Very late vasomotor responses and gene expression with bioresorbable scaffolds and metallic drug‐eluting stents

Objectives To investigate the long‐term vasomotor response and inflammatory changes in Absorb bioresorbable vascular scaffold (BVS) and metallic drug‐eluting stent (DES) implanted artery. Background Clinical evidence has demonstrated that compared to DES, BVS is associated with higher rates of targe...

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Veröffentlicht in:Catheterization and cardiovascular interventions 2021-10, Vol.98 (4), p.723-732, Article ccd.29819
Hauptverfasser: Koh, Jin‐Sin, Gogas, Bill D., Kumar, Sandeep, Benham, James J., Sur, Sanjoli, Spilias, Nikolaos, Kumar, Arnav, Giddens, Don P., Rapoza, Richard, Kereiakes, Dean J., Stone, Gregg, Jo, Hanjoong, Samady, Habib
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container_end_page 732
container_issue 4
container_start_page 723
container_title Catheterization and cardiovascular interventions
container_volume 98
creator Koh, Jin‐Sin
Gogas, Bill D.
Kumar, Sandeep
Benham, James J.
Sur, Sanjoli
Spilias, Nikolaos
Kumar, Arnav
Giddens, Don P.
Rapoza, Richard
Kereiakes, Dean J.
Stone, Gregg
Jo, Hanjoong
Samady, Habib
description Objectives To investigate the long‐term vasomotor response and inflammatory changes in Absorb bioresorbable vascular scaffold (BVS) and metallic drug‐eluting stent (DES) implanted artery. Background Clinical evidence has demonstrated that compared to DES, BVS is associated with higher rates of target lesion failure. However, it is not known whether the higher event rates observed with BVS are related to endothelial dysfunction or inflammation associated with polymer degradation. Methods Ten Absorb BVS and six Xience V DES were randomly implanted in the main coronaries of six nonatherosclerotic swine. At 4‐years, vasomotor response was evaluated in vivo by quantitative coronary angiography response to intracoronary infusion of Ach and ex vivo by the biomechanical response to prostaglandin F2‐α (PGF2‐α), substance P and bradykinin and gene expression analysis. Results Absorb BVS implanted arteries showed significantly restored vasoconstrictive responses after Ach compared to in‐stent Xience V. The contractility of Absorb BVS treated segments induced by PGF2‐α was significantly greater compared to Xience V treated segments and endothelial‐dependent vasorelaxation was greater with Absorb BVS compared to Xience V. Gene expression analyses indicated the pro‐inflammatory lymphotoxin‐beta receptor (LTβR) signaling pathway was significantly upregulated in arteries treated with a metallic stent compared to Absorb BVS treated arterial segments. Conclusions At 4 years, arteries treated with Absorb BVS compared with Xience V, demonstrate significantly greater restoration of vasomotor responses. Genetic analysis suggests mechanobiologic reparation of Absorb BVS treated arteries at 4 years as opposed to Xience V treated vessels.
