Effect of statin therapy on plasma proprotein convertase subtilisin kexin 9 (PCSK9) concentrations: a systematic review and meta-analysis of clinical trials

被引:87
作者
Sahebkar, A. [1 ,2 ]
Simental-Menda, L. E. [3 ]
Guerrero-Romero, F. [3 ]
Golledge, J. [4 ,5 ]
Watts, G. F. [6 ]
机构
[1] Mashhad Univ Med Sci, Biotechnol Res Ctr, Mashhad, Iran
[2] Univ Western Australia, Royal Perth Hosp, Sch Med & Pharmacol, Metab Res Ctr, Perth, WA 6009, Australia
[3] Mexican Social Secur Inst, Biomed Res Unit, Durango, CO, Mexico
[4] James Cook Univ, Coll Med & Dent, Queensland Res Ctr Peripheral Vasc Dis, Vasc Biol Unit, Townsville, Qld 4811, Australia
[5] Townsville Hosp, Dept Vasc & Endovasc Surg, Townsville, Qld, Australia
[6] Univ Western Australia, Royal Perth Hosp, Sch Med & Pharmacol, Lipid Disorders Clin,Cardiovasc Med, Perth, WA 6847, Australia
基金
美国国家科学基金会;
关键词
meta-analysis; statin; PCSK9; LOW-DENSITY-LIPOPROTEIN; DOSE ATORVASTATIN; LDL RECEPTOR; CHOLESTEROL; EZETIMIBE; SIMVASTATIN; METABOLISM; GENE; HYPERCHOLESTEROLEMIA; ROSUVASTATIN;
D O I
10.1111/dom.12536
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims: To evaluate the magnitude of the effect of statin therapy on plasma proprotein convertase subtilisin kexin 9 (PCSK9) levels through a systematic review and meta-analysis of clinical trials. Methods: A random-effects model (using DerSimonian-Laird method) and the generic inverse variance method were used for quantitative data synthesis. Heterogeneity was quantitatively assessed using the I-2 index. Sensitivity analyses were conducted using the one-study remove approach. Random-effects meta-regression was performed using an unrestricted maximum likelihood method to evaluate the association between statin-induced elevation of plasma PCSK9 concentrations with duration of treatment and magnitude of LDL cholesterol reduction. Results: A total of 15 clinical trials examining the effects of statin therapy on plasma PCSK9 levels were included. Meta-analysis of data from single-arm statin treatment arms [weighted mean difference (WMD) 40.72 ng/ml, 95% confidence interval (CI) 34.79, 46.65; p< 0.001] and randomized placebo-controlled trials (WMD 22.98 ng/ml, 95% CI 17.95, 28.01; p< 0.001) showed a significant increase in plasma PCSK9 concentrations after statin therapy, irrespective of the type of statin administered in either of the analyses (single-arm or randomized placebo-controlled trial). There was no significant elevation of plasma PCSK9 levels with statin/ezetimibe combination therapy compared with statin monotherapy (WMD 23.14 ng/ml, 95% CI -1.97, 48.25; p = 0.071); however, removal of one study in the meta-analysis yielded a significant result in the sensitivity analysis (WMD 31.41 ng/ml, 95% CI 7.86, 54.97; p = 0.009). Conclusions: This meta-analysis suggests that statin therapy causes a significant increase in plasma PCSK9 concentrations.
引用
收藏
页码:1042 / 1055
页数:14
相关论文
共 51 条
[1]  
[Anonymous], ETHN DIS
[2]   Dual regulation of the LDL receptor - Some clarity and new questions [J].
Attie, AD ;
Seidah, NG .
CELL METABOLISM, 2005, 1 (05) :290-292
[3]   Rosuvastatin, Proprotein Convertase Subtilisin/Kexin Type 9 Concentrations, and LDL Cholesterol Response: the JUPITER Trial [J].
Awan, Zuhier ;
Seidah, Nabil G. ;
MacFadyen, Jean G. ;
Benjannet, Suzanne ;
Chasman, Daniel I. ;
Ridker, Paul M. ;
Genest, Jacques .
CLINICAL CHEMISTRY, 2012, 58 (01) :183-189
[4]   Missense mutations in the PCSK9 gene are associated with hypocholesterolemia and possibly increased response to statin therapy [J].
Berge, KE ;
Ose, L ;
Leren, TP .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2006, 26 (05) :1094-1100
[5]   Evidence from a Randomized Trial That Simvastatin, but Not Ezetimibe, Upregulates Circulating PCSK9 Levels [J].
Berthold, Heiner K. ;
Seidah, Nabil G. ;
Benjannet, Suzanne ;
Gouni-Berthold, Ioanna .
PLOS ONE, 2013, 8 (03)
[6]   A 52-Week Placebo-Controlled Trial of Evolocumab in Hyperlipidemia [J].
Blom, Dirk J. ;
Hala, Tomas ;
Bolognese, Michael ;
Lillestol, Michael J. ;
Toth, Phillip D. ;
Burgess, Lesley ;
Ceska, Richard ;
Roth, Eli ;
Koren, Michael J. ;
Ballantyne, Christie M. ;
Monsalvo, Maria Laura ;
Tsirtsonis, Kate ;
Kim, Jae B. ;
Scott, Rob ;
Wasserman, Scott M. ;
Stein, Evan A. .
NEW ENGLAND JOURNAL OF MEDICINE, 2014, 370 (19) :1809-1819
[7]  
Borenstein M., 2013, BIOSTAT
[8]   Atorvastatin increases human serum levels of proprotein convertase subtilisin/kexin type 9 [J].
Careskey, Holly E. ;
Davis, R. Aleks ;
Alborn, William E. ;
Troutt, Jason S. ;
Cao, Guoqing ;
Konrad, Robert J. .
JOURNAL OF LIPID RESEARCH, 2008, 49 (02) :394-398
[9]   The effects of simvastatin treatment on plasma lipid-related biomarkers in men with dyslipidaemia [J].
Chen, Fabian ;
Maridakis, Vic ;
O'Neill, Edward A. ;
Hubbard, Brian K. ;
Strack, Alison ;
Beals, Chan ;
Herman, Gary A. ;
Wong, Peggy .
BIOMARKERS, 2011, 16 (04) :321-333
[10]   Sequence variations in PCSK9, low LDL, and protection against coronary heart disease [J].
Cohen, JC ;
Boerwinkle, E ;
Mosley, TH ;
Hobbs, HH .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (12) :1264-1272