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Mitral Valve Prolapse Induces Regionalized Myocardial Fibrosis

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Filamin‐A as a Balance between Erk/Smad Activities During Cardiac Valve Development
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A role for primary cilia in aortic valve development and disease
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TGF‐β Suppresses Ift88 Expression in Chondrocytic ATDC5 Cells
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Cardiac interstitium in health and disease: The fibrillar collagen network
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The extracellular matrix and ciliary signaling
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Macrophages Facilitate Electrical Conduction in the Heart
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TGF-β Signaling Is Associated with Endocytosis at the Pocket Region of the Primary Cilium
inferredcites →https://doi.org/10.1016/j.hrthm.2020.12.021openalex-snapshot
Systematic quantification of histologic ventricular fibrosis in isolated mitral valve prolapse and sudden cardiac death
inferredcites →https://doi.org/10.1016/j.jacc.2018.06.048openalex-snapshot
Myocardial Fibrosis in Patients With Primary Mitral Regurgitation With and Without Prolapse
inferredcites →https://doi.org/10.1016/j.jacc.2018.07.070openalex-snapshot
The Mitral Annulus Disjunction Arrhythmic Syndrome
inferredcites →https://doi.org/10.1016/j.jacc.2018.09.048openalex-snapshot
Arrhythmic Mitral Valve Prolapse
inferredcites →https://doi.org/10.1016/j.jacc.2018.11.018openalex-snapshot
Atrial Fibrillation and Mitral Valve Prolapse
inferredcites →https://doi.org/10.1016/j.jacc.2019.06.052openalex-snapshot
Long-Term Results of Mitral Valve Repair for Regurgitation Due to Leaflet Prolapse
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IFT88 influences chondrocyte actin organization and biomechanics
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Left ventricular dysfunction after mitral valve repair—the fallacy of “normal” preoperative myocardial function
inferredcites →https://doi.org/10.1016/j.jtcvs.2018.10.029openalex-snapshot
Measuring chordae tension during transapical neochordae implantation: Toward understanding objective consequences of mitral valve repair
inferredcites →https://doi.org/10.1016/j.jtcvs.2020.01.086openalex-snapshot
A novel cross-species model of Barlow's disease to biomechanically analyze repair techniques in an ex vivo left heart simulator
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Development of the post-natal growth plate requires intraflagellar transport proteins
inferredcites →https://doi.org/10.1016/j.ydbio.2020.03.003openalex-snapshot
Desert hedgehog-primary cilia cross talk shapes mitral valve tissue by organizing smooth muscle actin
inferredcites →https://doi.org/10.1016/j.yjmcc.2015.11.025openalex-snapshot
Mechanical control of cardiac myofibroblasts
inferredcites →https://doi.org/10.1016/j.yjmcc.2016.03.008openalex-snapshot
A computational model of cardiac fibroblast signaling predicts context-dependent drivers of myofibroblast differentiation
inferredcites →https://doi.org/10.1016/s0070-2153(08)00807-7openalex-snapshot
Chapter 7 Ciliary Function and Wnt Signal Modulation
inferredcites →https://doi.org/10.1016/s0140-6736(06)69208-8openalex-snapshot
Burden of valvular heart diseases: a population-based study
inferredcites →https://doi.org/10.1038/nature14670openalex-snapshot
Mutations in DCHS1 cause mitral valve prolapse
inferredcites →https://doi.org/10.1038/nature24676openalex-snapshot
IL-11 is a crucial determinant of cardiovascular fibrosis
inferredcites →https://doi.org/10.1038/ng.3383openalex-snapshot
Genetic association analyses highlight biological pathways underlying mitral valve prolapse
inferredcites →https://doi.org/10.1038/nrcardio.2015.161openalex-snapshot
Mitral valve disease—morphology and mechanisms
