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    <title>海洋之心 - 心肌病</title>
    <link>https://heart.lihaiyang.com</link>
    <description>心血管文献检索平台 - 最新收录论文</description>
    <language>zh-CN</language>
    <atom:link href="https://heart.lihaiyang.com/rss.php?category=%E5%BF%83%E8%82%8C%E7%97%85" rel="self" type="application/rss+xml"/>
        <item>
        <title>Effect of 2 Weeks of Time-Restricted Eating on Innate Immunity and Systemic Inflammation in Patients With a History of Myocardial Infarction: A Randomized-Controlled Crossover Study.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=187</link>
        <description>Preclinical evidence suggests that time-restricted eating (TRE) exerts beneficial metabolic and cardiovascular effects by ameliorating inflammation and modulating immune cell function. However, the effect in patients with established coronary artery disease remains unknown. In this prospective, rand</description>
        <pubDate>Fri, 20 Mar 2026 00:00:00 +0800</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.1161/JAHA.125.048092</guid>    </item>
        <item>
        <title>Rationale and Design of CARDIO-TTRansform, a Phase 3 Trial of Eplontersen in Transthyretin Amyloid Cardiomyopathy.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=2</link>
        <description>Transthyretin amyloidosis with cardiomyopathy is a progressive, fatal disease characterized by deposition of extracellular misfolded transthyretin (TTR) in the myocardium. Eplontersen is an N-acetylgalactosamine ligand-conjugated antisense oligonucleotide targeting hepatocyte TTR messenger RNA to re</description>
        <pubDate>Thu, 01 Jan 2026 00:00:00 +0800</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.1161/CIRCHEARTFAILURE.126.014205</guid>    </item>
        <item>
        <title>Integrating ECG and echocardiography to identify early-stage transthyretin amyloid cardiomyopathy.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=86</link>
        <description>Current diagnostic criteria for transthyretin amyloid (ATTR) cardiomyopathy (ATTR-CM) emphasize increased left ventricular (LV) wall thickness, potentially delaying recognition of early myocardial involvement. We evaluated whether combining ECG (S-wave amplitude in lead aVR, SaVR) with echocardiogra</description>
        <pubDate>Thu, 01 Jan 2026 00:00:00 +0800</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.1093/ehjimp/qyag058</guid>    </item>
        <item>
        <title>Adenovirus-Associated Viral Vector Based Gene Replacement Therapy for the treatment of Arrhythmogenic Cardiomyopathy.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=102</link>
        <description>Arrhythmogenic Cardiomyopathy (ACM) is a primary disorder of the myocardium characterized by a high propension for ventricular arrhythmias (VAs) and sudden cardiac death (SCD). Several genes have been associated with the development of aggressive forms of ACM, the most common of which is the one enc</description>
        <pubDate>Thu, 01 Jan 2026 00:00:00 +0800</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.1016/j.hrthm.2026.03.1942</guid>    </item>
        <item>
        <title>Long-Term Durability of Acoramidis Efficacy in Transthyretin Amyloid Cardiomyopathy: Open-Label Extension of the ATTRibute-CM Randomized Clinical Trial.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=113</link>
        <description>Transthyretin amyloid cardiomyopathy (ATTR-CM) is a progressive disorder caused by destabilization of serum transthyretin (sTTR). Acoramidis, an approved therapy that achieves near-complete (≥90%) sTTR stabilization, demonstrated clinical benefit through month 30 in ATTRibute-CM, which was increment</description>
        <pubDate>Thu, 01 Jan 2026 00:00:00 +0800</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.1001/jamacardio.2026.0819</guid>    </item>
        <item>
        <title>RBM20 Truncating Variants and Human Cardiomyopathy.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=116</link>
        <description>Genetic diagnosis has become increasingly important to guide clinical decision-making for patients with dilated cardiomyopathy (DCM). Pathogenic or likely pathogenic (P/LP) missense variants in the gene RBM20 cause a highly penetrant arrhythmogenic DCM, but the role of RBM20 truncating variants (RBM</description>
        <pubDate>Thu, 01 Jan 2026 00:00:00 +0800</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.1001/jamacardio.2026.0401</guid>    </item>
        <item>
        <title>[Inflammatory Heart Disease: The Role of Multimodality Cardiac Imaging in Myocarditis and Pericarditis].</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=18432</link>
