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数字语音生物标志物可测量左旋多巴对帕金森病的急性影响。

Digital speech biomarkers can measure acute effects of levodopa in Parkinson's disease.

作者信息

Sousa M, Krýže P, Amstutz D, Petermann K, Averna A, Castelli M, Magalhães A D, Jorge A, Švihlík J, Tykalová T, Illner V, Maradan-Gachet M E, Diamantaras A A, Waskönig J, Lachenmayer M L, Debove I, Tinkhauser G, Nef T, Rusz J, Krack P

机构信息

Department of Neurology, Bern University Hospital and University of Bern, Bern, Switzerland.

Graduate School of Health Sciences, University of Bern, Bern, Switzerland.

出版信息

NPJ Parkinsons Dis. 2025 Jul 1;11(1):184. doi: 10.1038/s41531-025-01045-5.

Abstract

Speech abnormalities in Parkinson's disease (PD) are heterogeneous and often considered resistant to levodopa. However, human hearing may miss subtle treatment-related speech changes. Digital speech biomarkers offer a sensitive alternative to measure such changes objectively. Speech was recorded in 51 PD patients during ON and OFF medication states and compared to 43 healthy controls matched for language and gender. Acute levodopa effects were significant in prosodic (F0 standard deviation, p = 0.03, effect size = 0.47), respiratory (intensity slope, p = 0.02, effect size = 0.49), and spectral domains (LTAS mean, p = 0.01, effect size = 0.35). Stepwise backward regression identified 8 biomarkers reflecting hypokinetic symptoms, 6 for dyskinetic symptoms, and 7 for medication-state transitions. Hypokinetic compound score correlated strongly with MDS-UPDRS-III changes (r = 0.70; MAE = 6.06/92), and the dyskinetic compound score with dyskinesia ratings (r = 0.50; MAE = 1.81/12). Medication-state transitions were detected with AUC = 0.86. This study highlights the potential of digital speech biomarkers to objectively measure levodopa-induced changes in PD symptoms and medication states.

摘要

帕金森病(PD)中的言语异常具有异质性,通常被认为对左旋多巴耐药。然而,人类听力可能会忽略与治疗相关的细微言语变化。数字语音生物标志物提供了一种敏感的替代方法来客观地测量此类变化。对51名PD患者在服药和未服药状态下的语音进行了记录,并与43名在语言和性别上匹配的健康对照者进行了比较。急性左旋多巴效应在韵律(F0标准差,p = 0.03,效应大小 = 0.47)、呼吸(强度斜率,p = 0.02,效应大小 = 0.49)和频谱域(长时平均谱,p = 0.01,效应大小 = 0.35)方面具有显著性。逐步向后回归确定了8个反映运动迟缓症状的生物标志物、6个反映运动障碍症状的生物标志物和7个反映药物状态转换的生物标志物。运动迟缓复合评分与MDS-UPDRS-III变化密切相关(r = 0.70;平均绝对误差 = 6.06/92),运动障碍复合评分与运动障碍评分密切相关(r = 0.50;平均绝对误差 = 1.81/12)。药物状态转换的检测曲线下面积(AUC)为0.86。本研究强调了数字语音生物标志物在客观测量左旋多巴引起的PD症状和药物状态变化方面的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c8c/12217330/014a837db858/41531_2025_1045_Fig1_HTML.jpg

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