inferredcites →https://doi.org/10.1038/nrd.2016.89openalex-snapshot
Novel therapeutic strategies targeting fibroblasts and fibrosis in heart disease
inferredcites →https://doi.org/10.1038/nrm3085openalex-snapshot
Ciliogenesis: building the cell's antenna
inferredcites →https://doi.org/10.1038/s41419-017-0174-5openalex-snapshot
Givinostat reduces adverse cardiac remodeling through regulating fibroblasts activation
inferredcites →https://doi.org/10.1038/s41467-020-15248-2openalex-snapshot
Wnt-PLC-IP3-Connexin-Ca2+ axis maintains ependymal motile cilia in zebrafish spinal cord
inferredcites →https://doi.org/10.1038/s41598-017-15649-2openalex-snapshot
The primary cilium is necessary for the differentiation and the maintenance of human adipose progenitors into myofibroblasts
inferredcites →https://doi.org/10.1038/s41598-019-41173-6openalex-snapshot
Mitral valve repair based on intraoperative objective measurement
inferredcites →https://doi.org/10.1038/s41598-020-62844-9openalex-snapshot
Connexin-43 reduction prevents muscle defects in a mouse model of manifesting Duchenne muscular dystrophy female carriers
inferredcites →https://doi.org/10.1038/srep35542openalex-snapshot
TGFβ1 – induced recruitment of human bone mesenchymal stem cells is mediated by the primary cilium in a SMAD3-dependent manner
inferredcites →https://doi.org/10.1074/jbc.m109902200openalex-snapshot
Intercellular Calcium Signaling in Astrocytes via ATP Release through Connexin Hemichannels
inferredcites →https://doi.org/10.1089/ten.tea.2014.0651openalex-snapshot
Inhibition of Connexin 43 Hemichannel-Mediated ATP Release Attenuates Early Inflammation During the Foreign Body Response
inferredcites →https://doi.org/10.1093/biosci/biu173openalex-snapshot
Mechanobiology of Ciliogenesis
inferredcites →https://doi.org/10.1093/ejcts/ezz258openalex-snapshot
Mitral chordae tendineae force profile characterization using a posterior ventricular anchoring neochordal repair model for mitral regurgitation in a three-dimensional-printed ex vivo left heart simulator
inferredcites →https://doi.org/10.1093/eurheartj/ehx391openalex-snapshot
2017 ESC/EACTS Guidelines for the management of valvular heart disease
inferredcites →https://doi.org/10.1093/eurheartj/ehz745.0365openalex-snapshot
P3500The primary cilium, a sensory apparatus of cells regulates the profibrotic capacity of fibroblasts in atrial fibrillation
inferredcites →https://doi.org/10.1096/fj.12-204677openalex-snapshot
ATP released from cardiac fibroblasts via connexin hemichannels activates profibrotic P2Y 2 receptors
inferredcites →https://doi.org/10.1126/science.1139740openalex-snapshot
Patched1 Regulates Hedgehog Signaling at the Primary Cilium
inferredcites →https://doi.org/10.1126/scitranslmed.aax0290openalex-snapshot
Primary cilia defects causing mitral valve prolapse
inferredcites →https://doi.org/10.1136/heartjnl-2016-309303openalex-snapshot
Diffuse myocardial fibrosis in patients with mitral valve prolapse and ventricular arrhythmia
inferredcites →https://doi.org/10.1136/heartjnl-2018-314269openalex-snapshot
Left ventricular mechanical dispersion predicts arrhythmic risk in mitral valve prolapse
inferredcites →https://doi.org/10.1161/circgen.119.002497openalex-snapshot
Genome-Wide Association Study–Driven Gene-Set Analyses, Genetic, and Functional Follow-Up Suggest GLIS1 as a Susceptibility Gene for Mitral Valve Prolapse
inferredcites →https://doi.org/10.1161/circresaha.115.303567openalex-snapshot
Differential Contribution of Monocytes to Heart Macrophages in Steady-State and After Myocardial Infarction
inferredcites →https://doi.org/10.1161/circresaha.115.306565openalex-snapshot
Cardiac Fibrosis
inferredcites →https://doi.org/10.1161/circulationaha.115.016291openalex-snapshot
Arrhythmic Mitral Valve Prolapse and Sudden Cardiac Death
inferredcites →https://doi.org/10.1161/circulationaha.117.028752openalex-snapshot
