Cleo Roberts Center, Banner Sun Health Research Institute, Sun City, AZ, United States.
Department of Neurology, Mayo Clinic College of Medicine, Scottsdale, AZ, United States.
Parkinsonism Relat Disord. 2018 Oct;55:92-96. doi: 10.1016/j.parkreldis.2018.05.020. Epub 2018 May 17.
Inability to accurately diagnose Lewy type alpha-synucleinopathy (LTS) pre-mortem has been a major obstacle to clinical care and research. Probable REM sleep behavior disorder (PRBD) diagnosed with support of instruments such as the Mayo Sleep Questionnaire (MSQ) may provide a cost effective means of predicting LTS. Since 2007, 602 subjects in the Arizona Study of Aging and Neurodegenerative Disorders had clinician assessment for PRBD (298 with, 304 without support of the MSQ), completed cognitive and movement examinations, and had neuropathological assessment. Mean age at death was 84.8 years. Histological evidence of LTS was found in 80/101(79.2%) cases with PRBD and 198/501 (39.5%) without PRBD (p < 0.001). Overall sensitivity for predicting LTS by PRBD diagnosis was 28.8%, specificity 93.5%, positive predictive value (PPV) 79.2%, negative predictive value (NPV) 60.5%. Diagnosis of PRBD was less frequently present in subjects without LTS [4/105 (3.8%) of healthy controls, 42/255 (16.5%) AD, 2/33 (6.1%) progressive supranuclear palsy (PSP) without LTS] than in subjects with LTS [11/46 (23.9%) DLB, 58/104 (55.8%) PD, and 4/16 (25.0%) PSP with LTS.] PRBD was not present in any of 46 subjects with incidental Lewy body disease (ILBD). MSQ-supported diagnosis of PRBD appears useful for predicting LTS in manifest neurodegenerative disease, but not necessarily ILBD. Additional prospective autopsy research, including well-characterized polysomnogram-confirmed RBD subjects, is needed to elucidate the earliest tissue abnormalities in the "idiopathic" (premotor/pre-dementia) stage of RBD.
无法在生前准确诊断路易体阿尔法-突触核蛋白病 (LTS) 一直是临床护理和研究的主要障碍。使用 Mayo 睡眠问卷 (MSQ) 等仪器诊断的可能 REM 睡眠行为障碍 (PRBD) 可能提供一种预测 LTS 的具有成本效益的方法。自 2007 年以来,亚利桑那州衰老和神经退行性疾病研究中的 602 名受试者接受了 PRBD 的临床评估(298 名有支持,304 名无支持的 MSQ),完成了认知和运动检查,并接受了神经病理学评估。死亡时的平均年龄为 84.8 岁。在有 PRBD 的 101 例(79.2%)和无 PRBD 的 501 例(39.5%)病例中均发现了 LTS 的组织学证据(p<0.001)。PRBD 诊断预测 LTS 的总灵敏度为 28.8%,特异性为 93.5%,阳性预测值 (PPV) 为 79.2%,阴性预测值 (NPV) 为 60.5%。在无 LTS 的受试者中,PRBD 的诊断频率较低[健康对照组的 105 例中 4 例(3.8%),AD 的 255 例中 42 例(16.5%),无 LTS 的 33 例中 2 例(6.1%)进展性核上性麻痹 (PSP)],而在有 LTS 的受试者中,PRBD 的诊断频率较高[DLB 的 46 例中 11 例(23.9%),PD 的 104 例中 58 例(55.8%),和有 LTS 的 16 例中 4 例(25.0%)PSP]。在 46 例偶然Lewy 体病 (ILBD) 患者中均未发现 PRBD。MSQ 支持的 PRBD 诊断似乎可用于预测明显神经退行性疾病中的 LTS,但不一定适用于 ILBD。需要进行更多的前瞻性尸检研究,包括经过充分特征描述的多导睡眠图确认的 RBD 受试者,以阐明 RBD 的“特发性”(运动前/痴呆前)阶段中最早的组织异常。