Effect of PCSK9 antibodies on coronary plaque regression and stabilization derived from intravascular imaging in patients with coronary artery disease: A meta-analysis

Despite extensive evidence demonstrating the beneficial effects of the additional PCSK9 antibodies with high-density statins treatment on cardiovascular clinical outcomes, the potent causes underlying these effects remain elusive. This meta-analysis aimed at exploring the underlying causes to assess...

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Veröffentlicht in:International journal of cardiology 2023-12, Vol.392, p.131330-131330, Article 131330
Hauptverfasser: Liu, Sen, Wang, Peijian, Liu, Cheng, Jin, Menglong, Wan, Jindong, Hou, Jixin, Yang, Yi, Wang, Dan, Liu, Ziyang, Fu, Zhenyan
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container_title International journal of cardiology
container_volume 392
creator Liu, Sen
Wang, Peijian
Liu, Cheng
Jin, Menglong
Wan, Jindong
Hou, Jixin
Yang, Yi
Wang, Dan
Liu, Ziyang
Fu, Zhenyan
description Despite extensive evidence demonstrating the beneficial effects of the additional PCSK9 antibodies with high-density statins treatment on cardiovascular clinical outcomes, the potent causes underlying these effects remain elusive. This meta-analysis aimed at exploring the underlying causes to assess the effect of PCSK9 antibodies on the regression and stabilization of coronary plaque derived from intravascular imaging in statin-treated patients with coronary artery disease (CAD). PubMed, Embase, and Cochrane Library were searched from inception to February 1, 2023, for randomized controlled trials (RCTs), nonrandomized studies without language restrictions if they described the association between PCSK9 antibodies with coronary plaque regression and stabilization evaluated by intravascular imaging in statin-treated patients with CAD. Meta-analyses were performed for mean difference (MD) and odds ratio (OR) using a random-effects model. This study followed the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) reporting guideline. A total of 9 studies (7 RCTs and 2 non-RCTs) with 2290 CAD patients were identified and included. Among statin-treated CAD patients, the addition use of PCSK9 antibodies was associated with IVUS-derived percent atheroma volume (PAV) (4 studies with 1875 participants; MD, −1.26; 95% CI, −1.51 to −1.00; P 
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This meta-analysis aimed at exploring the underlying causes to assess the effect of PCSK9 antibodies on the regression and stabilization of coronary plaque derived from intravascular imaging in statin-treated patients with coronary artery disease (CAD). PubMed, Embase, and Cochrane Library were searched from inception to February 1, 2023, for randomized controlled trials (RCTs), nonrandomized studies without language restrictions if they described the association between PCSK9 antibodies with coronary plaque regression and stabilization evaluated by intravascular imaging in statin-treated patients with CAD. Meta-analyses were performed for mean difference (MD) and odds ratio (OR) using a random-effects model. This study followed the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) reporting guideline. A total of 9 studies (7 RCTs and 2 non-RCTs) with 2290 CAD patients were identified and included. Among statin-treated CAD patients, the addition use of PCSK9 antibodies was associated with IVUS-derived percent atheroma volume (PAV) (4 studies with 1875 participants; MD, −1.26; 95% CI, −1.51 to −1.00; P < 0.01), total atheroma volume (TAV) (4 studies with 1875 participants; MD, −7.23; 95% CI, −11.28 to −3.18; P < 0.01), incidence of PAV regression (4 studies with 1875 participants; OR, 2.24; 95% CI, 1.81 to 2.77; P < 0.01) and incidence of TAV regression (3 studies with 1256 participants; OR, 1.66; 95% CI, 1.33 to 2.09; P < 0.01) in Caucasians instead of Asians from multiple countries; OCT-derived