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Effects of the high-density lipoprotein mimetic agent CER-001 on coronary atherosclerosis in patients with acute coronary syndromes: a randomized trial(†)
AIM: High-density lipoproteins (HDLs) have several potentially protective vascular effects. Most clinical studies of therapies targeting HDL have failed to show benefits vs. placebo. OBJECTIVE: To investigate the effects of an HDL-mimetic agent on atherosclerosis by intravascular ultrasonography (IV...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4258222/ https://www.ncbi.nlm.nih.gov/pubmed/24780501 http://dx.doi.org/10.1093/eurheartj/ehu171 |
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author | Tardif, Jean-Claude Ballantyne, Christie M. Barter, Philip Dasseux, Jean-Louis Fayad, Zahi A. Guertin, Marie-Claude Kastelein, John J. P. Keyserling, Constance Klepp, Heather Koenig, Wolfgang L'Allier, Philippe L. Lespérance, Jacques Lüscher, Thomas F. Paolini, John F. Tawakol, Ahmed Waters, David D. Pfeffer, M. Brown, V. Rouleau, J. Watkins, P. Wei, L.J. Gosselin, G. Chayer, C. Lanthier, S. Pelletier, G.B. Racine, N. Agarwal, H. Brilakis, E. Cannon, L. Carrié, D. Corbelli, J. Coste, P. de Winter, R. Diaz, A. Eisenberg, S. Ennis, B. Fajadet, J. Fam, N. Fortuin, D. Gessler, C. Grines, C. Guerra, D. Gum, H. Haldis, T. Heestermans, T. Herrman, J.P. Huynh, T. Kedhi, E. Koren, M. Kouz, S. Krolick, M. Kumkumian, G. Lavi, S. Li, R.J. Masud, ARZ McAlhany, C. McGrew, F.A. O'Shaughnessy, C. Oude Ophuis, A.J.M. Parr, K. Penny, W. Pesant, Y. Post, H. Robinson, S. Rodes-Cabau, J. Roy, A. Schulman, S. Spence, F. Stouffer, G. Stys, T. Sussex, B. Tahirkheli, N. Tardif, J-C. Grégoire, J. ten Berg, J. van Boven, A.J. von Birgelen, C. Weinstein, D. |
author_facet | Tardif, Jean-Claude Ballantyne, Christie M. Barter, Philip Dasseux, Jean-Louis Fayad, Zahi A. Guertin, Marie-Claude Kastelein, John J. P. Keyserling, Constance Klepp, Heather Koenig, Wolfgang L'Allier, Philippe L. Lespérance, Jacques Lüscher, Thomas F. Paolini, John F. Tawakol, Ahmed Waters, David D. Pfeffer, M. Brown, V. Rouleau, J. Watkins, P. Wei, L.J. Gosselin, G. Chayer, C. Lanthier, S. Pelletier, G.B. Racine, N. Agarwal, H. Brilakis, E. Cannon, L. Carrié, D. Corbelli, J. Coste, P. de Winter, R. Diaz, A. Eisenberg, S. Ennis, B. Fajadet, J. Fam, N. Fortuin, D. Gessler, C. Grines, C. Guerra, D. Gum, H. Haldis, T. Heestermans, T. Herrman, J.P. Huynh, T. Kedhi, E. Koren, M. Kouz, S. Krolick, M. Kumkumian, G. Lavi, S. Li, R.J. Masud, ARZ McAlhany, C. McGrew, F.A. O'Shaughnessy, C. Oude Ophuis, A.J.M. Parr, K. Penny, W. Pesant, Y. Post, H. Robinson, S. Rodes-Cabau, J. Roy, A. Schulman, S. Spence, F. Stouffer, G. Stys, T. Sussex, B. Tahirkheli, N. Tardif, J-C. Grégoire, J. ten Berg, J. van Boven, A.J. von Birgelen, C. Weinstein, D. |
author_sort | Tardif, Jean-Claude |
collection | PubMed |
description | AIM: High-density lipoproteins (HDLs) have several potentially protective vascular effects. Most clinical studies of therapies targeting HDL have failed to show benefits vs. placebo. OBJECTIVE: To investigate the effects of an HDL-mimetic agent on atherosclerosis by intravascular ultrasonography (IVUS) and quantitative coronary angiography (QCA). DESIGN AND SETTING: A prospective, double-blinded, randomized trial was conducted at 51 centres in the USA, the Netherlands, Canada, and France. Intravascular ultrasonography and QCA were performed to assess coronary atherosclerosis at baseline and 3 (2–5) weeks after the last study infusion. PATIENTS: Five hundred and seven patients were randomized; 417 and 461 had paired IVUS and QCA measurements, respectively. INTERVENTION: Patients were randomized to receive 6 weekly infusions of placebo, 3 mg/kg, 6 mg/kg, or 12 mg/kg CER-001. MAIN OUTCOME MEASURES: The primary efficacy parameter was the nominal change in the total atheroma volume. Nominal changes in