doi_str_mv 10.1002/ccd.29819
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Background Clinical evidence has demonstrated that compared to DES, BVS is associated with higher rates of target lesion failure. However, it is not known whether the higher event rates observed with BVS are related to endothelial dysfunction or inflammation associated with polymer degradation. Methods Ten Absorb BVS and six Xience V DES were randomly implanted in the main coronaries of six nonatherosclerotic swine. At 4‐years, vasomotor response was evaluated in vivo by quantitative coronary angiography response to intracoronary infusion of Ach and ex vivo by the biomechanical response to prostaglandin F2‐α (PGF2‐α), substance P and bradykinin and gene expression analysis. Results Absorb BVS implanted arteries showed significantly restored vasoconstrictive responses after Ach compared to in‐stent Xience V. The contractility of Absorb BVS treated segments induced by PGF2‐α was significantly greater compared to Xience V treated segments and endothelial‐dependent vasorelaxation was greater with Absorb BVS compared to Xience V. Gene expression analyses indicated the pro‐inflammatory lymphotoxin‐beta receptor (LTβR) signaling pathway was significantly upregulated in arteries treated with a metallic stent compared to Absorb BVS treated arterial segments. Conclusions At 4 years, arteries treated with Absorb BVS compared with Xience V, demonstrate significantly greater restoration of vasomotor responses. Genetic analysis suggests mechanobiologic reparation of Absorb BVS treated arteries at 4 years as opposed to Xience V treated vessels.</description><identifier>ISSN: 1522-1946</identifier><identifier>EISSN: 1522-726X</identifier><identifier>DOI: 10.1002/ccd.29819</identifier><identifier>PMID: 34164905</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley &amp; Sons, Inc</publisher><subject>Angiography ; Arteries ; bioresorbable scaffolds ; Bradykinin ; Contractility ; Gene expression ; Genetic analysis ; Implants ; Inflammation ; Lymphotoxin ; mechanobiology ; Polymers ; Signal transduction ; Stents ; Substance P ; Vasodilation ; vasomotor function ; Veins &amp; arteries</subject><ispartof>Catheterization and cardiovascular interventions, 2021-10, Vol.98 (4), p.723-732, Article ccd.29819</ispartof><rights>2021 Wiley Periodicals LLC.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3809-664f65851121dca93e25bf5ecb9bc54dea7b440b1dd8488aa8c6ca4b2aed8843</cites><orcidid>0000-0003-2920-7411</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fccd.29819$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fccd.29819$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,776,780,881,1411,27901,27902,45550,45551</link.rule.ids></links><search><creatorcontrib>Koh, Jin‐Sin</creatorcontrib><creatorcontrib>Gogas, Bill D.</creatorcontrib><creatorcontrib>Kumar, Sandeep</creatorcontrib><creatorcontrib>Benham, James J.</creatorcontrib><creatorcontrib>Sur, Sanjoli</creatorcontrib><creatorcontrib>Spilias, Nikolaos</creatorcontrib><creatorcontrib>Kumar, Arnav</creatorcontrib><creatorcontrib>Giddens, Don P.</creatorcontrib><creatorcontrib>Rapoza, Richard</creatorcontrib><creatorcontrib>Kereiakes, Dean J.</creatorcontrib><creatorcontrib>Stone, Gregg</creatorcontrib><creatorcontrib>Jo, Hanjoong</creatorcontrib><creatorcontrib>Samady, Habib</creatorcontrib><title>Very late vasomotor responses and gene expression with bioresorbable scaffolds and metallic drug‐eluting stents</title><title>Catheterization and cardiovascular interventions</title><description>Objectives To investigate the long‐term vasomotor response and inflammatory changes in Absorb bioresorbable vascular scaffold (BVS) and metallic drug‐eluting stent (DES) implanted artery. Background Clinical evidence has demonstrated that compared to DES, BVS is associated with higher rates of target lesion failure. However, it is not known whether the higher event rates observed with BVS are related to endothelial dysfunction or inflammation associated with polymer degradation. Methods Ten Absorb BVS and