构信息

Vanderbilt Memory and Alzheimer's Center, Vanderbilt University Medical Center, Nashville, TN, USA; Pharmacology Department, Vanderbilt University Medical Center, Nashville, TN, USA.

Vanderbilt Memory and Alzheimer's Center, Vanderbilt University Medical Center, Nashville, TN, USA; Department of Neurology, Vanderbilt University Medical Center, Nashville, TN, USA; Vanderbilt Genetics Institute, Vanderbilt University Medical Center, Nashville, TN, USA.

出版信息

Neurobiol Aging. 2022 Oct;118:88-98. doi: 10.1016/j.neurobiolaging.2022.06.013. Epub 2022 Jul 5.

Abstract

Cerebrospinal fluid (CSF) soluble triggering receptor expressed on myeloid cells-2 (sTREM2) is an emerging biomarker of neuroinflammation in Alzheimer's disease (AD). Yet, sTREM2 expression has not been systematically evaluated in relation to concomitant drivers of neuroinflammation. While associations between sTREM2 and tau in CSF are established, we sought to determine additional biological correlates of CSF sTREM2 during the prodromal stages of AD by evaluating CSF Aβ species (Aβ), a fluid biomarker of blood-brain barrier integrity (CSF/plasma albumin ratio), and CSF biomarkers of neurodegeneration measured in 155 participants from the Vanderbilt Memory and Aging Project. A novel association between high CSF levels of both sTREM2 and Aβ was observed and replicated in an independent dataset. Aβ levels, as well as the CSF/plasma albumin ratio, explained additional and unique variance in sTREM2 levels above and beyond that of CSF biomarkers of neurodegeneration. The component of sTREM2 levels correlated with Aβ levels best predicted future cognitive performance. We highlight potential contributions of Aβ homeostasis and blood-brain barrier integrity to elevated CSF sTREM2, underscoring novel biomarker associations relevant to disease progression and clinical outcome measures.

摘要

脑脊液(CSF)可溶性髓系细胞触发受体 2(sTREM2)是阿尔茨海默病(AD)神经炎症的新兴生物标志物。然而,sTREM2 的表达尚未与神经炎症的伴随驱动因素进行系统评估。虽然 CSF 中 sTREM2 与 tau 之间存在关联,但我们试图通过评估 CSF 中的 Aβ 种类(Aβ)、血脑屏障完整性的液体生物标志物(CSF/血浆白蛋白比)以及来自范德比尔特记忆和衰老项目的 155 名参与者的 CSF 神经退行性变生物标志物,来确定 AD 发生前阶段 CSF sTREM2 的其他生物学相关性。我们观察到 CSF 中 sTREM2 和 Aβ 水平均升高之间存在新的关联,并在独立数据集进行了复制。Aβ 水平以及 CSF/血浆白蛋白比在神经退行性变生物标志物的基础上进一步解释了 sTREM2 水平的额外和独特差异。与 Aβ 水平相关的 sTREM2 水平成分最佳预测了未来的认知表现。我们强调了 Aβ 动态平衡和血脑屏障完整性对 CSF sTREM2 升高的潜在贡献,突出了与疾病进展和临床结果测量相关的新型生物标志物关联。

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