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Machine Learning for Screening Microvascular Complications in Type 2 Diabetic Patients Using Demographic, Clinical, and Laboratory Profiles

Microvascular complications are one of the key causes of mortality among type 2 diabetic patients. This study was sought to investigate the use of a novel machine learning approach for predicting these complications using only the patient demographic, clinical, and laboratory profiles. A total of 96...

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Autores principales: Rashid, Mamunur, Alkhodari, Mohanad, Mukit, Abdul, Ahmed, Khawza Iftekhar Uddin, Mostafa, Raqibul, Parveen, Sharmin, Khandoker, Ahsan H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8879306/
https://www.ncbi.nlm.nih.gov/pubmed/35207179
http://dx.doi.org/10.3390/jcm11040903
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author Rashid, Mamunur
Alkhodari, Mohanad
Mukit, Abdul
Ahmed, Khawza Iftekhar Uddin
Mostafa, Raqibul
Parveen, Sharmin
Khandoker, Ahsan H.
author_facet Rashid, Mamunur
Alkhodari, Mohanad
Mukit, Abdul
Ahmed, Khawza Iftekhar Uddin
Mostafa, Raqibul
Parveen, Sharmin
Khandoker, Ahsan H.
author_sort Rashid, Mamunur
collection PubMed
description Microvascular complications are one of the key causes of mortality among type 2 diabetic patients. This study was sought to investigate the use of a novel machine learning approach for predicting these complications using only the patient demographic, clinical, and laboratory profiles. A total of 96 Bangladeshi participants with type 2 diabetes were recruited during their routine hospital visits. All patient profiles were assessed by using a chi-squared (χ(2)) test to statistically determine the most important markers in predicting three microvascular complications: cardiac autonomic neuropathy (CAN), diabetic peripheral neuropathy (DPN), and diabetic retinopathy (RET). A machine learning approach based on logistic regression, random forest (RF), and support vector machine (SVM) algorithms was then developed to ensure automated clinical testing for microvascular complications in diabetic patients. The highest prediction accuracies were obtained by RF using diastolic blood pressure, albumin–creatinine ratio, and gender for CAN testing (98.67%); microalbuminuria, smoking history, and hemoglobin A1C for DPN testing (67.78%); and hemoglobin A1C, microalbuminuria, and smoking history for RET testing (84.38%). This study suggests machine learning as a promising automated tool for predicting microvascular complications in diabetic patients using their profiles, which could help prevent those patients from further microvascular complications leading to early death.
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spelling pubmed-88793062022-02-26 Machine Learning for Screening Microvascular Complications in Type 2 Diabetic Patients Using Demographic, Clinical, and Laboratory Profiles Rashid, Mamunur Alkhodari, Mohanad Mukit, Abdul Ahmed, Khawza Iftekhar Uddin Mostafa, Raqibul Parveen, Sharmin Khandoker, Ahsan H. J Clin Med Article Microvascular complications are one of the key causes of mortality among type 2 diabetic patients. This study was sought to investigate the use of a novel machine learning approach for predicting these complications using only the patient demographic, clinical, and laboratory profiles. A total of 96 Bangladeshi participants with type 2 diabetes were recruited during their routine hospital visits. All patient profiles were assessed by using a chi-squared (χ(2)) test to statistically determine the most important markers in predicting three microvascular complications: cardiac autonomic neuropathy (CAN), diabetic peripheral neuropathy (DPN), and diabetic retinopathy (RET). A machine learning approach based on logistic regression, random forest (RF), and support vector machine (SVM) algorithms was then developed to ensure automated clinical testing for microvascular complications in diabetic patients. The highest prediction accuracies were obtained by RF using diastolic blood pressure, albumin–creatinine ratio, and gender for CAN testing (98.67%); microalbuminuria, smoking history, and hemoglobin A1C for DPN testing (67.78%); and hemoglobin A1C, microalbuminuria, and smoking history for RET testing (84.38%). This study suggests machine learning as a promising automated tool for predicting microvascular complications in diabetic patients using their profiles, which could help prevent those patients from further microvascular complications leading to early death. MDPI 2022-02-09 /pmc/articles/PMC8879306/ /pubmed/35207179 http://dx.doi.org/10.3390/jcm11040903 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Rashid, Mamunur
Alkhodari, Mohanad
Mukit, Abdul
Ahmed, Khawza Iftekhar Uddin
Mostafa, Raqibul
Parveen, Sharmin
Khandoker, Ahsan H.
Machine Learning for Screening Microvascular Complications in Type 2 Diabetic Patients Using Demographic, Clinical, and Laboratory Profiles
title Machine Learning for Screening Microvascular Complications in Type 2 Diabetic Patients Using Demographic, Clinical, and Laboratory Profiles
title_full Machine Learning for Screening Microvascular Complications in Type 2 Diabetic Patients Using Demographic, Clinical, and Laboratory Profiles
title_fullStr Machine Learning for Screening Microvascular Complications in Type 2 Diabetic Patients Using Demographic, Clinical, and Laboratory Profiles
title_full_unstemmed Machine Learning for Screening Microvascular Complications in Type 2 Diabetic Patients Using Demographic, Clinical, and Laboratory Profiles
title_short Machine Learning for Screening Microvascular Complications in Type 2 Diabetic Patients Using Demographic, Clinical, and Laboratory Profiles
title_sort machine learning for screening microvascular complications in type 2 diabetic patients using demographic, clinical, and laboratory profiles
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8879306/
https://www.ncbi.nlm.nih.gov/pubmed/35207179
http://dx.doi.org/10.3390/jcm11040903
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