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ORIGINAL RESEARCH article

Front. Cardiovasc. Med.

Sec. General Cardiovascular Medicine

The Value of Cardiac Magnetic Resonance Delayed Enhancement Combined with Tissue Tracking in Discriminating Cardiac Amyloidosis from Hypertrophic Cardiomyopathy

Provisionally accepted
Xiao-Gang  XueXiao-Gang Xue*Xiao-Yong  XuXiao-Yong XuXue-Yao  LinXue-Yao LinGao-Yan  WangGao-Yan WangHai-Bo  DongHai-Bo Dong
  • Ningbo Medical Centre Lihuili Hospital, Ningbo, China

The final, formatted version of the article will be published soon.

Purpose: Cardiac amyloidosis (CA) and hypertrophic cardiomyopathy (HCM) may both present with left ventricular hypertrophy, making differential diagnosis challenging. This study aimed to evaluate the value of cardiac magnetic resonance (CMR) delayed enhancement combined with tissue tracking (CMR-TT) in discriminating CA from HCM. Methods: Data from 30 patients with CA, 29 patients with HCM, and 20 normal controls (NC) were retrospectively analyzed. All subjects underwent CMR examinations. Tissue tracking techniques were adopted for CMR cine sequences to directly quantify global radial strain (GRS), global circumferential strain (GCS), and global longitudinal strain (GLS). Results: The most common delayed enhancement pattern in CA was linear subendocardial enhancement (76.7%). Half of the CA patients had delayed enhancement involving atria and right ventricle, while 33.3% exhibited the characteristic “chaotic sign.” The GRS and GCS values were significantly different between the CA group and the HCM group and between the CA group and the NC group (P<0.05). GLS differed significantly among the CA, HCM, and NC groups (P<0.05). ROC analysis revealed that GCS (AUC=0.748, P=0.001) and GLS (AUC=0.732, P=0.002) provided good diagnostic efficiency in differentiating CA from HCM. Conclusion: CMR delayed enhancement patterns combined with myocardial strain parameters, particularly GLS and GCS, can aid in the differential diagnosis of CA and HCM. Optimal cutoff values of GCS (–14.6%) and GLS (–9.22%) provide a noninvasive imaging approach with significant clinical implications for guiding treatment and improving prognosis.

Keywords: Amyloidosis, Hypertrophic Cardiomyopathy, Magnetic Resonance Imaging, Ventricular Function, Medicine

Received: 25 Sep 2025; Accepted: 25 Nov 2025.

Copyright: © 2025 Xue, Xu, Lin, Wang and Dong. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Xiao-Gang Xue

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