ArticleFrontiers in cardiovascular medicine2026
Sex differences in amyloid transthyretin cardiomyopathy National Amyloidosis Centre staging at diagnosis: an analysis from a large single-center cohort.
Article in Frontiers in cardiovascular medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Background: Amyloid transthyretin cardiomyopathy (ATTR-CM) is a progressive infiltrative cardiomyopathy that has seen significant advances in diagnosis and treatment over the last two decades. Sex differences in phenotype, treatment response, and long-term outcomes remain poorly understood. Our study aims to describe the factors that contribute to differences in phenotype and long-term outcomes between male and female patients. Methods: This was a single-center retrospective analysis of 334 patients with ATTR-CM seen at Northwestern Memorial Hospital, Chicago, IL, USA. The study included adults >18 years with an ATTR-CM diagnosis (wild-type, variant). Immunoglobulin light chain (AL) amyloidosis patients were excluded. Patients were classified as male or female based on the biological gender described in the electronic medical record. Male patients with ATTR-CM were compared with female patients with ATTR-CM. The National Amyloidosis Centre (NAC) stage was calculated using clinical parameters at the time of diagnosis. The primary outcome was all-cause mortality. Baseline characteristics were compared using chi-squared analysis. Associations were determined using Kaplan-Meier estimation and restricted mean survival time analysis (RMST). Results: The study included 334 patients with ATTR-CM-268 (80%) men and 66 (20%) women. Female patients were diagnosed at higher NAC stages ( Conclusions: Female patients present with ATTR-CM at significantly later NAC stages than men. Despite this, they have a similar mortality rate. Our findings may demonstrate that the NAC stage overestimates disease severity in female patients or, alternatively, that biological mechanisms confer a less aggressive disease phenotype in female patients despite advanced disease staging.
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