Light‐chain and transthyretin cardiac amyloidosis in severe aortic stenosis: prevalence, screening possibilities, and outcome. (20th February 2020)
- Record Type:
- Journal Article
- Title:
- Light‐chain and transthyretin cardiac amyloidosis in severe aortic stenosis: prevalence, screening possibilities, and outcome. (20th February 2020)
- Main Title:
- Light‐chain and transthyretin cardiac amyloidosis in severe aortic stenosis: prevalence, screening possibilities, and outcome
- Authors:
- Nitsche, Christian
Aschauer, Stefan
Kammerlander, Andreas A.
Schneider, Matthias
Poschner, Thomas
Duca, Franz
Binder, Christina
Koschutnik, Matthias
Stiftinger, Julian
Goliasch, Georg
Siller‐Matula, Jolanta
Winter, Max‐Paul
Anvari‐Pirsch, Anahit
Andreas, Martin
Geppert, Alexander
Beitzke, Dietrich
Loewe, Christian
Hacker, Marcus
Agis, Hermine
Kain, Renate
Lang, Irene
Bonderman, Diana
Hengstenberg, Christian
Mascherbauer, Julia - Abstract:
- Abstract: Aims: Concomitant cardiac amyloidosis (CA) in severe aortic stenosis (AS) is difficult to recognize, since both conditions are associated with concentric left ventricular thickening. We aimed to assess type, frequency, screening parameters, and prognostic implications of CA in AS. Methods and results: A total of 191 consecutive AS patients (81.2 ± 7.4 years; 50.3% female) scheduled for transcatheter aortic valve replacement (TAVR) were prospectively enrolled. Overall, 81.7% underwent complete assessment including echocardiography with strain analysis, electrocardiography (ECG), cardiac magnetic resonance imaging (CMR), 99m Tc‐DPD scintigraphy, serum and urine free light chain measurement, and myocardial biopsy in immunoglobulin light chain (AL)‐CA. Voltage/mass ratio (VMR; Sokolow–Lyon index on ECG/left ventricular mass index) and stroke volume index (SVi) were tested as screening parameters. Receiver operating characteristic curve, binary logistic regression, and Kaplan–Meier curve analyses were performed. CA was found in 8.4% of patients ( n = 16); 15 had transthyretin (TTR)‐CA and one AL‐CA. While global longitudinal strain by echo did not reliably differentiate AS from CA‐AS [area under the curve (AUC) 0.643], VMR as well as SVi showed good discriminative power (AUC 0.770 and 0.773, respectively), which was comparable to extracellular volume by CMR (AUC 0.756). Also, VMR and SVi were independently associated with CA by multivariate logistic regression analysisAbstract: Aims: Concomitant cardiac amyloidosis (CA) in severe aortic stenosis (AS) is difficult to recognize, since both conditions are associated with concentric left ventricular thickening. We aimed to assess type, frequency, screening parameters, and prognostic implications of CA in AS. Methods and results: A total of 191 consecutive AS patients (81.2 ± 7.4 years; 50.3% female) scheduled for transcatheter aortic valve replacement (TAVR) were prospectively enrolled. Overall, 81.7% underwent complete assessment including echocardiography with strain analysis, electrocardiography (ECG), cardiac magnetic resonance imaging (CMR), 99m Tc‐DPD scintigraphy, serum and urine free light chain measurement, and myocardial biopsy in immunoglobulin light chain (AL)‐CA. Voltage/mass ratio (VMR; Sokolow–Lyon index on ECG/left ventricular mass index) and stroke volume index (SVi) were tested as screening parameters. Receiver operating characteristic curve, binary logistic regression, and Kaplan–Meier curve analyses were performed. CA was found in 8.4% of patients ( n = 16); 15 had transthyretin (TTR)‐CA and one AL‐CA. While global longitudinal strain by echo did not reliably differentiate AS from CA‐AS [area under the curve (AUC) 0.643], VMR as well as SVi showed good discriminative power (AUC 0.770 and 0.773, respectively), which was comparable to extracellular volume by CMR (AUC 0.756). Also, VMR and SVi were independently associated with CA by multivariate logistic regression analysis ( P = 0.016 and P = 0.027, respectively). CA did not significantly affect survival 15.3 ± 7.9 months after TAVR ( P = 0.972). Conclusion: Both TTR‐ and AL‐CA can accompany severe AS. Parameters solely based on ECG and echocardiography allow for the identification of the majority of CA‐AS. In the present cohort, CA did not significantly worsen prognosis 15.3 months after TAVR. … (more)
- Is Part Of:
- European journal of heart failure. Volume 22:Number 10(2020)
- Journal:
- European journal of heart failure
- Issue:
- Volume 22:Number 10(2020)
- Issue Display:
- Volume 22, Issue 10 (2020)
- Year:
- 2020
- Volume:
- 22
- Issue:
- 10
- Issue Sort Value:
- 2020-0022-0010-0000
- Page Start:
- 1852
- Page End:
- 1862
- Publication Date:
- 2020-02-20
- Subjects:
- Aortic stenosis -- Cardiac amyloidosis -- Transcatheter aortic valve replacement -- Screening -- Prognosis
Heart failure -- Periodicals
Heart Failure -- Periodicals
Insuffisance cardiaque -- Périodiques
Heart failure
Periodicals
616.129005 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1879-0844 ↗
http://rave.ohiolink.edu/ejournals/issn/13889842/ ↗
http://www.sciencedirect.com/science/journal/13889842 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/ejhf.1756 ↗
- Languages:
- English
- ISSNs:
- 1388-9842
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3829.729860
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