        <description>Myocarditis and pericarditis represent a broad spectrum of inflammatory heart diseases and are important differential diagnoses in patients presenting with chest pain, heart failure, or arrhythmias. Diagnosis is often challenging due to non-specific clinical presentation and biomarkers. Growing reco</description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.23785/TU.2026.03.005</guid>    </item>
        <item>
        <title>Low-Level Domoic Acid Exposure Induces Age-like Cardiomyopathy in Young Adult and Aged Mice.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=18433</link>
        <description>Domoic acid (DA) is a well-known seafood toxin produced by some species of marine phytoplankton in the genus Pseudo-nitzschia during harmful algal blooms (HABs). Acute toxic exposures induce overt clinical signs of neuroexcitotoxicity, such as seizures in mammals due to overstimulation of glutamate </description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.3390/md24060210</guid>    </item>
        <item>
        <title>Hybrid Cardiac (68)Ga-FAPI-4 PET/MRI in Dilated Cardiomyopathy: A Feasibility and Pilot Study.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=11270</link>
        <description>Background Cardiac gallium 68-labeled fibroblast activation protein inhibitor (FAPI)-4 (68Ga-FAPI-4) PET/MRI allows simultaneous assessment of cardiac tissue characteristics, function, and molecular remodeling in myocardial diseases. An integrated workflow for nonischemic dilated cardiomyopathy (DCM</description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.1148/radiol.252706</guid>    </item>
        <item>
        <title>Synergistic Cardioprotection of Colchicine and Hyperbaric Oxygen Therapy in a Rat Model of Remote Ischemia-Reperfusion Injury.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=20230</link>
        <description>PURPOSE: Lower extremity ischemia-reperfusion injury (IRI) triggers systemic inflammation and oxidative stress, causing myocardial remote ischemia-reperfusion injury (MIRI). Current treatments are limited. METHODS: Male Sprague-Dawley rats (n = 6 per group) were assigned to Sham, I/R, I/R + colchici</description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.1111/fcp.70102</guid>    </item>
        <item>
        <title>Single-Dose Nivolumab as a Trigger of Myocarditis, Myositis, and Myasthenia Gravis Overlap Syndrome With Late Cardiac Death Despite Initial Recovery: A Case Report.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=33032</link>
        <description>BACKGROUND Immune checkpoint inhibitors (ICIs) have transformed the treatment of advanced malignancies but can cause life-threatening immune-related adverse events. Myocarditis, myositis, and myasthenia gravis (MMM) overlap syndrome is a rare, highly morbid complication with high mortality. Most cas</description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.12659/AJCR.953173</guid>    </item>
        <item>
        <title>Dynamic LVOT Obstruction as a Cause of Hemodynamic Instability in Takotsubo Syndrome.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=45832</link>
        <description>Takotsubo syndrome (TTS) frequently presents with chest pain, ST-segment elevation, and troponin elevation, closely mimicking acute coronary syndrome, and can be complicated by acute heart failure and cardiogenic shock. In a subset of patients, dynamic left ventricular outflow tract obstruction (LVO</description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.1177/23247096261475113</guid>    </item>
        <item>
        <title>Randomized Controlled Trial of Internet-Delivered Cognitive Behavioral Therapy After Myocardial Infarction With Nonobstructive Coronary Arteries or Takotsubo Syndrome.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=11275</link>
        <description>BACKGROUND: Patients with myocardial infarction with nonobstructive coronary arteries (MINOCA) or Takotsubo syndrome (TS) often suffer from poor mental health and low quality-of-life post event, with no current evidence-based treatments available. This study aimed to evaluate the effects of an inter</description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.1161/JAHA.125.047311</guid>    </item>
        <item>
        <title>Mechanisms and Intervention Strategies for Heat Stroke-Associated Myocardial Dysfunction: A Narrative Review.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=7692</link>