minimum fibrous cap thickness (FCT) (6 studies with 841 participants; MD, 25.16; 95% CI, 14.06 to 36.27; P < 0.01), incidence of thin-capped fibroatheroma (TCFA) regression (2 studies with 222 participants; OR, 2.56; 95% CI, 1.42 to 4.61; P < 0.01) and maximum lipid arc (4 studies with 280 participants; MD, −14.96; 95% CI, −22.10 to −7.83; P < 0.01) in Asians and Caucasians without races restrictions. PCSK9 antibodies resulted in significantly greater coronary plaque regression and stabilization in statin-treated CAD patients, mostly Caucasians from multiple countries. Further studies are needed to assess the effect for Asian patients. •There exist racial disparities of additional PCSK9 antibodies versus statin treatment alone on coronary plaque regression and stabilization.•The additional PCSK9 antibodies made great coronary plaque regression and stabilization in Caucasians.•The additional PCSK9 antibodies did not make coronary plaque regression in Asians.•Our findings about the effect of PCSK9 antibodies on coronary plaque contribute to reveal potent causes improving cardiovascular prognosis.]]></description><identifier>ISSN: 0167-5273</identifier><identifier>EISSN: 1874-1754</identifier><identifier>DOI: 10.1016/j.ijcard.2023.131330</identifier><language>eng</language><publisher>Elsevier B.V</publisher><subject>Coronary artery disease ; Coronary plaque ; Intravascular imaging ; Meta-analysis ; PCSK9 antibody</subject><ispartof>International journal of cardiology, 2023-12, Vol.392, p.131330-131330, Article 131330</ispartof><rights>2023 Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c288t-f24ceb1ec6c768381c7c9e02664ccb0f7885acc082f0ddb9196468dea04de5803</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S016752732301286X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids></links><search><creatorcontrib>Liu, Sen</creatorcontrib><creatorcontrib>Wang, Peijian</creatorcontrib><creatorcontrib>Liu, Cheng</creatorcontrib><creatorcontrib>Jin, Menglong</creatorcontrib><creatorcontrib>Wan, Jindong</creatorcontrib><creatorcontrib>Hou, Jixin</creatorcontrib><creatorcontrib>Yang, Yi</creatorcontrib><creatorcontrib>Wang, Dan</creatorcontrib><creatorcontrib>Liu, Ziyang</creatorcontrib><creatorcontrib>Fu, Zhenyan</creatorcontrib><title>Effect of PCSK9 antibodies on coronary plaque regression and stabilization derived from intravascular imaging in patients with coronary artery disease: A meta-analysis</title><title>International journal of cardiology</title><description><![CDATA[Despite extensive evidence demonstrating the beneficial effects of the additional PCSK9 antibodies with high-density statins treatment on cardiovascular clinical outcomes, the potent causes underlying these effects remain elusive. This meta-analysis aimed at exploring the underlying causes to assess the effect of PCSK9 antibodies on the regression and stabilization of coronary plaque derived from intravascular imaging in statin-treated patients with coronary artery disease (CAD). PubMed, Embase, and Cochrane Library were searched from inception to February 1, 2023, for randomized controlled trials (RCTs), nonrandomized studies without language restrictions if they described the association between PCSK9 antibodies with coronary plaque regression and stabilization evaluated by intravascular imaging in statin-treated patients with CAD. Meta-analyses were performed for mean difference (MD) and odds ratio (OR) using a random-effects model. This study followed the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) reporting guideline. A total of 9 studies (7 RCTs and 2 non-RCTs) with 2290 CAD patients were identified and included. Among statin-treated CAD patients, the addition use of PCSK9 antibodies was associated with IVUS-derived percent atheroma volume (PAV) (4 studies with 1875 participants; MD, −1.26; 95% CI, −1.51 to −1.00; P < 0.01), total atheroma volume (TAV) (4 studies with 1875 participants; MD, −7.23; 