six Xience V DES were randomly implanted in the main coronaries of six nonatherosclerotic swine. At 4‐years, vasomotor response was evaluated in vivo by quantitative coronary angiography response to intracoronary infusion of Ach and ex vivo by the biomechanical response to prostaglandin F2‐α (PGF2‐α), substance P and bradykinin and gene expression analysis. Results Absorb BVS implanted arteries showed significantly restored vasoconstrictive responses after Ach compared to in‐stent Xience V. The contractility of Absorb BVS treated segments induced by PGF2‐α was significantly greater compared to Xience V treated segments and endothelial‐dependent vasorelaxation was greater with Absorb BVS compared to Xience V. Gene expression analyses indicated the pro‐inflammatory lymphotoxin‐beta receptor (LTβR) signaling pathway was significantly upregulated in arteries treated with a metallic stent compared to Absorb BVS treated arterial segments. Conclusions At 4 years, arteries treated with Absorb BVS compared with Xience V, demonstrate significantly greater restoration of vasomotor responses. Genetic analysis suggests mechanobiologic reparation of Absorb BVS treated arteries at 4 years as opposed to Xience V treated vessels.</description><subject>Angiography</subject><subject>Arteries</subject><subject>bioresorbable scaffolds</subject><subject>Bradykinin</subject><subject>Contractility</subject><subject>Gene expression</subject><subject>Genetic analysis</subject><subject>Implants</subject><subject>Inflammation</subject><subject>Lymphotoxin</subject><subject>mechanobiology</subject><subject>Polymers</subject><subject>Signal transduction</subject><subject>Stents</subject><subject>Substance P</subject><subject>Vasodilation</subject><subject>vasomotor function</subject><subject>Veins &amp; arteries</subject><issn>1522-1946</issn><issn>1522-726X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp1kUtuFDEQhi0EIiGw4AaW2MBiEttju90bJDSEhxSJTYTYWX5UTxy57YndnWR2OQJn5CQYeoQEEqtylb_6q-wfoZeUnFJC2Jlz_pT1ivaP0DEVjK06Jr89Ppxpz-URelbrNSGkl6x_io7WnEreE3GMbr5C2eNoJsC3puYxT7ngAnWXU4WKTfJ4Cwkw3O9atYac8F2YrrANueW5WGMj4OrMMOTol4YRJhNjcNiXefvj4TvEeQppi-sEaarP0ZPBxAovDvEEXX44v9x8Wl18-fh58-5i5daK9Csp-SCFEpQy6p3p18CEHQQ421snuAfTWc6Jpd4rrpQxyklnuGUGvFJ8fYLeLrK72Y7gXRtdTNS7EkZT9jqboP--SeFKb_OtVoILLmUTeH0QKPlmhjrpMVQHMZoEea6aCc5V19FONfTVP-h1nktqr2tUp4ji7ecb9WahXMm1Fhj-LEOJ_uWjbj7q3z429mxh70KE_f9Bvdm8Xzp-Airkoio</recordid><startdate>202110</startdate><enddate>202110</enddate><creator>Koh, Jin‐Sin</creator><creator>Gogas, Bill D.</creator><creator>Kumar, Sandeep</creator><creator>Benham, James J.</creator><creator>Sur, Sanjoli</creator><creator>Spilias, Nikolaos</creator><creator>Kumar, Arnav</creator><creator>Giddens, Don P.</creator><creator>Rapoza, Richard</creator><creator>Kereiakes, Dean J.</creator><creator>Stone, Gregg</creator><creator>Jo, Hanjoong</creator><creator>Samady, Habib</creator><general>John Wiley &amp; Sons, Inc</general><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-2920-7411</orcidid></search><sort><creationdate>202110</creationdate><title>Very late vasomotor responses and gene expression with bioresorbable scaffolds and metallic drug‐eluting stents</title><author>Koh, Jin‐Sin ; Gogas, Bill D. ; Kumar, Sandeep ; Benham, James J. ; Sur, Sanjoli ; Spilias, Nikolaos ; Kumar, Arnav ; Giddens, Don P. ; Rapoza, Richard ; Kereiakes, Dean J. ; Stone, Gregg ; Jo, Hanjoong ; Samady, Habib</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3809-664f65851121dca93e25bf5ecb9bc54dea7b440b1dd8488aa8c6ca4b2aed8843</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Angiography</topic><topic>Arteries</topic><topic>bioresorbable scaffolds</topic><topic>Bradykinin</topic><topic>Contractility</topic><topic>Gene expression</topic><topic>Genetic analysis</topic><topic>Implants</topic><topic>Inflammation</topic><topic>Lymphotoxin</topic><topic>mechanobiology</topic><topic>Polymers</topic><topic>Signal transduction</topic><topic>Stents</topic><topic>Substance P</topic><topic>Vasodilation</topic><topic>vasomotor function</topic><topic>Veins &amp; arteries</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Koh, Jin‐Sin</creatorcontrib><creatorcontrib>Gogas, Bill D.