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脑血管成像生物标志物在检测脑淀粉样血管病中的应用。

Utility of cerebrovascular imaging biomarkers to detect cerebral amyloidosis.

作者信息

Howe Matthew D, Caruso Megan R, Manoochehri Masood, Kunicki Zachary J, Emrani Sheina, Rudolph James L, Huey Edward D, Salloway Stephen P, Oh Hwamee

出版信息

medRxiv. 2024 May 28:2024.05.28.24308056. doi: 10.1101/2024.05.28.24308056.

DOI:10.1101/2024.05.28.24308056
PMID:38853879
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11160821/
Abstract

INTRODUCTION

The relationship between cerebrovascular disease (CVD) and amyloid-β (Aβ) in Alzheimer disease (AD) is understudied. We hypothesized that magnetic resonance imaging (MRI)-based CVD biomarkers, including cerebral microbleeds (CMBs), ischemic infarction, and white matter hyperintensities (WMH), would correlate with Aβ positivity on positron emission tomography (Aβ-PET).

METHODS

We cross-sectionally analyzed data from the Alzheimer's Disease Neuroimaging Initiative (ADNI, N=1,352). Logistic regression was used to calculate odds ratios (ORs), with Aβ-PET positivity as the standard-of-truth.

RESULTS

Following adjustment, WMH (OR=1.25) and superficial CMBs (OR=1.45) remained positively associated with Aβ-PET positivity (p<.001). Deep CMBs and infarcts exhibited a varied relationship with Aβ-PET in cognitive subgroups. The combined diagnostic model, which included CVD biomarkers and other accessible measures, significantly predicted Aβ-PET (pseudo-R =.41).

DISCUSSION

The study highlights the translational value of CVD biomarkers in diagnosing AD, and underscores the need for more research on their inclusion in diagnostic criteria. ADNI-2 ( NCT01231971 ), ADNI-3 ( NCT02854033 ).

摘要

引言

脑血管疾病(CVD)与阿尔茨海默病(AD)中的β淀粉样蛋白(Aβ)之间的关系研究不足。我们假设基于磁共振成像(MRI)的CVD生物标志物,包括脑微出血(CMB)、缺血性梗死和白质高信号(WMH),将与正电子发射断层扫描(Aβ-PET)上的Aβ阳性相关。

方法

我们对来自阿尔茨海默病神经影像倡议(ADNI,N = 1352)的数据进行了横断面分析。使用逻辑回归计算比值比(OR),以Aβ-PET阳性作为真值标准。

结果

调整后,WMH(OR = 1.25)和浅表CMB(OR = 1.45)与Aβ-PET阳性仍呈正相关(p <.001)。深部CMB和梗死在认知亚组中与Aβ-PET表现出不同的关系。包括CVD生物标志物和其他可获取测量指标的联合诊断模型显著预测了Aβ-PET(伪R = 0.41)。

讨论

该研究强调了CVD生物标志物在AD诊断中的转化价值,并强调了对将其纳入诊断标准进行更多研究的必要性。ADNI-2(NCT01231971),ADNI-3(NCT02854033)。

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