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Cerebrospinal Fluid α-Synuclein Predicts Cognitive Decline in Parkinson Disease Progression in the DATATOP Cohort

机译:脑脊液α-突触核蛋白预测DATATOP队列中帕金森病进展的认知下降

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摘要

Most patients with Parkinson disease (PD) develop both cognitive and motor impairment, and biomarkers for progression are urgently needed. Although α-synuclein is altered in cerebrospinal fluid of patients with PD, it is not known whether it predicts motor or cognitive deterioration. We examined clinical data and α-synuclein in >300 unmedicated patients with PD who participated in the deprenyl and tocopherol antioxidative therapy of parkinsonism (DATATOP) study, with up to 8 years of follow-up. Longitudinal measures of motor and cognitive function were studied before (phase 1) and during (phase 2) levodopa therapy; cerebrospinal fluid was collected at the beginning of each phase. Correlations and linear mixed models were used to assess α-synuclein association with disease severity and prediction of progression in the subsequent follow-up period. Despite decreasing α-synuclein (phase 1 to phase 2 change of −0.05 ± 0.21 log-transformed values, P < 0.001), no correlations were observed between α-synuclein and motor symptoms. Longitudinally, lower α-synuclein predicted better preservation of cognitive function by several measures [Selective Reminding Test total recall α-synuclein × time interaction effect coefficient, −0.12 (P = 0.037); delayed recall, −0.05 (P = 0.002); New Dot Test, −0.03 (P = 0.002)]. Thus, α-synuclein, although not clinically useful for motor progression, might predict cognitive decline, and future longitudinal studies should include this outcome for further validation.
机译:大多数帕金森病(PD)患者都会出现认知功能障碍和运动障碍,因此迫切需要生物标志物以进行进展。尽管PD患者的脑脊液中α-突触核蛋白发生了改变,但尚不清楚其是否预测运动或认知功能下降。我们检查了超过300名进行了长达8年的随访的300例未接受药物治疗的PD患者的临床数据和α-突触核蛋白,这些患者接受了异戊二烯和生育酚抗氧化疗法的帕金森病研究(DATATOP)。在左旋多巴治疗之前(阶段1)和过程中(阶段2)研究了运动和认知功能的纵向测量。在每个阶段开始时收集脑脊液。相关性和线性混合模型用于评估α-突触核蛋白与疾病严重程度的关联以及在随后的随访期内的进展预测。尽管α-突触核蛋白减少(第1阶段到第2阶段的变化为-0.05±0.21对数转换值,P <0.001),但未观察到α-突触核蛋白与运动症状之间的相关性。纵向上,较低的α-突触核蛋白可以通过几种措施预测更好的认知功能保存[选择性提醒测试总回想度α-突触核蛋白×时间相互作用效应系数,-0.12(P = 0.037);延迟召回,-0.05(P = 0.002);新点测试,−0.03(P = 0.002)]。因此,尽管α-突触核蛋白在临床上对运动进展无用,但可能预示着认知功能下降,未来的纵向研究应将这一结果纳入进一步的验证。

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