</creatorcontrib><creatorcontrib>Kumar, Sandeep</creatorcontrib><creatorcontrib>Benham, James J.</creatorcontrib><creatorcontrib>Sur, Sanjoli</creatorcontrib><creatorcontrib>Spilias, Nikolaos</creatorcontrib><creatorcontrib>Kumar, Arnav</creatorcontrib><creatorcontrib>Giddens, Don P.</creatorcontrib><creatorcontrib>Rapoza, Richard</creatorcontrib><creatorcontrib>Kereiakes, Dean J.</creatorcontrib><creatorcontrib>Stone, Gregg</creatorcontrib><creatorcontrib>Jo, Hanjoong</creatorcontrib><creatorcontrib>Samady, Habib</creatorcontrib><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Catheterization and cardiovascular interventions</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Koh, Jin‐Sin</au><au>Gogas, Bill D.</au><au>Kumar, Sandeep</au><au>Benham, James J.</au><au>Sur, Sanjoli</au><au>Spilias, Nikolaos</au><au>Kumar, Arnav</au><au>Giddens, Don P.</au><au>Rapoza, Richard</au><au>Kereiakes, Dean J.</au><au>Stone, Gregg</au><au>Jo, Hanjoong</au><au>Samady, Habib</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Very late vasomotor responses and gene expression with bioresorbable scaffolds and metallic drug‐eluting stents</atitle><jtitle>Catheterization and cardiovascular interventions</jtitle><date>2021-10</date><risdate>2021</risdate><volume>98</volume><issue>4</issue><spage>723</spage><epage>732</epage><pages>723-732</pages><artnum>ccd.29819</artnum><issn>1522-1946</issn><eissn>1522-726X</eissn><abstract>Objectives To investigate the long‐term vasomotor response and inflammatory changes in Absorb bioresorbable vascular scaffold (BVS) and metallic drug‐eluting stent (DES) implanted artery. Background Clinical evidence has demonstrated that compared to DES, BVS is associated with higher rates of target lesion failure. However, it is not known whether the higher event rates observed with BVS are related to endothelial dysfunction or inflammation associated with polymer degradation. Methods Ten Absorb BVS and six Xience V DES were randomly implanted in the main coronaries of six nonatherosclerotic swine. At 4‐years, vasomotor response was evaluated in vivo by quantitative coronary angiography response to intracoronary infusion of Ach and ex vivo by the biomechanical response to prostaglandin F2‐α (PGF2‐α), substance P and bradykinin and gene expression analysis. Results Absorb BVS implanted arteries showed significantly restored vasoconstrictive responses after Ach compared to in‐stent Xience V. The contractility of Absorb BVS treated segments induced by PGF2‐α was significantly greater compared to Xience V treated segments and endothelial‐dependent vasorelaxation was greater with Absorb BVS compared to Xience V. Gene expression analyses indicated the pro‐inflammatory lymphotoxin‐beta receptor (LTβR) signaling pathway was significantly upregulated in arteries treated with a metallic stent compared to Absorb BVS treated arterial segments. Conclusions At 4 years, arteries treated with Absorb BVS compared with Xience V, demonstrate significantly greater restoration of vasomotor responses. Genetic analysis suggests mechanobiologic reparation of Absorb BVS treated arteries at 4 years as opposed to Xience V treated vessels.</abstract><cop>Hoboken, USA</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>34164905</pmid><doi>10.1002/ccd.29819</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0003-2920-7411</orcidid><oa>free_for_read</oa></addata></record>
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source Wiley Online Library Journals Frontfile Complete
subjects Angiography
Arteries
bioresorbable scaffolds
Bradykinin
Contractility
Gene expression
Genetic analysis
Implants
Inflammation
Lymphotoxin
mechanobiology
Polymers
Signal transduction
Stents
Substance P
Vasodilation
vasomotor function
Veins & arteries
title Very late vasomotor responses and gene expression with bioresorbable scaffolds and metallic drug‐eluting stents
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