{"title":"A novel assessment of anthracycline-induced cardiotoxicity: topological flow data analysis in childhood cancer survivors.","authors":"Tatsuki Nishiyama, Ken Takahashi, Yusuke Akatsuka, Hirohisa Kago, Azusa Akiya, Yu Hosono, Sachie Shigemitsu, Akinori Yaguchi, Osamu Tomita, Junya Fujimura, Masahiro Saito, Keiichi Itatani, Takashi Sakajo, Hiromichi Shoji","doi":"10.1152/ajpheart.00136.2025","DOIUrl":null,"url":null,"abstract":"<p><p>Anthracycline chemotherapy improves survival rates in childhood cancer patients but poses a significant risk of late-onset cardiotoxicity, potentially leading to cardiac dysfunction and heart failure. Recently, flow dynamics parameters derived from two-dimensional fluid dynamics may be sensitive indicators of cardiac dysfunction. Topological flow data analysis (TFDA) mathematically defines vortical flow structures and offers a novel approach to cardiac function assessment. This study aimed to use TFDA to analyze the left ventricular flow patterns in 90 childhood cancer survivors (CCSs) treated with anthracyclines (median age 15.1 yr) and 90 age-matched control subjects. The TFDA parameters, including vortex number, size, circulation, width of mitral inflow, and saddle points, were calculated and compared across the three age subgroups: <i>C1</i> (4-12 yr), <i>C2</i> (13-19 yr), and <i>C3</i> (20-36 yr). The CCSs in <i>group C3</i> exhibited a reduced left ventricular ejection fraction within the normal range, and the longitudinal strain decreased in <i>groups C2</i> and <i>C3</i>. Regarding TFDA parameters, the number of abnormal vortices in the early diastolic frames increased across all CCSs, with significant reductions in the width of the effective mitral inflow in <i>groups C2</i> and <i>C3</i>. Systolic circulation was reduced across all CCSs, and diastolic circulation was decreased in <i>groups C2</i> and <i>C3</i>, which correlated with age, time since chemotherapy, and cumulative anthracycline dose. TFDA parameters identified cardiac dysfunction before conventional echocardiographic markers, highlighting its potential as a novel and sensitive tool for the early detection and long-term monitoring of cardiotoxicity in CCSs and supporting its integration into clinical practice.<b>NEW & NOTEWORTHY</b> This study suggests that topological flow data analysis (TFDA) is a novel and sensitive method for assessing cardiotoxicity in childhood cancer survivors. By analyzing vortical flow parameters, including circulation and abnormal vortices, TFDA detected anthracycline-induced cardiotoxicity earlier than conventional echocardiographic indicators. The findings reveal age- and dose-dependent cardiac dysfunction, emphasizing TFDA's potential as a highly sensitive tool for long-term cardiovascular monitoring and early intervention in high-risk populations.</p>","PeriodicalId":7692,"journal":{"name":"American journal of physiology. Heart and circulatory physiology","volume":" ","pages":"H41-H50"},"PeriodicalIF":4.1000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"American journal of physiology. Heart and circulatory physiology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1152/ajpheart.00136.2025","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/5/2 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CARDIAC & CARDIOVASCULAR SYSTEMS","Score":null,"Total":0}
引用次数: 0
Abstract
Anthracycline chemotherapy improves survival rates in childhood cancer patients but poses a significant risk of late-onset cardiotoxicity, potentially leading to cardiac dysfunction and heart failure. Recently, flow dynamics parameters derived from two-dimensional fluid dynamics may be sensitive indicators of cardiac dysfunction. Topological flow data analysis (TFDA) mathematically defines vortical flow structures and offers a novel approach to cardiac function assessment. This study aimed to use TFDA to analyze the left ventricular flow patterns in 90 childhood cancer survivors (CCSs) treated with anthracyclines (median age 15.1 yr) and 90 age-matched control subjects. The TFDA parameters, including vortex number, size, circulation, width of mitral inflow, and saddle points, were calculated and compared across the three age subgroups: C1 (4-12 yr), C2 (13-19 yr), and C3 (20-36 yr). The CCSs in group C3 exhibited a reduced left ventricular ejection fraction within the normal range, and the longitudinal strain decreased in groups C2 and C3. Regarding TFDA parameters, the number of abnormal vortices in the early diastolic frames increased across all CCSs, with significant reductions in the width of the effective mitral inflow in groups C2 and C3. Systolic circulation was reduced across all CCSs, and diastolic circulation was decreased in groups C2 and C3, which correlated with age, time since chemotherapy, and cumulative anthracycline dose. TFDA parameters identified cardiac dysfunction before conventional echocardiographic markers, highlighting its potential as a novel and sensitive tool for the early detection and long-term monitoring of cardiotoxicity in CCSs and supporting its integration into clinical practice.NEW & NOTEWORTHY This study suggests that topological flow data analysis (TFDA) is a novel and sensitive method for assessing cardiotoxicity in childhood cancer survivors. By analyzing vortical flow parameters, including circulation and abnormal vortices, TFDA detected anthracycline-induced cardiotoxicity earlier than conventional echocardiographic indicators. The findings reveal age- and dose-dependent cardiac dysfunction, emphasizing TFDA's potential as a highly sensitive tool for long-term cardiovascular monitoring and early intervention in high-risk populations.
期刊介绍:
The American Journal of Physiology-Heart and Circulatory Physiology publishes original investigations, reviews and perspectives on the physiology of the heart, vasculature, and lymphatics. These articles include experimental and theoretical studies of cardiovascular function at all levels of organization ranging from the intact and integrative animal and organ function to the cellular, subcellular, and molecular levels. The journal embraces new descriptions of these functions and their control systems, as well as their basis in biochemistry, biophysics, genetics, and cell biology. Preference is given to research that provides significant new mechanistic physiological insights that determine the performance of the normal and abnormal heart and circulation.