Shapley Regression for Rare Disease Diagnosis Support: a case study on APDS
- URL: http://arxiv.org/abs/2605.08897v1
- Date: Sat, 09 May 2026 11:30:54 GMT
- Title: Shapley Regression for Rare Disease Diagnosis Support: a case study on APDS
- Abstract summary: Activated PI3K8 Syndrome (APDS) is a rare genetic immune disorder caused by variants in PIK3CD or PIK3R1.<n>Shapley regression is a novel game-theoretic model replacing the linear predictor with a k-additive cooperative game.
- Score: 3.4842393087897015
- License: http://creativecommons.org/licenses/by/4.0/
- Abstract: Activated PI3K8 Syndrome (APDS) is a rare genetic immune disorder caused by variants in PIK3CD or PIK3R1, with highly heterogeneous symptoms that often delay diagnosis. Early recognition is hampered by overlapping clinical presentations and limited clinician awareness, motivating systematic, data-driven approaches to detect APDS-associated phenotypic patterns in routine electronic health records. Traditional linear scoring systems cannot capture complex symptom interactions, while deep learning models, though expressive, often lack interpretability. To bridge this gap, we propose Shapley regression, a novel game-theoretic model replacing the linear predictor with a k-additive cooperative game, explicitly modeling co-occurrence of symptoms while maintaining the transparency and convexity of logistic regression. We carry out an empirical study of our lightweight method on eight public biomedical datasets, showing that a 2-additive model with $l_{2}$ regularization achieves an optimal trade-off between predictive power and noise robustness. We also apply it to a real-world cohort of 222 patients, on which Shapley regression accurately distinguished APDS cases from matched controls, confirming and validating phenotypes known to be associated with APDS, and facilitating the exploration of pairwise interactions between symptoms, validated by clinical experts.
Related papers
- RareDxR1: Autonomous Medical Reasoning for Rare Disease Diagnosis Beyond Human Annotation [18.759964003865278]
We introduce RareDxR1, an end-to-end reasoning-centric large language model for open-domain rare disease diagnosis.<n>We synergize knowledge internalization with autonomous evolutionary learning, thereby bypassing reliance on structured phenotypes and closed-set decision-making.<n> Experimental results demonstrate that RareDxR1 achieves state-of-the-art accuracy across different benchmarks, marking a significant breakthrough in open-domain rare disease diagnosis.
arXiv Detail & Related papers (2026-06-30T20:25:53Z) - Explainable Retinal Imaging for Prediction of Multi-Organ Dysfunction in Type 2 Diabetes [2.153295259565971]
System-level abnormality indices were constructed to quantify organ-specific dysfunction.<n>Supervised machine learning models were trained to predict multi-system dysregulation.<n>Hyperglycaemia, renal impairment, dyslipidaemia, and inflammation were the dominant drivers of multi-system risk.
arXiv Detail & Related papers (2026-05-24T07:31:57Z) - Toward Personalized Digital Twins for Cognitive Decline Assessment: A Multimodal, Uncertainty-Aware Framework [0.2566571621858396]
The PCD-DT framework provides a principled starting point for personalized in silico modeling in neurodegenerative disease.<n>This work positions PCD-DT as a foundational step toward clinically deployable, uncertainty-aware digital twin systems.
arXiv Detail & Related papers (2026-04-29T21:40:55Z) - Predicting Neuromodulation Outcome for Parkinson's Disease with Generative Virtual Brain Model [95.41752463487008]
Parkinson's disease affects over ten million people worldwide.<n>Inter-individual variability limits empirical treatment selection, increasing non-negligible surgical risk and cost.<n>We bridge this gap with a pretraining-finetuning framework to predict outcomes directly from resting-state fMRI.
arXiv Detail & Related papers (2026-03-31T02:36:10Z) - Clinical Cognition Alignment for Gastrointestinal Diagnosis with Multimodal LLMs [63.535652574541764]
Multimodal Large Language Models (MLLMs) have demonstrated remarkable potential in medical image analysis.<n>Their application in gastrointestinal endoscopy is currently hindered by two critical limitations.<n>We propose a novel Clinical-Cognitive-Aligned (CogAlign) framework to address these challenges.
