Lenka Abhishek, Isonaka Risa, Holmes Courtney, Goldstein David S
Baylor College of Medicine.
National Institute of Neurological Disorders and Stroke Intramural Research Program.
Res Sq. 2023 Jul 17:rs.3.rs-3157807. doi: 10.21203/rs.3.rs-3157807/v1.
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.
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.
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.
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.
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。
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。
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。
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。