Treatment of patients with cardiovascular disease with L-4F, an apo-A1 mimetic, did not improve select biomarkers of HDL function

被引:123
作者
Watson, Catherine E. [1 ]
Weissbach, Nicole [1 ]
Kjems, Lise [1 ]
Ayalasomayajula, Surya [2 ]
Zhang, Yiming [2 ]
Chang, Ih [2 ]
Navab, Mohamad [3 ]
Hama, Susan [3 ]
Hough, Greg [3 ]
Reddy, Srinivasa T. [3 ]
Soffer, Daniel [4 ]
Rader, Daniel J. [4 ]
Fogelman, Alan M. [3 ]
Schecter, Alison [1 ]
机构
[1] Novartis Inst Biomed Res, Cambridge, MA 02139 USA
[2] Novartis Inst Biomed Res, E Hanover, NJ 07936 USA
[3] Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Los Angeles, CA 90095 USA
[4] Univ Penn, Sch Med, Inst Translat Med & Therapeut, Philadelphia, PA 19104 USA
关键词
apolipoprotein; atherosclerosis; high density lipoprotein; C-reactive protein; coronary heart disease; diabetes; HIGH-DENSITY-LIPOPROTEIN; E-NULL MICE; APOA-I; CHOLESTEROL LEVELS; AMINO-ACIDS; PEPTIDES; PLASMA; D-4F;
D O I
10.1194/jlr.M011098
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
L-4F, an apolipoprotein A-I (apoA-I) mimetic peptide (also known as APL180), was administered daily by either intravenous (IV) infusion for 7 days or by subcutaneous (SC) injection for 28 days in patients with coronary heart disease in two distinct clinical studies. L-4F was well tolerated at all doses tested. Despite achieving plasma levels (mean maximal plasma concentration of 2,907 ng/ml and 395 ng/ml, following IV infusion and SC injection, respectively), that were effective in previously published animal models, treatment with L-4F, as assessed by biomarkers of HDL function such as HDL-inflammatory index (HII), and paraoxonase activity, did not improve. Paradoxically, there was a 49% increase in high-sensitivity C-reactive protein (hs-CRP) levels after seven IV infusions of 30 mg L-4F (P < 0.05; compared with placebo) and a trend for hs-CRP increase in subjects receiving 30 mg SC injection for 28 days. In a subsequent, ex vivo study, addition of L-4F at concentrations of 150, 375, or 1,000 ng/ml to plasma from subjects prior to L-4F treatment resulted in significant dose-dependent HII improvement. In conclusion, in vivo L-4F treatment, delivered by either SC injection or IV infusion, did not improve HDL functional biomarkers despite achieving plasma levels that improved identical biomarkers ex vivo and in animal models.-Watson, C. E., N. Weissbach, L. Kjems, S. Ayalasomayajula, Y. Zhang, I. Chang, M. Navab, S. Hama, G. Hough, S. T. Reddy, D. Soffer, D. J. Rader, A. M. Fogelman, and A. Schecter. Treatment of patients with cardiovascular disease with L-4F, an apo-A1 mimetic, did not improve select biomarkers of HDL function. J. Lipid Res. 2011. 52: 361-373.
引用
收藏
页码:361 / 373
页数:13
相关论文
共 17 条
[1]   Inflammatory/antiinflammatory properties of high-density lipoprotein distinguish patients from control subjects better than high-density lipoprotein cholesterol levels and are favorably affected by simvastatin treatment [J].
Ansell, BJ ;
Navab, M ;
Hama, S ;
Kamranpour, N ;
Fonarow, G ;
Hough, G ;
Rahmani, S ;
Mottahedeh, R ;
Dave, R ;
Reddy, ST ;
Fogelman, AM .
CIRCULATION, 2003, 108 (22) :2751-2756
[2]   Safety, pharmacokinetics, and pharmacodynamics of oral apoA-I mimetic peptide D-4F in high-risk cardiovascular patients [J].
