A machine learning prediction model for Cardiac Amyloidosis using routine blood tests in patients with left ventricular hypertrophy

Abstract Current approaches for cardiac amyloidosis (CA) identification are time-consuming, labor-intensive, and present challenges in sensitivity and accuracy, leading to limited treatment efficacy and poor prognosis for patients. In this retrospective study, we aimed to leverage machine learning (...

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Main Authors: Yuling Pan, Qingkun Fan, Yu Liang, Yunfan Liu, Haihang You, Chunzi Liang
Format: Article
Language:English
Published: Nature Portfolio 2024-11-01
Series:Scientific Reports
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Online Access:https://doi.org/10.1038/s41598-024-77466-8
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author Yuling Pan
Qingkun Fan
Yu Liang
Yunfan Liu
Haihang You
Chunzi Liang
author_facet Yuling Pan
Qingkun Fan
Yu Liang
Yunfan Liu
Haihang You
Chunzi Liang
author_sort Yuling Pan
collection DOAJ
description Abstract Current approaches for cardiac amyloidosis (CA) identification are time-consuming, labor-intensive, and present challenges in sensitivity and accuracy, leading to limited treatment efficacy and poor prognosis for patients. In this retrospective study, we aimed to leverage machine learning (ML) to create a diagnostic model for CA using data from routine blood tests. Our dataset included 6,563 patients with left ventricular hypertrophy, 261 of whom had been diagnosed with CA. We divided the dataset into training and testing cohorts, applying ML algorithms such as logistic regression, random forest, and XGBoost for automated learning and prediction. Our model’s diagnostic accuracy was then evaluated against CA biomarkers, specifically serum-free light chains (FLCs). The model’s interpretability was elucidated by visualizing the feature importance through the gain map. XGBoost outperformed both random forest and logistic regression in internal validation on the testing cohort, achieving an area under the curve (AUC) of 0.95 (95%CI: 0.92–0.97), sensitivity of 0.92 (95%CI: 0.86–0.98), specificity of 0.95 (95%CI: 0.94–0.97), and an F1 score of 0.89 (95%CI: 0.85–0.92). Its performance was also superior to the serum FLC-kappa and FLC-lambda combination (AUC of 0.88). Furthermore, XGBoost identified unique biomarker signatures indicative of multisystem dysfunction in CA patients, with significant changes in eGFR, FT3, cTnI, ANC, and NT-proBNP. This study develops a highly sensitive and accurate ML model for CA detection using routine clinical laboratory data, effectively streamlining diagnostic procedures, and providing valuable clinical insights and guiding future research into disease mechanisms.
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spelling doaj-art-63bbe87d07984ac1bd45de8fe24f58bb2025-08-20T02:32:52ZengNature PortfolioScientific Reports2045-23222024-11-0114111110.1038/s41598-024-77466-8A machine learning prediction model for Cardiac Amyloidosis using routine blood tests in patients with left ventricular hypertrophyYuling Pan0Qingkun Fan1Yu Liang2Yunfan Liu3Haihang You4Chunzi Liang5School of Laboratory Medicine, Hubei University of Chinese MedicineDepartment of Medical Laboratory, Wuhan Asia Heart HospitalSchool of Laboratory Medicine, Hubei University of Chinese MedicineUniversity of TorontoInstitute of Computing Technology, Chinese Academy of SciencesSchool of Laboratory Medicine, Hubei University of Chinese MedicineAbstract Current approaches for cardiac amyloidosis (CA) identification are time-consuming, labor-intensive, and present challenges in sensitivity and accuracy, leading to limited treatment efficacy and poor prognosis for patients. In this retrospective study, we aimed to leverage machine learning (ML) to create a diagnostic model for CA using data from routine blood tests. Our dataset included 6,563 patients with left ventricular hypertrophy, 261 of whom had been diagnosed with CA. We divided the dataset into training and testing cohorts, applying ML algorithms such as logistic regression, random forest, and XGBoost for automated learning and prediction. Our model’s diagnostic accuracy was then evaluated against CA biomarkers, specifically serum-free light chains (FLCs). The model’s interpretability was elucidated by visualizing the feature importance through the gain map. XGBoost outperformed both random forest and logistic regression in internal validation on the testing cohort, achieving an area under the curve (AUC) of 0.95 (95%CI: 0.92–0.97), sensitivity of 0.92 (95%CI: 0.86–0.98), specificity of 0.95 (95%CI: 0.94–0.97), and an F1 score of 0.89 (95%CI: 0.85–0.92). Its performance was also superior to the serum FLC-kappa and FLC-lambda combination (AUC of 0.88). Furthermore, XGBoost identified unique biomarker signatures indicative of multisystem dysfunction in CA patients, with significant changes in eGFR, FT3, cTnI, ANC, and NT-proBNP. This study develops a highly sensitive and accurate ML model for CA detection using routine clinical laboratory data, effectively streamlining diagnostic procedures, and providing valuable clinical insights and guiding future research into disease mechanisms.https://doi.org/10.1038/s41598-024-77466-8Cardiac amyloidosisMachine learningRoutine blood testsMulti-system dysfunction profilePrediction model
spellingShingle Yuling Pan
Qingkun Fan
Yu Liang
Yunfan Liu
Haihang You
Chunzi Liang
A machine learning prediction model for Cardiac Amyloidosis using routine blood tests in patients with left ventricular hypertrophy
Scientific Reports
Cardiac amyloidosis
Machine learning
Routine blood tests
Multi-system dysfunction profile
Prediction model
title A machine learning prediction model for Cardiac Amyloidosis using routine blood tests in patients with left ventricular hypertrophy
title_full A machine learning prediction model for Cardiac Amyloidosis using routine blood tests in patients with left ventricular hypertrophy
title_fullStr A machine learning prediction model for Cardiac Amyloidosis using routine blood tests in patients with left ventricular hypertrophy
title_full_unstemmed A machine learning prediction model for Cardiac Amyloidosis using routine blood tests in patients with left ventricular hypertrophy
title_short A machine learning prediction model for Cardiac Amyloidosis using routine blood tests in patients with left ventricular hypertrophy
title_sort machine learning prediction model for cardiac amyloidosis using routine blood tests in patients with left ventricular hypertrophy
topic Cardiac amyloidosis
Machine learning
Routine blood tests
Multi-system dysfunction profile
Prediction model
url https://doi.org/10.1038/s41598-024-77466-8
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