主観評価なしで運動障害を測定するAIモデルを開発 (New AI Model Measures Motor Impairment Without Subjectivity)

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2026-05-12 マサチューセッツ大学アマースト校

米マサチューセッツ大学の研究チームは、運動機能障害を客観的に評価できる新しいAIモデルを開発した。パーキンソン病や脳卒中後遺症などの患者評価では、従来、医師による主観的判断に依存する部分が大きく、診断や治療効果判定のばらつきが課題だった。研究では、患者の動作データをAIで解析し、歩行や手の動き、姿勢変化などから運動障害の程度を定量化する手法を構築。人間の評価者間で生じる差を減らし、一貫した評価が可能になることを示した。研究チームは、この技術により、早期診断やリハビリ効果の継続的モニタリングが容易になると期待している。また、遠隔医療や在宅診療との組み合わせによって、患者負担軽減や医療アクセス改善にも役立つ可能性がある。AIを活用した客観的医療評価システムとして注目される成果である。

高齢男性が平行棒につかまりながら数歩歩く様子を、セラピストが注意深く見守っている。写真提供:ゲッティイメージズ<関連情報>

ウェアラブルデバイスを用いた運動失調症評価のための対照学習モデル Contrastive Learning Model for Wearable-Based Ataxia Assessment

Juhyeon Lee; Brandon Oubre; Jean-Francois Daneault; Christopher D. Stephen; Jeremy D. Schmahmann; Anoopum S. Gupta
IEEE Transactions on Biomedical Engineering  Published:10 September 2025
DOI:https://doi.org/10.1109/TBME.2025.3608674

Abstract

Objective: Frequent and objective assessment of ataxia severity is essential for tracking disease progression and evaluating the effectiveness of potential treatments. Wearable-based assessments have emerged as a promising solution. However, existing methods rely on inertial data features directly correlated with subjective and coarse clinician-evaluated rating scales, which serve as imperfect gold standards. This approach may introduce biases and restrict flexibility in feature design. To address these limitations, this study introduces a novel contrastive learning-based model that leverages motor severity differences in wearable inertial data to learn relevant features. Methods: The model was trained on inertial data collected from 87 individuals with diagnostically heterogeneous ataxias and 44 healthy participants performing the finger-to-nose task. A pairwise contrastive loss function was proposed to learn representations capturing relative differences in ataxia severity, which were evaluated through downstream regression and classification tasks. Results: The learned features demonstrated strong cross-sectional (r = 0.84) and longitudinal (r = 0.68) associations with clinical scores and robust measurement reliability (intraclass correlation coefficient = 0.96). Additionally, the model exhibited strong known-group validity, distinguishing between ataxia and healthy phenotypes with an area under the receiver operating characteristic curve of 0.95. Conclusion: The proposed contrastive model captures robust representations of disease severity with reduced reliance on clinical scales, outperforming state-of-the-art methods that derive features directly from clinical scores. Significance: Combining wearable sensors with contrastive learning enables a more objective, scalable, and frequent method for assessing ataxia severity, with the potential to enhance patient monitoring and improve clinical trial efficiency.

 

医療・健康
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