Lipoprotein(a) in patients with aortic stenosis: Insights from cardiovascular magnetic resonance

Aortic stenosis is the most common age-related valvular pathology. Patients with aortic stenosis and myocardial fibrosis have worse outcome but the underlying mechanism is unclear. Lipoprotein(a) is associated with adverse cardiovascular risk and is elevated in patients with aortic stenosis. Althoug...

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Published in:PloS one Vol. 12; no. 7; p. e0181077
Main Authors: Vassiliou, Vassilios S, Flynn, Paul D, Raphael, Claire E, Newsome, Simon, Khan, Tina, Ali, Aamir, Halliday, Brian, Studer Bruengger, Annina, Malley, Tamir, Sharma, Pranev, Selvendran, Subothini, Aggarwal, Nikhil, Sri, Anita, Berry, Helen, Donovan, Jackie, Lam, Willis, Auger, Dominique, Cook, Stuart A, Pennell, Dudley J, Prasad, Sanjay K
Format: Journal Article
Language:English
Published: United States Public Library of Science 13-07-2017
Public Library of Science (PLoS)
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Summary:Aortic stenosis is the most common age-related valvular pathology. Patients with aortic stenosis and myocardial fibrosis have worse outcome but the underlying mechanism is unclear. Lipoprotein(a) is associated with adverse cardiovascular risk and is elevated in patients with aortic stenosis. Although mechanistic pathways could link Lipoprotein(a) with myocardial fibrosis, whether the two are related has not been previously explored. In this study, we investigated whether elevated Lipoprotein(a) was associated with the presence of myocardial replacement fibrosis. A total of 110 patients with mild, moderate and severe aortic stenosis were assessed by late gadolinium enhancement (LGE) cardiovascular magnetic resonance to identify fibrosis. Mann Whitney U tests were used to assess for evidence of an association between Lp(a) and the presence or absence of myocardial fibrosis and aortic stenosis severity and compared to controls. Univariable and multivariable linear regression analysis were undertaken to identify possible predictors of Lp(a). Thirty-six patients (32.7%) had no LGE enhancement, 38 (34.6%) had midwall enhancement suggestive of midwall fibrosis and 36 (32.7%) patients had subendocardial myocardial fibrosis, typical of infarction. The aortic stenosis patients had higher Lp(a) values than controls, however, there was no significant difference between the Lp(a) level in mild, moderate or severe aortic stenosis. No association was observed between midwall or infarction pattern fibrosis and Lipoprotein(a), in the mild/moderate stenosis (p = 0.91) or severe stenosis patients (p = 0.42). There is no evidence to suggest that higher Lipoprotein(a) leads to increased myocardial midwall or infarction pattern fibrosis in patients with aortic stenosis.
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Competing Interests: Professor Pennell is a consultant to ApoPharma, director of Cardiovascular Imaging Solutions., London, United Kingdom and reports personal fees from Siemens outside the submitted work. Dr Prasad reports personal fees from Bayer outside the submitted work. This does not alter our adherence to PLOS ONE policies on sharing data and materials. The other authors have declared that no competing interests exist.
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0181077