High-Pressure Distention of the Saphenous Vein During Preparation Results in Increased Markers of Inflammation: A Potential Mechanism for Graft Failure
Background Coronary artery disease is the single leading cause of death in the United States. Commonly it is treated with coronary bypass grafting using the saphenous vein (SV) or internal mammary artery (IMA) as a conduit. Unfortunately, the SV has much lower patency rates compared with the IMA. Se...
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Veröffentlicht in: | The Annals of thoracic surgery 2012-02, Vol.93 (2), p.552-558 |
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creator | Khaleel, Maseeha S., MD Dorheim, Tracy A., MD Duryee, Michael J., MS Durbin, Harold E., PA-C Bussey, Walter D., PA-C Garvin, Robert P., BA Klassen, Lynell W., MD Thiele, Geoffrey M., PhD Anderson, Daniel R., MD, PhD |
description | Background Coronary artery disease is the single leading cause of death in the United States. Commonly it is treated with coronary bypass grafting using the saphenous vein (SV) or internal mammary artery (IMA) as a conduit. Unfortunately, the SV has much lower patency rates compared with the IMA. Several hypotheses exist as to why occlusion occurs more commonly in SV grafts than in IMA grafts. However detailed studies in this area have been limited. This study investigates the effects of pressure distention on inflammation in SV conduit used in coronary artery bypass grafting (CABG). Methods Saphenous vein distention pressure was measured intraoperatively during 48 CABG procedures. A segment of SV was excised from the conduit before distention. Because the vein was used for coronary artery grafting, sequential pieces were archived for evaluation. Real-time polymerase chain reaction (RT-PCR) and immunohistochemical analyses were performed to investigate a change in the expression of biomarkers. Results Upregulation of various biomarkers occurred. These biomarkers included scavenger receptors A and B (SR-A, SR-B), toll-like receptors 2 and 4 (TLR2, TLR4), platelet endothelial cell adhesion molecule (PECAM), vascular cell adhesion molecule (VCAM), and intercellular cell adhesion molecule (ICAM) in segments of SV that were subjected to distention. Immunohistochemical results mirrored RT-PCR findings. A significant correlation was observed between biomarkers and pressure values. Conclusions These studies demonstrate that markers of inflammation are upregulated in response to SV distention. The data suggest that the pressure used in graft preparation procedures should be regulated to avoid inflammation and its potential to induce graft failure. |
doi_str_mv | 10.1016/j.athoracsur.2011.10.035 |
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Commonly it is treated with coronary bypass grafting using the saphenous vein (SV) or internal mammary artery (IMA) as a conduit. Unfortunately, the SV has much lower patency rates compared with the IMA. Several hypotheses exist as to why occlusion occurs more commonly in SV grafts than in IMA grafts. However detailed studies in this area have been limited. This study investigates the effects of pressure distention on inflammation in SV conduit used in coronary artery bypass grafting (CABG). Methods Saphenous vein distention pressure was measured intraoperatively during 48 CABG procedures. A segment of SV was excised from the conduit before distention. Because the vein was used for coronary artery grafting, sequential pieces were archived for evaluation. Real-time polymerase chain reaction (RT-PCR) and immunohistochemical analyses were performed to investigate a change in the expression of biomarkers. Results Upregulation of various biomarkers occurred. These biomarkers included scavenger receptors A and B (SR-A, SR-B), toll-like receptors 2 and 4 (TLR2, TLR4), platelet endothelial cell adhesion molecule (PECAM), vascular cell adhesion molecule (VCAM), and intercellular cell adhesion molecule (ICAM) in segments of SV that were subjected to distention. Immunohistochemical results mirrored RT-PCR findings. A significant correlation was observed between biomarkers and pressure values. Conclusions These studies demonstrate that markers of inflammation are upregulated in response to SV distention. The data suggest that the pressure used in graft preparation procedures should be regulated to avoid inflammation and its potential to induce graft failure.