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241. Race- and Sex-Specific Age at Which Coronary Artery Calcium Becomes Detectable Among Young Adults.

作者: Yvette A Yeboah-Kordieh.;Ellen Boakye.;Albert D Osei.;Omar Dzaye.;Zeina A Dardari.;Joao A C Lima.;Alan Rozanski.;Daniel S Berman.;Matthew J Budoff.;Michael D Miedema.;Khurram Nasir.;John A Rumberger.;Leslee J Shaw.;David R Jacobs.;Michael J Blaha.
来源: Circ Cardiovasc Imaging. 2025年18卷3期e016599页
Coronary artery calcium (CAC) is an excellent predictor of atherosclerotic cardiovascular disease (ASCVD) risk. Limited data exist on the age at which CAC transitions to nonzero among young adults. We aimed to assess the prevalence of CAC by the number of ASCVD risk factors and use this data to model the race- and sex-specific ages at which young adults transition to a CAC >0.

242. Association Between Use of WATCHMAN Device and 1-Year Mortality Using High-Dimensional Propensity Scores to Reduce Confounding.

作者: Julie Z Zhao.;Mohammed Ruzieh.;Fanxing Du.;Yi Lian.;Andrew J Foy.;Robert W Platt.;Mark S Segal.;Janie Coulombe.;Almut G Winterstein.;Tianze Jiao.
来源: Circ Cardiovasc Qual Outcomes. 2025年18卷4期e011188页
Previous observational studies showed left atrial appendage occlusions with the WATCHMAN device reduced 1-year mortality, which conflicted with evidence generated from randomized controlled trials. We proposed to use the high-dimensional propensity score (hdPS) to assist in nonactive comparator selection (prevalent user of medication) and compared 1-year mortality between patients with atrial fibrillation who received the WATCHMAN device (percutaneous left atrial appendage occlusion device [pLAAO]) and direct oral anticoagulants in 2 matched cohorts based on (1) traditional propensity score (PS) and (2) integrating traditional PS with information learned from hdPS.

243. Impact of Multimorbidity on Mortality in Heart Failure With Mildly Reduced and Preserved Ejection Fraction.

作者: Mingming Yang.;Toru Kondo.;Pooja Dewan.;Akshay S Desai.;Carolyn S P Lam.;Martin P Lefkowitz.;Milton Packer.;Jean L Rouleau.;Muthiah Vaduganathan.;Michael R Zile.;Pardeep S Jhund.;Lars Køber.;Scott D Solomon.;John J V McMurray.
来源: Circ Heart Fail. 2025年18卷3期e011598页
How different combinations of comorbidities influence risk at the patient level and population level in patients with heart failure with mildly reduced ejection fraction/heart failure with preserved ejection fraction is unknown. We aimed to investigate the prevalence of different combinations of cardiovascular and noncardiovascular comorbidities (ie, multimorbidity) and associated risk of death at the patient level and population level.

244. Challenges Related to Out-of-Pocket Costs in Heart Failure Management.

作者: Birju R Rao.;Larry A Allen.;Alexander T Sandhu.;Neal W Dickert.
来源: Circ Heart Fail. 2025年18卷3期e011584页
High out-of-pocket costs and financial toxicity related to heart failure treatment are substantial concerns. Two of 4 pillars of guideline-directed medical therapy for heart failure with reduced ejection fraction, for example, carry high costs that may attenuate their uptake. Furthermore, heart failure rarely occurs in isolation. Many patients have other comorbidities that require treatment, further driving up patients' out-of-pocket costs. Developing treatment plans that improve mortality without subjecting patients to financial toxicity can be challenging for several reasons. First, patients with heart failure can accrue out-of-pocket costs from multiple domains and can depend on a variety of insurance and pharmacy-related factors that can make determining patient-specific out-of-pocket cost estimates complicated. Second, strategies to mitigate financial toxicity involve health policy-level interventions and patient-level interventions. These have their own unique sets of challenges. Third, integrating out-of-pocket costs into shared decision-making requires nuanced and challenging discussions about whether a therapy is worth the cost. Though shared decision-making has been advocated, there are little data on how to best conduct these discussions. Health policies like the Inflation Reduction Act of 2022 may provide relief to some patients, and efforts to improve transparency have the potential to be beneficial. Over the long term, policy solutions such as value-based insurance design and patient engagement solutions that emphasize enhancing shared decision-making have important potential to yield durable results.

