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Updated: Nov 30, 2025

Ultrasonic Assessment of Myocardial Microstructure
Published on: January 14, 2014
A simple echocardiographic score to rule out cardiac amyloidosis
Alberto Aimo1, Vladyslav Chubuchny2, Giuseppe Vergaro1,2
1Institute of Life Sciences, Scuola Superiore Sant'Anna, Pisa, Italy.
Insights
The novel AMYLoidosis Index (AMYLI) score effectively screens for cardiac amyloidosis (CA). A low AMYLI score can reliably rule out CA in patients, aiding early diagnosis and treatment initiation.
Area of Science:
- Cardiology
- Medical Diagnostics
- Biomarkers
Background:
- Early diagnosis of cardiac amyloidosis (CA) is crucial for timely treatment and improved patient outcomes.
- Existing scoring systems like AL and IWT have limitations and include complex variables.
- There is a need for simpler, effective screening tools for CA.
Purpose of the Study:
- To develop and validate a simple screening score for cardiac amyloidosis (CA).
- To assess the diagnostic performance of the novel AMYLoidosis Index (AMYLI) score.
- To determine the utility of AMYLI in different patient subsets.
Main Methods:
- A new score, AMYLoidosis Index (AMYLI), was created using relative wall thickness (RWT) and E/e' ratio.
- The diagnostic performance of AMYLI was evaluated in original and validation cohorts.
- Specific cut-off values were determined for ruling out CA in general and specific patient groups.
Main Results:
- The AMYLI score demonstrated high accuracy in diagnosing CA across cohorts.
- A threshold of <2.22 for AMYLI effectively ruled out CA in the general population (LR- 0.0).
- Specific cut-offs of <2.36 and <2.22 were identified for AL CA and unexplained hypertrophy subsets, respectively.
Conclusions:
- The AMYLI score (RWT*E/e') shows promise as an initial screening tool for CA.
- Low AMYLI values can reliably exclude CA diagnosis in various clinical scenarios.
- AMYLI offers a simplified approach to CA screening, potentially improving early detection rates.
Background:
Early diagnosis of cardiac amyloidosis (CA) is warranted to initiate specific treatment and improve outcome. The amyloid light chain (AL) and inferior wall thickness (IWT) scores have been proposed to assess patients referred by haematologists or with unexplained left ventricular (LV) hypertrophy, respectively. These scores are composed of 4 or 5 variables, respectively, including strain data.
Methods:
Based on 2 variables common to the AL and IWT scores, we defined a simple score named AMYLoidosis Index (AMYLI) as the product of relative wall thickness (RWT) and E/e' ratio, and assessed its diagnostic performance.
Results:
In the original cohort (n = 251), CA was ultimately diagnosed in 111 patients (44%). The 2.22 value was selected as rule-out cut-off (negative likelihood ratio [LR-] 0.0). In the haematology subset, AL CA was diagnosed in 32 patients (48%), with 2.36 as rule-out cut-off (LR- 0.0). In the hypertrophy subset, ATTR CA was diagnosed in 79 patients (43%), with 2.22 as the best rule-out cut-off (LR- 0.0). In the validation cohort (n = 691), the same cut-offs proved effective: indeed, there were no patients with CA in the whole population or in the haematology or hypertrophy subsets scoring < 2.22, <2.36 or < 2.22, respectively.
Conclusions:
The AMYLI score (RWT*E/e') may have a role as an initial screening tool for CA. A < 2.22 value excludes the diagnosis in patients undergoing a diagnostic screening for CA, while a < 2.36 and a < 2.22 value may be better considered in the subsets with suspected cardiac AL amyloidosis or unexplained hypertrophy, respectively.
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