95% CI, −11.28 to −3.18; P < 0.01), incidence of PAV regression (4 studies with 1875 participants; OR, 2.24; 95% CI, 1.81 to 2.77; P < 0.01) and incidence of TAV regression (3 studies with 1256 participants; OR, 1.66; 95% CI, 1.33 to 2.09; P < 0.01) in Caucasians instead of Asians from multiple countries; OCT-derived minimum fibrous cap thickness (FCT) (6 studies with 841 participants; MD, 25.16; 95% CI, 14.06 to 36.27; P < 0.01), incidence of thin-capped fibroatheroma (TCFA) regression (2 studies with 222 participants; OR, 2.56; 95% CI, 1.42 to 4.61; P < 0.01) and maximum lipid arc (4 studies with 280 participants; MD, −14.96; 95% CI, −22.10 to −7.83; P < 0.01) in Asians and Caucasians without races restrictions. PCSK9 antibodies resulted in significantly greater coronary plaque regression and stabilization in statin-treated CAD patients, mostly Caucasians from multiple countries. Further studies are needed to assess the effect for Asian patients. •There exist racial disparities of additional PCSK9 antibodies versus statin treatment alone on coronary plaque regression and stabilization.•The additional PCSK9 antibodies made great coronary plaque regression and stabilization in Caucasians.•The additional PCSK9 antibodies did not make coronary plaque regression in Asians.•Our findings about the effect of PCSK9 antibodies on coronary plaque contribute to reveal potent causes improving cardiovascular prognosis.]]></description><subject>Coronary artery disease</subject><subject>Coronary plaque</subject><subject>Intravascular imaging</subject><subject>Meta-analysis</subject><subject>PCSK9 antibody</subject><issn>0167-5273</issn><issn>1874-1754</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9kcGKFDEQhhtRcFx9Aw85eukx6c6k0x6EZdhVcUFBPYfqpDJm6EnGVGZkfCFf0wwtePNU8NdfVfz1Nc1LwdeCC_V6vw57C9mtO971a9GLvuePmpXQg2zFsJGPm1W1De2mG_qnzTOiPedcjqNeNb_vvEdbWPLs8_bLx5FBLGFKLiCxFJlNOUXIF3ac4ccJWcZdRqJQWxAdowJTmMMvKFfFYQ5ndMzndGAhlgxnIHuaIbNwgF2Iu6qyYzVjLMR-hvL93wHIBWtxgRAI37BbdsACLUSYLxToefPEw0z44m-9ab7d333dvm8fPr37sL19aG2ndWl9Jy1OAq2yg9K9FnawI_JOKWntxP2g9Qas5brz3LlpFKOSSjsELh1uNO9vmlfL3mNONTAVcwhkcZ4hYjqR6bQSPZe96qpVLlabE1FGb4655swXI7i5cjF7s3AxVy5m4VLH3i5jWGOcA2ZDtj7Eogu5kjAuhf8v-APgl5yB</recordid><startdate>20231201</startdate><enddate>20231201</enddate><creator>Liu, Sen</creator><creator>Wang, Peijian</creator><creator>Liu, Cheng</creator><creator>Jin, Menglong</creator><creator>Wan, Jindong</creator><creator>Hou, Jixin</creator><creator>Yang, Yi</creator><creator>Wang, Dan</creator><creator>Liu, Ziyang</creator><creator>Fu, Zhenyan</creator><general>Elsevier B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20231201</creationdate><title>Effect of PCSK9 antibodies on coronary plaque regression and stabilization derived from intravascular imaging in patients with coronary artery disease: A meta-analysis</title><author>Liu, Sen ; Wang, Peijian ; Liu, Cheng ; Jin, Menglong ; Wan, Jindong ; Hou, Jixin ; Yang, Yi ; Wang, Dan ; Liu, Ziyang ; Fu, Zhenyan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c288t-f24ceb1ec6c768381c7c9e02664ccb0f7885acc082f0ddb9196468dea04de5803</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Coronary artery disease</topic><topic>Coronary plaque</topic><topic>Intravascular imaging</topic><topic>Meta-analysis</topic><topic>PCSK9 antibody</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Sen</creatorcontrib><creatorcontrib>Wang, Peijian</creatorcontrib><creatorcontrib>Liu, Cheng</creatorcontrib><creatorcontrib>Jin, Menglong</creatorcontrib><creatorcontrib>Wan, Jindong</creatorcontrib><creatorcontrib>Hou, Jixin</creatorcontrib><creatorcontrib>Yang, Yi</creatorcontrib><creatorcontrib>Wang, Dan</creatorcontrib><creatorcontrib>Liu, Ziyang</creatorcontrib><creatorcontrib>Fu, Zhenyan</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of cardiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Sen</au><au>Wang, Peijian</au><au>Liu, Cheng</au><au>Jin, Menglong</au><au>Wan, Jindong</au><au>Hou, Jixin</au><au>Yang, Yi</au><au>Wang, Dan</au><au>Liu, Ziyang</au><au>Fu, Zhenyan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of PCSK9 antibodies on coronary plaque regression and stabilization derived from intravascular imaging in patients with coronary artery disease: A meta-analysis</atitle><jtitle>International journal of cardiology</jtitle><date>2023-12-01</date><risdate>2023</risdate><volume>392</volume><spage>131330</spage><epage>131330</epage><pages>131330-131330</pages><artnum>131330</artnum><issn>0167-5273</issn><eissn>1874-1754</eissn><abstract><![CDATA[Despite extensive evidence demonstrating the beneficial effects of the additional PCSK9 antibodies with high-density statins treatment on cardiovascular clinical outcomes, the potent causes underlying these effects remain elusive. This meta-analysis aimed at exploring the underlying causes to assess the effect of PCSK9 antibodies on the regression and stabilization of coronary plaque derived from intravascular imaging in statin-treated patients with coronary artery disease (CAD). PubMed, Embase, and Cochrane Library were searched from inception to February 1, 2023, for randomized controlled trials (RCTs), nonrandomized studies without language restrictions if they described the association between PCSK9 antibodies with coronary plaque regression and stabilization evaluated by intravascular imaging in statin-treated patients with CAD. Meta-analyses were performed for mean difference (MD) and odds ratio (OR) using a random-effects model. This study followed the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) reporting guideline. A total of 9 studies (7 RCTs and 2 non-RCTs) with 2290 CAD patients were identified and included. Among statin-treated CAD patients, the addition use of PCSK9 antibodies was associated with IVUS-derived percent atheroma volume (PAV) (4 studies with 1875 participants; MD, −1.26; 95% CI, −1.51 to −1.00; P < 0.01), total atheroma volume (TAV) (4 studies with 1875 participants; MD, −7.23; 95% CI, −11.28 to −3.18; P < 0.01), incidence of PAV regression (4 studies with 1875 participants; OR, 2.24; 95% CI, 1.81 to 2.77; P < 0.01) and incidence of TAV regression (3 studies with 1256 participants; OR, 1.66; 95% CI, 1.33 to 2.09; P < 0.01) in Caucasians instead of Asians from multiple countries; OCT-derived minimum fibrous cap thickness (FCT) (6 studies with 841 participants; MD, 25.16; 95% CI, 14.06 to 36.27; P < 0.01), incidence of thin-capped fibroatheroma (TCFA) regression (2 studies with 222 participants; OR, 2.56; 95% CI, 1.42 to 4.61; P < 0.01) and maximum lipid arc (4 studies with 280 participants; MD, −14.96; 95% CI, −22.10 to −7.83; P < 0.01) in Asians and Caucasians without races restrictions. PCSK9 antibodies resulted in significantly greater coronary plaque regression and stabilization in statin-treated CAD patients, mostly Caucasians from multiple countries. Further studies are needed to assess the effect for Asian patients. •There exist racial disparities of additional PCSK9 antibodies versus statin treatment alone on coronary plaque regression and stabilization.•The additional PCSK9 antibodies made great coronary plaque regression and stabilization in Caucasians.•The additional PCSK9 antibodies did not make coronary plaque regression in Asians.•Our findings about the effect of PCSK9 antibodies on coronary plaque contribute to reveal potent causes improving cardiovascular prognosis.]]></abstract><pub>Elsevier B.V</pub><doi>10.1016/j.ijcard.2023.131330</doi><tpages>1</tpages></addata></record>
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subjects Coronary artery disease
Coronary plaque
Intravascular imaging
Meta-analysis
PCSK9 antibody
title Effect of PCSK9 antibodies on coronary plaque regression and stabilization derived from intravascular imaging in patients with coronary artery disease: A meta-analysis
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