ReviewCurrent cardiology reports2026
Non-Dilated Left Ventricular Cardiomyopathy (NDLVC): A Name, Multiple Souls.
Review in Current cardiology reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Non-Dilated Left Ventricular Cardiomyopathy: Exploring the Spectrum from Phenotype to Disease Entity.Journal of clinical medicine · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
10 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
purpose of reviewNon-dilated left ventricular cardiomyopathy (NDLVC) is a newly recognized cardiomyopathy phenotype, characterized by systolic dysfunction and/or non-ischemic myocardial scar, in the absence of ventricular dilatation. This review summarizes current evidence on its epidemiology, imaging features, genetic background, arrhythmic substrate, differential diagnosis, risk stratification, and management. RECENT
findingsAdvanced cardiac magnetic resonance has demonstrated that late gadolinium enhancement, particularly septal and ring-like pattern, is common in NDLVC and predicts malignant ventricular arrhythmias (MVA) and evolution to dilated phenotype. High-risk genotypes (e.g., DSP, FLNC, LMNA, PLN) and myocardial inflammation further increase arrhythmic and heart failure risk. Novel tools, including the NDLVC-5-year risk score, allow improved individualized prediction, especially when combined with genotype-specific score. NDLVC resulting from the complex interplay between genetic background and environmental factors may lead to arrhythmias and heart failure. A multimodal, phenotype-first approach integrating imaging, genetics, and electrophysiology is essential for accurate diagnosis, risk stratification, and personalized management.
Indexed as
Identifiers
41915332What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.