认知障碍患者的脑淀粉样血管病--脑脊液生物标记物

IF 2.2 4区 医学 Q3 CLINICAL NEUROLOGY
Dementia and Geriatric Cognitive Disorders Pub Date : 2024-01-01 Epub Date: 2024-06-18 DOI:10.1159/000539884
Kasia Gustaw Rothenberg, Lynn Bekris, James B Leverenz, Jenny Wu, Jonathan Lee, Volodymyr Statsevych, Paul Ruggieri, Stephen E Jones
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引用次数: 0

摘要

简介脑淀粉样血管病(CAA)的特征是淀粉样β(Aβ)沉积在脑血管中,导致出血现象和认知障碍。基于磁共振成像(MRI)的标准可以诊断出体内可能存在的 CAA,但这种诊断并不能预测 CAA 的最终发展:我们对 464 名认知障碍患者进行了一项回顾性队列研究,这些患者的数据被纳入脑健康生物库。我们评估了有CAA和无CAA患者的去识别参数,包括性别、年龄、认知评分、APOE状态和脑脊液(CSF)中Aβ 1-40、Aβ 1-42、磷酸化tau和总tau的水平。结果发现,在46例CAA患者中,53例存在Aβ 1-40和Aβ 1-42水平的Aβ 1-40和Aβ 1-42水平的Aβ 1-40和Aβ 1-42水平的Aβ 1-42水平:464例患者中有53例(11.5%)存在CAA。有 CAA 的患者 P-tau 水平明显更高(115 vs 84.3 pg/ml p=0.038)。在单变量分析中,年龄越大(OR, 1.036; 95% CI: 1.008, 1.064; p = 0.011)、脑脊液中 Aβ 1-40 水平越低(OR, 0.685; 95% CI: 0.534, 0.878; p = 0.003),患 CAA 的风险越高。在多变量分析中,Aβ 1-40 的 CSF 水平降低,患 CAA 的风险仍然较高(OR,0.681;95% CI:0.531,0.874;p = 0.003):这些研究结果表明,CSF中的Aβ 1-40水平可能是痴呆症患者CAA的一个有用的分子生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cerebral Amyloid Angiopathy in Patients with Cognitive Impairment: Cerebrospinal Fluid Biomarkers.

Introduction: Cerebral amyloid angiopathy (CAA) is characterized by amyloid β (Aβ) deposition in brain vessels, leading to hemorrhagic phenomena and cognitive impairment. Magnetic resonance imaging (MRI)-based criteria allow a diagnosis of probable CAA in vivo, but such a diagnosis cannot predict the eventual development of CAA.

Methods: We conducted a retrospective cohort study of 464 patients with cognitive disorders whose data were included in a brain health biobank. De-identified parameters including sex, age, cognitive score, APOE status, and cerebrospinal fluid (CSF) levels of Aβ 1-40, Aβ 1-42, phosphorylated tau, and total tau were assessed in those with and without CAA. Odds ratios (ORs) and 95% confidence intervals (CIs) were determined.

Results: CAA was present in 53 of 464 (11.5%) patients. P-tau level was significantly higher in those with CAA (115 vs. 84.3 pg/mL p = 0.038). In univariate analyses, the risk of developing CAA was higher with increased age (OR, 1.036; 95% CI: 1.008, 1.064; p = 0.011) and decreased CSF level of Aβ 1-40 (OR, 0.685; 95% CI: 0.534, 0.878; p = 0.003). In multivariate analyses, the risk of CAA remained higher with a decreased CSF level of Aβ 1-40 (OR, 0.681; 95% CI: 0.531, 0.874; p = 0.003).

Conclusion: These findings suggest that Aβ 1-40 levels in the CSF might be a useful molecular biomarker of CAA in patients with dementia.

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来源期刊
CiteScore
4.70
自引率
0.00%
发文量
46
审稿时长
2 months
期刊介绍: As a unique forum devoted exclusively to the study of cognitive dysfunction, ''Dementia and Geriatric Cognitive Disorders'' concentrates on Alzheimer’s and Parkinson’s disease, Huntington’s chorea and other neurodegenerative diseases. The journal draws from diverse related research disciplines such as psychogeriatrics, neuropsychology, clinical neurology, morphology, physiology, genetic molecular biology, pathology, biochemistry, immunology, pharmacology and pharmaceutics. Strong emphasis is placed on the publication of research findings from animal studies which are complemented by clinical and therapeutic experience to give an overall appreciation of the field.
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