Fibroblast Primary Cilia Are Required for Cardiac Fibrosis
inferredcites →https://doi.org/10.1161/circulationaha.118.034075openalex-snapshot
Mitral Valve Prolapse, Ventricular Arrhythmias, and Sudden Death
inferredcites →https://doi.org/10.1161/circulationaha.119.038376openalex-snapshot
Defects in the Exocyst-Cilia Machinery Cause Bicuspid Aortic Valve Disease and Aortic Stenosis
inferredcites →https://doi.org/10.1161/circulationaha.119.039710openalex-snapshot
Disruption of Ca 2+ i Homeostasis and Connexin 43 Hemichannel Function in the Right Ventricle Precedes Overt Arrhythmogenic Cardiomyopathy in Plakophilin-2–Deficient Mice
inferredcites →https://doi.org/10.1161/circulationaha.120.050214openalex-snapshot
Replacement Myocardial Fibrosis in Patients With Mitral Valve Prolapse
inferredcites →https://doi.org/10.1161/jaha.119.012385openalex-snapshot
Interaction of α Carboxyl Terminus 1 Peptide With the Connexin 43 Carboxyl Terminus Preserves Left Ventricular Function After Ischemia‐Reperfusion Injury
inferredcites →https://doi.org/10.1242/dmm.003194openalex-snapshot
The ADPKD genespkd1a/bandpkd2regulate extracellular matrix formation
inferredcites →https://doi.org/10.3390/jcdd2030200openalex-snapshot
Increased Infiltration of Extra-Cardiac Cells in Myxomatous Valve Disease
inferredcites →https://doi.org/10.7554/elife.42670openalex-snapshot
Connexin-43-dependent ATP release mediates macrophage activation during sepsis
inferredcites →https://doi.org/10.7554/elife.62856openalex-snapshot
Fibroblast mechanotransduction network predicts targets for mechano-adaptive infarct therapies

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4797658openalex-extracted
Primary Cilia Confer TGFβ1-Dependent Resistance in Rat Cardiac Fibroblasts after X-Ray Injury
inferred← citeshttps://doi.org/10.1002/ccd.31158openalex-snapshot
A modified Carpentier classification in transcatheter edge‐to‐edge repair for mitral regurgitation
inferred← citeshttps://doi.org/10.1002/cpz1.1025openalex-snapshot
In Vitro Assessment of Cardiac Fibroblast Activation at Physiologic Stiffness
inferred← citeshttps://doi.org/10.1007/s00330-023-10413-9openalex-snapshot
Imaging for the assessment of the arrhythmogenic potential of mitral valve prolapse
inferred← citeshttps://doi.org/10.1007/s10554-023-02985-wopenalex-snapshot
Left ventricular fibrosis and CMR tissue characterization of papillary muscles in mitral valve prolapse patients
inferred← citeshttps://doi.org/10.1007/s13258-025-01626-xopenalex-snapshot
Whole exome sequencing of 80 cases of sporadic mitral valve prolapse reveals novel disease-associated genes and variants in a Southern Chinese population
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2025.119919openalex-snapshot
Connexin 43 dephosphorylation mediates the Dchs1/YAP/TEAD signaling pathway to induce cardiac fibrosis
inferred← citeshttps://doi.org/10.1016/j.cjca.2026.07.004openalex-snapshot
Extra-Mitral Abnormalities in Nonsyndromic Mitral Valve Prolapse Assessed By Means of Cardiovascular Magnetic Resonance
inferred← citeshttps://doi.org/10.1016/j.cmpb.2025.109151openalex-snapshot
Magnetic resonance-based computational modelling of healthy and prolapsing mitral valves to quantify the load transfer between the mitral apparatus and the ventricular myocardium
inferred← citeshttps://doi.org/10.1016/j.cpcardiol.2023.101724openalex-snapshot
Arrhythmogenic Mitral Valve Prolapse and Sudden Cardiac Death: An Update and Current Perspectives
inferred← citeshttps://doi.org/10.1016/j.jacc.2022.09.044openalex-snapshot
Research Opportunities in the Treatment of Mitral Valve Prolapse
inferred← citeshttps://doi.org/10.1016/j.jaccas.2025.103685openalex-snapshot
Reversed Remodeling Unveils Mitral Annular Disjunction
inferred← citeshttps://doi.org/10.1016/j.jocmr.2024.101056openalex-snapshot
Mitral annulus disjunction in consecutive patients undergoing cardiovascular magnetic resonance: Where is the boundary between normality and disease?
