Key result
Elevated bio-ADM predicts higher all-cause death and MACE in cardiac amyloidosis.
Why the study?
Bio-ADM predicts clinical outcomes in heart failure, but its prognostic role in cardiac amyloidosis was unknown.
Does elevated bio-ADM predict all-cause death and major adverse cardiovascular events in patients with cardiac amyloidosis?
Does elevated bio-ADM predict all-cause death and major adverse cardiovascular events in patients with cardiac amyloidosis?
Bio-ADM is a strong independent prognostic biomarker in cardiac amyloidosis that significantly improves risk stratification when added to established staging systems for ATTR-CA.
May aid risk stratification beyond current systems in cardiac amyloidosis; extends heart failure data but leaves open prospective validation.
Background Bio‐ADM (bioactive adrenomedullin) is a vasoactive peptide hormone that predicts clinical outcomes in heart failure—the main driver of adverse outcomes in cardiac amyloidosis (CA). This prospective observational study sought to assess the prognostic role of bio‐ADM in CA. Methods Patients with CA were enrolled from amyloid centers in Germany (observation cohort), Japan, and the United States (combined validation cohort). Bio‐ADM was quantified using the sphingotest bio‐ADM assay. Associations of bio‐ADM with all‐cause death and major adverse cardiovascular events over 2 years were assessed using Kaplan–Meier and Cox regression analyses. Likelihood ratio chi‐square tests for nested models evaluated whether adding bio‐ADM improves validated prognostic staging systems. Results In both the German observation cohort (n=86) and the combined validation cohort from Japan and the United States (n=124), elevated bio‐ADM (>29 pg/mL) was associated with more frequent all‐cause death and major adverse cardiovascular events. Bio‐ADM remained independently associated with impaired overall ( P <0.001) and major adverse cardiovascular events‐free survival ( P <0.001) after adjustment for age, sex, and established prognostic biomarkers in the entire cohort. Adding categorized bio‐ADM (>29 pg/mL) significantly improved the prognostic accuracy of the National Amyloidosis Centre (C‐index 0.674 to 0.787; P =0.002) and MayoATTR (C‐index 0.662 to 0.757; P <0.001) staging systems for cardiac transthyretin amyloidosis. Adding bio‐ADM to staging systems for cardiac immunoglobulin light chain amyloidosis yielded no significant changes. Conclusions Bio‐ADM is a promising prognostic biomarker, especially in cardiac transthyretin amyloidosis, where it improved risk stratification when added to established staging systems. Further research is needed to clarify its role as part of staging systems for cardiac immunoglobulin light chain amyloidosis.
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Müller et al. (2025) studied this question. Elevated bio‐ADM levels (>29 pg/mL) predicted higher rates of all-cause death and major adverse cardiovascular events in patients with cardiac amyloidosis.
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