per cent atheroma volume on IVUS and coronary scores on QCA were also pre-specified endpoints. RESULTS: The nominal change in the total atheroma volume (adjusted means) was −2.71, −3.13, −1.50, and −3.05 mm(3) with placebo, CER-001 3 mg/kg, 6 mg/kg, and 12 mg/kg, respectively (primary analysis of 12 mg/kg vs. placebo: P = 0.81). There was also no difference among groups for the nominal change in per cent atheroma volume (0.02, −0.02, 0.01, and 0.19%; nominal P = 0.53 for 12 mg/kg vs. placebo). Change in the coronary artery score was −0.022, −0.036, −0.022, and −0.015 mm (nominal P = 0.25, 0.99, 0.55), and change in the cumulative coronary stenosis score was −0.51, 2.65, 0.71, and −0.77% (compared with placebo, nominal P = 0.85 for 12 mg/kg and nominal P = 0.01 for 3 mg/kg). The number of patients with major cardiovascular events was 10 (8.3%), 16 (13.3%), 17 (13.7%), and 12 (9.8%) in the four groups. CONCLUSION: CER-001 infusions did not reduce coronary atherosclerosis on IVUS and QCA when compared with placebo. Whether CER-001 administered in other regimens or to other populations could favourably affect atherosclerosis must await further study. Name of the trial registry: Clinicaltrials.gov; Registry's URL: http://clinicaltrials.gov/ct2/show/NCT01201837?term=cer-001&rank=2; Trial registration number: NCT01201837. |
format | Online Article Text |
id | pubmed-4258222 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-42582222014-12-08 Effects of the high-density lipoprotein mimetic agent CER-001 on coronary atherosclerosis in patients with acute coronary syndromes: a randomized trial(†) Tardif, Jean-Claude Ballantyne, Christie M. Barter, Philip Dasseux, Jean-Louis Fayad, Zahi A. Guertin, Marie-Claude Kastelein, John J. P. Keyserling, Constance Klepp, Heather Koenig, Wolfgang L'Allier, Philippe L. Lespérance, Jacques Lüscher, Thomas F. Paolini, John F. Tawakol, Ahmed Waters, David D. Pfeffer, M. Brown, V. Rouleau, J. Watkins, P. Wei, L.J. Gosselin, G. Chayer, C. Lanthier, S. Pelletier, G.B. Racine, N. Agarwal, H. Brilakis, E. Cannon, L. Carrié, D. Corbelli, J. Coste, P. de Winter, R. Diaz, A. Eisenberg, S. Ennis, B. Fajadet, J. Fam, N. Fortuin, D. Gessler, C. Grines, C. Guerra, D. Gum, H. Haldis, T. Heestermans, T. Herrman, J.P. Huynh, T. Kedhi, E. Koren, M. Kouz, S. Krolick, M. Kumkumian, G. Lavi, S. Li, R.J. Masud, ARZ McAlhany, C. McGrew, F.A. O'Shaughnessy, C. Oude Ophuis, A.J.M. Parr, K. Penny, W. Pesant, Y. Post, H. Robinson, S. Rodes-Cabau, J. Roy, A. Schulman, S. Spence, F. Stouffer, G. Stys, T. Sussex, B. Tahirkheli, N. Tardif, J-C. Grégoire, J. ten Berg, J. van Boven, A.J. von Birgelen, C. Weinstein, D. Eur Heart J FASTTrack Clinical Research AIM: High-density lipoproteins (HDLs) have several potentially protective vascular effects. Most clinical studies of therapies targeting HDL have failed to show benefits vs. placebo. OBJECTIVE: To investigate the effects of an HDL-mimetic agent on atherosclerosis by intravascular ultrasonography (IVUS) and quantitative coronary angiography (QCA). DESIGN AND SETTING: A prospective, double-blinded, randomized trial was conducted at 51 centres in the USA, the Netherlands, Canada, and France. Intravascular ultrasonography and QCA were performed to assess coronary atherosclerosis at baseline and 3 (2–5) weeks after the last study infusion. PATIENTS: Five hundred and seven patients were randomized; 417 and 461 had paired IVUS and QCA measurements, respectively. INTERVENTION: Patients were randomized to receive 6 weekly infusions of placebo, 3 mg/kg, 6 mg/kg, or 12 mg/kg CER-001. MAIN OUTCOME MEASURES: The primary efficacy parameter was the nominal change in the total atheroma volume. Nominal changes in per cent atheroma volume on IVUS and coronary scores on QCA were also pre-specified endpoints. RESULTS: The nominal change in the total atheroma volume (adjusted means) was −2.71, −3.13, −1.50, and −3.05 