161. Characterization of Aortic Valve Stenosis by CT Angiography in a Diverse US Cohort.
作者: Daniel Lorenzatti.;Annalisa Filtz.;Pamela Pina.;Jolien Geers.;Jake Gilman.;Jonathan Daich.;Paul Ippolito.;Abdullah Aftab.;Aldo L Schenone.;Carlos A Gongora.;Justin Johannesen.;Andrea Scotti.;Edwin C Ho.;Mario J Garcia.;Azeem Latib.;Carlos J Rodriguez.;Daniel S Berman.;Marie-Annick Clavel.;Philippe Pibarot.;Robert O Bonow.;Piotr J Slomka.;Marc R Dweck.;Damini Dey.;Leandro Slipczuk.
来源: Circ Cardiovasc Imaging. 2025年18卷6期e017858页
Aortic stenosis (AS) involves calcific and fibrotic degeneration of the valve tissue. The only noninvasive method for evaluating both processes is contrast-enhanced computed tomography angiography. We aimed to explore the differences in aortic valve (AV) tissue composition across sex, race/ethnicity, and AS hemodynamic phenotype in US patients referred for transcatheter AV replacement planning.
163. Data Interoperability and Harmonization in Cardiovascular Genomic and Precision Medicine.
作者: C Anwar A Chahal.;Fares Alahdab.;Babken Asatryan.;Daniel Addison.;Nay Aung.;Mina K Chung.;Spiros Denaxas.;Jessilyn Dunn.;Jennifer L Hall.;Nathalie Pamir.;David J Slotwiner.;Jose D Vargas.;Antonis A Armoundas.
来源: Circ Genom Precis Med. 2025年18卷3期e004624页
Despite advances in cardiovascular care and improved outcomes, fragmented healthcare systems, nonequitable access to health care, and nonuniform and unbiased collection and access to healthcare data have exacerbated disparities in healthcare provision and further delayed the technological-enabled implementation of precision medicine. Precision medicine relies on a foundation of accurate and valid omics and phenomics that can be harnessed at scale from electronic health records. Big data approaches in noncardiovascular healthcare domains have helped improve efficiency and expedite the development of novel therapeutics; therefore, applying such an approach to cardiovascular precision medicine is an opportunity to further advance the field. Several endeavors, including the American Heart Association Precision Medicine platform and public-private partnerships (such as BigData@Heart in Europe), as well as cloud-based platforms, such as Terra used for the National Institutes of Health All of Us, are attempting to temporally and ontologically harmonize data. This state-of-the-art review summarizes best practices used in cardiovascular genomic and precision medicine and provides recommendations for systems' requirements that could enhance and accelerate the integration of these platforms.
164. Developments in Digital Wearable in Heart Failure and the Rationale for the Design of TRUE-HF (Ted Rogers Understanding of Exacerbations in Heart Failure) Apple CPET Study.
作者: Yasbanoo Moayedi.;Farid Foroutan.;Yuan Gao.;Ben Kim.;Enza De Luca.;Margaret Brum.;Darshan H Brahmbhatt.;Joe Duhamel.;Anne Simard.;Christopher McIntosh.;Heather J Ross.
来源: Circ Heart Fail. 2025年18卷6期e012204页
Heart failure (HF) is a highly prevalent condition characterized by exercise intolerance, an important metric for ambulatory prognostication. However, current methods to assess exercise capacity are often limited to tertiary HF centers, lacking scalability or accessibility. Wearable devices can enable near-continuous dynamic biometrics including exercise tolerance.
165. Proteomic Analysis of Valsartan for Attenuating Disease Evolution in Early Sarcomeric Hypertrophic Cardiomyopathy (VANISH) Clinical Trial.