245. 2025 ACC/AHA/ACEP/NAEMSP/SCAI Guideline for the Management of Patients With Acute Coronary Syndromes: A Report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines.

作者: Sunil V Rao.;Michelle L O'Donoghue.;Marc Ruel.;Tanveer Rab.;Jaqueline E Tamis-Holland.;John H Alexander.;Usman Baber.;Heather Baker.;Mauricio G Cohen.;Mercedes Cruz-Ruiz.;Leslie L Davis.;James A de Lemos.;Tracy A DeWald.;Islam Y Elgendy.;Dmitriy N Feldman.;Abhinav Goyal.;Ijeoma Isiadinso.;Venu Menon.;David A Morrow.;Debabrata Mukherjee.;Elke Platz.;Susan B Promes.;Sigrid Sandner.;Yader Sandoval.;Rachel Schunder.;Binita Shah.;Jason P Stopyra.;Amy W Talbot.;Pam R Taub.;Marlene S Williams.
来源: Circulation. 2025年151卷13期e771-e862页
The "2025 ACC/AHA/ACEP/NAEMSP/SCAI Guideline for the Management of Patients With Acute Coronary Syndromes" incorporates new evidence since the "2013 ACCF/AHA Guideline for the Management of ST-Elevation Myocardial Infarction" and the corresponding "2014 AHA/ACC Guideline for the Management of Patients With Non-ST-Elevation Acute Coronary Syndromes" and the "2015 ACC/AHA/SCAI Focused Update on Primary Percutaneous Coronary Intervention for Patients With ST-Elevation Myocardial Infarction." The "2025 ACC/AHA/ACEP/NAEMSP/SCAI Guideline for the Management of Patients With Acute Coronary Syndromes" and the "2021 ACC/AHA/SCAI Guideline for Coronary Artery Revascularization" retire and replace, respectively, the "2016 ACC/AHA Guideline Focused Update on Duration of Dual Antiplatelet Therapy in Patients With Coronary Artery Disease."

246. Evaluating Percutaneous Coronary Intervention Safety, Quality, and Appropriateness Across Michigan Using Blinded Cross-Institutional Peer Review.

作者: Stephanie M Spehar.;Milan Seth.;John F Collins.;Simon R Dixon.;Elizabeth Pielsticker.;Daniel Lee.;Mark Zainea.;Thomas LaLonde.;Dilip Arora.;Devraj Sukul.;Hitinder S Gurm.
来源: Circ Cardiovasc Qual Outcomes. 2025年18卷4期e011031页
Several quality improvement initiatives have focused on the quality gap in percutaneous coronary intervention (PCI), yet significant variations in quality persist. Our objective was to use a novel blinded peer review system to evaluate PCI quality, safety, and appropriateness across Michigan.

247. Evaluating the Appropriate Use Criteria for Coronary Revascularization in Stable Ischemic Heart Disease Using Randomized Data From the ISCHEMIA Trial.

作者: James Slater.;David J Maron.;Philip G Jones.;Sripal Bangalore.;Harmony R Reynolds.;Zhuxuan Fu.;Gregg W Stone.;Ruth Kirby.;Judith S Hochman.;John A Spertus.; .
来源: Circ Cardiovasc Qual Outcomes. 2025年18卷3期e010849页
The appropriate use criteria for revascularization of stable ischemic heart disease have not been evaluated using randomized data. Using data from the randomized ISCHEMIA trial (International Study of Comparative Health Effectiveness with Medical and Invasive Approaches; July 2012 to January 2018, 37 countries), the health status benefits of an invasive strategy over a conservative one were examined within appropriate use criteria scenarios.