Bloedon, LeAnne T. ;
Dunbar, Richard ;
Duffy, Danielle ;
Pinell-Salles, Paula ;
Norris, Robert ;
DeGroot, Bruce J. ;
Movva, Rajesh ;
Navab, Mohamad ;
Fogelman, Alan M. ;
Rader, Daniel J. .
JOURNAL OF LIPID RESEARCH, 2008, 49 (06) :1344-1352
[3]   TURNOVER OF SYNTHETIC CLASS-A AMPHIPATHIC PEPTIDE ANALOGS OF EXCHANGEABLE APOLIPOPROTEINS IN RATS - CORRELATION WITH PHYSICAL-PROPERTIES [J].
GARBER, DW ;
VENKATACHALAPATHI, YV ;
GUPTA, KB ;
IBDAH, J ;
PHILLIPS, MC ;
HAZELRIG, JB ;
SEGREST, JP ;
ANANTHARAMAIAH, GM .
ARTERIOSCLEROSIS AND THROMBOSIS, 1992, 12 (08) :886-894
[4]   D-4F and statins synergize to render HDL antiinflammatory in mice and monkeys and cause lesion regression in old apolipoprotein E-null mice [J].
Navab, M ;
Anantharamaiah, GM ;
Hama, S ;
Hough, G ;
Reddy, ST ;
Frank, JS ;
Garber, DW ;
Handattu, S ;
Fogelman, AM .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2005, 25 (07) :1426-1432
[5]   Apolipoprotein A-I mimetic peptides [J].
Navab, M ;
Anantharamaiah, GM ;
Reddy, ST ;
Hama, S ;
Hough, G ;
Grijalva, VR ;
Yu, N ;
Ansell, BJ ;
Datta, G ;
Garber, DW ;
Fogelman, AM .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2005, 25 (07) :1325-1331
[6]   Oral D-4F causes formation of pre-β high-density lipoprotein and improves high-density lipoprotein-mediated cholesterol efflux and reverse cholesterol transport from macrophages in apolipoprotein E-null mice [J].
Navab, M ;
Anantharamaiah, GM ;
Reddy, ST ;
Hama, S ;
Hough, G ;
Grijalva, VR ;
Wagner, AC ;
Frank, JS ;
Datta, G ;
Garber, D ;
Fogelman, AM .
CIRCULATION, 2004, 109 (25) :3215-3220
[7]   Oral administration of an apo A-I mimetic peptide synthesized from D-amino acids dramatically reduces atherosclerosis in mice independent of plasma cholesterol [J].
Navab, M ;
Anantharamaiah, GM ;
Hama, S ;
Garber, DW ;
Chaddha, M ;
Hough, G ;
Lallone, R ;
Fogelman, AM .
CIRCULATION, 2002, 105 (03) :290-292
[8]   Structure and Function of HDL Mimetics [J].
Navab, Mohamad ;
Shechter, Ishaiahu ;
Anantharamaiah, G. M. ;
Reddy, Srinivasa T. ;
Van Lenten, Brian J. ;
Fogelman, Alan M. .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2010, 30 (02) :164-168
[9]   HDL as a Biomarker, Potential Therapeutic Target, and Therapy [J].
Navab, Mohamad ;
Anantharamaiah, G. M. ;
Reddy, Srinivasa T. ;
Van Lenten, Brian J. ;
Al Fogelman, Alan .
DIABETES, 2009, 58 (12) :2711-2717
[10]   A novel method for oral delivery of apolipoprotein mimetic peptides synthesized from all L-amino acids [J].
Navab, Mohamad ;
Ruchala, Piotr ;
Waring, Alan J. ;
Lehrer, Robert I. ;
Hama, Susan ;
Hough, Greg ;
Palgunachari, Mayakonda N. ;
Anantharamaiah, G. M. ;
Fogelman, Alan M. .
JOURNAL OF LIPID RESEARCH, 2009, 50 (08) :1538-1547