arXiv:2606.25270cs.LG2026-06

用逆强化学习提取帕金森病患者打字时的可解释运动偏好指标。

Inverse Reinforcement Learning for Interpretable Keystroke Biomarkers in Parkinson's Disease

论文配图:Inverse Reinforcement Learning for Interpretable Keystroke Biomarkers in Parkinson's Disease
图 1 · 摘自论文原文
  • 通过逆强化学习从原始打字时间中恢复个体化运动速度偏好权重。
  • 该权重与运动严重程度相关(r=-0.607,p<0.001),跨子组重复验证。
  • 结果可解释且具高重测信度(ICC=0.903),适用于临床研究与远程监测。

打字动态提供了被动评估运动功能的窗口,但现有方法仅提取平均打字统计量并训练分类器进行帕金森病(PD)与健康对照区分,牺牲了可解释性,且极少报告可靠性。本文采用最大熵逆强化学习(IRL)处理原始打字时间,无需临床标签即可恢复每位受试者的速度偏好权重(w_speed),反映其对快速动作的隐含代价。在neuroQWERTY MIT-CSXPD数据集(85名受试者,42名PD)上,诊断并修正了初始四参数分解中的特征共线性问题,得到可识别的三参数模型。恢复的w_speed与UPDRS-III运动评分显著相关(r=-0.607,95% CI [-0.770, -0.364],p<0.001,n=42),在两个独立子队列中复现(r=-0.720,r=-0.588),且在控制飞行时间均值与标准差后仍保持显著偏相关(r=-0.371,p=0.016)。该方法优于SHAP和LASSO在相同代理特征上的表现(r=+0.362,r=+0.410),并提供个体化可解释输出。模型无监督AUC为0.605,留一法交叉验证AUC达0.750(95% CI [0.644, 0.847]),证实其判别价值。跨诊室测试-重测信度极高(ICC(2,1)=0.903,95% CI [0.842, 0.971]),是首个报告正式可靠性的打字-PD研究。另外两个恢复权重(一致性、手交替)未通过混杂因素检验,增强了存活信号的可信度。在独立的mPower智能手机敲击数据(n=200)上实现跨模态外部验证(r=-0.639,p=2.52e-24,OR=14.19),确认了跨设备、跨国家的收敛效度。

原文摘要 · Abstract (English)

Keystroke dynamics offer a passive window into motor function, but existing work extracts aggregate typing statistics and trains classifiers for PD/control discrimination, foregoing interpretability and rarely reporting reliability. We instead apply maximum-entropy inverse reinforcement learning (IRL) to raw keystroke timing, recovering a per-subject speed-preference weight (w_speed) reflecting the implicit cost assigned to fast movement, without any clinical label during fitting. On the neuroQWERTY MIT-CSXPD dataset (85 subjects, 42 PD), we diagnose and correct a feature collinearity failure in an initial four-parameter decomposition, yielding an identifiable three-parameter model. The recovered w_speed correlates with UPDRS-III motor severity at r=-0.607 (95% CI [-0.770,-0.364], p<0.001, n=42), replicates across two independent sub-cohorts (r=-0.720, r=-0.588), and retains significant partial correlation after controlling for mean and SD of flight time (r=-0.371, p=0.016). It outperforms SHAP and LASSO on the same proxy features (r=+0.362 and r=+0.410) while additionally providing per-subject, interpretable output. A model-free AUC of 0.605 and LOO-CV AUC of 0.750 (95% CI [0.644,0.847]) confirm discriminative value. Test-retest reliability across clinic sessions yields ICC(2,1)=0.903 (95% CI [0.842,0.971]); no prior keystroke-PD study has reported formal reliability. Two other recovered weights (consistency, hand-alternation) did not survive confound checks, strengthening credibility of the surviving signal. Cross-modality external validation on independent mPower smartphone tapping data (n=200) recovers the same signal (r=-0.639, p=2.52e-24, OR=14.19), confirming convergent validity across modality, device, and country.

帕金森病可解释性逆强化学习生物标志物

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