248. Succinylation of SERCA2a at K352 Promotes Its Ubiquitinoylation and Degradation by Proteasomes in Sepsis-Induced Heart Dysfunction.

作者: Ni Yang.;Linus Li.;Xiao-Lu Shi.;Yong-Ping Liu.;Ri Wen.;Yu-Hang Yang.;Tao Zhang.;Xin-Ru Yang.;Yang-Fan Xu.;Chun-Feng Liu.;Wanshan Ning.;Tie-Ning Zhang.
来源: Circ Heart Fail. 2025年18卷4期e012180页
Intracellular Ca2+ cycling governs effective myocardial systolic contraction and diastolic relaxation. SERCA2a (sarco/endoplasmic reticulum Ca2+ ATPase type 2a), which plays a crucial role in controlling intracellular Ca2+ signaling and myocardial cell function, is downregulated and inactivated during sepsis-induced heart dysfunction. However, the cause of this dysregulation remains unclear. In this study, we investigated the effect of lysine succinylation in lipopolysaccharide-induced septic heart dysfunction through global succinylome analysis of myocardial tissues from septic rats.

249. Multicenter Results of a Novel Pediatric Pacemaker in Neonates and Infants.

作者: Charles I Berul.;Lindsey Haack.;Elizabeth D Sherwin.;Robert D Whitehill.;Dustin Nash.;Soham Dasgupta.;Christopher Johnsrude.;Stephanie F Chandler.;Marc D LeGras.;Bradley C Clark.;Erick Jimenez.;Heather M Giacone.;Scott Ceresnak.;Garbiñe Goya.;Lanier B Jackson.;Tam Dan Pham.;Santiago O Valdes.;Edward Rhee.;Rachel Brucker.;Sonja Olson.;Teri Whitman.
来源: Circ Arrhythm Electrophysiol. 2025年18卷3期e013436页
To address the unmet need for a smaller pacemaker for babies, a specially modified implantable pulse generator was developed containing a Medtronic Micra subassembly in a polymer header connecting to a bipolar epicardial lead. The aim of this study was to report midterm follow-up data and outcomes of patients who underwent implantation of this device.

250. Predicted Risk of Ventricular Arrhythmias in a Genome-First Population With Genetic Risk for Arrhythmogenic Right Ventricular Cardiomyopathy.

作者: Eric D Carruth.;Brittney Murray.;Crystal Tichnell.;Katelyn Young.;Hugh Calkins.;Cynthia A James.;Christopher M Haggerty.
来源: Circ Arrhythm Electrophysiol. 2025年18卷3期e013231页
Population genomic screening for desmosome variants associated with arrhythmogenic right ventricular cardiomyopathy (ARVC) may facilitate early disease detection and protective intervention. The validated ARVC risk calculator offers a novel means to risk stratify individuals with diagnosed ARVC, but predicted risk in the context of genomic screening identification has not been explored.

251. Left Ventricular Entry to Reduce Brain Lesions During Catheter Ablation: A Randomized Trial.

作者: Gregory M Marcus.;Roderick Tung.;Edward P Gerstenfeld.;Trisha F Hue.;Feng Lin.;Jing Cheng.;J Peter Weiss.;Wendy S Tzou.;Henry Hsia.;Ashkan Ehdaie.;Daniel H Cooper.;T Jared Bunch.;Jeffrey Arkles.;Babak Nazer.;Adam Lee.;Alexios Hadjis.;Duy T Nguyen.;Mihail G Chelu.;Joshua Moss.;Jonathan C Hsu.;Miguel Valderrábano.;Prashant D Bhave.;Andrew D Beaser.;Arvindh Kanagasundram.;Oussama Wazni.;Jason Bradfield.;Grace Wall.;Kathleen Chang.;Michelle Yang.;Gabrielle Montenegro.;Sabrina Jarrott.;Joel H Kramer.;Anthony S Kim.;Yvonne M Morris.;William P Dillon.
来源: Circulation. 2025年151卷15期1051-1059页
Catheter ablation of ventricular arrhythmias, one of the most rapidly growing procedures in cardiac electrophysiology, is associated with magnetic resonance imaging-detected brain lesions in more than half of cases. Although a retrograde aortic approach is conventional, modern tools enable entry through a transseptal approach that may avoid embolization of debris from the arterial system. We sought to test the hypothesis that a transseptal puncture would mitigate brain injury compared with a retrograde aortic approach.