inferred← citeshttps://doi.org/10.1016/j.jocmr.2024.101117openalex-snapshot
Interstitial fibrosis and arrhythmic mitral valve prolapse: Unraveling sex-based differences
inferred← citeshttps://doi.org/10.1016/j.jocmr.2024.101137openalex-snapshot
Cardiovascular magnetic resonance in patients with mitral valve prolapse
inferred← citeshttps://doi.org/10.1016/j.jtcvs.2023.04.026openalex-snapshot
Neochordal Goldilocks: Analyzing the biomechanics of neochord length on papillary muscle forces suggests higher tolerance to shorter neochordae
inferred← citeshttps://doi.org/10.1016/j.jvc.2025.10.007openalex-snapshot
Distribution of ionized calcium–binding adaptor molecule 1–positive macrophages and papillary muscle fibrosis in dogs with myxomatous mitral valve disease
inferred← citeshttps://doi.org/10.1038/s41572-023-00478-7openalex-snapshot
Degenerative mitral regurgitation
inferred← citeshttps://doi.org/10.1038/s41598-025-33951-2openalex-snapshot
Left atrioventricular coupling in isolated pediatric mitral valve prolapse with preserved ejection fraction and moderate regurgitation
inferred← citeshttps://doi.org/10.1053/j.semtcvs.2025.03.005openalex-snapshot
Arrhythmic Mitral Valve Prolapse: Pathophysiology, Diagnostics, and Management Strategies
inferred← citeshttps://doi.org/10.1063/5.0248930openalex-snapshot
Modeling the fluid dynamics of mitral valve for clinical applications and surgical mitral valve repair
inferred← citeshttps://doi.org/10.1080/15569527.2026.2715412openalex-snapshot
Evaluation of facial cutaneous aging in individuals with mitral valve prolapse
inferred← citeshttps://doi.org/10.1093/ehjopen/oeae034openalex-snapshot
Gene expression and ultra-structural evidence for metabolic derangement in the primary mitral regurgitation heart
inferred← citeshttps://doi.org/10.1093/ehjqcco/qcaf016openalex-snapshot
Prevalence, progression, and clinical outcomes of mitral valve prolapse: a systematic review and meta-analysis
inferred← citeshttps://doi.org/10.1093/ejcts/ezae312openalex-snapshot
Presentation and outcomes of women and men undergoing surgery for degenerative mitral regurgitation
inferred← citeshttps://doi.org/10.1093/eurheartj/ehag242openalex-snapshot
Is true -MAD what we are truly looking for in arrhythmic risk stratification?
inferred← citeshttps://doi.org/10.1111/ahg.12534openalex-snapshot
Functions of cilia in cardiac development and disease
inferred← citeshttps://doi.org/10.1111/echo.15657openalex-snapshot
Secondary leaflet tethering in patients with severe degenerative mitral regurgitation and its association with the severity of mitral regurgitation
inferred← citeshttps://doi.org/10.1111/echo.15894openalex-snapshot
Cardiac magnetic resonance imaging in the evaluation and management of mitral valve prolapse – a comprehensive review
inferred← citeshttps://doi.org/10.1148/ryct.230247openalex-snapshot
Arrhythmic Mitral Valve Prolapse Phenotype: An Unsupervised Machine Learning Analysis Using a Multicenter Cardiac MRI Registry
inferred← citeshttps://doi.org/10.1161/circimaging.122.014963openalex-snapshot
Abnormal Mechanics Relate to Myocardial Fibrosis and Ventricular Arrhythmias in Patients With Mitral Valve Prolapse
inferred← citeshttps://doi.org/10.1161/circimaging.124.017313openalex-snapshot
Multimodality Imaging of Arrhythmic Risk in Mitral Valve Prolapse
inferred← citeshttps://doi.org/10.1161/circinterventions.122.011928openalex-snapshot
Native and Post-Repair Residual Mitral Valve Prolapse Increases Forces Exerted on the Papillary Muscles: A Possible Mechanism for Localized Fibrosis?