        <description>INTRODUCTION: Heatstroke is a life-threatening condition defined by a core body temperature exceeding 40° C and central nervous system dysfunction. Its onset is potentiated by high heat and humidity, especially if superimposed upon high thermal loads due to exertion or to impaired ability to sweat a</description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.5811/westjem.53045</guid>    </item>
        <item>
        <title>Twenty-Year Follow-up After Combined Heart and Kidney Transplant: A Case Report.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=23830</link>
        <description>Combined heart and kidney transplant is a rare but valuable treatment option for selected patients with end -stage cardiac and renal failure. We present the long -term outcome of a 27 -year -old man with pulmonary stenosis previously treated with valvuloplasty in 1998, who subsequently developed end</description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.6002/ect.2026.0088</guid>    </item>
        <item>
        <title>[Cardiogenetics in clinical practice : challenges, indications, and perspectives].</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=23831</link>
        <description>Cardiogenetics plays an increasingly important role in managing cardiovascular diseases, owing to the major impact of genetic data on diagnosis, risk stratification, therapeutic decision-making, and family-based prevention. Many cardiomyopathies, channelopathies, and other entities have a genetic ba</description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.53738/REVMED.2026.22.969.48836</guid>    </item>
        <item>
        <title>Overcoming barriers to early diagnosis and treatment of p.Val142Ile amyloid transthyretin (ATTR) cardiomyopathy.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=23832</link>
        <description>The most common hereditary transthyretin (ATTRv) amyloidosis variant in the United States, Val122Ile (p.Val142Ile), is predominantly detected in populations of African ancestry. In this narrative review, we highlight the current challenges and discuss priority focus areas to improve the timely diagn</description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.1007/s10741-026-10651-1</guid>    </item>
        <item>
        <title>Expanding the Recessive Spectrum of Dilated Cardiomyopathy: RNA-Level Validation of a Homozygous CTNNA3 Splice-Site Variant.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=36632</link>
        <description>CTNNA3 encodes αT-catenin, an intercalated disc (ICD) protein essential for cardiomyocyte coupling. Human omics studies have shown reduced CTNNA3 expression, ICD ultrastructural disruption, and dilated cardiomyopathy (DCM)-associated hyperphosphorylation of αT-catenin. Direct RNA-level evidence link</description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.1155/humu/2079958</guid>    </item>
        <item>
        <title>Early Detection of Acute Myocarditis in the Pediatric Population Using Clinically Accessible Data.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=43032</link>
        <description>BACKGROUND: Early diagnosis of acute myocarditis (AMC) is crucial due to its rapid progression and high mortality rate. Initial symptoms such as fever, abdominal pain, and vomiting are nonspecific and pose challenges for clinicians in distinguishing AMC from acute gastroenteritis (AGE). METHODS: We </description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.1111/ped.70492</guid>    </item>
        <item>
        <title>Association of the triglyceride-glucose index with subclinical left ventricular dysfunction in type 2 diabetes mellitus: mediation by myocardial energetic efficiency and resting perfusion.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=49432</link>
        <description>BACKGROUND: The triglyceride-glucose(TyG) index, a surrogate marker of insulin resistance, has been linked to cardiac dysfunction; however, its underlying associated pathways in patients with type 2 diabetes mellitus(T2DM) remain unclear. This study used cardiac magnetic resonance(CMR) to explore th</description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.1186/s12933-026-03308-8</guid>    </item>
        <item>
        <title>Exploring the role of CaMKII in exercise-induced cardioprotection.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=49433</link>
        <description>Regular physical exercise can induce a multifaceted cardioprotective phenotype characterized by improved Ca2⁺ handling, mitochondrial resilience, redox buffering, autonomic regulation, and resistance to ischemia-reperfusion injury. Ca2⁺/calmodulin-dependent protein kinase II (CaMKII), particularly c</description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.1007/s13577-026-01425-w</guid>    </item>
