MIRA: Myocardial insulin resistance app for clinical practice

IF 4.8 2区 医学 Q1 COMPUTER SCIENCE, INTERDISCIPLINARY APPLICATIONS Computer methods and programs in biomedicine Pub Date : 2025-02-14 DOI:10.1016/j.cmpb.2025.108674
Queralt Martín-Saladich , Rafael Simó , José Raul Herance , Miguel A. González Ballester
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Abstract

Background and Objective

Type 2 diabetes (T2D) is a prevalent disease characterized by insulin resistance (IR), leading to energy disruptions in myocardial cells and increasing cardiovascular (CV) risk. Current diagnostic methods are either systemic, thus lacking tissue-specific information, or invasive. The hyperinsulinemic euglycemic clamp (HEC) combined with [18F]FDG-PET images, only used in clinical trials, allow to assess regional IR and identify phenotypes within T2D, linking myocardial IR to higher CV risk. However, phenotyping is not easily accessible, creating a need for alternative assessment tools. Thus, we propose a myocardial IR model to address these gaps and improve T2D management.

Methods

The study included forty-two patients with T2D who enrolled in a clinical trial (NCT02248311) and who underwent biochemical analyses, anthropometric measurements and [18F]FDG PET/CT imaging before and after HEC with. Patients were phenotyped into mIR and mIS according to poor or good uptake after HEC, respectively. The proposed predictive model was based on stepwise regression including feature selection to provide an estimate of myocardial IS and thus IR=1/IS by using biochemical parameters in T2D. A software application, the myocardial IR app (MIRA), was developed using MATLAB.

Results

MIRA was developed as a myocardial IR estimator (R2=0.97, p=7.1 × 10–7, error=1.24) for patients with T2D. Moreover, since HEC is not allowed in rutinary clinical practice, the application includes a prediction of the expected myocardial HEC [18F]FDG uptake from baseline uptake (r=0.52, p=5 × 10–4, R2=0.60). The app also yields the patient's phenotype, either mIR or mIS, according to poor or good uptake after HEC. Enhanced CV risk exposure due to altered T2D biomarkers and associated to mIR is also provided with highlighted features.

Conclusions

We hereby present MIRA, a myocardial IR calculation app to manage myocardial-specific affectation in T2D, as well as to provide with patient phenotyping and CV risk assessment.
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MIRA:心肌胰岛素抵抗临床应用程序
背景与目的2型糖尿病(T2D)是一种以胰岛素抵抗(IR)为特征的常见病,可导致心肌细胞能量中断并增加心血管(CV)风险。目前的诊断方法要么是系统性的,因此缺乏组织特异性信息,要么是侵入性的。高胰岛素正糖钳(HEC)结合[18F]FDG-PET图像,仅用于临床试验,可以评估区域IR并识别T2D内的表型,将心肌IR与更高的CV风险联系起来。然而,表现型不容易获得,创造了对替代评估工具的需求。因此,我们提出心肌IR模型来解决这些差距并改善T2D管理。方法本研究纳入了42例T2D患者,他们参加了一项临床试验(NCT02248311),并在HEC前后进行了生化分析、人体测量和[18F]FDG PET/CT成像。根据HEC后摄取不良或良好的情况,患者分别表型为mIR和mIS。所提出的预测模型基于逐步回归,包括特征选择,以提供心肌IS的估计,从而通过使用T2D的生化参数提供IR=1/IS。利用MATLAB开发了心肌IR应用程序(MIRA)。结果smira可作为t2dm患者的心肌IR估计指标(R2=0.97, p=7.1 × 10-7,误差=1.24)。此外,由于HEC在常规临床实践中是不允许的,该应用包括从基线摄取预测心肌HEC [18F]FDG摄取(r=0.52, p=5 × 10-4, R2=0.60)。该应用程序还根据HEC后摄取不良或良好的情况显示患者的表型,mIR或mIS。由于T2D生物标志物改变并与mIR相关而增加的CV风险暴露也具有突出的特征。我们在此提出MIRA,一款心肌IR计算应用程序,用于管理T2D中心肌特异性影响,并提供患者表型和CV风险评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Computer methods and programs in biomedicine
Computer methods and programs in biomedicine 工程技术-工程:生物医学
CiteScore
12.30
自引率
6.60%
发文量
601
审稿时长
135 days
期刊介绍: To encourage the development of formal computing methods, and their application in biomedical research and medical practice, by illustration of fundamental principles in biomedical informatics research; to stimulate basic research into application software design; to report the state of research of biomedical information processing projects; to report new computer methodologies applied in biomedical areas; the eventual distribution of demonstrable software to avoid duplication of effort; to provide a forum for discussion and improvement of existing software; to optimize contact between national organizations and regional user groups by promoting an international exchange of information on formal methods, standards and software in biomedicine. Computer Methods and Programs in Biomedicine covers computing methodology and software systems derived from computing science for implementation in all aspects of biomedical research and medical practice. It is designed to serve: biochemists; biologists; geneticists; immunologists; neuroscientists; pharmacologists; toxicologists; clinicians; epidemiologists; psychiatrists; psychologists; cardiologists; chemists; (radio)physicists; computer scientists; programmers and systems analysts; biomedical, clinical, electrical and other engineers; teachers of medical informatics and users of educational software.
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