mm(3) with placebo, CER-001 3 mg/kg, 6 mg/kg, and 12 mg/kg, respectively (primary analysis of 12 mg/kg vs. placebo: P = 0.81). There was also no difference among groups for the nominal change in per cent atheroma volume (0.02, −0.02, 0.01, and 0.19%; nominal P = 0.53 for 12 mg/kg vs. placebo). Change in the coronary artery score was −0.022, −0.036, −0.022, and −0.015 mm (nominal P = 0.25, 0.99, 0.55), and change in the cumulative coronary stenosis score was −0.51, 2.65, 0.71, and −0.77% (compared with placebo, nominal P = 0.85 for 12 mg/kg and nominal P = 0.01 for 3 mg/kg). The number of patients with major cardiovascular events was 10 (8.3%), 16 (13.3%), 17 (13.7%), and 12 (9.8%) in the four groups. CONCLUSION: CER-001 infusions did not reduce coronary atherosclerosis on IVUS and QCA when compared with placebo. Whether CER-001 administered in other regimens or to other populations could favourably affect atherosclerosis must await further study. Name of the trial registry: Clinicaltrials.gov; Registry's URL: http://clinicaltrials.gov/ct2/show/NCT01201837?term=cer-001&rank=2; Trial registration number: NCT01201837. Oxford University Press 2014-12-07 2014-04-29 /pmc/articles/PMC4258222/ /pubmed/24780501 http://dx.doi.org/10.1093/eurheartj/ehu171 Text en © The Author 2014. Published by Oxford University Press on behalf of the European Society of Cardiology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | FASTTrack Clinical Research Tardif, Jean-Claude Ballantyne, Christie M. Barter, Philip Dasseux, Jean-Louis Fayad, Zahi A. Guertin, Marie-Claude Kastelein, John J. P. Keyserling, Constance Klepp, Heather Koenig, Wolfgang L'Allier, Philippe L. Lespérance, Jacques Lüscher, Thomas F. Paolini, John F. Tawakol, Ahmed Waters, David D. Pfeffer, M. Brown, V. Rouleau, J. Watkins, P. Wei, L.J. Gosselin, G. Chayer, C. Lanthier, S. Pelletier, G.B. Racine, N. Agarwal, H. Brilakis, E. Cannon, L. Carrié, D. Corbelli, J. Coste, P. de Winter, R. Diaz, A. Eisenberg, S. Ennis, B. Fajadet, J. Fam, N. Fortuin, D. Gessler, C. Grines, C. Guerra, D. Gum, H. Haldis, T. Heestermans, T. Herrman, J.P. Huynh, T. Kedhi, E. Koren, M. Kouz, S. Krolick, M. Kumkumian, G. Lavi, S. Li, R.J. Masud, ARZ McAlhany, C. McGrew, F.A. O'Shaughnessy, C. Oude Ophuis, A.J.M. Parr, K. Penny, W. Pesant, Y. Post, H. Robinson, S. Rodes-Cabau, J. Roy, A. Schulman, S. Spence, F. Stouffer, G. Stys, T. Sussex, B. Tahirkheli, N. Tardif, J-C. Grégoire, J. ten Berg, J. van Boven, A.J. von Birgelen, C. Weinstein, D. Effects of the high-density lipoprotein mimetic agent CER-001 on coronary atherosclerosis in patients with acute coronary syndromes: a randomized trial(†) |
title | Effects of the high-density lipoprotein mimetic agent CER-001 on coronary atherosclerosis in patients with acute coronary syndromes: a randomized trial(†) |
title_full | Effects of the high-density lipoprotein mimetic agent CER-001 on coronary atherosclerosis in patients with acute coronary syndromes: a randomized trial(†) |
title_fullStr | Effects of the high-density lipoprotein mimetic agent CER-001 on coronary atherosclerosis in patients with acute coronary syndromes: a randomized trial(†) |
title_full_unstemmed | Effects of the high-density lipoprotein mimetic agent CER-001 on coronary atherosclerosis in patients with acute coronary syndromes: a randomized trial(†) |
title_short | Effects of the high-density lipoprotein mimetic agent CER-001 on coronary atherosclerosis in patients with acute coronary syndromes: a randomized trial(†) |
title_sort | effects of the high-density lipoprotein mimetic agent cer-001 on coronary atherosclerosis in patients with acute coronary syndromes: a randomized trial(†) |
topic | FASTTrack Clinical Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4258222/ https://www.ncbi.nlm.nih.gov/pubmed/24780501 http://dx.doi.org/10.1093/eurheartj/ehu171 |
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