University of Pennsylvania, Department of Neurology, Philadelphia, PA, 19104, United States.
University of Pennsylvania, Department of Neurology, Philadelphia, PA, 19104, United States; Michael J. Crescenz VA Medical Center, Parkinson's Disease Research, Education, and Clinical Center, Philadelphia, PA, 19104, United States.
Parkinsonism Relat Disord. 2022 Jul;100:33-36. doi: 10.1016/j.parkreldis.2022.05.022. Epub 2022 Jun 8.
Motor features of Parkinson's disease (PD) are heterogeneous and well-studied; non-tremor features of postural instability and gait dysfunction (PIGD) have been linked to worse outcomes and Alzheimer's disease (AD) co-pathology. However, these features are understudied in Lewy body dementias (LBD). Here we perform retrospective analysis of a unique cohort of LBD (n = 30) with Unified Parkinson's Disease Rating Scale (UPDRS) data collected at baseline in proximity to cerebrospinal fluid collection to test the hypothesis that LBD patients with a positive AD biomarker profile (LBD + AD = 13) would have higher PIGD burden compared with LBD patients without AD biomarker positivity (LBD-AD = 17). We find novel evidence for selective impairment of PIGD burden in LBD + AD vs LBD-AD (OR = 1.95, 95%CI = 1.02-3.70, p = 0.04) and a direct association of increasing CSF tau/Aβ ratio with increasing PIGD disability in the total cohort (β = 0.23, SE = 0.08, p = 0.01). This unique biomarker stratification approach suggests AD co-pathology may contribute to PIGD motor signs in LBD.
帕金森病(PD)的运动特征具有异质性,并且已经得到了充分的研究;姿势不稳和步态功能障碍(PIGD)等非震颤特征与较差的预后和阿尔茨海默病(AD)共病有关。然而,这些特征在路易体痴呆症(LBD)中研究较少。在这里,我们对一组独特的 LBD 患者(n=30)进行了回顾性分析,这些患者在靠近脑脊液采集时收集了基线统一帕金森病评定量表(UPDRS)数据,以检验以下假设:具有 AD 生物标志物阳性特征的 LBD 患者(LBD+AD=13)与没有 AD 生物标志物阳性特征的 LBD 患者(LBD-AD=17)相比,PIGD 负担更高。我们发现了新的证据,表明 LBD+AD 与 LBD-AD 相比,PIGD 负担存在选择性损伤(OR=1.95,95%CI=1.02-3.70,p=0.04),并且在总队列中,CSF tau/Aβ 比值的增加与 PIGD 残疾的增加呈直接关联(β=0.23,SE=0.08,p=0.01)。这种独特的生物标志物分层方法表明,AD 共病可能导致 LBD 中的 PIGD 运动体征。