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Article

Diagnostic Value of Native T1 and T2 Mapping in Differentiating Clinically Suspected Amyloidosis and Hypertrophic Cardiomyopathy

1
Department of Radiology, School of Medicine, Ankara University, Hacettepe Mahallesi A. Adnan Saygun Cad. No: 35, 06230 Altındağ, Ankara, Türkiye
2
Department of Radiology, Tosya State Hospital, A.Raşit Urkaya Sok., Dilküşah Mahallesi No: 2, 37300 Tosya, Kastamonu, Türkiye
3
Department of Cardiology, School of Medicine, Ankara University, Hacettepe Mahallesi A. Adnan Saygun Cad. No: 35, 06230 Altındağ, Ankara, Türkiye
*
Author to whom correspondence should be addressed.
Diagnostics 2026, 16(10), 1558; https://doi.org/10.3390/diagnostics16101558
Submission received: 12 April 2026 / Revised: 4 May 2026 / Accepted: 18 May 2026 / Published: 20 May 2026
(This article belongs to the Section Medical Imaging and Theranostics)

Abstract

Background/Objectives: Differentiating clinically suspected cardiac amyloidosis from hypertrophic cardiomyopathy (HCM) remains a significant clinical challenge, especially when contrast-enhanced imaging is contraindicated. This study evaluated the potential diagnostic utility of non-contrast cardiac MRI parameters, specifically native T1 and T2 mapping, as supportive indicators in this differential diagnosis. Methods: This retrospective single-center study included 20 patients with clinically suspected amyloidosis (based on combined clinical and echocardiographic assessment), 20 patients with HCM, and 20 healthy controls. Cine imaging and native T1/T2 mapping were analyzed. Myocardial, blood-pool, and liver T1/T2 values, along with morphological parameters, were recorded. N-terminal pro–B-type natriuretic peptide (NT-proBNP) and troponin levels, when available, were documented retrospectively for descriptive purposes. Receiver operating characteristic (ROC) analyses were performed to assess the discriminatory performance of imaging parameters. Results: Patients in the suspected amyloidosis group demonstrated significantly higher myocardial, blood-pool, and liver T1 values, as well as higher myocardial T2 values, compared with both the HCM and control groups (p < 0.001). Myocardial T1 showed strong discriminatory performance for differentiating suspected amyloidosis from controls (cut-off 1061 ms, AUC = 0.975). In distinguishing suspected amyloidosis from HCM, blood-pool T1 (AUC = 0.900) and myocardial T1 (AUC = 0.938) provided the highest diagnostic performance. Additionally, elevated NT-proBNP (>1000 pg/mL in 93% of tested cases) and troponin levels were observed in the suspected amyloidosis group, consistent with increased myocardial stress. Conclusions: Native T1 and T2 mapping may offer valuable supportive information in differentiating clinically suspected amyloidosis from HCM on non-contrast MRI. Myocardial and blood-pool T1 values appear to provide complementary tissue characterization, which may be particularly useful when gadolinium administration or invasive procedures are not feasible. These findings suggest a role for non-contrast mapping in the diagnostic workup but require further validation in larger, biopsy-confirmed multicenter cohorts.
Keywords: amyloidosis; hypertrophic cardiomyopathy; cardiac MRI; T1 mapping; T2 mapping amyloidosis; hypertrophic cardiomyopathy; cardiac MRI; T1 mapping; T2 mapping

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MDPI and ACS Style

Unal, S.; Uzun, C.; Bozer Uludag, S.; Yamak, C.; Tan, T.S.; Peker, E. Diagnostic Value of Native T1 and T2 Mapping in Differentiating Clinically Suspected Amyloidosis and Hypertrophic Cardiomyopathy. Diagnostics 2026, 16, 1558. https://doi.org/10.3390/diagnostics16101558

AMA Style

Unal S, Uzun C, Bozer Uludag S, Yamak C, Tan TS, Peker E. Diagnostic Value of Native T1 and T2 Mapping in Differentiating Clinically Suspected Amyloidosis and Hypertrophic Cardiomyopathy. Diagnostics. 2026; 16(10):1558. https://doi.org/10.3390/diagnostics16101558

Chicago/Turabian Style

Unal, Sena, Caglar Uzun, Sena Bozer Uludag, Cuneyt Yamak, Turkan Seda Tan, and Elif Peker. 2026. "Diagnostic Value of Native T1 and T2 Mapping in Differentiating Clinically Suspected Amyloidosis and Hypertrophic Cardiomyopathy" Diagnostics 16, no. 10: 1558. https://doi.org/10.3390/diagnostics16101558

APA Style

Unal, S., Uzun, C., Bozer Uludag, S., Yamak, C., Tan, T. S., & Peker, E. (2026). Diagnostic Value of Native T1 and T2 Mapping in Differentiating Clinically Suspected Amyloidosis and Hypertrophic Cardiomyopathy. Diagnostics, 16(10), 1558. https://doi.org/10.3390/diagnostics16101558

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