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孤立性快速眼动睡眠行为障碍中的5-羟色胺转运体密度

Serotonin transporter density in isolated rapid eye movement sleep behavioral disorder.

作者信息

Garwood Mark, Vijayakumar Punithavathy, Bohnen Nicolaas I, Koeppe Robert A, Kotagal Vikas

机构信息

Department of Neurology, University of Michigan, Ann Arbor, MI, United States.

Division of Nuclear Medicine, Department of Radiology, University of Michigan, Ann Arbor, MI, United States.

出版信息

Front Sleep. 2024;2. doi: 10.3389/frsle.2023.1298854. Epub 2024 Jan 29.

Abstract

BACKGROUND/OBJECTIVE: The serotoninergic nervous system is known to play a role in the maintenance of rapid eye movement (REM) sleep. Serotoninergic projections are known to be vulnerable in synucleinopathies. To date, positron emission tomography (PET) studies using serotonin-specific tracers have not been reported in isolated REM sleep behavior disorder (iRBD).

METHODS

We conducted a cross-sectional imaging study using serotonin transporter (SERT) C-3-amino-4-(2-dimethylaminomethyl-phenylsulfaryl)-benzonitrile (DASB) PET to identify differences in serotonin system integrity between 11 participants with iRBD and 16 older healthy controls.

RESULTS

Participants with iRBD showed lower DASB distribution volume ratios (DVRs) in the total neocortical mantle [1.13 (SD: 0.07) vs. 1.19 (SD: 0.06); = 2.33, = 0.028)], putamen [2.07 (SD: 0.19) vs. 2.25 (SD: 0.18); = 2.55, = 0.017], and insula [1.26 (SD: 0.11) vs. 1.39 (SD: 0.09); = 3.58, = 0.001]. Paradoxical increases relative to controls were seen in cerebellar hemispheres [0.98 (SD: 0.04) vs. 0.95 (SD: 0.02); = 2.93, = 0.007)]. No intergroup differences were seen in caudate, substantia nigra, or other brainstem regions with the exception of the dorsal mesencephalic raphe [3.08 (SD: 0.53) vs. 3.47 (SD: 0.48); = 2.00, = 0.056] that showed a non-significant trend toward lower values in iRBD.

CONCLUSIONS

Insular, neocortical, and striatal serotoninergic terminal loss may be common in prodromal synucleinopathies before the onset of parkinsonism or dementia. Given our small sample size, these results should be interpreted as hypothesis-generating/exploratory in nature.

摘要

背景/目的:已知血清素能神经系统在快速眼动(REM)睡眠的维持中起作用。已知血清素能投射在突触核蛋白病中易受影响。迄今为止,尚未有关于使用血清素特异性示踪剂的正电子发射断层扫描(PET)研究在孤立性快速眼动睡眠行为障碍(iRBD)中的报道。

方法

我们进行了一项横断面成像研究,使用血清素转运体(SERT)C - 3 - 氨基 - 4 -(2 - 二甲基氨基甲基 - 苯基硫芳基)- 苄腈(DASB)PET来确定11名iRBD参与者和16名老年健康对照者之间血清素系统完整性的差异。

结果

iRBD参与者在整个新皮质脑壳中的DASB分布体积比(DVRs)较低[1.13(标准差:0.07)对1.19(标准差:0.06);t = 2.33,P = 0.028],壳核[2.07(标准差:0.19)对2.25(标准差:0.18);t = 2.55,P = 0.017],以及脑岛[1.26(标准差:0.11)对1.39(标准差:0.09);t = 3.58,P = 0.001]。与对照组相比,小脑半球出现了反常增加[0.98(标准差:0.04)对0.95(标准差:0.02);t = 2.93,P = 0.007]。在尾状核、黑质或其他脑干区域,除了中脑背侧缝际核[3.08(标准差:0.53)对3.47(标准差:0.48);t = 2.00,P = 0.056]外,未观察到组间差异,该区域在iRBD中显示出值较低的非显著趋势。

结论

在帕金森病或痴呆症发作前的前驱性突触核蛋白病中,脑岛、新皮质和纹状体血清素能终末丧失可能很常见。鉴于我们的样本量较小,这些结果本质上应被解释为产生假设/探索性的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d329/11101191/d8867d226414/nihms-1968638-f0001.jpg

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