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

Sena Unal1, Caglar Uzun1, Sena Bozer Uludag2

  • 1Department of Radiology, School of Medicine, Ankara University, Hacettepe Mahallesi A. Adnan Saygun Cad. No: 35, 06230 Altındağ, Ankara, Türkiye.

Insights

Non-contrast cardiac MRI using native T1 and T2 mapping shows promise in distinguishing cardiac amyloidosis from hypertrophic cardiomyopathy (HCM). These techniques offer valuable supportive data when contrast agents are not an option.

Area of Science:

  • Cardiovascular Imaging
  • Magnetic Resonance Imaging
  • Biomarkers

Background:

  • Differentiating cardiac amyloidosis from hypertrophic cardiomyopathy (HCM) is clinically challenging, particularly when contrast-enhanced MRI is contraindicated.
  • Non-contrast cardiac MRI parameters, specifically native T1 and T2 mapping, were evaluated for their diagnostic utility.

Purpose of the Study:

  • To assess the diagnostic performance of non-contrast cardiac MRI parameters (native T1 and T2 mapping) in differentiating clinically suspected cardiac amyloidosis from HCM.
  • To explore the utility of these parameters in scenarios where contrast agents cannot be used.

Main Methods:

  • Retrospective single-center study involving 20 patients with suspected amyloidosis, 20 with HCM, and 20 healthy controls.
  • Analysis of cine imaging and native T1/T2 mapping, including myocardial, blood-pool, and liver values.
  • Receiver operating characteristic (ROC) analyses to determine discriminatory performance.

Main Results:

  • Patients with suspected amyloidosis exhibited significantly higher myocardial, blood-pool, and liver T1 values, and higher myocardial T2 values compared to HCM and control groups (p < 0.001).
  • Myocardial T1 (AUC = 0.938) and blood-pool T1 (AUC = 0.900) showed strong discriminatory performance for differentiating suspected amyloidosis from HCM.
  • Elevated NT-proBNP and troponin levels were observed in the suspected amyloidosis group, indicating myocardial stress.

Conclusions:

  • Native T1 and T2 mapping can provide valuable supportive information for differentiating suspected cardiac amyloidosis from HCM using non-contrast MRI.
  • Myocardial and blood-pool T1 values offer complementary tissue characterization, beneficial when gadolinium contrast or invasive procedures are not feasible.
  • Further validation in larger, multicenter, biopsy-confirmed cohorts is warranted to establish the role of non-contrast mapping in the diagnostic workup.

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