arXiv Detail & Related papers (2026-03-21T07:47:37Z) - Investigating the Impact of Histopathological Foundation Models on Regressive Prediction of Homologous Recombination Deficiency [52.50039435394964]
We systematically evaluate foundation models for regression-based tasks.<n>We extract patch-level features from whole slide images (WSI) using five state-of-the-art foundation models.<n>Models are trained to predict continuous HRD scores based on these extracted features across breast, endometrial, and lung cancer cohorts.
arXiv Detail & Related papers (2026-01-29T14:06:50Z) - A Weakly Supervised Transformer for Rare Disease Diagnosis and Subphenotyping from EHRs with Pulmonary Case Studies [28.253741893497136]
We propose WEST (WEakly Supervised Transformer for rare disease phenotyping and subphenotyping from EHRs) to enable large-scale phenotyping.<n>We evaluate WEST on two rare pulmonary diseases using EHR data from Boston Children's Hospital and show that it outperforms existing methods in phenotype classification, identification of clinically meaningful subphenotypes, and prediction of disease progression.
arXiv Detail & Related papers (2025-07-01T23:11:20Z) - CTPD: Cross-Modal Temporal Pattern Discovery for Enhanced Multimodal Electronic Health Records Analysis [50.56875995511431]
We introduce a Cross-Modal Temporal Pattern Discovery (CTPD) framework, designed to efficiently extract meaningful cross-modal temporal patterns from multimodal EHR data.<n>Our approach introduces shared initial temporal pattern representations which are refined using slot attention to generate temporal semantic embeddings.
arXiv Detail & Related papers (2024-11-01T15:54:07Z) - Clustering of Disease Trajectories with Explainable Machine Learning: A Case Study on Postoperative Delirium Phenotypes [13.135589459700865]
We propose an approach that combines supervised machine learning for personalized POD risk prediction with unsupervised clustering techniques to uncover potential POD phenotypes.
We show that clustering patients in the SHAP feature importance space successfully recovers the true underlying phenotypes, outperforming clustering in the raw feature space.
arXiv Detail & Related papers (2024-05-06T10:05:46Z) - Bayesian Models of Functional Connectomics and Behavior [0.0]
We present a fully bayesian formulation for joint representation learning and prediction.
We present preliminary results on a subset of a publicly available clinical rs-fMRI study on patients with Autism Spectrum Disorder.
arXiv Detail & Related papers (2023-01-15T20:42:31Z) - Bayesian Networks for the robust and unbiased prediction of depression
and its symptoms utilizing speech and multimodal data [65.28160163774274]
We apply a Bayesian framework to capture the relationships between depression, depression symptoms, and features derived from speech, facial expression and cognitive game data collected at thymia.
arXiv Detail & Related papers (2022-11-09T14:48:13Z) - DxFormer: A Decoupled Automatic Diagnostic System Based on
Decoder-Encoder Transformer with Dense Symptom Representations [26.337392652262103]
A diagnosis-oriented dialogue system queries the patient's health condition and makes predictions about possible diseases through continuous interaction with the patient.
We propose a decoupled automatic diagnostic framework DxFormer, which divides the diagnosis process into two steps: symptom inquiry and disease diagnosis.
Our proposed model can effectively learn doctors' clinical experience and achieve the state-of-the-art results in terms of symptom recall and diagnostic accuracy.
arXiv Detail & Related papers (2022-05-08T01:52:42Z) - Learning Dynamic and Personalized Comorbidity Networks from Event Data
using Deep Diffusion Processes [102.02672176520382]
Comorbid diseases co-occur and progress via complex temporal patterns that vary among individuals.
In electronic health records we can observe the different diseases a patient has, but can only infer the temporal relationship between each co-morbid condition.
We develop deep diffusion processes to model "dynamic comorbidity networks"
arXiv Detail & Related papers (2020-01-08T15:47:08Z)
This list is automatically generated from the titles and abstracts of the papers in this site.
This site does not guarantee the quality of this site (including all information) and is not responsible for any consequences.