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May 29, 2026Journal of Thoracic Imaging0 citations

The Diagnostic and Prognostic Value of Multi-Chamber Strain Analysis by Cardiac MRI in Amyloidosis

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SCSushmita Keerthi ChilkuriImaging CenterRDRomina DSouzaUniversity of TorontoCHC HouboisSunnybrook Health Science Centre

Key Result

Multi-chamber strain analysis by CMR identified LV GLS (HR 5.27; P=0.016) and LA reservoir strain (HR 0.025; P=0.03) as strong independent predictors of MACE in cardiac amyloidosis.

Key Points

  • To assess the diagnostic and prognostic value of multi-chamber strain analysis in cardiac amyloidosis.
  • Retrospective study involving 47 patients
  • Utilized cardiac MRI to quantify strain and assess native T1 and late gadolinium enhancement
  • Analyzed strain parameters using Cox regression and receiver operating characteristic curves.
  • LV strain indices showed high diagnostic accuracy (AUC=0.897; cutoff=-12.9) and significant correlations with native T1 and QALE (P<0.05)
  • RV GLS (AUC=0.687; cutoff=-12.5) independently predicted MACE with HR=1.05; P<0.05
  • Multivariable Cox regression identified LV GLS (HR=5.27; P=0.016) and LA reservoir strain (HR=0.025; P=0.03) as strong independent prognostic indicators.

Study Design

Type

Cohort (n=47)

Structured PICO

Does multi-chamber strain analysis by cardiac MRI improve diagnostic accuracy and predict major adverse cardiovascular events in patients with cardiac amyloidosis?

P
Population
47 patients evaluated for cardiac amyloidosis
I
Intervention
Multi-chamber myocardial strain analysis by cardiac magnetic resonance (CMR) imaging, integrated with native T1 mapping and late gadolinium enhancement (LGE)
O
Outcome
Diagnostic accuracy for cardiac amyloidosis and prediction of major adverse cardiovascular events (MACE)surrogate

Multi-chamber strain analysis by CMR, particularly LV GLS and LA reservoir strain, provides strong independent prognostic value for predicting MACE in patients with cardiac amyloidosis.

Main Result

Effect estimate: HR 5.27

p-value: p=0.016

Abstract

PURPOSE: To evaluate the diagnostic and prognostic utility of multi-chamber myocardial strain, and its correlation with native T1 mapping and late gadolinium enhancement (LGE) imaging, by cardiac magnetic resonance (CMR) in cardiac amyloidosis. MATERIALS AND METHODS: A total of 47 patients were retrospectively included and the strain of the ventricles and atria were quantified. Native T1 and Query Amyloid Late Enhancement (QALE) values were assessed. Follow-up data on major adverse cardiovascular events (MACE) were retrieved from medical records. Spearman correlations between strain, LGE, and mapping were assessed. The strain parameters were analyzed using receiver operating characteristic curves and Cox regression analysis. RESULTS: LV strain indices, RV GLS, RV GRS, LA reservoir, LA conduit strain, and RA reservoir strain demonstrated diagnostic ability (P<0.05), with the highest diagnostic accuracy for LV GCS (AUC=0.897; cutoff=-12.9). Native T1 and QALE showed moderate correlations with LV and LA strain, reflecting amyloid infiltration and fibrosis-related dysfunction. For prognosis, RV GLS (AUC=0.687; cutoff=-12.5) and RA conduit strain (AUC=0.737; cutoff=+10) independently predicted MACE on univariable Cox analysis (HR=1.05 and 0.96; P<0.05). Importantly, multivariable Cox regression identified LV GLS (HR=5.27; P=0.016) and LA reservoir strain (HR=0.025; P=0.03) as strong independent predictors of MACE. CONCLUSION: Multi-chamber strain, and its integration with T1 and QALE, enhances diagnostic accuracy and prognostic precision in cardiac amyloidosis, enabling earlier recognition of myocardial dysfunction.

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Cite This Study

Chilkuri et al. (2026) conducted a cohort in Cardiac amyloidosis (n=47). Multi-chamber myocardial strain by CMR was evaluated on Major adverse cardiovascular events (MACE) (HR 5.27, p=0.016). Multi-chamber strain analysis by CMR identified LV GLS (HR 5.27; P=0.016) and LA reservoir strain (HR 0.025; P=0.03) as strong independent predictors of MACE in cardiac amyloidosis.

synapsesocial.com/papers/6a192da0fab5b468c4416810https://doi.org/10.1097/rti.0000000000000878
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