</description><identifier>ISSN: 0003-4975</identifier><identifier>EISSN: 1552-6259</identifier><identifier>DOI: 10.1016/j.athoracsur.2011.10.035</identifier><identifier>PMID: 22206954</identifier><identifier>CODEN: ATHSAK</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Aged ; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Biological and medical sciences ; Biomarkers ; Cardiology. Vascular system ; Cardiothoracic Surgery ; Cell Adhesion Molecules - analysis ; Cell Adhesion Molecules - biosynthesis ; Cell Adhesion Molecules - genetics ; Coronary Artery Bypass - methods ; Coronary Disease - surgery ; Female ; Graft Occlusion, Vascular - etiology ; Graft Occlusion, Vascular - metabolism ; Humans ; Hyperplasia ; Male ; Medical sciences ; Middle Aged ; Phlebitis - etiology ; Phlebitis - metabolism ; Pneumology ; Pressure - adverse effects ; Real-Time Polymerase Chain Reaction ; Receptors, Scavenger - analysis ; Receptors, Scavenger - biosynthesis ; Receptors, Scavenger - genetics ; RNA, Messenger - analysis ; Saphenous Vein - metabolism ; Saphenous Vein - pathology ; Saphenous Vein - transplantation ; Surgery ; Tissue and Organ Harvesting - adverse effects ; Tissue and Organ Harvesting - methods ; Toll-Like Receptors - analysis ; Toll-Like Receptors - biosynthesis ; Toll-Like Receptors - genetics ; Up-Regulation ; Vascular Patency</subject><ispartof>The Annals of thoracic surgery, 2012-02, Vol.93 (2), p.552-558</ispartof><rights>The Society of Thoracic Surgeons</rights><rights>2012 The Society of Thoracic Surgeons</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2012 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c574t-966eedcdcaa498a8db8bf18a53d768ae1685b578017e681e3a8dbd7100ac6f103</citedby><cites>FETCH-LOGICAL-c574t-966eedcdcaa498a8db8bf18a53d768ae1685b578017e681e3a8dbd7100ac6f103</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,782,786,27933,27934</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=25600181$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22206954$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Khaleel, Maseeha S., MD</creatorcontrib><creatorcontrib>Dorheim, Tracy A., MD</creatorcontrib><creatorcontrib>Duryee, Michael J., MS</creatorcontrib><creatorcontrib>Durbin, Harold E., PA-C</creatorcontrib><creatorcontrib>Bussey, Walter D., PA-C</creatorcontrib><creatorcontrib>Garvin, Robert P., BA</creatorcontrib><creatorcontrib>Klassen, Lynell W., MD</creatorcontrib><creatorcontrib>Thiele, Geoffrey M., PhD</creatorcontrib><creatorcontrib>Anderson, Daniel R., MD, PhD</creatorcontrib><title>High-Pressure Distention of the Saphenous Vein During Preparation Results in Increased Markers of Inflammation: A Potential Mechanism for Graft Failure</title><title>The Annals of thoracic surgery</title><addtitle>Ann Thorac Surg</addtitle><description>Background Coronary artery disease is the single leading cause of death in the United States. Commonly it is treated with coronary bypass grafting using the saphenous vein (SV) or internal mammary artery (IMA) as a conduit. Unfortunately, the SV has much lower patency rates compared with the IMA. Several hypotheses exist as to why occlusion occurs more commonly in SV grafts than in IMA grafts. However detailed studies in this area have been limited. This study investigates the effects of pressure distention on inflammation in SV conduit used in coronary artery bypass grafting (CABG). Methods Saphenous vein distention pressure was measured intraoperatively during 48 CABG procedures. A segment of SV was excised from the conduit before distention. Because the vein was used for coronary artery grafting, sequential pieces were archived for evaluation. Real-time polymerase chain reaction (RT-PCR) and immunohistochemical analyses were performed to investigate a change in the expression of biomarkers. Results Upregulation of various biomarkers occurred. These biomarkers included scavenger receptors A and B (SR-A, SR-B), toll-like receptors 2 and 4 (TLR2, TLR4), platelet endothelial cell adhesion molecule (PECAM), vascular cell adhesion molecule (VCAM), and intercellular cell adhesion molecule (ICAM) in segments of SV that were subjected to distention. Immunohistochemical results mirrored RT-PCR findings. A significant correlation was observed between biomarkers and pressure values. Conclusions These studies demonstrate that markers of inflammation are upregulated in response to SV distention. The data suggest that the pressure used in graft preparation procedures should be regulated to avoid inflammation and its potential to induce graft failure.