Prognostic Value of Compact Myocardial Thinning in Patients With Left Ventricular Noncompaction.

Am J Cardiol

Division of Cardiovascular Medicine, Department of Medicine, Stanford University, Stanford, California; Stanford University, Cardiovascular Institute, Stanford, California; Department of Radiology, Stanford University, Stanford, California. Electronic address:

Published: August 2025


Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Clinical presentations of left ventricular noncompaction (LVNC) range from asymptomatic cases to ventricular tachyarrhythmia (VT), heart failure (HF), and cerebrovascular accidents (CVA). In this multicenter study, we explored the associations between clinical and imaging characteristics and outcomes of LVNC patients and validated the predictive value of myocardial thinning identified on cardiac magnetic resonance imaging (CMR) as previously described. About 214 adult patients (54% male, mean age 41 ± 16 years) meeting the imaging criteria for LVNC were identified. Myocardial thinning was defined as a 50% or greater diameter reduction of the compacted myocardium compared to a contiguous segment on CMR. The primary endpoint was the occurrence of a major adverse cardiovascular event (MACE), defined as a composite of all-cause mortality, HF hospitalization, left ventricular assist device (LVAD) or heart transplant, cardiac resynchronization therapy (CRT), CVA/transient ischemic attacks (TIA), VT and appropriate implantable cardioverter defibrillator (ICD) therapy. Focal myocardial thinning was observed in 42 patients (20%). Over a median follow-up time of 7 years (IQR, 4 to 10 years), 54 patients (24%) experienced a primary outcome. Patients with myocardial thinning had more cumulative adverse events than those without myocardial thinning (chi-square = 29.516, log-rank < 0.001), even after matching for medical risk score. In a multivariate Cox regression model, myocardial thinning remained associated with outcomes: HR 3.052 (95% CI: 1.569 to 5.937, p = 0.001). Myocardial thinning is associated with adverse cardiovascular events in LVNC patients. Incorporating myocardial thinning into medical risk assessments can improve the prediction and management of adverse outcomes in these patients.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12380258PMC
http://dx.doi.org/10.1016/j.amjcard.2025.04.018DOI Listing

Publication Analysis

Top Keywords

myocardial thinning
36
left ventricular
12
myocardial
9
thinning
9
patients
8
ventricular noncompaction
8
lvnc patients
8
adverse cardiovascular
8
medical risk
8
prognostic compact
4

Similar Publications

Loss of actin cytoskeleton control can hinder integral developmental and physiological processes and can be the basis for a subset of developmental defects. SHROOM3 is an actin binding protein, best characterized as being essential for neural tube closure in vertebrates. Shroom3 expression has also been identified in the developing heart, with some associated congenital heart defects.

View Article and Find Full Text PDF

Echocardiography-guided intramyocardial injection (EGI) is a minimally invasive technique for delivering stem cell therapies in preclinical myocardial infarction (MI) models. Compared to traditional open-chest approaches, EGI offers improved clinical translatability, reduced invasiveness, and minimized physiological impact on the animal. While EGI is well established in murine models, its application in rats remains limited due to anatomical and technical challenges.

View Article and Find Full Text PDF

Diabetes is closely associated with the onset and prognosis of myocardial infarction (MI). However, current treatment strategies primarily focus on addressing MI, often neglecting the detrimental effects of hyperglycemia, a hallmark of diabetes. Hyperglycemia disrupts the crucial transition of macrophages from the M1 to M2 phenotype, thereby exacerbating MI-induced tissue damage and impeding myocardial repair.

View Article and Find Full Text PDF

Macro- and microinjury define the heart failure progression after permanent coronary ligation or ischemia-reperfusion in young healthy mice.

Am J Physiol Heart Circ Physiol

August 2025

Division of Cardiovascular Sciences, Department of Internal Medicine, Morsani College of Medicine, Heart Institute, University of South Florida, Tampa, Florida, United States.

Heart failure (HF) is a major outcome in cardiovascular disease resulting from myocardial infarction (MI). Preclinical studies use MI-induced HF rodent models with either permanent coronary occlusion (PO) or transient ligation to induce ischemia-reperfusion (I/R). Comparisons of inflammation-resolution signaling in these models are understudied.

View Article and Find Full Text PDF

Fibroblasts are crucial for cardiac repair after myocardial infarction (MI). In response to signaling cues, they differentiate to phenotypes with robust capacities to synthesize and secrete extracellular matrix (ECM) and signaling molecules. Although activated fibroblast phenotypes are associated with pronounced changes in metabolism, it remains unclear how the metabolic network upholds the effector functions of fibroblasts in the infarcted heart.

View Article and Find Full Text PDF