Seyed Arsalan Seyedi , Juan P. González-Rivas , Pranav Mellacheruvu , Ananya Mellacheruvu , Seyed Pedram Aledavood , Jeffrey I. Mechanick
{"title":"Cardiometabolic Risk Reduction with Digital Twinning: A Narrative Review","authors":"Seyed Arsalan Seyedi , Juan P. González-Rivas , Pranav Mellacheruvu , Ananya Mellacheruvu , Seyed Pedram Aledavood , Jeffrey I. Mechanick","doi":"10.1016/j.ahj.2025.07.033","DOIUrl":null,"url":null,"abstract":"<div><div>Digital twin (DT) technology—real-time, data-driven virtual models of individuals—offers transformative potential in managing cardiometabolic-based chronic disease (CMBCD), a progressive continuum including abnormal adiposity (ABCD), hypertension (HBCD), dysglycemia (DBCD), dyslipidemia (LBCD), residual risk states, and cardiovascular diseases (CVDs). Type 2 diabetes (T2D), central in this cascade, requires individualized, integrative strategies where DT may serve as a precision-medicine tool. A systematic search across PubMed, Embase, Web of Science, Scopus, and Cochrane identified 12 eligible studies. Due to data duplication (five studies using the same cohort) and lack of homogeneity, meta-analysis was not feasible, prompting a narrative synthesis. DT-guided interventions were categorized across the CMBCD spectrum: (1) ABCD – DT reduced visceral fat and lowered BMI by 1.8 kg/m²; (2) DBCD – HbA1c dropped up to 1.8%, 89% achieved glycemic targets, fewer medications were used, time-in-range improved from 69.7% (±30.7) to 86.9% (±24.5), time-above-range decreased (p<0.001), and time-below-range slightly increased (p<0.001); (3) HBCD – normal blood pressure cases increased from 108 (46.4%) to 147 (63.1%), outperforming standard care, with 30 patients stopping antihypertensive drugs; (4) LBCD – triglycerides dropped 18.8% and HDL increased 6.8% (p<0.001); (5) Residual risk – DT improved liver fat/fibrosis (via imaging and fibrosis scores), and predicted CKD with area under the curves (AUCs) range from 0.80 to 0.86, retinopathy (AUC: 0.84), and cataracts (AUC: 0.93); (6) CVD outcomes – early trials show improved risk factors and medication de-escalation. DT appears promising for cardiometabolic risk management and personalized T2D care. Broader validation in diverse populations and refined implementation strategies are needed for clinical integration.</div></div>","PeriodicalId":7868,"journal":{"name":"American heart journal","volume":"290 ","pages":"Pages 10-11"},"PeriodicalIF":3.5000,"publicationDate":"2025-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"American heart journal","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S000287032500242X","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CARDIAC & CARDIOVASCULAR SYSTEMS","Score":null,"Total":0}
引用次数: 0
Abstract
Digital twin (DT) technology—real-time, data-driven virtual models of individuals—offers transformative potential in managing cardiometabolic-based chronic disease (CMBCD), a progressive continuum including abnormal adiposity (ABCD), hypertension (HBCD), dysglycemia (DBCD), dyslipidemia (LBCD), residual risk states, and cardiovascular diseases (CVDs). Type 2 diabetes (T2D), central in this cascade, requires individualized, integrative strategies where DT may serve as a precision-medicine tool. A systematic search across PubMed, Embase, Web of Science, Scopus, and Cochrane identified 12 eligible studies. Due to data duplication (five studies using the same cohort) and lack of homogeneity, meta-analysis was not feasible, prompting a narrative synthesis. DT-guided interventions were categorized across the CMBCD spectrum: (1) ABCD – DT reduced visceral fat and lowered BMI by 1.8 kg/m²; (2) DBCD – HbA1c dropped up to 1.8%, 89% achieved glycemic targets, fewer medications were used, time-in-range improved from 69.7% (±30.7) to 86.9% (±24.5), time-above-range decreased (p<0.001), and time-below-range slightly increased (p<0.001); (3) HBCD – normal blood pressure cases increased from 108 (46.4%) to 147 (63.1%), outperforming standard care, with 30 patients stopping antihypertensive drugs; (4) LBCD – triglycerides dropped 18.8% and HDL increased 6.8% (p<0.001); (5) Residual risk – DT improved liver fat/fibrosis (via imaging and fibrosis scores), and predicted CKD with area under the curves (AUCs) range from 0.80 to 0.86, retinopathy (AUC: 0.84), and cataracts (AUC: 0.93); (6) CVD outcomes – early trials show improved risk factors and medication de-escalation. DT appears promising for cardiometabolic risk management and personalized T2D care. Broader validation in diverse populations and refined implementation strategies are needed for clinical integration.
期刊介绍:
The American Heart Journal will consider for publication suitable articles on topics pertaining to the broad discipline of cardiovascular disease. Our goal is to provide the reader primary investigation, scholarly review, and opinion concerning the practice of cardiovascular medicine. We especially encourage submission of 3 types of reports that are not frequently seen in cardiovascular journals: negative clinical studies, reports on study designs, and studies involving the organization of medical care. The Journal does not accept individual case reports or original articles involving bench laboratory or animal research.