        <item>
        <title>Spatiotemporal Analysis of Mortality from Cardiomyopathies in Brazil between 2001 and 2021.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=44832</link>
        <description>BACKGROUND: Brazil presents regional variations in mortality from cardiomyopathies, influenced by demographic characteristics, socioeconomic inequalities, and differences in access to health services. Between 2001 and 2021, 272,448 deaths from the disease were recorded in the country. OBJECTIVE: To </description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.36660/abc.20260064</guid>    </item>
        <item>
        <title>Non-invasive pressure-volume loop analysis in left ventricular load manipulation.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=32033</link>
        <description>BACKGROUND: Clinical monitoring of patients with heart failure or cardiomyopathy is facilitated by detailed assessment of cardiac loading conditions. Specifically, alterations in preload and afterload may unmask pathology through effects on ventricular pressure-volume (PV) relations. Therefore, the </description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.1111/cpf.70081</guid>    </item>
        <item>
        <title>Adeno-Associated Virus Vector Mediated Gene Therapy: A Promising Approach to Transform Hypertrophic Cardiomyopathy Treatment.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=12070</link>
        <description>Hypertrophic cardiomyopathy (HCM) is a genetically heterogeneous myocardial disease that usually arises from mutations in key sarcomeric proteins, particularly MYBPC3 and MYH7. Current pharmacological treatments, such as myosin inhibitors, calcium channel blockers, and β-blockers, reduce symptoms bu</description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.1002/biot.70262</guid>    </item>
        <item>
        <title>Exploration and prospect of core research hotspots in sepsis-induced myocardial injury based on bibliometrics.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=46632</link>
        <description>OBJECTIVE: Sepsis-associated myocardial injury (SICM) is one of the most common and severe complications of sepsis. The present study aimed to analyze research trends, collaborative networks, and knowledge dissemination in SICM over the past decade using bibliometric methods, thereby providing a ref</description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.1097/MD.0000000000050014</guid>    </item>
        <item>
        <title>[Research progress in Lyme carditis].</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=33833</link>
        <description>莱姆病是由蜱虫传播、伯氏疏螺旋体感染所致的自然疫源性疾病，莱姆病心脏炎是其严重的心血管并发症，发生率为1%~10%。该病以房室传导阻滞及心肌炎症为主要表现，主要累及心脏传导系统，可引发心律失常甚至猝死。诊断需结合流行病学史、临床症状与血清学检测，推荐采用“酶免疫分析联合C6肽检测、心电图初筛，蛋白免疫印迹法最终确证”的流程，并注意与病毒性心肌炎等疾病鉴别。2024年美国疾病控制与预防中心/欧洲心脏病学会采纳改良用药方案中指出，轻中度患者可口服多西环素；临时起搏器应用具有明确适应证，而永久起搏器需谨慎使用。预防以加强野外蜱虫防护为核心，目前VLA15疫苗已进入Ⅲ期临床试验阶段。未来研究将聚焦缩短</description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.3760/cma.j.cn112148-20260113-00030</guid>    </item>
        <item>
        <title>Knowledge mapping of targeted therapy for hypertrophic cardiomyopathy: A bibliometric analysis of myosin inhibitor research.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=46633</link>
        <description>BACKGROUND: Targeted therapy using myosin inhibitors represents a groundbreaking advancement in the management of hypertrophic cardiomyopathy (HCM). This study conducts a comprehensive bibliometric analysis to map the research landscape indexed in the Web of Science Core Collection, identify key tre</description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.1097/MD.0000000000050034</guid>    </item>
        <item>
        <title>[Research progress of mitochondria-associated endoplasmic reticulum membranes in sepsis-induced cardiomyopathy].</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=33834</link>
        <description>线粒体相关内质网膜（MAMs）是线粒体与内质网通过物理接触形成的特殊功能结构域，介导两大细胞器间的物质转运与信息交流，在空间分布与生物学功能上均实现高度偶联。脓毒症心肌病是脓毒症进程中出现的可逆性心肌功能损伤。现有研究表明MAMs可通过调控钙信号传导、自噬、线粒体动力学、内质网应激及炎症等关键通路，参与脓毒症心肌病的发生与发展。该文就MAMs的结构特征、生物学功能及其在脓毒症心肌病中的作用机制作一综述，以期为该病的防治提供潜在新靶点。.</description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.3760/cma.j.cn112148-20260319-00188</guid>    </item>
        <item>
        <title>Suppression of Post-Ischemic Cardiac Remodelling and Inflammatory Response by a Novel Sphingolipid Modifier, CIN038.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=33836</link>
