Abstract
Evidence that elevated lipoprotein(a) (Lp[a]) levels contribute to cardiovascular disease (CVD) and calcific aortic valve stenosis (CAVS) is substantial. Development of isoform-independent assays, in concert with genetic, epidemiological, translational, and pathophysiological insights, have established Lp(a) as an independent, genetic, and likely causal risk factor for CVD and CAVS. These observations are consistent across a broad spectrum of patients, risk factors, and concomitant therapies, including patients with low-density lipoprotein cholesterol 80%. These approaches will allow testing of the "Lp(a) hypothesis" in clinical trials. This review summarizes the current landscape of Lp(a), discusses…
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1,103
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- FWCI
- 72.56
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Authors
1Topics & keywords
Topics
Keywords
- PCSK9
- Medicine
- Lipoprotein(a)
- Kexin
- Context (archaeology)
- Internal medicine
- Lipoprotein
- Residual risk
UN Sustainable Development Goals
- Good health and well-being
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