252. Aortic Valve Calcification Is Induced by the Loss of ALDH1A1 and Can Be Prevented by Agonists of Retinoic Acid Receptor Alpha: Preclinical Evidence for Drug Repositioning.

作者: Mickael Rosa.;Annabelle Dupont.;David M Smadja.;Jérôme Soquet.;Johan Abdoul.;Thibault Pamart.;Flavien Vincent.;Christina Le Tanno.;Eloise Borowczak.;Timothée Bigot.;Alexandre Ung.;Bertrand Vaast.;Mélanie Daniel.;Ramadan Jashari.;Frédéric Mouquet.;Cedric Delhaye.;Yoann Sottejeau.;Jeanne Rancic.;Delphine Corseaux.;Francis Juthier.;Bart Staels.;Sophie Susen.;Eric Van Belle.
来源: Circulation. 2025年151卷18期1329-1341页
To date, the only effective treatment of severe aortic stenosis is valve replacement. With the introduction of transcatheter aortic valve replacement and extending indications to younger patients, the use of bioprosthetic valves (BPVs) has considerably increased. The main inconvenience of BPVs is their limited durability because of mechanisms similar as the fibro-calcifying processes observed in native aortic stenosis. One of the major gaps of the field is to identify therapeutic targets to prevent or slow the fibro-calcifying process leading to severe and symptomatic aortic stenosis.

253. Artificial Intelligence to Enhance Precision Medicine in Cardio-Oncology: A Scientific Statement From the American Heart Association.

作者: Rohan Khera.;Aarti H Asnani.;Jacob Krive.;Daniel Addison.;Han Zhu.;Alexi Vasbinder.;Matthew R Fleming.;Rima Arnaout.;Pedram Razavi.;Tochukwu M Okwuosa.; .
来源: Circ Genom Precis Med. 2025年18卷2期e000097页
Artificial intelligence is poised to transform cardio-oncology by enabling personalized care for patients with cancer, who are at a heightened risk of cardiovascular disease due to both the disease and its treatments. The rising prevalence of cancer and the availability of multiple new therapeutic options has resulted in improved survival among patients with cancer and has expanded the scope of cardio-oncology to not only short-term but also long-term cardiovascular risks resulting from both cancer and its treatments. However, there is considerable heterogeneity in cardiovascular risk, driven by the nature of the malignancy as well as each individual's unique characteristics. The use of novel therapies, such as targeted therapies and immune checkpoint inhibitors, across multiple cancer groups has also broadened the populations among which cardiotoxicity has become an important consideration of therapy. Therefore, the ability to understand and personalize cardiovascular risk management in patients with cancer is a key target for artificial intelligence, which can deduce and respond to complex patterns within the data. These advances necessitate an overview of established biomarkers of risk, spanning advanced imaging, diagnostic testing, and multi-omics, the evidence supporting their use, and the proven and proposed role of artificial intelligence in refining this risk to attain greater precision in risk prediction and management in cardio-oncologic care.

254. Reactivation of Oxidized Soluble Guanylate Cyclase as a Novel Treatment Strategy to Slow Progression of Calcific Aortic Valve Stenosis: Preclinical and Randomized Clinical Trials to Assess Safety and Efficacy.

