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Enhancing Hypertension Risk Diagnosis Using a Hybrid Machine Learning Framework: Leveraging Body Composition Data.

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  • معلومة اضافية
    • المصدر:
      Publisher: Wiley Country of Publication: United States NLM ID: 101600173 Publication Model: eCollection Cited Medium: Internet ISSN: 2314-6141 (Electronic) NLM ISO Abbreviation: Biomed Res Int Subsets: MEDLINE
    • بيانات النشر:
      Publication: 2024- : [Hoboken, NJ] : Wiley
      Original Publication: New York, NY : Hindawi Pub. Co.
    • الموضوع:
    • نبذة مختصرة :
      Hypertension, widely recognized as the "silent killer," remains a leading cause of cardiovascular, renal, and neurological complications worldwide. This study proposes a dual-scenario hybrid machine learning framework for hypertension risk prediction using noninvasive body composition features, aimed at enhancing both interpretability and predictive reliability. In Scenario 1, an unsupervised clustering analysis inspired by self-labeling principles was performed exclusively on hypertensive individuals, where five physiological subgroups were identified via K-Means clustering and validated using Silhouette (0.3371), Davies-Bouldin (1.0094), and Calinski-Harabasz (720.10) indices. Significant intercluster variability (p < 0.001) was observed across key indicators such as FATP, RLFATP, LLFATP, FATM, and age. Among the tested models, the support vector machine (SVM) with random oversampling achieved the best performance (accuracy = 99.08%, F1 = 98.04%, AUC = 99.98%), confirming effective subgroup discrimination. In Scenario 2, a comprehensive binary classification between healthy and hypertensive subjects was conducted using five models-ExtraTrees, KNN, SVM, Gaussian Naive Bayes, and Decision Tree-across multiple configurations. The cluster-augmented dataset yielded the best results, with the ExtraTrees classifier achieving superior performance (accuracy = 98.23%, recall = 98.30%, precision = 98.17%, F1 = 98.23%, AUC = 99.87%). Clustering and feature selection both improved generalization, particularly for ensemble-based learners. Overall, Scenario 2 demonstrated the highest predictive accuracy and stability, whereas Scenario 1 provided valuable interpretability through subgroup discovery. These findings highlight that integrating unsupervised clustering with supervised classification offers a robust and explainable framework for personalized hypertension risk prediction, contributing to early detection and precision healthcare.
      (Copyright © 2026 Abdul Wahid Mirzaye et al. BioMed Research International published by John Wiley & Sons Ltd.)
    • نبذة مختصرة :
      The authors declare no conflicts of interest.
    • References:
      Environ Pollut. 2018 Feb;233:670-678. (PMID: 29121602)
      Clin Hypertens. 2021 Jan 1;27(1):1. (PMID: 33384019)
      Biomed Res Int. 2026 Feb 01;2026:6335947. (PMID: 41635286)
      Hypertension. 2003 Dec;42(6):1206-52. (PMID: 14656957)
      IEEE J Biomed Health Inform. 2025 Jan;29(1):5-16. (PMID: 38598377)
      J Neurosci Methods. 2016 Jan 15;257:97-108. (PMID: 26432931)
      Int J Cardiol Hypertens. 2020 Mar 19;5:100027. (PMID: 33447756)
      J Am Heart Assoc. 2020 Jul 7;9(13):e015533. (PMID: 32573312)
      Am J Obstet Gynecol MFM. 2021 Jan;3(1):100250. (PMID: 33451620)
      Environ Sci Pollut Res Int. 2024 Jan;31(3):4595-4605. (PMID: 38105323)
      Hypertens Res. 2024 Mar;47(3):700-707. (PMID: 38216731)
      Circulation. 2016 Aug 9;134(6):441-50. (PMID: 27502908)
      IEEE Trans Neural Netw Learn Syst. 2018 Aug;29(8):3524-3537. (PMID: 28816682)
    • Contributed Indexing:
      Keywords: Gaussian naive Bayes; K-Means clustering; SMOTE technique; body composition data; hypertension diagnosis; random search optimization
    • الموضوع:
      Date Created: 20260204 Date Completed: 20260204 Latest Revision: 20260416
    • الموضوع:
      20260417
    • الرقم المعرف:
      PMC12862000
    • الرقم المعرف:
      10.1155/bmri/6335947
    • الرقم المعرف:
      41635286