Yoo Sang-Won, Oh Yoon-Sang, Ryu Dong-Woo, Ha Seunggyun, Kim Yuna, Yoo Ji-Yeon, Kim Joong-Seok
Department of Neurology, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Division of Nuclear Medicine, Department of Radiology, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
NPJ Parkinsons Dis. 2023 Jun 21;9(1):96. doi: 10.1038/s41531-023-00546-5.
In Parkinson's disease (PD), cardiovascular dysautonomia accumulates with disease progression, but studies are lacking on the natural history behind each subtype except orthostatic hypotension. This study investigated the early natural history of orthostatic blood pressure (BP) subtypes in PD. Two hundred sixty-seven early PD patients were included. Their cardiovascular functions were assessed by head-up tilt-test and I-metaiodobenzylguanidine scintigraphy. All patients were classified as having supine hypertension (SH), orthostatic hypertension (OHT), delayed orthostatic hypotension (dOH), or orthostatic hypotension (OH) according to consensus criteria. The patients were assigned to one of three groups: extreme BP dysregulation (BP), mild BP dysregulation (BP), and no BP dysregulation (BP) according to their orthostatic BP subtypes. The autonomic functions of 237 patients were re-assessed after approximately 3 years. Among initially enrolled subjects, 61.8% of the patients showed orthostatic BP dysregulation: 29.6% in the BP group and 32.2% in the BP group. At follow-up, the BP group increased in number, while the BP group diminished. Two-thirds of the initial BP patients maintained their initial subtype at follow-up. In comparison, 40.7% of the initial BP patients progressed to the BP group, and 32.4% and 14.7% of the initial BP group progressed to BP and BP groups, respectively. Cardiac denervation was most severe in the BP group, and a linear gradient of impairment was observed across the subtypes. In conclusion, various forms of positional BP dysregulation were observed during the early disease stage. SH and OH increased with disease progression, while OHT and dOH decreased, converting primarily to SH and/or OH.
在帕金森病(PD)中,心血管自主神经功能障碍会随着疾病进展而累积,但除体位性低血压外,关于每种亚型背后的自然病史的研究尚缺。本研究调查了PD患者体位性血压(BP)亚型的早期自然病史。纳入了267例早期PD患者。通过头高位倾斜试验和间碘苄胍闪烁扫描评估他们的心血管功能。根据共识标准,将所有患者分为仰卧位高血压(SH)、体位性高血压(OHT)、迟发性体位性低血压(dOH)或体位性低血压(OH)。根据体位性BP亚型,将患者分为三组之一:极端BP失调(BP)、轻度BP失调(BP)和无BP失调(BP)。约3年后对237例患者的自主神经功能进行了重新评估。在最初纳入的受试者中,61.8%的患者表现出体位性BP失调:BP组为29.6%,BP组为32.2%。在随访时,BP组人数增加,而BP组人数减少。三分之二的初始BP患者在随访时维持其初始亚型。相比之下,40.7%的初始BP患者进展为BP组,初始BP组分别有32.4%和14.7%进展为BP组和BP组。心脏去神经支配在BP组最为严重,并且在各亚型中观察到损伤的线性梯度。总之,在疾病早期阶段观察到了各种形式的体位性BP失调。SH和OH随着疾病进展而增加,而OHT和dOH减少,主要转变为SH和/或OH。