作者: Bin Zhang.;Maurice Enriquez-Sarano.;Hartzell V Schaff.;Hector I Michelena.;Carolyn M Roos.;Michael A Hagler.;Heyu Zhang.;Grace Casaclang-Verzosa.;Runqing Huang.;Anna Bartoo.;Sushant Ranadive.;Michael J Joyner.;Sorin Pislaru.;Vuyisile T Nkomo.;Walter K Kremers.;Philip A Araoz.;Gurpreet Singh.;Michael A Walters.;Jon Hawkinson.;Kevin Y Cunningham.;Jaeyun Sung.;Brandon Dunagan.;Zi Ye.;Jordan D Miller.
来源: Circulation. 2025年151卷13期913-930页
Pharmacological treatments for fibrocalcific aortic valve stenosis (FCAVS) have been elusive for >50 years. Here, we tested the hypothesis that reactivation of oxidized sGC (soluble guanylate cyclase), the primary receptor for nitric oxide, with ataciguat is a safe and efficacious strategy to slow progression of FCAVS.

255. Oxidative Stress Causes Mitochondrial and Electrophysiologic Dysfunction to Promote Atrial Fibrillation in Pitx2+/- Mice.

作者: Tuerdi Subati.;Kyungsoo Kim.;Zhenjiang Yang.;Matthew B Murphy.;Joseph C Van Amburg.;Isis L Christopher.;Owen P Dougherty.;Kaylen K Woodall.;Charles D Smart.;Joyce E Johnson.;Agnes B Fogo.;Venkataraman Amarnath.;Vineet Agrawal.;Joey V Barnett.;Jeffrey E Saffitz.;Katherine T Murray.
来源: Circ Arrhythm Electrophysiol. 2025年18卷3期e013199页
The strongest genetic risk factors for atrial fibrillation (AF) are DNA variants on chromosome 4q25 near the transcription factor gene PITX2 (Pitx2:Paired-like homeodomain transcription factor 2). Mice deficient in Pitx2 (Pitx2+/-) have increased AF susceptibility, although the molecular mechanism(s) remains controversial. Pitx2 encodes a transcription factor that activates an antioxidant response to promote cardiac repair. Increased reactive oxygen species causing oxidation of polyunsaturated fatty acids generates reactive lipid dicarbonyl moieties that adduct to proteins and other macromolecules to promote cellular injury. We tested the hypothesis that oxidative stress, and specifically isolevuglandins, the most reactive lipid dicarbonyls identified, are increased in the setting of Pitx2 deficiency to promote proarrhythmic remodeling and AF.

256. Subcutaneous Implantable Defibrillators in Young Patients: Arrhythmias, Complications, and Physical Activity.

作者: Pietro Francia.;Matteo Ziacchi.;Federico Migliore.;Paolo De Filippo.;Antonio Dello Russo.;Stefano Viani.;Antonio Rapacciuolo.;Giulio Falasconi.;Carmen Adduci.;Giovanni Bisignani.;Luca Checchi.;Giuseppe Busacca.;Luca Santini.;Carlo Lavalle.;Valeria Ilia Calvi.;Antonio Curcio.;Massimo Silvetti.;Antonio Pangallo.;Marco Carbonaro.;Davide Giorgi.;Raimondo Pittorru.;Mariolina Lovecchio.;Sergio Valsecchi.;Mauro Biffi.;Antonio D'Onofrio.;Antonio Pelliccia.; .
来源: Circ Arrhythm Electrophysiol. 2025年18卷3期e013365页
The safety of subcutaneous implantable cardioverter defibrillator (S-ICD) recipients who lead active lifestyles and engage in recreational sports is unknown. We aimed to evaluate the association between lifestyle and recreational sports and the occurrence of arrhythmia- and device-related complications, appropriate and inappropriate shocks in S-ICD recipients.

257. Variations in the Medical Device Authorization and Reimbursement Landscape: A Case Study of 2 Cardiovascular Devices Across 4 Countries.

