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Mixed-location cerebral microbleeds as a biomarker of neurodegeneration in a memory clinic population

机译:混合位置的脑微出血是记忆诊所人群神经变性的生物标志物

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摘要

Cerebral microbleeds (CMBs) in the lobar and deep locations are associated with two distinct pathologies: cerebral amyloid angiopathy and hypertensive arteriopathy. However, the role of mixed-location CMBs in neurodegeneration remains unexplored. We investigated the associations between strictly lobar, strictly deep and mixed-location CMBs with markers of neurodegeneration. This study recruited 477 patients from a memory clinic who underwent 3T MRI scans. CMBs were categorized into strictly lobar, strictly deep and mixed-location. Cortical thickness, white matter volume and subcortical structural volumes were quantified using Free-Surfer. Linear regression models were performed to assess the association between CMBs and cerebral atrophy, and the mean difference (β) and 95% confidence intervals (CIs) were reported. In the regression analyses, mixed-location CMBs were associated with smaller cortical thickness of limbic region [β= -0.01; 95% CI= -0.02, -0.00, p=0.007) as well as with smaller accumbens volume [β= -0.01; 95% CI= -0.02, -0.00, p=0.004) and presubiculum region of hippocampus [β= -0.01; 95% CI= -0.02, -0.00, p=0.002). Strictly lobar CMBs were associated with smaller total white matter volume [β= -0.03; 95% CI= -0.04, -0.01, p<0.001] and with region specific white matter volumes. The underlying mechanism requires further research and may involve shared mechanisms of vascular dysfunction and neurodegeneration.
机译:大叶和深部的脑微出血(CMB)与两种不同的病理相关:脑淀粉样血管病和高血压性动脉病。然而,混合位置CMBs在神经退行性变中的作用尚待探索。我们调查了严格的大叶,严格的深度和混合位置CMBs与神经变性标记之间的关联。这项研究从一家记忆诊所招募了477位接受3T MRI扫描的患者。 CMB分为严格的大叶,严格的深度和混合位置。皮质厚度,白质体积和皮质下结构体积使用Free-Surfer进行定量。进行线性回归模型以评估CMB与脑萎缩之间的关联,并报告了平均差异(β)和95%置信区间(CIs)。在回归分析中,混合位置的CMB与边缘区域的皮质厚度较小相关[β= -0.01; 95%CI = -0.02,-0.00,p = 0.007)以及较小的伏安体积[β= -0.01; 95%CI = -0.02,-0.00,p = 0.004)和海马前丘脑区[β= -0.01; 95%CI = -0.02,-0.00,p = 0.002)。严格的大叶CMB与较小的总白质体积相关[β= -0.03; 95%CI = -0.04,-0.01,p <0.001],且具有特定区域的白质体积。潜在的机制需要进一步研究,并可能涉及血管功能障碍和神经变性的共同机制。

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