Evidence map›Paper›PMID 40156690›Full record

ArticleThe international journal of cardiovascular imaging2025

Correlation between left ventricular hypertrophy, myocardial fibrosis, and left atrial function in non-obstructive hypertrophic cardiomyopathy: insights from CMR-FT imaging.

Yan Zheng, Ma Liyuan, Qian Wu, Huairong Zhang, Yuan Li, Rui Li, Li Zhu

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Article in The international journal of cardiovascular imaging, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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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.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Yan ZhengDepartment of Radiology, General Hospital of Ningxia Medical University, Yichuan, 750004, China.
Ma LiyuanThe First Clinical Medical College of Ningxia Medical University, Yinchuan, 750004, China.
Qian WuDepartment of Radiology, General Hospital of Ningxia Medical University, Yichuan, 750004, China.
Huairong ZhangDepartment of Radiology, General Hospital of Ningxia Medical University, Yichuan, 750004, China.
Yuan LiDepartment of Radiology, General Hospital of Ningxia Medical University, Yichuan, 750004, China.
Rui LiDepartment of Radiology, General Hospital of Ningxia Medical University, Yichuan, 750004, China.
Li ZhuDepartment of Radiology, General Hospital of Ningxia Medical University, Yichuan, 750004, China. zhuli72@163.com.ORCID http://orcid.org/0009-0008-4755-9246

Funding

Central guidance for Ningxia Hui Autonomous Region in 2023 2023FRD05010National Key Research and Development Program of China 2022YFC2010003
6 · The paper itself

Abstract

Nonobstructive hypertrophic cardiomyopathy (NOHCM) is associated with left ventricular (LV) hypertrophy and myocardial fibrosis, which progressively impair left atrial (LA) function. This study evaluated the impact of LV hypertrophy and fibrosis on LA dysfunction using cardiac magnetic resonance (CMR) imaging and feature-tracking (FT) strain analysis in 99 NOHCM patients, who were stratified into four groups based on the extent of late gadolinium enhancement (LGE): no fibrosis (LGE < 7%), mild fibrosis (7% ≤ LGE < 15%), moderate fibrosis (15% ≤ LGE < 30%), and severe fibrosis (LGE ≥ 30%). LA functional parameters, including reservoir strain (εs), conduit strain (εe), and pump strain (εa), showed significant reductions with increasing LGE burden (P < 0.05), with functional decline detectable even in mild fibrosis cases despite preserved LV ejection fraction. LV morphological and functional indices, such as global peak wall thickness (GPWT), LV end-systolic volume (LVESV), and LGE percentage, negatively correlated with LA strain metrics (r = -0.2 to -0.7, P < 0.05). Strain analysis demonstrated high reproducibility (ICC > 0.75). These findings highlight the clinical significance of CMR-FT as a sensitive and reliable tool for early detection of LA dysfunction in NOHCM patients, even before significant LV structural changes occur. The ability of CMR-FT to identify subtle changes in LA mechanics could provide valuable insights for risk stratification and guide early intervention strategies, ultimately improving clinical outcomes in this patient population.

Indexed as

Atrial Function, LeftCardiomyopathy, HypertrophicHypertrophy, Left VentricularMagnetic Resonance Imaging, CineMyocardiumVentricular Function, LeftAdultAgedBiomechanical PhenomenaContrast MediaFemaleFibrosisHumansMaleMiddle AgedPredictive Value of TestsContrast MediaCardiac magnetic resonance imaging (CMR)Hypertrophic cardiomyopathyLate gadolinium enhancement (LGE)Left atrial functionMyocardial fibrosis

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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.