Key result
A high likelihood of concomitant cardiac amyloidosis in patients undergoing TAVI was associated with higher 3-year mortality (44% vs 29%), which was attenuated after adjustment for baseline risk (HR 1.2, p=0.065).
Why the study?
Data on the prevalence of coexisting aortic stenosis and transthyretin cardiac amyloidosis across AS flow groups are limited.
Does the likelihood of concomitant cardiac amyloidosis affect procedural outcomes and long-term survival in patients undergoing TAVI for severe aortic stenosis?
Cohort (n=2,764)
No
Does the likelihood of concomitant cardiac amyloidosis affect procedural outcomes and long-term survival in patients undergoing TAVI for severe aortic stenosis?
Hazard Ratio: 1.2 (95% CI 0.99–1.53)
Absolute Event Rate: 44% vs 29%
p-value: p=0.065
In patients undergoing TAVI, a high likelihood of concomitant cardiac amyloidosis is present in about 9% of cases across all flow groups and is associated with increased mortality that is largely driven by baseline comorbidities rather than the dual pathology itself.
Background: Aortic stenosis (AS) and transthyretin cardiac amyloidosis (CA) may coexist with overlapping clinical and imaging features. Data on the prevalence of this dual pathology (AS-CA) across AS flow groups are limited. This study assessed the likelihood of AS-CA in different AS flow groups and its association with outcomes after transcatheter aortic valve implantation (TAVI). Methods: We retrospectively analyzed 2764 patients (median age 82 years, 55% male) undergoing TAVI for severe native AS between 2017 and 2022). High likelihood of AS-CA was defined as RAISE score ≥ 3 points together with a T-AMYLO score ≥ 3 + red-flag criteria, or a T-AMYLO score ≥ 7 points. Procedural outcomes and long-term survival were evaluated. Conclusion: Dual pathology of AS-CA is likely present in approximately 9% of TAVI patients and is not confined to specific AS flow groups. Although procedural outcomes are comparable, AS-CA is associated with increased mortality, largely driven by baseline risk. Further studies are needed to improve diagnostic strategies and clarify the underlying mechanisms.
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Schwarting et al. (2026) conducted a cohort in Severe native aortic stenosis (n=2,764). High likelihood of concomitant cardiac amyloidosis (AS-CA) vs. Lone aortic stenosis was evaluated on 3-year all-cause mortality (adjusted for STS score) (HR 1.2, 95% CI 0.99-1.53, p=0.065). A high likelihood of concomitant cardiac amyloidosis in patients undergoing TAVI was associated with higher 3-year mortality (44% vs 29%), which was attenuated after adjustment for baseline risk (HR 1.2, p=0.065).
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