作者: Marta M Williams.;Nathan R Smith.;Carin A Uyl-de Groot.;Corstiaan A den Uil.;Joseph S Ross.;Mohamed O Mohamed.;Mamas A Mamas.;Amitava Banerjee.;Dennis T Ko.;Bruce Landon.;Peter Cram.
来源: Circ Cardiovasc Qual Outcomes. 2025年18卷4期e011636页
The authorization process and coverage/reimbursement mechanisms for medical devices play critical roles in device adoption and usage. However, international variation in these processes remains poorly characterized, especially with regard to data transparency and the effects of reimbursement on usage.

258. Characteristics of Patients With the Arrhythmogenic Mitral Valve Prolapse Syndrome and Sudden Cardiac Arrest and Sustained Ventricular Arrhythmias.

作者: Apurba Chakrabarti.;John R Giudicessi.;Fatima M Ezzeddine.;Francesca N Delling.;Shalini Dixit.;Yoo Jin Lee.;Daniele Muser.;Silvia Magnani.;Aniek Van Wijngaarden.;Nina Ajmone Marsan.;Marc A Miller.;Jonathan Gandhi.;Maria G Trivieri.;Jonaz Font.;Raphael Martins.;James A McCaffrey.;Pasquale Santangeli.;Francis E Marchlinski.;Himal Chapagain.;Don Mathew.;Krishna Kancharla.;Faisal F Syed.;Ahad Abid.;Lukasz Cerbin.;Wendy S Tzou.;Lohit Garg.;Domenico G Della Rocca.;Andrea Natale.;Sanghamitra Mohanty.;Seth H Sheldon.;Ling Kuo.;Kristina H Haugaa.;Eivind W Aabel.;Andres Enriquez.;Shingo Maeda.;Amrish Deshmukh.;Michael Ghannam.;Frank Bogun.;Michael J Ackerman.;Jackson J Liang.
来源: Circ Arrhythm Electrophysiol. 2025年18卷3期e013099页
Patients with arrhythmogenic mitral valve prolapse syndrome are at increased risk for life-threatening ventricular arrhythmias, but studies have been limited by small sample sizes. We sought to assemble an international arrhythmogenic mitral valve prolapse syndrome registry to delineate the clinical, imaging, and treatment characteristics of patients with arrhythmogenic mitral valve prolapse syndrome who survived sudden cardiac arrest (SCA) or had sustained ventricular tachycardia (VT) or ventricular fibrillation.

259. Fast Degradation of MecciRNAs by SUPV3L1/ELAC2 Provides a Novel Opportunity to Tackle Heart Failure With Exogenous MecciRNA.

作者: Xu Liu.;Qinwei Wang.;Xinya Li.;Yan Yang.;Yuqi Deng.;Xiaolin Wang.;Peipei Wang.;Liang Chen.;Likun Ma.;Ge Shan.
来源: Circulation. 2025年151卷17期1272-1290页
Circular RNAs derived from both nuclear and mitochondrial genomes are identified in animal cells. Mitochondria-encoded circular RNAs (mecciRNAs) are attracting more attention, and several members of mecciRNAs have already been recognized in regulating mitochondrial functions. Mitochondria dysfunctions are well-known to participate in heart failure (HF). This study was designed to investigate the RNA metabolism of mecciRNAs and the relevant roles and potential application of mecciRNAs in HF.

260. Sane Approach to Optimizing the Workload in Remote Monitoring of Cardiovascular Implantable Electronic Devices.

作者: Markus Sane.;Toni Jäntti.;Annukka Marjamaa.;Elina Pennanen.;Charlotte Aura.;Eeva Torvinen.;Leena Karjalainen.;Pekka Raatikainen.;Jarkko Karvonen.
来源: Circ Arrhythm Electrophysiol. 2025年18卷3期e013078页
Remote monitoring offers an effective and safe method for monitoring patients with cardiovascular implantable electronic devices. The downside of remote monitoring is the overflow of the data. Since many of the remote monitoring transmissions are nonactionable, optimizing alert transmissions could partly overcome this problem.
共有 34033 条符合本次的查询结果, 用时 4.8469275 秒