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心脏18F-多巴胺正电子发射断层扫描可预测单纯自主神经功能衰竭的表型转化类型。

Cardiac 18F-Dopamine Positron Emission Tomography Predicts the Type of Phenoconversion of Pure Autonomic Failure.

作者信息

Lenka Abhishek, Isonaka Risa, Holmes Courtney, Goldstein David S

机构信息

Baylor College of Medicine.

National Institute of Neurological Disorders and Stroke Intramural Research Program.

出版信息

Res Sq. 2023 Jul 17:rs.3.rs-3157807. doi: 10.21203/rs.3.rs-3157807/v1.

Abstract

BACKGROUND

Pure autonomic failure (PAF) is a rare disease characterized clinically by neurogenic orthostatic hypotension (nOH) and biochemically by peripheral noradrenergic deficiency. Clinically diagnosed PAF can evolve ("phenoconvert") to a central Lewy body disease (LBD, e.g., Parkinson's disease (PD) or dementia with Lewy bodies (DLB)) or to the non-LBD synucleinopathy multiple system atrophy (MSA). We examined whether cardiac F-dopamine positron emission tomography (PET) predicts the trajectory of phenoconversion in PAF. Since cardiac F-dopamine-derived radioactivity always is decreased in LBDs with nOH and usually is normal in MSA, we hypothesized that PAF patients with low cardiac F-dopamine-derived radioactivity may phenoconvert to a central LBD but do not phenoconvert to MSA.

METHODS

We reviewed data from all the patients seen at the National Institutes of Health Clinical Center from 1994 to 2023 with a clinical diagnosis of PAF and data about serial F-dopamine PET.

RESULTS

Twenty patients met the above criteria. Of 15 with low cardiac F-dopamine-derived radioactivity, 6 (40%) phenoconverted to PD or DLB and none to MSA. Of 5 patients with consistently normal F-dopamine PET, 4 phenoconverted to MSA, and the other at autopsy had neither a central LBD nor MSA.

CONCLUSION

In this case series, 40% of patients with nOH and low cardiac F-dopamine-derived radioactivity phenoconverted to PD or DLB during follow-up; none phenoconverted to MSA. Cardiac F-DA PET therefore can predict the type of phenoconversion in PAF. This capability could refine eligibility criteria for entry into disease-modification trials aiming to prevent evolution of PAF to symptomatic central LBDs.

摘要

背景

纯自主神经功能衰竭(PAF)是一种罕见疾病,临床特征为神经源性直立性低血压(nOH),生化特征为外周去甲肾上腺素能缺乏。临床诊断的PAF可演变为(“表型转换”)中枢性路易体病(LBD,如帕金森病(PD)或路易体痴呆(DLB))或非LBD突触核蛋白病多系统萎缩(MSA)。我们研究了心脏F-多巴胺正电子发射断层扫描(PET)是否能预测PAF的表型转换轨迹。由于在伴有nOH的LBD中,源自心脏F-多巴胺的放射性总是降低的,而在MSA中通常是正常的,我们推测心脏F-多巴胺衍生放射性低的PAF患者可能会表型转换为中枢性LBD,但不会表型转换为MSA。

方法

我们回顾了1994年至2023年在美国国立卫生研究院临床中心就诊的所有临床诊断为PAF的患者的数据以及关于连续F-多巴胺PET的数据。

结果

20名患者符合上述标准。在15名心脏F-多巴胺衍生放射性低的患者中,6名(40%)表型转换为PD或DLB,无一人转换为MSA。在5名F-多巴胺PET始终正常的患者中,4名表型转换为MSA,另一名在尸检时既没有中枢性LBD也没有MSA。

结论

在这个病例系列中,40%的伴有nOH且心脏F-多巴胺衍生放射性低的患者在随访期间表型转换为PD或DLB;无一人表型转换为MSA。因此,心脏F-DA PET可以预测PAF的表型转换类型。这种能力可以完善进入旨在预防PAF演变为有症状中枢性LBD的疾病修饰试验的入选标准。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fde1/10371148/1502052c28ac/nihpp-rs3157807v1-f0001.jpg

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