Yoritaka Asako, Hayashi Tetsuo, Fusegi Keiko, Nakayama Sachiko, Haneda Jun, Hattori Nobutaka
Department of Neurology, Juntendo University Koshigaya Hospital, Saitama 343-0032, Japan.
Department of Radiology, Koshigaya Municipal Hospital, Saitama 343-8577, Japan.
Parkinsons Dis. 2024 May 30;2024:5550362. doi: 10.1155/2024/5550362. eCollection 2024.
Patients with Parkinson's disease (PD) experience significantly reduced quality of life when PD is complicated with Pisa syndrome (PS). PS is a postural abnormality associated with a lateral bending of the trunk, causing the patient to lean to one side. Microsaccades during fixation are transmitted to the visual cortex, and this gaze movement may be impaired in PD. We aimed to detect presymptomatic signs of PS. We enrolled 50 patients with PD without dementia and investigated the visual systems in patients with concurrent PD and PS based on a Romberg ratio of<1.0. Gaze analysis, pupil diameter, stabilization tests, neuropsychological tests, and cerebral perfusion scintigraphy were reviewed and statistically analyzed. Two years later, we divided the patients into three groups as follows: PISA++ (patients who had PS at enrollment), PISA-+ (patients without PS that developed PS during the 2-year period), and PISA-- (patients without PS that did not develop PS during the 2-year period). The PISA-+ group exhibited a significantly higher daily levodopa dose and longer fixations, as well as lower position discrimination, Wechsler Adult Intelligence Scale-Third Edition blocking, and blood flow in the left supramarginal and orbital gyri than that in the PISA-- group. The PISA++ group showed a significantly longer fixation time and lower Mini-Mental State Examination score, Romberg ratio of area, amplitude, velocity of microsaccades, and blood flow in the left precuneus and cuneus than that in the PISA-+ group. Before the onset of PS, hypoperfusion occurred in the correlative visual cortex and the position discrimination test. Patients with PS have reduced saccades and slow microsaccades.
帕金森病(PD)患者并发 Pisa 综合征(PS)时,生活质量会显著下降。PS 是一种与躯干侧弯相关的姿势异常,导致患者向一侧倾斜。注视期间的微扫视会传递到视觉皮层,而这种注视运动在 PD 患者中可能受损。我们旨在检测 PS 的症状前体征。我们招募了 50 名无痴呆的 PD 患者,并根据 Romberg 比率<1.0 对同时患有 PD 和 PS 的患者的视觉系统进行了研究。对注视分析、瞳孔直径、稳定性测试、神经心理学测试和脑灌注闪烁扫描进行了回顾和统计分析。两年后,我们将患者分为三组:PISA++(入组时患有 PS 的患者)、PISA-+(入组时无 PS 但在两年期间发展为 PS 的患者)和 PISA--(入组时无 PS 且在两年期间未发展为 PS 的患者)。与 PISA--组相比,PISA-+组的每日左旋多巴剂量显著更高、注视时间更长,同时位置辨别能力、韦氏成人智力量表第三版阻滞能力以及左缘上回和眶回的血流更低。与 PISA-+组相比,PISA++组的注视时间显著更长、简易精神状态检查表得分更低、微扫视面积的 Romberg 比率、幅度、速度以及左楔前叶和楔叶的血流更低。在 PS 发作前,相关视觉皮层出现灌注不足以及位置辨别测试异常。患有 PS 的患者扫视减少且微扫视缓慢。