作者: Constantin-Cristian Topriceanu.;Christoffer Rasmus Vissing.;Anna Axelsson Raja.;Sharlene M Day.;Mark W Russell.;Kenneth Zahka.;Alexandre C Pereira.;Steven D Colan.;Anne M Murphy.;Charles Canter.;Richard G Bach.;Matthew T Wheeler.;Joseph W Rossano.;Anjali T Owens.;Luisa Mestroni.;Matthew R G Taylor.;James C Moon.;Gabriella Captur.;Amit R Patel.;Ivan Wilmot.;Jonathan H Soslow.;Jason R Becker.;Christine E Seidman.;Neal K Lakdawala.;Henning Bundgaard.;Usman A Tahir.;Carolyn Y Ho.
来源: Circ Heart Fail. 2025年18卷6期e012393页
In hypertrophic cardiomyopathy (HCM), the mechanisms through which pathogenic sarcomere variants (G+) lead to left ventricular hypertrophy (LVH) are not understood.
166. Response to Letter Regarding Article, "Abnormal Exercise Electrocardiography With Normal Stress Echocardiography Is Associated With Subclinical Coronary Atherosclerosis".168. Interrupted Inferior Vena Cava, Partial Anomalous Pulmonary Venous Return and Extra-Mediastinal Superior Vena Cava: A Rare Case of Multilevel Congenital Anomalous Venous Return.
作者: Francisco Javier Ruperti-Repilado.;Gorka Gómez Ciriz.;Begoña Manso-García.
来源: Circ Cardiovasc Imaging. 2025年e017917页 169. Doughnut Sign: A Mixed Plaque Phenotype Unraveled Only by the Photon Counting CCTA.
作者: Pruthvi C Revaiah.;Patrick W Serruys.;Sean O Hynes.;Christos V Bourantas.;Helle Precht.;Yoshinobu Onuma.;Erica Maffei.;Filippo Cademartiri.
来源: Circ Cardiovasc Imaging. 2025年e017925页 170. Letter by Barbieri et al Regarding Article, "Abnormal Exercise Electrocardiography With Normal Stress Echocardiography Is Associated With Subclinical Coronary Atherosclerosis".
作者: Andrea Barbieri.;Francesca Bursi.;Francesca Mantovani.
来源: Circ Cardiovasc Imaging. 2025年18卷6期e018294页 171. Letter by Skalidis et al Regarding Article, "Comparing the Efficacy of Sirolimus and Paclitaxel-Eluting Balloon Catheters in the Treatment of Coronary In-Stent Restenosis: A Prospective Randomized Study (TIS 2 Study)".180. Evidence Generation and Implementation of Transcatheter Interventions for Atrioventricular Valvular Heart Disease in Heart Failure: Current Status and Future Directions.
作者: Marco Metra.;Daniela Tomasoni.;Marianna Adamo.;Stefan D Anker.;Antoni Bayes-Genis.;Ralph Stephan von Bardeleben.;Michael Böhm.;Erwan Donal.;Gerasimos S Filippatos.;Francesco Maisano.;Piotr Ponikowski.;Gianluigi Savarese.;Fabien Praz.;Javed Butler.
来源: Circulation. 2025年151卷18期1342-1363页
Mitral regurgitation and tricuspid regurgitation are the most common valvular heart diseases in patients with heart failure and have independent prognostic value. Transcatheter interventions are now available for the treatment of valvular heart disease, and their efficacy and safety have been tested in randomized controlled trials. However, evidence is still limited and sometimes inconclusive because several aspects of these trials limit their interpretation or consistency. These include heterogeneity in the pathogenesis and clinical characteristics of patients, the dynamic nature of secondary atrioventricular valve disease severity, the role of heart failure medications and devices, dependency on procedural results and operators' skills, smaller number of patients enrolled and the power to detect differences in trials, and limitations to use patients' reported outcomes with unblinded study protocols. These specific aspects of trials in patients with atrioventricular valve disease are reviewed in this article with a focus on possible solutions to generate further evidence for the efficacy and safety for transcatheter treatments of atrioventricular valve disease in patients with heart failure.
|