Cardiac MRI for clinical dilated cardiomyopathy: Improved diagnostic power via combined T1, T2, and ECV

S-Q Jia; S-Y Lv; Y-H Jin; Y Zhao; L-P Tian; M-M Chang; C-L Yan; X-L Qi

doi:10.1016/j.radi.2024.04.005

Cardiac MRI for clinical dilated cardiomyopathy: Improved diagnostic power via combined T1, T2, and ECV

Radiography (Lond). 2024 Apr 23;30(3):926-931. doi: 10.1016/j.radi.2024.04.005. Online ahead of print.

Authors

S-Q Jia¹, S-Y Lv¹, Y-H Jin², Y Zhao¹, L-P Tian³, M-M Chang³, C-L Yan⁴, X-L Qi⁵

Affiliations

¹ Department of Clinical Medicine, Jining Medical University, Jining 272000, Shandong, China.
² Department of Radiology, Chenzhou First People's Hospital, Chenzhou 423000, Hunan, China.
³ Department of Radiology, Jining First People's Hospital Affiliated to Shandong First Medical University, Jining 272000, Shandong, China.
⁴ Department of Radiology, Jining First People's Hospital Affiliated to Shandong First Medical University, Jining 272000, Shandong, China. Electronic address: yclky2012@126.com.
⁵ Department of Radiology, Jining First People's Hospital Affiliated to Shandong First Medical University, Jining 272000, Shandong, China. Electronic address: qixianlong@126.com.

PMID: 38657385
DOI: 10.1016/j.radi.2024.04.005

Abstract

Introduction: Early diagnosis of patients with dilated cardiomyopathy (DCM) remains challenging. Cardiac MR can correlate myocardial changes with their pathological basis. There have been some previous studies on the effect of T1 mapping in DCM, but there is limited data on the incremental value of T2 mapping for DCM in routine clinical practice. This study will examine whether the combination of MRI T1 and T2 mapping offers greater advantages in the diagnosis of DCM.

Methods: The study included 28 patients with DCM and 21 healthy controls. CMR evaluation included late gadolinium enhancement (LGE), T1 mapping, extracellular volume (ECV) fraction and T2 mapping. The DCM group was divided into LGE (+) and LGE (-) subgroups. The main modes of LGE are subendocardial, midwall, subepicardial, or transmural. T1 values, T2 values, and ECV in the 16 segments myocardial levels were measured by post-processing software. Student's t-tests or Mann-Whitney U test was used to compare between two groups, and one-way ANOVA or Kruskal-Wallis H test was used to compare between multiple groups, with p values corrected by Bonferroni. The difference was considered statistically significant at P < 0.05. ROC curve analysis was used to compare the area under the curve (AUC) of each index and its combined value, and the cut-off value, sensitivity and specificity were determined by Jordan's index.

Results: Mean native myocardial T1, ECV and T2 were significantly higher in the DCM group compared to controls (p ≤ 0.001, respectively). The best cut-off values for T1, T2 and ECV to discriminate DCM from controls were 1184 ms, 40.9 ms and 29.2%, respectively. The AUC of T1, ECV and T2 were 0.87, 0.89, and 0.83, respectively. The combined AUC of the three values was 0.96.

Conclusion: Native T1 value and ECV overcome some of the limitations of LGE, and the T2 helps to understand the extent of myocardial damage. The combination of T1 and T2 mapping techniques can reveal fibrotic and oedematous changes in the early stages of DCM, providing a more comprehensive assessment of DCM and better guidance for individualised clinical management of patients.

Implications for practice: We suggest that the addition of T2 mapping to the routine CMR examination of patients with suspected DCM, and the combined assessment of T1mapping and T2 mapping can provide complementary information about the disease and improve the early diagnosis of DCM.

Keywords: Cardiovascular magnetic resonance; Dilated cardiomyopathy; Extracellular volume fraction; T1 mapping; T2 mapping.