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C-reactive protein and coronary atheroma regression following statin therapy: A meta-regression of randomized controlled trials
OBJECTIVE: Several clinical trials have indicated that statins stabilize and reverse atherosclerotic plaque. However, different studies have provided inconsistent findings regarding mechanisms and influencing factors of plaque regression under statin therapy. Apart from lipid-lowering effect, statin...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9691666/ https://www.ncbi.nlm.nih.gov/pubmed/36440015 http://dx.doi.org/10.3389/fcvm.2022.989527 |
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author | Gao, Darui Hua, Rong Jiesisibieke, Dina Ma, Yanjun Li, Chenglong Wu, Sijing Ma, Qian Xie, Wuxiang |
author_facet | Gao, Darui Hua, Rong Jiesisibieke, Dina Ma, Yanjun Li, Chenglong Wu, Sijing Ma, Qian Xie, Wuxiang |
author_sort | Gao, Darui |
collection | PubMed |
description | OBJECTIVE: Several clinical trials have indicated that statins stabilize and reverse atherosclerotic plaque. However, different studies have provided inconsistent findings regarding mechanisms and influencing factors of plaque regression under statin therapy. Apart from lipid-lowering effect, statins have pleiotropic effects including anti inflammation in humans. In this study, meta-analysis and meta-regression were used to determine the effects of statin medications on coronary plaque volume. Meanwhile, to assess whether statins promote plaque regression effect was related to their anti-inflammatory ability, the impact of CRP/hsCRP reduction during statin therapy on plaque regression was investigated. METHODS: Up to June 15, 2022, a systematic PubMed, EMBASE, and Cochrane search was performed for randomized controlled trials that assessed treatment effect using total atheroma volume (TAV), percent atheroma volume (PAV), or plaque volume (PV). Only CRP/hsCRP and LDL-C values reported before and after treatment were considered. RESULTS: 12 studies (2,812 patients with heart and/or vascular disease) fulfilled the inclusion criteria and were included in the systematic review. A meta-analysis of 15 statin-treated arms reported a significant reduction in change of TAV/PV [standardized mean difference (SMD): –0.27, 95% confidence intervals (–CI): –0.42, –0.12, p < 0.001], compared with the control arms. Another meta-analysis of 7 trials also found that patients in the intervention group had a significant reduction in change of PAV (SMD: -0.16, 95% CI: –0.29, –0.03, p = 0.019), compared with those in the control group. Meta-regressionanalysis revealed that the percent change of CRP/hsCRP was significantly associated with SMD in change of TAV/PV after adjusting for percent change of LDL-C, age, gender and study duration. Meta-regression analysis showed that percent change of CRP/hsCRP statistically influenced SMD in change of PAV, when percent change of CRP/hsCRP was included separately. However, the percent change of CRP/hsCRP was not significantly associated with SMD of PAV change after adjusting for all covariates. CONCLUSION: In conclusion, statin therapy is beneficial for plaque regression. Statins promote plaque regression, which might be associated to their anti-inflammatory ability. |
format | Online Article Text |
id | pubmed-9691666 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96916662022-11-26 C-reactive protein and coronary atheroma regression following statin therapy: A meta-regression of randomized controlled trials Gao, Darui Hua, Rong Jiesisibieke, Dina Ma, Yanjun Li, Chenglong Wu, Sijing Ma, Qian Xie, Wuxiang Front Cardiovasc Med Cardiovascular Medicine OBJECTIVE: Several clinical trials have indicated that statins stabilize and reverse atherosclerotic plaque. However, different studies have provided inconsistent findings regarding mechanisms and influencing factors of plaque regression under statin therapy. Apart from lipid-lowering effect, statins have pleiotropic effects including anti inflammation in humans. In this study, meta-analysis and meta-regression were used to determine the effects of statin medications on coronary plaque volume. Meanwhile, to assess whether statins promote plaque regression effect was related to their anti-inflammatory ability, the impact of CRP/hsCRP reduction during statin therapy on plaque regression was investigated. METHODS: Up to June 15, 2022, a systematic PubMed, EMBASE, and Cochrane search was performed for randomized controlled trials that assessed treatment effect using total atheroma volume (TAV), percent atheroma volume (PAV), or plaque volume (PV). Only CRP/hsCRP and LDL-C values reported before and after treatment were considered. RESULTS: 12 studies (2,812 patients with heart and/or vascular disease) fulfilled the inclusion criteria and were included in the systematic review. A meta-analysis of 15 statin-treated arms reported a significant reduction in change of TAV/PV [standardized mean difference (SMD): –0.27, 95% confidence intervals (–CI): –0.42, –0.12, p < 0.001], compared with the control arms. Another meta-analysis of 7 trials also found that patients in the intervention group had a significant reduction in change of PAV (SMD: -0.16, 95% CI: –0.29, –0.03, p = 0.019), compared with those in the control group. Meta-regressionanalysis revealed that the percent change of CRP/hsCRP was significantly associated with SMD in change of TAV/PV after adjusting for percent change of LDL-C, age, gender and study duration. Meta-regression analysis showed that percent change of CRP/hsCRP statistically influenced SMD in change of PAV, when percent change of CRP/hsCRP was included separately. However, the percent change of CRP/hsCRP was not significantly associated with SMD of PAV change after adjusting for all covariates. CONCLUSION: In conclusion, statin therapy is beneficial for plaque regression. Statins promote plaque regression, which might be associated to their anti-inflammatory ability. Frontiers Media S.A. 2022-11-11 /pmc/articles/PMC9691666/ /pubmed/36440015 http://dx.doi.org/10.3389/fcvm.2022.989527 Text en Copyright © 2022 Gao, Hua, Jiesisibieke, Ma, Li, Wu, Ma and Xie. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cardiovascular Medicine Gao, Darui Hua, Rong Jiesisibieke, Dina Ma, Yanjun Li, Chenglong Wu, Sijing Ma, Qian Xie, Wuxiang C-reactive protein and coronary atheroma regression following statin therapy: A meta-regression of randomized controlled trials |
title | C-reactive protein and coronary atheroma regression following statin therapy: A meta-regression of randomized controlled trials |
title_full | C-reactive protein and coronary atheroma regression following statin therapy: A meta-regression of randomized controlled trials |
title_fullStr | C-reactive protein and coronary atheroma regression following statin therapy: A meta-regression of randomized controlled trials |
title_full_unstemmed | C-reactive protein and coronary atheroma regression following statin therapy: A meta-regression of randomized controlled trials |
title_short | C-reactive protein and coronary atheroma regression following statin therapy: A meta-regression of randomized controlled trials |
title_sort | c-reactive protein and coronary atheroma regression following statin therapy: a meta-regression of randomized controlled trials |
topic | Cardiovascular Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9691666/ https://www.ncbi.nlm.nih.gov/pubmed/36440015 http://dx.doi.org/10.3389/fcvm.2022.989527 |
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