Heart failure & cardiomyopathiesCross-sectional study

First clinical experience with the Transthyretin Amyloidosis-Quality of Life questionnaire (ATTR-QoL): associations with clinical characteristics and established patient-reported outcomes

Eur Heart J Qual Care Clin OutcomesPublished

  • cross-sectional study
  • consecutive ATTR patients
  • Columbia University

Authors' conclusion

ATTR-QOL, as a disease-specific PRO, effectively captures the multidimensional impact of ATTR and is associated with clinical parameters and functionality in patients with ATTR.

Study context

Population
Consecutive ATTR patients at Columbia University between 3/2024 and 1/2025 who completed the ATTR-QOLpatients included · cardiomyopathy 137 · mixed 48 · neuropathy 9
Participants
194 patients
Exposure
ATTR-QOL against clinical parameters, functionality testing (6-minute walk test, Short Physical Performance Battery Test) and established patient-reported outcome (PROs) (Kansas City Cardiomyopathy Questionnaire (KCCQ), SF36v2, COMPASS-31)

Main finding

As reported in the abstract

Convergent validity of ATTR-QOL
  • ATTR-QOL exhibited good convergent validity with clinical parameters, functionality testing, and established quality of life (QOL) tools

Observational data: associations, not effects.

Further findings

Known-groups discriminant validity of ATTR-QOL

ATTR-QOL demonstrated strong known-groups discriminant validity, differentiating between various clinical and functional groups and established PRO categories

Disease stage (National Amyloidosis Centre (NAC))

NAC Stage 1
70%
NAC Stage 2
22%
NAC Stage 3
8%
All on disease-modifying treatment

Original publication

First clinical experience with the Transthyretin Amyloidosis-Quality of Life questionnaire (ATTR-QoL): associations with clinical characteristics and established patient-reported outcomes. Eur Heart J Qual Care Clin Outcomes. Published 12 February 2026. doi:10.1093/ehjqcco/qcag015

Summarised from the published abstract; every number is checked against it