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High Prevalence of Cardiac Amyloidosis in Clinically Significant Aortic Stenosis: A Meta-Analysis
Samiullah Arshad1, Ythan H Goldberg2, Huzefa Bhopalwala3
1Department of Medicine, University of Kentucky, Lexington, KY, USA.
Insights
Screening aortic stenosis (AS) patients for transthyretin cardiac amyloidosis (CA) is crucial, as 11% have concomitant CA. Coexisting AS and CA are linked to worse outcomes and distinct clinical, imaging, and mortality profiles.
Area of Science:
- Cardiology
- Cardiovascular Research
- Medical Diagnostics
Background:
- Growing evidence highlights the coexistence of aortic stenosis (AS) and transthyretin cardiac amyloidosis (CA).
- Failure to screen AS patients for CA during clinical encounters represents a missed diagnostic opportunity.
Purpose of the Study:
- To determine the prevalence of CA in patients with AS.
- To compare clinical, imaging, and mortality characteristics between patients with AS and concomitant CA (AS-CA) versus AS alone.
Main Methods:
- A systematic survey of studies reporting CA prevalence in AS patients was conducted.
- Meta-regression analysis was performed on studies comparing AS-CA patients with AS-alone patients.
Main Results:
- Nine studies encompassing 1,321 AS patients revealed an 11% prevalence of CA (131 patients).
- AS-CA patients were older, more male, and exhibited higher rates of carpal tunnel syndrome and right bundle branch block.
- Echocardiographic findings in AS-CA included thicker interventricular septum, higher LVMI, and reduced myocardial contraction and stroke volume indices, with a higher incidence of low-flow low-gradient AS.
Conclusions:
- Transthyretin cardiac amyloidosis is highly prevalent in patients with aortic stenosis.
- AS-CA is associated with significantly worse clinical, imaging, and biochemical parameters compared to AS alone.
- Patients with AS-CA demonstrated higher all-cause mortality (33% vs. 22%) at one-year follow-up.
Background:
There is growing evidence of coexistence of aortic stenosis (AS) and transthyretin cardiac amyloidosis (CA). Not screening AS patients at the time of hospital/clinic visit for CA represents a lost opportunity.
Methods:
We surveyed studies that reported the prevalence of CA among AS patients. Studies that compared patients with aortic stenosis with cardiac amyloidosis (AS-CA) and AS alone were further analyzed, and meta-regression was performed.
Results:
We identified nine studies with 1,321 patients of AS, of which 131 patients had concomitant CA, with a prevalence of 11%. When compared to AS-alone, the patients with AS-CA were older, more likely to be males, had higher prevalence of carpal tunnel syndrome, right bundle branch block. On echocardiogram, patients with AS-CA had thicker interventricular septum, higher left ventricular mass index (LVMI), lower myocardial contraction fraction, and lower stroke volume index. Classical low-flow low-gradient (LFLG) physiology was more common among patients with AS-CA. Patients with AS-CA had higher all-cause mortality than patients with AS alone (33% vs. 22%, P = 0.02) in a follow-up period of at least 1 year.
Conclusions:
CA has a high prevalence in patients with AS and is associated with worse clinical, imaging, and biochemical parameters than patients with AS alone.
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