A new method for measurement of total plasma PCSK9: clinical applications

被引:195
作者
Dubuc, Genevieve [1 ]
Tremblay, Michel [1 ]
Pare, Guillaume [4 ]
Jacques, Helene [1 ]
Hamelin, Josee [2 ]
Benjannet, Suzanne [2 ]
Boulet, Lucie [1 ]
Genest, Jacques [3 ]
Bernier, Lise [1 ]
Seidah, Nabil G. [2 ]
Davignon, Jean [1 ]
机构
[1] Clin Res Inst Montreal, Hyperlipidemia & Atherosclerosis Res Grp, Montreal, PQ H2W 1R7, Canada
[2] Clin Res Inst Montreal, Biochem Neuroendocrinol Lab, Montreal, PQ H2W 1R7, Canada
[3] McGill Univ, Royal Victoria Hosp, Cardiovasc Genet Lab, Div Cardiol,Hlth Ctr, Montreal, PQ H3A 1A1, Canada
[4] Harvard Univ, Brigham & Womens Hosp, Sch Med, Div Prevent Med, Boston, MA 02115 USA
关键词
proprotein convertase subtilisin/kexin type 9; LDL-cholesterol; hypercholesterolemia; hypocholesterolemia; ELISA; novel natural mutation; cardiovascular disease; DENSITY-LIPOPROTEIN-RECEPTOR; AUTOSOMAL-DOMINANT HYPERCHOLESTEROLEMIA; FAMILIAL COMBINED HYPERLIPIDEMIA; CORONARY-HEART-DISEASE; LDL RECEPTOR; PROPROTEIN CONVERTASES; LIVER-REGENERATION; APOLIPOPROTEIN-B; STATIN THERAPY; TARGET GENES;
D O I
10.1194/jlr.M900273-JLR200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The proprotein convertase subtilisin kexin-9 (PCSK9) circulates in plasma as mature and furin-cleaved forms. A polyclonal antibody against human PCSK9 was used to develop an ELISA that measures total plasma PCSK9 rather than only the mature form. A cross-sectional study evaluated plasma levels in normal (n = 254) and hypercholesterolemic (n = 200) subjects treated or untreated with statins or statin plus ezetimibe. In controls, mean plasma PCSK9 (89.5 +/- 31.9 ng/ml) correlated positively with age, total cholesterol, LDL-cholesterol (LDL-C), triglycerides, and fasting glucose. Sequencing PCSK9 from individuals at the extremes of the normal PCSK9 distribution identified a new loss-of-function R434W variant associated with lower levels of circulating PCSK9 and LDL-C. In hypercholesterolemic subjects, PCSK9 levels were higher than in controls (99.3 +/- 31.7 ng/ml, P < 0.04) and increased in proportion to the statin dose, combined or not with ezetimibe. In treated patients (n = 139), those with familial hypercholesterolemia (FH; due to LDL receptor gene mutations) had higher PCSK9 values than non-FH (147.01 +/- 42.5 vs. 127.2 +/- 40.8 ng/ml, P < 0.005), but LDL-C reduction correlated positively with achieved plasma PCSK9 levels to a similar extent in both subsets (r = 0.316, P < 0.02 in FH and r = 0.275, P < 0.009 in non-FH). The detection of circulating PCSK9 in both FH and non-FH subjects means that this assay could be used to monitor response to therapy in a wide range of patients.-Dubuc, G., M. Tremblay, G. Pare, H. Jacques, J. Hamelin, S. Benjannet, L. Boulet, J. Genest, L. Bernier, N. G. Seidah, and J. Davignon. A new method for measurement of total plasma PSCK9: clinical applications. J. Lipid Res. 2010. 51: 140-149.
引用
收藏
页码:140 / 149
页数:10
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