        <description>In patients with myocardial infarction (MI), the level of sphingolipids, such as ceramide (Cer), is elevated and is associated with an increased risk of progression towards heart failure (HF). Dihydroceramide desaturase 1 (DES1) catalyses the conversion of dihydroceramide (dhCer) into Cer in the de </description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.3390/ijms27135776</guid>    </item>
        <item>
        <title>Circulating β-Hydroxybutyrate in Glycemic Progression and Diabetic Cardiomyopathy: Adaptive Signal or Maladaptive Substrate?</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=33837</link>
        <description>Circulating ketone bodies (KBs), particularly β-hydroxybutyrate (β-HB), have emerged as metabolites with dual roles as both oxidative fuels and metabolic signaling molecules. Beyond serving as an alternative energy substrate, β-HB regulates diverse pathways involved in oxidative stress, inflammation</description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.3390/ijms27135716</guid>    </item>
        <item>
        <title>The Pivotal Role of Plant Derivatives and Eicosanoid Signaling Modulation in Counteracting Cardiomiopathy.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=8494</link>
        <description>Eicosanoids and their receptors act as key regulators of inflammation, calcium homeostasis, mitochondrial function, and cardiomyocyte survival, thereby contributing to the onset and progression of cardiac dysfunction. This review aims to summarize the evidence to underscore the pivotal role of eicos</description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.3390/ijms27114849</guid>    </item>
        <item>
        <title>Validity testing of the novel European Society of Cardiology EURObservational Research Programme PPCM Registry score to predict left ventricular recovery in a cohort of Ugandan women with PPCM.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=13870</link>
        <description>BACKGROUND: Recently under the European Society of Cardiology (ESC) EURObservational Research Programme (EORP) PPCM registry the first predictive score was derived. This study sought to test the validity of this predictive score in a cohort of women with PPCM in Uganda. METHODS: 80 PPCM cases enroll</description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.5830/CVJA-2025-099</guid>    </item>
        <item>
        <title>Asprosin Protects H9C2 Cells From Ferroptosis Following Hypoxia/Reoxygenation by Promoting Mitophagy.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=33839</link>
        <description>BACKGROUND: Acute myocardial infarction is a leading cause of death globally. Percutaneous coronary intervention is the primary treatment to restore blood flow to the affected myocardium, but reperfusion can cause myocardial injury, affecting the prognosis of patients with acute myocardial infarctio</description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.1155/cdr/8401037</guid>    </item>
        <item>
        <title>Cardiac MRI Monitoring of Myocardial Tissue Changes in a Myocarditis Mouse Model with Histologic Validation.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=8496</link>
        <description>Purpose To evaluate multiparametric cardiac MRI for assessing myocardial inflammation, fibrosis, and spatiotemporal distribution in autoimmune myocarditis, with histologic reference. Materials and Methods This study (December 2022 to January 2024) included 84 BALB/c mice (42 with experimental autoim</description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.1148/ryct.250488</guid>    </item>
        <item>
        <title>The immune-cardiovascular metabolic circuitry in myocardial ischemia-reperfusion injury: from metabolic signal release to spatiotemporal reprogramming.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=8497</link>
        <description>Myocardial ischemia-reperfusion injury (MIRI) remains a major driver of infarct expansion, adverse remodeling, and poor outcomes after reperfusion therapy, yet mechanism-based treatments remain limited. Emerging evidence suggests that MIRI is not simply the additive result of oxidative stress and st</description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.3389/fimmu.2026.1848067</guid>    </item>
        <item>
        <title>Neurogenic shock to the heart: a rare case of meningitis-triggered reverse takotsubo cardiomyopathy.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=8498</link>
