Evidence map›Paper›PMID 42206034›Full record

ArticleFrontiers in immunology2026

Predictive value of thyroid autoantibodies for coronary heart disease severity in individuals with normal thyroid function based on machine learning and SHAP interpretation.

Nana Liang, Huiru Ma, Xingyue Wang, Jie Meng, Zixuan Ru, Na Lv, Kerou Li, Hong Qiao

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Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

8 authors.

Nana LiangThe Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Huiru MaThe Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Xingyue WangThe Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Jie MengThe Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Zixuan RuThe Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Na LvThe Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Kerou LiThe Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Hong QiaoThe Second Affiliated Hospital of Harbin Medical University, Harbin, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Assessing the severity of coronary heart disease (CHD) is critical for clinical decision-making. Thyroid autoantibodies are associated with cardiovascular disease, but their ability to predict CHD severity remains unclear. This study aimed to systematically elucidate the predictive value of thyroid autoantibodies for CHD severity using machine learning methods. Methods: This retrospective study included 942 patients hospitalized in the cardiovascular department between January 2024 and June 2025, comprising 590 patients with severe lesions and 352 with nonsevere lesions. Traditional statistical analysis employed correlation analysis and multivariate logistic regression. Eight machine learning models were subsequently constructed and compared: logistic regression (LR), support vector machine (SVM), K-nearest neighbors (KNN), adaptive boosting (AdaBoost), multilayer perceptron (MLP), random forest (RF), gradient boosting (GB), and XGBoost (XGB). The optimal model was determined using Shapley additive propagation (SHAP), and the robustness of the core findings was validated through hierarchical analysis and subgroup feature importance comparisons. Results: Multivariate logistic regression revealed that log anti-TPO was an independent risk factor for severe coronary lesions (OR = 2.19; 95% CI: 1.87-2.57; P<0.001), whereas log anti-Tg shows a negative correlation after adjustment (OR = 0.72; 95% CI: 0.61-0.85; P<0.001). However, given the significant multicollinearity between the two variables (r = 0.55), this negative correlation strongly suggests that it is a statistical artifact. The gradient boosting tree performed best (AUROC:0.855). SHAP analysis consistently confirmed three key predictive features: log anti-TPO, log anti-Tg, and glycated hemoglobin (HbA1c). SHAP dependency plots further revealed a distinct threshold effect for log anti-TPO, while elevated log anti-Tg was associated with reduced risk, However, this negative association is likely a statistical artifact rather than an independent protective effect. Stratified analysis and sex-specific feature importance assessments confirmed that log anti-TPO demonstrated a highly robust and significant predictive value across all the subgroups, ranking as the primary predictor in both the male and female cohorts. Conclusion: The presence of thyroid autoantibodies represents an independent key predictor of CHD severity. Thyroid peroxidase antibodies (TPO-Ab) serve as a strong risk marker, The gradient boosting tree model demonstrated optimal predictive performance when these biomarkers were integrated.

Indexed as

AutoantibodiesCoronary DiseaseMachine LearningThyroid GlandAgedBiomarkersBoosting Machine Learning AlgorithmsClassification AlgorithmsFemaleHumansMaleMiddle AgedPredictive Learning ModelsPredictive Value of TestsRandom ForestRetrospective StudiesAutoantibodiesBiomarkerscardiovascular diseasemachine learningSHAPTgAbTPOAb

Identifiers

PMID42206034
PMCPMC13201438

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.