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Cited by 313

The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.

Atorvastatin increases human serum levels of proprotein convertase subtilisin/kexin type 9

Open access
Careskey, Holly E., Davis, R. Aleks, Alborn, William E., Troutt, Jason S., Cao, Guoqing, Konrad, Robert J.·2008·Journal of Lipid Research

Abstract

Proprotein convertase subtilisin/kexin type 9 (PCSK9) has gained attention as a key regulator of serum low density lipoprotein cholesterol (LDL-C) levels. This novel protease causes the degradation of hepatic low density lipoprotein receptors. In humans, gain-of-function mutations in PCSK9 cause a form of familial hypercholesterolemia, whereas loss-of-function mutations result in significantly decreased LDL-C levels and cardiovascular risk. Previous studies have demonstrated that statins upregulate PCSK9 mRNA expression in cultured cells and animal models. In light of these observations, we studied the effect of atorvastatin on circulating PCSK9 protein levels in humans using a sandwich ELISA to quantitate serum PCSK9 levels in patients treated with atorvastatin or placebo for 16 weeks. We observed that atorvastatin (40 mg/day) significantly increased circulating PCSK9 levels by 34% compared with baseline and placebo and decreased LDL-C levels by 42%. These results suggest that the addition of a PCSK9 inhibitor to statin therapy may result in even further LDL-C decreases.

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Crossref · 10.1194/jlr.m700437-jlr200

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Metadata

Authors
Careskey, H. E., Davis, R. A., Alborn, W. E., Troutt, J. S., Cao, G., & Konrad, R. J.
Venue
Journal of Lipid Research
Publisher
Elsevier BV
Published
2008-02
Volume
49
Issue
2
Pages
394-398
ISSN
0022-2275 (ISSN-L)
OpenAlex
W2119708151
Cited by
313
References
4
FWCI
11.01
Type
journal article
Language
en
Open access
hybrid

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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