        <description>Reverse takotsubo cardiomyopathy, a rare variant of stress-induced cardiomyopathy, is characterized by basal hypokinesis with apical sparing and can be associated with neurological insults. Prompt recognition is essential to avoid unnecessary invasive interventions and to guide appropriate supportiv</description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.1080/08998280.2025.2605609</guid>    </item>
        <item>
        <title>[Lactate induces gastric mucosal injury by promoting M1 polarization of macrophages via the cardio-gastric axis].</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=18230</link>
        <description>OBJECTIVES: To investigate the role of lactate in myocardial ischemia-reperfusion (MIR)-induced gastric mucosal injury. METHODS: Thirty C57BL/6J mice were randomized into sham-operated group, MIR (45 min ischemia and 2 h reperfusion) group, and MIR+LDHAI group, and gastric mucosal injury was assesse</description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.12122/j.issn.1673-4254.2026.06.07</guid>    </item>
        <item>
        <title>Tongmai Yangxin pills alleviate myocardial ischemia-reperfusion injury by enhancing mitochondrial function via activating the ERK signaling pathway.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=18231</link>
        <description>BACKGROUND: To explore the mechanism of Tongmai yangxin pills (TMYX) for improving myocardial ischemia-reperfusion injury (MIRI) in rats. METHODS: In a SD rat model of MIRI, the therapeutic effects of TMYX were evaluated by cardiac echography, measurement of myocardial infarction area, and examinati</description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.12122/j.issn.1673-4254.2026.06.01</guid>    </item>
        <item>
        <title>Iron overload cardiomyopathy.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=52032</link>
        <description>Iron overload cardiomyopathy (IOC) remains an important cause of morbidity and mortality in patients with hereditary haemochromatosis and transfusion-dependent conditions such as haemoglobinopathies. The condition arises when excess iron, due to increased intestinal iron absorption or repetitive tra</description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.1007/s10741-026-10663-x</guid>    </item>
        <item>
        <title>Artificial Intelligence-Enhanced Electrocardiography Analysis for Diagnosing Chagas Disease.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=39233</link>
        <description>BACKGROUND: Chagas disease affects millions worldwide and remains a leading cause of cardiomyopathy in Latin America. Early diagnosis remains challenging in endemic regions. Artificial intelligence (AI)-based electrocardiography (ECG) analysis may offer a low-cost strategy for large-scale screening </description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.36660/abc.20260032</guid>    </item>
        <item>
        <title>Heart Transplant for Noncompaction Cardiomyopathy in NONO-Related Syndromic Intellectual Disability.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=32834</link>
        <description>INTRODUCTION: Loss-of-function variants in NONO cause an X-linked syndromic neurodevelopmental disorder (MRXS34), characterized by developmental delay, corpus callosum abnormalities, dysmorphic features, feeding difficulties, and congenital heart disease, most commonly left ventricular noncompaction</description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.1002/mgg3.70261</guid>    </item>
        <item>
        <title>Comprehensive biophysical and structural profiling of alpha-actinin-2 variants reveals mechanistic diversity in hypertrophic cardiomyopathy.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=39234</link>
        <description>Hypertrophic cardiomyopathy (HCM) is a genetic disease associated with sudden cardiac death. Variants in alpha-actinin-2 (ACTN2), a Z-disc protein that anchors actin thin filaments have been implicated in HCM, yet their structural consequences remain poorly defined. Here, we characterise seventeen H</description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.1038/s41467-026-75392-z</guid>    </item>
        <item>
        <title>Beyond epilepsy: convulsive syncope revealing restrictive cardiomyopathy in a child.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=39235</link>
        <description>Seizure-like episodes may occasionally arise from cardiovascular causes rather than primary neurological disease, leading to diagnostic delay. We report an adolescent girl who presented with recurrent generalised tonic episodes with cyanosis and transient loss of consciousness. Initial evaluation fo</description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.1136/bcr-2026-274228</guid>    </item>
