Development and validation of an echocardiographic nomogram for identifying cardiac amyloidosis in patients with left

Shichu Liang1, Zhiyue Liu1, Fanfan Shi2

  • 1Department of Cardiology, West China Hospital, Sichuan University, No.37 GuoXue Alley, Chengdu, 610041, China.

PubMed

Insights

This study developed a highly accurate echocardiographic model to identify cardiac amyloidosis (CA) in patients with left ventricular hypertrophy (LVH). The nomogram aids in early CA detection and guides further diagnostic steps.

Area of Science:

  • Cardiology
  • Medical Imaging
  • Diagnostic Tools

Background:

  • Echocardiography is the primary non-invasive method for screening cardiac amyloidosis (CA).
  • Cardiac amyloidosis-associated left ventricular hypertrophy (CA-LVH) requires effective identification strategies.
  • Developing a predictive model using echocardiographic parameters is crucial for early diagnosis.

Purpose of the Study:

  • To establish a cohort of CA-LVH within a hospital population.
  • To develop an echocardiographic identification model for CA using readily available parameters.
  • To improve the diagnostic accuracy of CA screening in patients with LVH.

Main Methods:

  • Retrospective nested cohort study of clinical and echocardiographic data (2008-2023).
  • Calculation of relative wall thickness (RWT) and asymmetric hypertrophy.
  • Development of the AMYLI score and a nomogram model based on logistic regression analysis.

Main Results:

  • A multivariable logistic regression identified key predictive factors for CA in LVH patients.
  • These factors included LVID, LVEF, AMYLI score, asymmetric hypertrophy, granular sparkling, pericardial effusion, and valvular regurgitation.
  • The constructed nomogram model demonstrated high accuracy (0.91-0.92) and sensitivity (0.90-0.91).

Conclusions:

  • The developed nomogram shows significant predictive accuracy for CA in LVH.
  • This tool can enhance CA screening using routine echocardiography.
  • It strategically guides further diagnostic evaluations for suspected cardiac amyloidosis.
Abstract