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阿尔茨海默病和帕金森病患者体液中的可溶性 TREM2。

Soluble TREM2 in body fluid in Alzheimer's disease and Parkinson's disease.

机构信息

Department of Neurology, Tianjin Huanhu Hospital, No. 6 Jizhao Road, Tianjin, 300222, China.

Department of Neurology, the Fourth Affiliated Hospital of Nanjing Medical University, Nanjing, 210031, Jiangsu, China.

出版信息

Neurol Sci. 2023 Aug;44(8):2743-2751. doi: 10.1007/s10072-023-06729-5. Epub 2023 Mar 13.

DOI:10.1007/s10072-023-06729-5
PMID:36913148
Abstract

BACKGROUND

Previous studies showed conflicting results regarding soluble triggering receptor expressed on myeloid cells 2 (sTREM2) level alteration in body fluid in Alzheimer's disease (AD) and Parkinson's disease (PD).

METHODS

We applied the STATA 12.0 software to compute standard mean difference (SMD) and 95% confidence interval (CI).

RESULTS

The study showed elevated sTREM2 level in cerebrospinal fluid (CSF) in AD, mild cognitive impairment (MCI), and preclinical AD (pre-AD) patients, compared to healthy controls (HCs) with random effects models (AD: SMD 0.28, 95% CI 0.12 to 0.44, I = 77.6%, p < 0.001; MCI: SMD 0.29, 95% CI 0.09 to 0.48, I = 89.7%, p < 0.001; pre-AD: SMD 0.24, 95% CI 0.00 to 0.48, I = 80.8%, p < 0.001). The study showed no significant difference in sTREM2 level in plasma between AD patients and HCs with a random effects model (SMD 0.06, 95% CI - 0.16 to 0.28, I = 65.6%, p = 0.008). The study showed no significant difference in sTREM2 level in CSF or plasma between PD patients and HCs with random effects models (CSF: SMD 0.33, 95% CI - 0.02 to 0.67, I = 85.6%, p < 0.001; plasma: SMD 0.37, 95% CI - 0.17 to 0.92, I = 77.8%, p = 0.011).

CONCLUSIONS

In conclusion, the study highlighted the CSF sTREM2 as a promising biomarker in the different clinical stages of AD. More studies were essential to explore the CSF and plasmatic concentrations of sTREM2 alteration in PD.

摘要

背景

先前的研究表明,可溶性髓系细胞触发受体 2(sTREM2)在阿尔茨海默病(AD)和帕金森病(PD)患者体液中的水平变化存在相互矛盾的结果。

方法

我们应用 STATA 12.0 软件计算标准均数差(SMD)和 95%置信区间(CI)。

结果

研究显示,与健康对照组(HCs)相比,AD、轻度认知障碍(MCI)和临床前 AD(pre-AD)患者的脑脊液(CSF)中 sTREM2 水平升高,采用随机效应模型(AD:SMD 0.28,95%CI 0.12 至 0.44,I=77.6%,p<0.001;MCI:SMD 0.29,95%CI 0.09 至 0.48,I=89.7%,p<0.001;pre-AD:SMD 0.24,95%CI 0.00 至 0.48,I=80.8%,p<0.001)。采用随机效应模型,研究显示 AD 患者和 HCs 之间的血浆 sTREM2 水平无显著差异(SMD 0.06,95%CI-0.16 至 0.28,I=65.6%,p=0.008)。采用随机效应模型,研究显示 PD 患者和 HCs 之间的 CSF 或血浆 sTREM2 水平无显著差异(CSF:SMD 0.33,95%CI-0.02 至 0.67,I=85.6%,p<0.001;血浆:SMD 0.37,95%CI-0.17 至 0.92,I=77.8%,p=0.011)。

结论

总之,该研究强调了 CSF sTREM2 作为 AD 不同临床阶段有前途的生物标志物。有必要开展更多研究来探索 PD 中 CSF 和血浆 sTREM2 浓度的变化。

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Microglial Activation, Tau Pathology, and Neurodegeneration Biomarkers Predict Longitudinal Cognitive Decline in Alzheimer's Disease Continuum.小胶质细胞激活、tau病理改变及神经退行性变生物标志物可预测阿尔茨海默病连续体中的纵向认知衰退。
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The Association of CSF sTREM2 With Cognitive Decline and Its Dynamic Change in Parkinson's Disease: Analysis of the PPMI Cohort.
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Microglia, Trem2, and Neurodegeneration.小胶质细胞、TREM2与神经退行性变
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脑脊液可溶性触发受体表达分子2与帕金森病认知功能减退的相关性及其动态变化:PPMI队列分析
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