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C-reactive protein levels and plaque regression with evolocumab: Insights from GLAGOV
OBJECTIVE: On-treatment levels of high sensitivity C-reactive protein (hsCRP) in statin-treated patients predict plaque progression and the prospective risk of atherosclerotic cardiovascular events. Proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors produce additional LDL-C lowering, r...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8315612/ https://www.ncbi.nlm.nih.gov/pubmed/34327467 http://dx.doi.org/10.1016/j.ajpc.2020.100091 |
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author | Nelson, Adam J. Puri, Rishi Brennan, Danielle M. Anderson, Todd J. Cho, Leslie Ballantyne, Christie M. Kastelein, John JP. Koenig, Wolfgang Kassahun, Helina Somaratne, Ransi M. Wasserman, Scott M. Nissen, Steven E. Nicholls, Stephen J. |
author_facet | Nelson, Adam J. Puri, Rishi Brennan, Danielle M. Anderson, Todd J. Cho, Leslie Ballantyne, Christie M. Kastelein, John JP. Koenig, Wolfgang Kassahun, Helina Somaratne, Ransi M. Wasserman, Scott M. Nissen, Steven E. Nicholls, Stephen J. |
author_sort | Nelson, Adam J. |
collection | PubMed |
description | OBJECTIVE: On-treatment levels of high sensitivity C-reactive protein (hsCRP) in statin-treated patients predict plaque progression and the prospective risk of atherosclerotic cardiovascular events. Proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors produce additional LDL-C lowering, reduce plaque burden and improve cardiovascular outcomes in statin-treated patients. It is unknown whether residual systemic inflammation attenuates their favorable effects on plaque burden. METHODS: GLAGOV compared the effects of treatment for 78 weeks with evolocumab or placebo on progression of coronary atherosclerosis in statin-treated patients with coronary artery disease. Clinical demographics, biochemistry and changes in both the burden (percentage atheroma volume (PAV), total atheroma volume (TAV), n = 413) and composition (n = 162) of coronary plaque were evaluated in evolocumab-treated patients according to baseline hsCRP strata (<1, 1–3, >3 mg/L). RESULTS: The study cohort comprised 413 evolocumab-treated patients (32% low [<1 mg/L], 41% intermediate [1–3 mg/L] and 27% high [>3 mg/L] baseline hsCRP levels). Patients in the highest hsCRP stratum were more likely to be female and had a higher prevalence of diabetes, hypertension, and the metabolic syndrome. LDL-C levels were similar across the groups, however participants with higher hsCRP levels had higher triglyceride and lower HDL-C levels at baseline. At follow-up, the change in PAV from baseline (−0.87% [low] vs. −0.84% [intermediate] vs. −1.22% [high], p = 0.46) and the proportion of patients experiencing any degree of regression (65.9% vs. 63.5% vs. 63.1%, p = 0.88) was similar across hsCRP strata and when evaluated by levels of achieved LDL-C. There were no serial differences in plaque composition by hsCRP strata. CONCLUSION: The ability of evolocumab to induce regression in statin-treated patients is not attenuated by the presence of enhanced systemic inflammation. This underscores the potential benefits of intensive lipid lowering, even in the presence of heightened inflammatory states. |
format | Online Article Text |
id | pubmed-8315612 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-83156122021-07-28 C-reactive protein levels and plaque regression with evolocumab: Insights from GLAGOV Nelson, Adam J. Puri, Rishi Brennan, Danielle M. Anderson, Todd J. Cho, Leslie Ballantyne, Christie M. Kastelein, John JP. Koenig, Wolfgang Kassahun, Helina Somaratne, Ransi M. Wasserman, Scott M. Nissen, Steven E. Nicholls, Stephen J. Am J Prev Cardiol Original Research OBJECTIVE: On-treatment levels of high sensitivity C-reactive protein (hsCRP) in statin-treated patients predict plaque progression and the prospective risk of atherosclerotic cardiovascular events. Proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors produce additional LDL-C lowering, reduce plaque burden and improve cardiovascular outcomes in statin-treated patients. It is unknown whether residual systemic inflammation attenuates their favorable effects on plaque burden. METHODS: GLAGOV compared the effects of treatment for 78 weeks with evolocumab or placebo on progression of coronary atherosclerosis in statin-treated patients with coronary artery disease. Clinical demographics, biochemistry and changes in both the burden (percentage atheroma volume (PAV), total atheroma volume (TAV), n = 413) and composition (n = 162) of coronary plaque were evaluated in evolocumab-treated patients according to baseline hsCRP strata (<1, 1–3, >3 mg/L). RESULTS: The study cohort comprised 413 evolocumab-treated patients (32% low [<1 mg/L], 41% intermediate [1–3 mg/L] and 27% high [>3 mg/L] baseline hsCRP levels). Patients in the highest hsCRP stratum were more likely to be female and had a higher prevalence of diabetes, hypertension, and the metabolic syndrome. LDL-C levels were similar across the groups, however participants with higher hsCRP levels had higher triglyceride and lower HDL-C levels at baseline. At follow-up, the change in PAV from baseline (−0.87% [low] vs. −0.84% [intermediate] vs. −1.22% [high], p = 0.46) and the proportion of patients experiencing any degree of regression (65.9% vs. 63.5% vs. 63.1%, p = 0.88) was similar across hsCRP strata and when evaluated by levels of achieved LDL-C. There were no serial differences in plaque composition by hsCRP strata. CONCLUSION: The ability of evolocumab to induce regression in statin-treated patients is not attenuated by the presence of enhanced systemic inflammation. This underscores the potential benefits of intensive lipid lowering, even in the presence of heightened inflammatory states. Elsevier 2020-10-06 /pmc/articles/PMC8315612/ /pubmed/34327467 http://dx.doi.org/10.1016/j.ajpc.2020.100091 Text en © 2020 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Research Nelson, Adam J. Puri, Rishi Brennan, Danielle M. Anderson, Todd J. Cho, Leslie Ballantyne, Christie M. Kastelein, John JP. Koenig, Wolfgang Kassahun, Helina Somaratne, Ransi M. Wasserman, Scott M. Nissen, Steven E. Nicholls, Stephen J. C-reactive protein levels and plaque regression with evolocumab: Insights from GLAGOV |
title | C-reactive protein levels and plaque regression with evolocumab: Insights from GLAGOV |
title_full | C-reactive protein levels and plaque regression with evolocumab: Insights from GLAGOV |
title_fullStr | C-reactive protein levels and plaque regression with evolocumab: Insights from GLAGOV |
title_full_unstemmed | C-reactive protein levels and plaque regression with evolocumab: Insights from GLAGOV |
title_short | C-reactive protein levels and plaque regression with evolocumab: Insights from GLAGOV |
title_sort | c-reactive protein levels and plaque regression with evolocumab: insights from glagov |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8315612/ https://www.ncbi.nlm.nih.gov/pubmed/34327467 http://dx.doi.org/10.1016/j.ajpc.2020.100091 |
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