A Study of the Relationship Between Uric Acid and Substantia Nigra Brain Connectivity in Patients With REM Sleep Behavior Disorder and Parkinson's Disease

被引:16
|
作者
Ellmore, Timothy M. [1 ]
Suescun, Jessika [2 ]
Castriotta, Richard J. [3 ]
Schiess, Mya C. [2 ]
机构
[1] CUNY, Dept Psychol, New York, NY 10021 USA
[2] Univ Texas Houston, McGovern Med Sch Houston, Dept Neurol, Houston, TX USA
[3] Univ Southern Calif, Keck Sch Med, Dept Clin Med, Los Angeles, CA 90007 USA
来源
FRONTIERS IN NEUROLOGY | 2020年 / 11卷
关键词
uric acid; REM sleep behavior disorder; parkinson's disease; resting state; functional connectivity; LEFT-HEMISPHERIC PREDOMINANCE; FUNCTIONAL CONNECTIVITY; PLASMA URATE; SERUM URATE; DELAYED EMERGENCE; RISK; MOVEMENT; PROGRESSION; MEN; DYSFUNCTION;
D O I
10.3389/fneur.2020.00815
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Low levels of the natural antioxidant uric acid (UA) and the presence of REM sleep behavior disorder (RBD) are both associated with an increased likelihood of developing Parkinson's disease (PD). RBD and PD are also accompanied by basal ganglia dysfunction including decreased nigrostriatal and nigrocortical resting state functional connectivity. Despite these independent findings, the relationship between UA and substantia nigra (SN) functional connectivity remains unknown. In the present study, voxelwise analysis of covariance was used in a cross-sectional design to explore the relationship between UA and whole-brain SN functional connectivity using the eyes-open resting state fMRI method in controls without RBD, patients with idiopathic RBD, and PD patients with and without RBD. The results showed that controls exhibited a positive relationship between UA and SN functional connectivity with left lingual gyrus. The positive relationship was reduced in patients with RBD and PD with RBD, and the relationship was found to be negative in PD patients. These results are the first to show differential relationships between UA and SN functional connectivity among controls, prodromal, and diagnosed PD patients in a ventral occipital region previously documented to be metabolically and structurally altered in RBD and PD. More investigation, including replication in longitudinal designs with larger samples, is needed to understand the pathophysiological significance of these changes.
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页数:14
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