E08脑血流量与疾病严重程度和亨廷顿病前期/早期认知缺陷相关

H. Furby, James Ralph, A. Rosser, P. O'Callaghan, K. Murphy, R. Wise, J. Steventon
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引用次数: 0

摘要

临床前和死后研究显示HD患者大脑中存在脑血管异常。动脉自旋标记(ASL) MRI可用于无创测量HD脑中的脑血流量(CBF),这是一种已知反映脑血管健康的因素。据报道,早期HD患者皮层和皮层下灰质(GM)区域的CBF降低,CBF的减少超过了GM体积的变化(Chen et al., 2012)。脑血流减少可能导致神经元功能障碍和认知能力下降。CBF的改变需要在病程早期进行检测。目的通过使用ASL MRI测量脑血流量(CBF)来评估HD前/早期症状队列的早期脑血管病理征象。方法在卡迪夫大学脑研究成像中心(CUBRIC)进行3T MRI检查。招募了14名hd前/早期基因携带者和19名匹配的对照志愿者。ASL MRI用于量化全球灰质(GM)和皮质下区域(尾状核、壳核、丘脑和海马)的CBF。通过T1加权解剖扫描测量GM体积。认知测试包括SDMT、STROOP、Trailmaking、SCOLP、Forward digit span和verbal流畅性测试。结果/结局HD携带者的右侧丘脑和右侧尾状核CBF低于对照组,但在整个GM中没有(p<0.05)。然而,总体GM和左丘脑CBF与疾病负担评分(年龄x (CAG−35.5))相关,其中疾病晚期患者CBF升高。HD携带者的尾状体、壳核和丘脑的体积明显低于对照组,但海马体没有。区域容积不能预测脑血流差异。HD组的认知表现普遍较低,双侧尾状核CBF预测SDMT和SCOLP任务的表现,但这一效应在两组中相似。结论在hd前/早期可以检测到明显的CBF改变。脑血流与认知有关,与GM体积无关。不同皮质下区域的CBF减少表明早期异常不是全局性的,可能首先发生在HD的局部关键区域。与疾病相关的CBF增加可能反映了早期代偿性CBF升高。CBF如何与HD病理相关仍有待阐明。研究结果强调了ASL MRI作为HD病理的非侵入性测量的附加价值,补充了典型的解剖MRI方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
E08 Cerebral blood flow is associated with disease severity and cognitive defecits in pre/early huntington’s disease
Background Preclinical and post-mortem studies reveal cerebrovascular abnormalities in the HD brain. Arterial spin labelling (ASL) MRI can be used to non-invasively measure cerebral blood flow (CBF) in the HD brain, a factor known to reflect cerebrovascular health. Lower CBF has been reported in cortical and subcortical grey matter (GM) regions in early HD patients and reductions in CBF exceed changes in GM volume (Chen et al., 2012). Reduced CBF may contribute to neuronal dysfunction and cognitive performance. Alterations in CBF need to be probed earlier in the disease course. Aims To assess early signs of cerebrovascular pathology in a pre-/early-symptomatic HD cohort, by measuring cerebral blood flow (CBF) using ASL MRI. Methods 3T MRI was performed at Cardiff University Brain Research Imaging Centre (CUBRIC). Fourteen pre-/early-HD gene carriers and 19 matched control volunteers were recruited. ASL MRI was used to quantify CBF across global grey matter (GM) and subcortical regions (caudate, putamen, thalamus and hippocampus). GM volume was measured from T1 weighted anatomical scans. Cognitive tests included the SDMT, STROOP, Trailmaking, SCOLP, Forward digit span and verbal fluency tests. Results/outcome CBF was lower in HD carriers than controls in the right thalamus and right caudate, but not across global GM (p<0.05). However, global GM and left thalamus CBF was related to disease burden score (Age x (CAG −35.5), where those later in the disease showed elevated CBF. Volume was significantly lower in HD carriers than controls in caudate, putamen and thalamus, but not the hippocampus. Regional volume did not predict CBF differences. Cognitive performance was generally lower in HD group, and bilateral caudate CBF predicted performance on SDMT and SCOLP tasks, but this effect was similar in both groups. Conclusions Apparent alterations in CBF can be detected in pre-/early-HD. CBF was related to cognition, but not to GM volume. A CBF reduction in distinct subcortical regions suggest that early abnormalities are not global, and may first occur locally in key regions in HD. A disease related increase in CBF may reflect an early compensatory elevation in CBF. How CBF is related to HD pathology remains to be elucidated. Findings highlight the additional value of ASL MRI as a non-invasive measure of HD pathology that complements typical anatomical MRI approaches.
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