多巴胺能
壳核
多巴胺转运体
多巴胺
白质
帕金森病
心理学
尾状核
磁共振弥散成像
神经科学
内科学
医学
疾病
磁共振成像
放射科
作者
Seok Chung,Yae Ji Kim,Yun Joong Kim,Hye Sun Lee,Seong Jin Jeong,JI-MAN HONG,Young H. Sohn,Mijin Yun,Yong Jeong,Phil Ho Lee
出处
期刊:Neurology
[Lippincott Williams & Wilkins]
日期:2022-10-04
卷期号:99 (24): e2672-e2682
标识
DOI:10.1212/wnl.0000000000201269
摘要
Individual variability in nigrostriatal dopaminergic denervation is an important factor underlying clinical heterogeneity in Parkinson's disease (PD). This study aimed to explore whether the pattern of striatal dopamine depletion was associated with white matter (WM) networks in PD.A total of 240 newly diagnosed PD patients who underwent 18F-FP-CIT PET scans and brain diffusion tensor imaging at initial assessment were enrolled in this study. We measured 18F-FP-CIT tracer uptake as an indirect marker for striatal dopamine depletion. Factor analysis-derived striatal dopamine loss patterns were estimated in each patient to calculate the composite scores of four striatal subregion factors (caudate, more- and less-affected sensorimotor striata, and anterior putamen) based on the availability of striatal dopamine transporter. The WM structural networks that were correlated with the composite scores of each striatal subregion factor were identified using a network-based statistic analysis.A higher composite score of caudate (i.e., relatively preserved dopaminergic innervation in the caudate) was associated with a strong structural connectivity in a single subnetwork comprising the left caudate and left frontal gyri. Selective dopamine loss in the caudate was associated with strong connectivity in the structural subnetwork whose hub nodes were bilateral thalami and left insula, which were connected to the anterior cingulum. However, no subnetworks were correlated with the composite scores of other striatal subregion factors. The connectivity strength of the network with a positive correlation with the composite score of caudate affected the frontal/executive function either directly or indirectly through the mediation of dopamine depletion in the caudate.
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