arXiv:2608.16507cs.AI2026-08

用大模型模拟临床专家,提升罕见病长期数据建模的准确性与可解释性。

Large language models as synthetic clinical experts to inform longitudinal rare-disease modeling

论文配图:Large language models as synthetic clinical experts to inform longitudinal rare-disease modeling
图 1 · 摘自论文原文
  • 用大模型生成临床判断,指导变分自编码器学习低维表征
  • 将原始与重构数据的疾病类型不一致率从11%降至7%
  • 适合需要结合医学知识的罕见病长期研究者使用

由于信息有限,罕见病纵向数据建模可受益于临床知识的整合。然而,获取并形式化临床专家知识极具挑战,尤其受限于专家时间。为此,我们利用大语言模型(LLMs)作为合成临床专家,在变分自编码器基础上学习就诊级观测的低维潜在表示。具体地,离线查询LLMs以获得患者观察的文本描述对应的判断(如疑似临床类别),再训练一个可微分的代理模型,并将其判断结果融入损失函数,以鼓励重建保持原始输入的临床标签分布。在脊髓性肌萎缩症(SMA)患儿运动功能纵向评估中的应用表明,该方法能将就诊级临床特征映射为低维表示,并通过多变量混合效应模型关联。合成专家损失有效减少数值相近但临床意义不同的重建,例如跨疾病类型边界的情况。最终,原始与重构的SMA类型标签不一致率由约11%降至7%。相较无监督潜在表示和数据级基线,引入合成专家的潜在表示显著提升了运动功能里程碑预测性能。结果表明,将大模型嵌入建模过程可使临床知识融入表征学习,增强罕见病纵向数据的临床一致性。

原文摘要 · Abstract (English)

Due to the limited amount of information, modeling longitudinal rare-disease data can benefit from integrating clinical knowledge. Yet, elicitation of expert knowledge and formalization for model fitting is challenging, in particular due to limited time of clinical experts. To nevertheless make domain knowledge accessible during model fitting, we use large language models (LLMs) as synthetic clinical experts to supervise a variational-autoencoder-based approach that learns low-dimensional latent summaries of visit-level observations. Specifically, LLMs are queried offline on textual descriptions of patient observations to obtain judgments, e.g., the suspected clinical category. To improve the variational autoencoder fit, we train a differentiable surrogate model on these judgments and augment the loss function to encourage reconstructions that preserve the clinical-label distribution of their corresponding input profile. In an application to longitudinal motor-function assessments from children with spinal muscular atrophy, we map visit-level clinical profiles to low-dimensional representations that are linked by a multivariate mixed-effects model. The synthetic expert loss discourages reconstructions that remain numerically close in data space but alter the clinical interpretation of the reconstructed motor function profile, such as by crossing a disease-type boundary. We thus reduced disagreement between original and reconstructed SMA type labels from about 11 to 7 percent. Furthermore, informing the latent representation by the synthetic expert improved prediction of motor function milestones compared with unsupervised latent representations and a data-level baseline. These results suggest that incorporating LLMs into model fitting can make clinical knowledge available to representation learning and improve clinical faithfulness for longitudinal rare-disease data.

罕见病建模大模型临床知识潜变量

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