TY - JOUR
T1 - The PCSK9 decade
AU - Lambert, Gilles
AU - Sjouke, Barbara
AU - Choque, Benjamin
AU - Kastelein, John J. P.
AU - Hovingh, G. Kees
PY - 2012
Y1 - 2012
N2 - PCSK9 proprotein convertase subtilisin/kexin type (PCSK9) is a crucial protein in LDL cholesterol (LDL-C) metabolism by virtue of its pivotal role in the degradation of the LDL receptor. In recent years, both in vitro and in vivo studies have greatly supplemented our understanding of the (patho) physiological role of PCSK9 in human biology. In the current review, we summarize studies published or in print before May 2012 concerning the physiological role of PCSK9 in cholesterol metabolism. Moreover, we briefly describe the clinical phenotypes encountered in carriers of mutations in the gene encoding PCSK9. As PCSK9 has emerged as a novel target for LDL-C lowering therapy, methods to inhibit PCSK9 will also be reviewed. Initial data from investigations of PCSK9 inhibition in humans are promising and indicate that PCSK9 inhibition may be a viable new therapeutic option for the treatment of dyslipidemia and associated cardiovascular diseases.-Lambert, G., B. Sjouke, B. Choque, J. J. P. Kastelein, and G. K. Hovingh. The PCSK9 decade. J. Lipid Res. 2012. 53: 2515-2524
AB - PCSK9 proprotein convertase subtilisin/kexin type (PCSK9) is a crucial protein in LDL cholesterol (LDL-C) metabolism by virtue of its pivotal role in the degradation of the LDL receptor. In recent years, both in vitro and in vivo studies have greatly supplemented our understanding of the (patho) physiological role of PCSK9 in human biology. In the current review, we summarize studies published or in print before May 2012 concerning the physiological role of PCSK9 in cholesterol metabolism. Moreover, we briefly describe the clinical phenotypes encountered in carriers of mutations in the gene encoding PCSK9. As PCSK9 has emerged as a novel target for LDL-C lowering therapy, methods to inhibit PCSK9 will also be reviewed. Initial data from investigations of PCSK9 inhibition in humans are promising and indicate that PCSK9 inhibition may be a viable new therapeutic option for the treatment of dyslipidemia and associated cardiovascular diseases.-Lambert, G., B. Sjouke, B. Choque, J. J. P. Kastelein, and G. K. Hovingh. The PCSK9 decade. J. Lipid Res. 2012. 53: 2515-2524
U2 - https://doi.org/10.1194/jlr.R026658
DO - https://doi.org/10.1194/jlr.R026658
M3 - Review article
C2 - 22811413
VL - 53
SP - 2515
EP - 2524
JO - Journal of lipid research
JF - Journal of lipid research
SN - 0022-2275
IS - 12
ER -