TY - JOUR
T1 - Sequential classification approach for enhancing the assessment of cardiac autonomic neuropathy
AU - Abdelwanis, Moustafa
AU - Moawad, Karim Ahmed
AU - Mohammed, Shahmir
AU - Hummieda, Ammar
AU - Syed, Shayaan
AU - Maalouf, Maher
AU - Jelinek, Herbert F.
N1 - Publisher Copyright:
© 2025 The Authors
PY - 2025/5
Y1 - 2025/5
N2 - Cardiac autonomic neuropathy (CAN) is a progressive condition associated with chronic diseases like diabetes, requiring regular reviews. Current CAN diagnostic methods are often time-consuming and lack precision. This study presents a novel, two-stage classification model designed to improve CAN diagnostic efficiency. Using a dataset of 1335 patient entries, including inflammatory markers and autonomic function tests (CARTs), the model first classifies patients based on six inflammatory markers– Interleukin-6 (IL-6), C-reactive protein (CRP), Interleukin-1 beta (IL-1beta), Interleukin-10 (IL-10), Monocyte Chemoattractant Protein-1 (MCP-1), and Insulin-like growth factor-1 (IGF-1). In this initial stage, the model achieves 0.893 accuracy for 31.46% of cases in the three-class CAN model at a 0.80 threshold. For cases requiring further assessment, the second stage incorporates CARTs, improving overall accuracy to 0.933. Notably, 98.87% of cases are accurately classified using only a subset of CARTs, with just 1.12% needing all five tests. Additionally, we developed a web application that utilizes Shapley plots to visualize and explain the contribution of each marker, facilitating interpretation for clinical use. This two-stage approach underscores the diagnostic relevance of inflammatory markers, providing clinicians with a streamlined, resource-efficient tool for timely CAN diagnosis and intervention.
AB - Cardiac autonomic neuropathy (CAN) is a progressive condition associated with chronic diseases like diabetes, requiring regular reviews. Current CAN diagnostic methods are often time-consuming and lack precision. This study presents a novel, two-stage classification model designed to improve CAN diagnostic efficiency. Using a dataset of 1335 patient entries, including inflammatory markers and autonomic function tests (CARTs), the model first classifies patients based on six inflammatory markers– Interleukin-6 (IL-6), C-reactive protein (CRP), Interleukin-1 beta (IL-1beta), Interleukin-10 (IL-10), Monocyte Chemoattractant Protein-1 (MCP-1), and Insulin-like growth factor-1 (IGF-1). In this initial stage, the model achieves 0.893 accuracy for 31.46% of cases in the three-class CAN model at a 0.80 threshold. For cases requiring further assessment, the second stage incorporates CARTs, improving overall accuracy to 0.933. Notably, 98.87% of cases are accurately classified using only a subset of CARTs, with just 1.12% needing all five tests. Additionally, we developed a web application that utilizes Shapley plots to visualize and explain the contribution of each marker, facilitating interpretation for clinical use. This two-stage approach underscores the diagnostic relevance of inflammatory markers, providing clinicians with a streamlined, resource-efficient tool for timely CAN diagnosis and intervention.
KW - Cardiac autonomic neuropathy
KW - Diabetes
KW - Explainable artificial intelligence
KW - Hierarchical models
KW - Inflammation
UR - http://www.scopus.com/inward/record.url?scp=105000304795&partnerID=8YFLogxK
U2 - 10.1016/j.compbiomed.2025.109999
DO - 10.1016/j.compbiomed.2025.109999
M3 - Article
C2 - 40112561
AN - SCOPUS:105000304795
SN - 0010-4825
VL - 190
JO - Computers in Biology and Medicine
JF - Computers in Biology and Medicine
M1 - 109999
ER -