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Diagnostic Performance of the Mayo ATTR-CM Score in Diverse Populations: Comparison With the AMY Score
Patricia Carey1, Nelson I Barrera2, Gregorio Tersalvi1
1Mayo Clinic, Rochester, Minnesota, USA.
Insights
The Mayo ATTR-CM score effectively identifies transthyretin amyloid cardiomyopathy (ATTR-CM) in diverse populations, outperforming the AMY score. This tool aids in earlier ATTR-CM detection across various patient groups.
Area of Science:
- Cardiology
- Medical Diagnostics
- Genetics
Background:
- Existing transthyretin amyloid cardiomyopathy (ATTR-CM) risk scores (Mayo ATTR-CM and AMY) were primarily developed in White male cohorts with preserved ejection fraction (EF).
- The performance of these scores in diverse racial, ethnic, and sex populations, and across the full EF spectrum, remains uncertain.
Purpose of the Study:
- To validate and compare the performance of the Mayo ATTR-CM and AMY scores.
- To assess score performance across racially, ethnically, and sex-diverse populations.
- To evaluate score performance across the full ejection fraction (EF) spectrum.
Main Methods:
- Two cohorts were analyzed: a Mayo Clinic referral cohort (n=1,553) and the SCAN-MP community-based study of Black or Caribbean Hispanic individuals (n=646).
- Score calculations followed published methods.
- Discrimination was assessed using receiver operating characteristic-area under the curve (AUC), with comparisons via DeLong's test.
Main Results:
- The Mayo ATTR-CM score showed superior discrimination in both cohorts (AUC 0.86 Mayo; 0.81 SCAN-MP) compared to the AMY score (AUC 0.67 Mayo; 0.70 SCAN-MP).
- Performance of the Mayo ATTR-CM score remained robust in individuals with EF <40% and in women.
- The AMY score exhibited lower sensitivity across both cohorts.
Conclusions:
- The Mayo ATTR-CM score demonstrates strong and consistent performance across diverse populations, including women, Black, and Hispanic individuals, and those with reduced EF.
- The Mayo ATTR-CM score outperforms the AMY score.
- Automated implementation of the Mayo ATTR-CM score, using routinely available data, may facilitate earlier ATTR-CM detection.
Background:
The Mayo transthyretin amyloid cardiomyopathy (ATTR-CM) and AMY scores were developed to identify patients at risk for ATTR-CM. However, both were derived largely from White male cohorts with preserved ejection fraction (EF ≥40%) and their performance in more diverse populations is uncertain.
Objectives:
The objective of the study was to validate and compare performance of the Mayo ATTR-CM and AMY scores across racially, ethnically, and sex-diverse populations, and across the EF spectrum.
Methods:
Two complementary cohorts were evaluated: a Mayo Clinic cardiac amyloid radionuclide imaging referral cohort (n = 1,553; 449 [29%] ATTR-CM) and Screening for Cardiac Amyloidosis With Nuclear Imaging in Minority Populations (SCAN-MP), a prospective community-based study of Black or Caribbean Hispanic individuals (n = 646; 43 [6.6%] ATTR-CM). Scores were calculated as published. Discrimination was assessed using receiver operating characteristic-area under the curve (AUC), with comparisons performed using DeLong's nonparametric method.
Results:
The Mayo ATTR-CM score demonstrated superior discrimination in both cohorts (AUC: 0.86; 95% CI: 0.84-0.88 Mayo; AUC: 0.81; 95% CI: 0.75-0.87 SCAN-MP) compared with AMY (AUC: 0.67; 95% CI: 0.64-0.70 Mayo; AUC: 0.70; 95% CI: 0.62-0.78 SCAN-MP; DeLong P < 0.001 for both). Performance remained robust among individuals with EF <40% and among women. The AMY score showed lower sensitivity across cohorts. Among individuals exceeding score cutoffs, the probability of ATTR-CM ranged from ∼1 in 2 in the Mayo cohort to ∼1 in 6 in SCAN-MP.
Conclusions:
The Mayo ATTR-CM score demonstrates strong, consistent performance across diverse populations, including women, Black, and Hispanic individuals, and those with reduced EF, and outperforms the AMY score. Its reliance on routinely available clinical and echocardiographic data supports automated implementation and may facilitate earlier detection of ATTR-CM.
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