</description><subject>Aged</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Biological and medical sciences</subject><subject>Biomarkers</subject><subject>Cardiology. Vascular system</subject><subject>Cardiothoracic Surgery</subject><subject>Cell Adhesion Molecules - analysis</subject><subject>Cell Adhesion Molecules - biosynthesis</subject><subject>Cell Adhesion Molecules - genetics</subject><subject>Coronary Artery Bypass - methods</subject><subject>Coronary Disease - surgery</subject><subject>Female</subject><subject>Graft Occlusion, Vascular - etiology</subject><subject>Graft Occlusion, Vascular - metabolism</subject><subject>Humans</subject><subject>Hyperplasia</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Phlebitis - etiology</subject><subject>Phlebitis - metabolism</subject><subject>Pneumology</subject><subject>Pressure - adverse effects</subject><subject>Real-Time Polymerase Chain Reaction</subject><subject>Receptors, Scavenger - analysis</subject><subject>Receptors, Scavenger - biosynthesis</subject><subject>Receptors, Scavenger - genetics</subject><subject>RNA, Messenger - analysis</subject><subject>Saphenous Vein - metabolism</subject><subject>Saphenous Vein - pathology</subject><subject>Saphenous Vein - transplantation</subject><subject>Surgery</subject><subject>Tissue and Organ Harvesting - adverse effects</subject><subject>Tissue and Organ Harvesting - methods</subject><subject>Toll-Like Receptors - analysis</subject><subject>Toll-Like Receptors - biosynthesis</subject><subject>Toll-Like Receptors - genetics</subject><subject>Up-Regulation</subject><subject>Vascular Patency</subject><issn>0003-4975</issn><issn>1552-6259</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNksFu1DAQhiMEokvhFZAviFMW24kThwNSaWm7UisqClytWWfSeJs4iydB6pPwuji7C5U4cbLs-eaf8fyTJEzwpeCieLdZwtgOASxNYSm5EPF5yTP1JFkIpWRaSFU9TRac8yzNq1IdJS-INvEqY_h5ciSl5EWl8kXy69LdtelNQIpSyM4cjehHN3g2NGxskd3CtkU_TMS-o_PsbArO37GYsIUAO_AL0tSNxGJ05W1AIKzZNYR7DDSrrHzTQd_v4PfshN0MuxLQsWu0LXhHPWuGwC4CNCM7B9fFTl4mzxroCF8dzuPk2_mnr6eX6dXni9XpyVVqVZmPaVUUiLWtLUBeadD1Wq8boUFldVloQFFotVal5qLEQgvMZqQuBedgi0bw7Dh5u9fdhuHHhDSa3pHFrgOP8dOmEqVWWioVSb0nbRiIAjZmG1wP4cEIbmZXzMY8umJmV-ZIdCWmvj4UmdY91n8T_9gQgTcHAMhC1wTw1tEjpwrOhRaR-7jnMI7kp8NgyDr0FmsX0I6mHtz_dPPhHxHbOe9i3Xt8QNoMU_Bx5EYYkoab23mL5iUSgkslc579BupPx9c</recordid><startdate>20120201</startdate><enddate>20120201</enddate><creator>Khaleel, Maseeha S., MD</creator><creator>Dorheim, Tracy A., MD</creator><creator>Duryee, Michael J., MS</creator><creator>Durbin, Harold E., PA-C</creator><creator>Bussey, Walter D., PA-C</creator><creator>Garvin, Robert P., BA</creator><creator>Klassen, Lynell W., MD</creator><creator>Thiele, Geoffrey M., PhD</creator><creator>Anderson, Daniel R., MD, PhD</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20120201</creationdate><title>High-Pressure Distention of the Saphenous Vein During Preparation Results in Increased Markers of Inflammation: A Potential Mechanism for Graft Failure</title><author>Khaleel, Maseeha S., MD ; Dorheim, Tracy A., MD ; Duryee, Michael J., MS ; Durbin, Harold E., PA-C ; Bussey, Walter D., PA-C ; Garvin, Robert P., BA ; Klassen, Lynell W., MD ; Thiele, Geoffrey M., PhD ; Anderson, Daniel R., MD, PhD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c574t-966eedcdcaa498a8db8bf18a53d768ae1685b578017e681e3a8dbd7100ac6f103</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Aged</topic><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Biological and medical sciences</topic><topic>Biomarkers</topic><topic>Cardiology. Vascular system</topic><topic>Cardiothoracic Surgery</topic><topic>Cell Adhesion Molecules - analysis</topic><topic>Cell Adhesion Molecules - biosynthesis</topic><topic>Cell Adhesion Molecules - genetics</topic><topic>Coronary Artery Bypass - methods</topic><topic>Coronary Disease - surgery</topic><topic>Female</topic><topic>Graft Occlusion, Vascular - etiology</topic><topic>Graft Occlusion, Vascular - metabolism</topic><topic>Humans</topic><topic>Hyperplasia</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Phlebitis - etiology</topic><topic>Phlebitis - metabolism</topic><topic>Pneumology</topic><topic>Pressure - adverse effects</topic><topic>Real-Time Polymerase Chain Reaction</topic><topic>Receptors, Scavenger - analysis</topic><topic>Receptors, Scavenger - biosynthesis</topic><topic>Receptors, Scavenger - genetics</topic><topic>RNA, Messenger - analysis</topic><topic>Saphenous Vein - metabolism</topic><topic>Saphenous Vein - pathology</topic><topic>Saphenous Vein - transplantation</topic><topic>Surgery</topic><topic>Tissue and Organ Harvesting - adverse effects</topic><topic>Tissue and Organ Harvesting - methods</topic><topic>Toll-Like Receptors - analysis</topic><topic>Toll-Like Receptors - biosynthesis</topic><topic>Toll-Like Receptors - genetics</topic><topic>Up-Regulation</topic><topic>Vascular Patency</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Khaleel, Maseeha S., MD</creatorcontrib><creatorcontrib>Dorheim, Tracy A., MD</creatorcontrib><creatorcontrib>Duryee, Michael J., MS</creatorcontrib><creatorcontrib>Durbin, Harold E., PA-C</creatorcontrib><creatorcontrib>Bussey, Walter D., PA-C</creatorcontrib><creatorcontrib>Garvin, Robert P., BA</creatorcontrib><creatorcontrib>Klassen, Lynell W., MD</creatorcontrib><creatorcontrib>Thiele, Geoffrey M., PhD</creatorcontrib><creatorcontrib>Anderson, Daniel R., MD, PhD</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The Annals of thoracic surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Khaleel, Maseeha S., MD</au><au>Dorheim, Tracy A., MD</au><au>Duryee, Michael J., MS</au><au>Durbin, Harold E., PA-C</au><au>Bussey, Walter D., PA-C</au><au>Garvin, Robert P., BA</au><au>Klassen, Lynell W., MD</au><au>Thiele, Geoffrey M., PhD</au><au>Anderson, Daniel R., MD, PhD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>High-Pressure Distention of the Saphenous Vein During Preparation Results in Increased Markers of Inflammation: A Potential Mechanism for Graft Failure</atitle><jtitle>The Annals of thoracic surgery</jtitle><addtitle>Ann Thorac Surg</addtitle><date>2012-02-01</date><risdate>2012</risdate><volume>93</volume><issue>2</issue><spage>552</spage><epage>558</epage><pages>552-558</pages><issn>0003-4975</issn><eissn>1552-6259</eissn><coden>ATHSAK</coden><abstract>Background Coronary artery disease is the single leading cause of death in the United States. Commonly it is treated with coronary bypass grafting using the saphenous vein (SV) or internal mammary artery (IMA) as a conduit. Unfortunately, the SV has much lower patency rates compared with the IMA. Several hypotheses exist as to why occlusion occurs more commonly in SV grafts than in IMA grafts. However detailed studies in this area have been limited. This study investigates the effects of pressure distention on inflammation in SV conduit used in coronary artery bypass grafting (CABG). Methods Saphenous vein distention pressure was measured intraoperatively during 48 CABG procedures. A segment of SV was excised from the conduit before distention. Because the vein was used for coronary artery grafting, sequential pieces were archived for evaluation. Real-time polymerase chain reaction (RT-PCR) and immunohistochemical analyses were performed to investigate a change in the expression of biomarkers. Results Upregulation of various biomarkers occurred. These biomarkers included scavenger receptors A and B (SR-A, SR-B), toll-like receptors 2 and 4 (TLR2, TLR4), platelet endothelial cell adhesion molecule (PECAM), vascular cell adhesion molecule (VCAM), and intercellular cell adhesion molecule (ICAM) in segments of SV that were subjected to distention. Immunohistochemical results mirrored RT-PCR findings. A significant correlation was observed between biomarkers and pressure values. Conclusions These studies demonstrate that markers of inflammation are upregulated in response to SV distention. The data suggest that the pressure used in graft preparation procedures should be regulated to avoid inflammation and its potential to induce graft failure.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>22206954</pmid><doi>10.1016/j.athoracsur.2011.10.035</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Biological and medical sciences Biomarkers Cardiology. Vascular system Cardiothoracic Surgery Cell Adhesion Molecules - analysis Cell Adhesion Molecules - biosynthesis Cell Adhesion Molecules - genetics Coronary Artery Bypass - methods Coronary Disease - surgery Female Graft Occlusion, Vascular - etiology Graft Occlusion, Vascular - metabolism Humans Hyperplasia Male Medical sciences Middle Aged Phlebitis - etiology Phlebitis - metabolism Pneumology Pressure - adverse effects Real-Time Polymerase Chain Reaction Receptors, Scavenger - analysis Receptors, Scavenger - biosynthesis Receptors, Scavenger - genetics RNA, Messenger - analysis Saphenous Vein - metabolism Saphenous Vein - pathology Saphenous Vein - transplantation Surgery Tissue and Organ Harvesting - adverse effects Tissue and Organ Harvesting - methods Toll-Like Receptors - analysis Toll-Like Receptors - biosynthesis Toll-Like Receptors - genetics Up-Regulation Vascular Patency |
title | High-Pressure Distention of the Saphenous Vein During Preparation Results in Increased Markers of Inflammation: A Potential Mechanism for Graft Failure |
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