        <item>
        <title>Cardiac imaging in Chagas cardiomyopathy for phenotypic characterisation and risk stratification.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=7492</link>
        <description>Chagas disease, caused by Trypanosoma cruzi, remains one of the leading infectious causes of non-ischemic cardiomyopathy worldwide. Although an estimated 6-7 million individuals are chronically infected, 20-30% will develop Chagas cardiomyopathy (CCM), a progressive myocardial disease characterised </description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.1007/s10741-026-10645-z</guid>    </item>
        <item>
        <title>From Genotype to Phenotype: Investigating SLC22A5 Variants and Their Significance in Carnitine Deficiency: A Systematic Review Study.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=39236</link>
        <description>Primary carnitine deficiency (PCD) is an autosomal recessive disorder caused by mutations in the SLC22A5 gene, which encodes the organic cation transporter 2 (OCTN2). These mutations impair carnitine transport and fatty acid metabolism, leading to a wide range of clinical symptoms, from mild fatigue</description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.1111/jcmm.71273</guid>    </item>
        <item>
        <title>Thick filament molecular interfaces play a critical role in the pathogenesis of hypertrophic cardiomyopathy.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=21830</link>
        <description>Hypertrophic cardiomyopathy (HCM) variants in genes encoding the myosin heavy chain (MHC) (MYH7), myosin light chains (MYL2 and MYL3), and cardiac myosin binding protein-C (cMyBP-C, MYBPC3) lead to cardiac hypertrophy, with abnormal contractility, relaxation, and energy consumption. Here, we defined</description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.1073/pnas.2529234123</guid>    </item>
        <item>
        <title>Rippling muscle disease due to a CAV3 mutation with myocarditis-like presentation in an adolescent.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=41032</link>
        <description>BACKGROUND: This case report describes a rare presentation of rippling muscle disease (RMD) due to a pathogenic CAV3 variant, manifesting with myocarditis-like cardiac involvement in an adolescent patient. To the best of our knowledge, this represents an exceedingly rare pediatric case of RMD associ</description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.24953/turkjpediatr.2026.7755</guid>    </item>
        <item>
        <title>Mavacamten's Dose-Time Dynamics and Predictive Factors in Hypertrophic Obstructive Cardiomyopathy Cardiac Remodeling.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=34633</link>
        <description>BACKGROUND: Hypertrophic obstructive cardiomyopathy (HOCM) causes dynamic left ventricular outflow tract (LVOT) obstruction and disabling symptoms; many patients do not respond to conventional agents. Mavacamten, a selective cardiac myosin inhibitor, improves gradients, but the dose-time response in</description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.1111/echo.70540</guid>    </item>
        <item>
        <title>A platelet-monocyte pyroptotic axis mediates uremic cardiomyopathy: critical role of PF4 and hematopoietic caspase-1.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=27210</link>
        <description>BACKGROUND: Cardiovascular disease is the leading cause of death in end-stage renal disease (ESRD). While platelet activation and monocyte inflammation are hallmarks of uremia, how platelet-derived factors drive monocyte-mediated cardiac remodeling remains elusive. We investigated the role of platel</description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.1007/s00011-026-02311-9</guid>    </item>
        <item>
        <title>Potential Mechanisms of Trimetazidine and Coenzyme Q10 Against Antipsychotic-Induced Myocarditis: A Network Pharmacology, Molecular Docking, and Molecular Dynamics Simulation Study.</title>
        <link>https://heart.lihaiyang.com/?p=detail&amp;id=27212</link>
        <description>BACKGROUND: Antipsychotic-induced myocarditis is a rare but potentially fatal adverse event associated with antipsychotic treatment. Trimetazidine (TMZ) and coenzyme Q10 (CoQ10) have shown potential cardioprotective effects. Thus, they may represent adjunctive therapeutic candidates for antipsychoti</description>
        <pubDate>Mon, 30 Nov -001 00:00:00 +0805</pubDate>
        <category>心肌病</category>
        <guid>https://doi.org/10.1002/cns.71009</guid>    </item>
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