inferred← citeshttps://doi.org/10.1161/circinterventions.125.016161openalex-snapshot
Aberrant, Elevated Papillary Muscle and LV Wall Forces Associated With Mitral Valve Prolapse Are Normalized by Surgical Neochordal Repair but Not by Transcatheter Edge-to-Edge Repair
inferred← citeshttps://doi.org/10.1161/jaha.125.045002openalex-snapshot
Sex‐Based Differences in Outcomes Following Mitral Valve Surgery: A Contemporary Analysis From 2 Institutions
inferred← citeshttps://doi.org/10.3389/fcvm.2022.862044openalex-snapshot
Left Ventricular Remodeling in Non-syndromic Mitral Valve Prolapse: Volume Overload or Concomitant Cardiomyopathy?
inferred← citeshttps://doi.org/10.3389/fcvm.2023.1057986openalex-snapshot
Histopathological insights into mitral valve prolapse-induced fibrosis
inferred← citeshttps://doi.org/10.3389/fcvm.2023.1077788openalex-snapshot
Genetics and pathophysiology of mitral valve prolapse
inferred← citeshttps://doi.org/10.3389/fcvm.2023.1093060openalex-snapshot
The evolving role of cardiovascular magnetic resonance in the assessment of mitral valve prolapse
inferred← citeshttps://doi.org/10.3390/bioengineering10050601openalex-snapshot
Utilization of Engineering Advances for Detailed Biomechanical Characterization of the Mitral–Ventricular Relationship to Optimize Repair Strategies: A Comprehensive Review
inferred← citeshttps://doi.org/10.3390/ijms24087142openalex-snapshot
Serum Proteomic Profiles Reflect the Stages of Myxomatous Mitral Valve Disease in Dogs
inferred← citeshttps://doi.org/10.3390/ijms242316928openalex-snapshot
Defect of TIMP4 Is Associated with High Myopia and Participates in Rat Ocular Development in a Dose-Dependent Manner
inferred← citeshttps://doi.org/10.3390/ijms27031498openalex-snapshot
Atrial Fibrillation and Primary Cilia-Associated Genes: The Role of CEP68
inferred← citeshttps://doi.org/10.3390/jcdd10040181openalex-snapshot
Left Ventricle Segmental Longitudinal Strain and Regional Myocardial Work Index Could Help Determine Mitral Valve Prolapse Patients with Increased Risk of Ventricular Arrhythmias
inferred← citeshttps://doi.org/10.3390/jcdd13090437openalex-snapshot
Arrhythmic Mitral Valve Prolapse as a Regional Stretch-Induced Cardiomyopathy with Fibro-Inflammatory Signature: A Conceptual Review
inferred← citeshttps://doi.org/10.3390/jcm12237441openalex-snapshot
The Potential of Intertwining Gene Diagnostics and Surgery for Mitral Valve Prolapse
inferred← citeshttps://doi.org/10.3390/jcm14072277openalex-snapshot
Does Preliminary Chest Shape Assessment Improve the Prognostic Risk Stratification of Individuals with Mitral Annular Disjunction? A Case Report and Narrative Review
inferred← citeshttps://doi.org/10.3390/jcm15020865openalex-snapshot
The Arrhythmogenic Spectrum of Mitral Valve Disease: Pathophysiology, Risk Stratification, and Surgical Management
inferred← citeshttps://doi.org/10.3390/medsci11010013openalex-snapshot
The Importance of Mitral Valve Prolapse Doming Volume in the Assessment of Left Ventricular Stroke Volume with Cardiac MRI
inferred← citeshttps://doi.org/10.4103/rcm.rcm_38_24openalex-snapshot
Aplastic Posterior Mitral Leaflet with an Unusual Clinical Course
inferred← citeshttps://doi.org/10.64898/2026.04.09.26350328openalex-snapshot
Genetic Architecture and Myocardial Fibrotic Remodeling in Mitral Valve Prolapse
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