Machine learning in lymphocyte and immune biomarker analysis for childhood thyroid diseases in China

Abstract Objective This study aims to characterize and analyze the expression of representative biomarkers like lymphocytes and immune subsets in children with thyroid disorders. It also intends to develop and evaluate a machine learning model to predict if patients have thyroid disorders based on t...

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Main Authors: Ruizhe Yang, Wei Li, Qing Niu, WenTao Yang, Wei Gu, Xu Wang
Format: Article
Language:English
Published: BMC 2025-03-01
Series:BMC Pediatrics
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Online Access:https://doi.org/10.1186/s12887-024-05368-9
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author Ruizhe Yang
Wei Li
Qing Niu
WenTao Yang
Wei Gu
Xu Wang
author_facet Ruizhe Yang
Wei Li
Qing Niu
WenTao Yang
Wei Gu
Xu Wang
author_sort Ruizhe Yang
collection DOAJ
description Abstract Objective This study aims to characterize and analyze the expression of representative biomarkers like lymphocytes and immune subsets in children with thyroid disorders. It also intends to develop and evaluate a machine learning model to predict if patients have thyroid disorders based on their clinical characteristics, ultimately providing insights to enhance the clinical guidelines for the pathogenesis of childhood thyroid disorders. Method This cross-sectional study conducted in China examined diagnosed cases to describe the characteristics and expression of lymphocyte and immune subsets as predicted by the model. The study included two groups of children: 139 who were hospitalized in the Department of Endocrinology and a control group consisting of 283 children who underwent routine health checks at the Department of Children Healthcare. Cases were classified into three groups based on diagnoses: Graves’ disease (GD), Hashimoto’s thyroiditis (HT), and hypothyroidism. By employing 11 readily obtainable serum biochemical indicators within three days of admission, the median concentrations and percentages of subset measurements were analyzed. Additionally, nine machine learning (ML) algorithms were utilized to construct prediction models. Various evaluation metrics, including the area under the receiver operating characteristic curve (AUC), were employed to compare predictive performance. Results GD cases had increased levels of CD3-CD19 + and CD3 + CD4 + T lymphocytes, and a higher CD4+/CD8 + ratio. In both GD and HT, the levels of complement C3c, IgA, and IgG were higher than those in the control group. HT cases also had an increasing percentage of CD3-CD16 + 56 + T lymphocytes. Most immune markers increased in hypothyroidism, except for some T lymphocyte percentages and the CD4+/CD8 + ratio. To reduce age-related bias, propensity score matching was used, yielding consistent results. Among the nine machine learning models evaluated, logistic regression showed the best performance, being useful in clinical practice. Conclusions Specific lymphocytes with different biomarkers are positively correlated with autoimmune thyroid disease (AITD) in children. Complement proteins C3c and C4, along with IgG, IgA, IgM, and T/B cells, are significant in childhood thyroid diseases. Our best model can effectively distinguish these conditions, but to enhance accuracy, more detailed information such as clinical images might be needed.
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spelling doaj-art-e90c4f070e514c6eb414eca77a596d5e2025-08-20T02:10:10ZengBMCBMC Pediatrics1471-24312025-03-0125111110.1186/s12887-024-05368-9Machine learning in lymphocyte and immune biomarker analysis for childhood thyroid diseases in ChinaRuizhe Yang0Wei Li1Qing Niu2WenTao Yang3Wei Gu4Xu Wang5Department of Public Health, Children’s Hospital of Nanjing Medical UniversityDepartment of Science and Technology, Children’s Hospital of Nanjing Medical UniversitySchool of Pediatrics, Nanjing Medical UniversitySchool of Pediatrics, Nanjing Medical UniversityDepartment of Endocrinology, Children’s Hospital of Nanjing Medical UniversityDepartment of Science and Technology, Children’s Hospital of Nanjing Medical UniversityAbstract Objective This study aims to characterize and analyze the expression of representative biomarkers like lymphocytes and immune subsets in children with thyroid disorders. It also intends to develop and evaluate a machine learning model to predict if patients have thyroid disorders based on their clinical characteristics, ultimately providing insights to enhance the clinical guidelines for the pathogenesis of childhood thyroid disorders. Method This cross-sectional study conducted in China examined diagnosed cases to describe the characteristics and expression of lymphocyte and immune subsets as predicted by the model. The study included two groups of children: 139 who were hospitalized in the Department of Endocrinology and a control group consisting of 283 children who underwent routine health checks at the Department of Children Healthcare. Cases were classified into three groups based on diagnoses: Graves’ disease (GD), Hashimoto’s thyroiditis (HT), and hypothyroidism. By employing 11 readily obtainable serum biochemical indicators within three days of admission, the median concentrations and percentages of subset measurements were analyzed. Additionally, nine machine learning (ML) algorithms were utilized to construct prediction models. Various evaluation metrics, including the area under the receiver operating characteristic curve (AUC), were employed to compare predictive performance. Results GD cases had increased levels of CD3-CD19 + and CD3 + CD4 + T lymphocytes, and a higher CD4+/CD8 + ratio. In both GD and HT, the levels of complement C3c, IgA, and IgG were higher than those in the control group. HT cases also had an increasing percentage of CD3-CD16 + 56 + T lymphocytes. Most immune markers increased in hypothyroidism, except for some T lymphocyte percentages and the CD4+/CD8 + ratio. To reduce age-related bias, propensity score matching was used, yielding consistent results. Among the nine machine learning models evaluated, logistic regression showed the best performance, being useful in clinical practice. Conclusions Specific lymphocytes with different biomarkers are positively correlated with autoimmune thyroid disease (AITD) in children. Complement proteins C3c and C4, along with IgG, IgA, IgM, and T/B cells, are significant in childhood thyroid diseases. Our best model can effectively distinguish these conditions, but to enhance accuracy, more detailed information such as clinical images might be needed.https://doi.org/10.1186/s12887-024-05368-9Childhood AITDImmune biomarkerPropensity score matchMachine learningExplainable prediction model
spellingShingle Ruizhe Yang
Wei Li
Qing Niu
WenTao Yang
Wei Gu
Xu Wang
Machine learning in lymphocyte and immune biomarker analysis for childhood thyroid diseases in China
BMC Pediatrics
Childhood AITD
Immune biomarker
Propensity score match
Machine learning
Explainable prediction model
title Machine learning in lymphocyte and immune biomarker analysis for childhood thyroid diseases in China
title_full Machine learning in lymphocyte and immune biomarker analysis for childhood thyroid diseases in China
title_fullStr Machine learning in lymphocyte and immune biomarker analysis for childhood thyroid diseases in China
title_full_unstemmed Machine learning in lymphocyte and immune biomarker analysis for childhood thyroid diseases in China
title_short Machine learning in lymphocyte and immune biomarker analysis for childhood thyroid diseases in China
title_sort machine learning in lymphocyte and immune biomarker analysis for childhood thyroid diseases in china
topic Childhood AITD
Immune biomarker
Propensity score match
Machine learning
Explainable prediction model
url https://doi.org/10.1186/s12887-024-05368-9
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