Anti-Inflammatory Effect of Cardiac Resynchronization Therapy
Background: Congestive heart failure (CHF) is associated with persistent immune activation. Medical therapy has been shown to exert only limited anti‐inflammatory effects. Cardiac resynchronization therapy (CRT) reduces morbidity and mortality in a subset of patients with heart failure, but it is no...
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Veröffentlicht in: | Pacing and clinical electrophysiology 2006-07, Vol.29 (7), p.753-758 |
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description | Background: Congestive heart failure (CHF) is associated with persistent immune activation. Medical therapy has been shown to exert only limited anti‐inflammatory effects. Cardiac resynchronization therapy (CRT) reduces morbidity and mortality in a subset of patients with heart failure, but it is not known whether this treatment affects the immune system as well. To test this hypothesis, eight patients with heart failure scheduled for CRT were investigated for immune activation before and 6 months after CRT treatment.
Methods and Results: After 6 months, all patients had improved in NYHA‐class and LVEF, and there was a statistically significant reduction in serum N‐terminal pro brain natriuretic peptide (BNP). Furthermore, there was a statistically significant reduction in plasma levels of the chemokines monocyte chemoattractant protein 1 (MCP‐1) and interleukin 8 (IL‐8) and the cytokine interleukin 6 (IL‐6). We observed no changes in the levels of interleukin 1β (IL‐1β), tumor necrosis factor α (TNF‐α), interleukin 10 (IL‐10), or complement activation products. There was a significant correlation between changes in BNP and IL‐6 (r = 0.74, P = 0.037).
Conclusion: Although based upon a limited number of patients, this report indicates that CRT reduces peripheral markers of immune activation in patients with CHF. Further large scale studies are warranted to verify these findings. |
doi_str_mv | 10.1111/j.1540-8159.2006.00430.x |
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Methods and Results: After 6 months, all patients had improved in NYHA‐class and LVEF, and there was a statistically significant reduction in serum N‐terminal pro brain natriuretic peptide (BNP). Furthermore, there was a statistically significant reduction in plasma levels of the chemokines monocyte chemoattractant protein 1 (MCP‐1) and interleukin 8 (IL‐8) and the cytokine interleukin 6 (IL‐6). We observed no changes in the levels of interleukin 1β (IL‐1β), tumor necrosis factor α (TNF‐α), interleukin 10 (IL‐10), or complement activation products. There was a significant correlation between changes in BNP and IL‐6 (r = 0.74, P = 0.037).
Conclusion: Although based upon a limited number of patients, this report indicates that CRT reduces peripheral markers of immune activation in patients with CHF. Further large scale studies are warranted to verify these findings.</description><identifier>ISSN: 0147-8389</identifier><identifier>EISSN: 1540-8159</identifier><identifier>DOI: 10.1111/j.1540-8159.2006.00430.x</identifier><identifier>PMID: 16884512</identifier><language>eng</language><publisher>Malden, USA: Blackwell Publishing Inc</publisher><subject>Aged ; Aged, 80 and over ; Cardiac Pacing, Artificial ; congestive heart failure ; Female ; Heart Failure - immunology ; Heart Failure - therapy ; Humans ; immunology ; Inflammation - blood ; Interleukin-6 - blood ; Interleukin-8 - blood ; Male ; Membrane Cofactor Protein - blood ; Middle Aged ; Natriuretic Peptide, Brain - blood ; pacing ; Statistics, Nonparametric</subject><ispartof>Pacing and clinical electrophysiology, 2006-07, Vol.29 (7), p.753-758</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4050-4be658d8ba6db3f952f9523455e4dd1f241f59b726ee2113b40cf2fc5022bc583</citedby><cites>FETCH-LOGICAL-c4050-4be658d8ba6db3f952f9523455e4dd1f241f59b726ee2113b40cf2fc5022bc583</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1540-8159.2006.00430.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1540-8159.2006.00430.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16884512$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>LAPPEGÅRD, KNUT T.</creatorcontrib><creatorcontrib>BJØRNSTAD, HANNE</creatorcontrib><title>Anti-Inflammatory Effect of Cardiac Resynchronization Therapy</title><title>Pacing and clinical electrophysiology</title><addtitle>Pacing Clin Electrophysiol</addtitle><description>Background: Congestive heart failure (CHF) is associated with persistent immune activation. Medical therapy has been shown to exert only limited anti‐inflammatory effects. Cardiac resynchronization therapy (CRT) reduces morbidity and mortality in a subset of patients with heart failure, but it is not known whether this treatment affects the immune system as well. To test this hypothesis, eight patients with heart failure scheduled for CRT were investigated for immune activation before and 6 months after CRT treatment.
Methods and Results: After 6 months, all patients had improved in NYHA‐class and LVEF, and there was a statistically significant reduction in serum N‐terminal pro brain natriuretic peptide (BNP). Furthermore, there was a statistically significant reduction in plasma levels of the chemokines monocyte chemoattractant protein 1 (MCP‐1) and interleukin 8 (IL‐8) and the cytokine interleukin 6 (IL‐6). We observed no changes in the levels of interleukin 1β (IL‐1β), tumor necrosis factor α (TNF‐α), interleukin 10 (IL‐10), or complement activation products. There was a significant correlation between changes in BNP and IL‐6 (r = 0.74, P = 0.037).
Conclusion: Although based upon a limited number of patients, this report indicates that CRT reduces peripheral markers of immune activation in patients with CHF. Further large scale studies are warranted to verify these findings.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Cardiac Pacing, Artificial</subject><subject>congestive heart failure</subject><subject>Female</subject><subject>Heart Failure - immunology</subject><subject>Heart Failure - therapy</subject><subject>Humans</subject><subject>immunology</subject><subject>Inflammation - blood</subject><subject>Interleukin-6 - blood</subject><subject>Interleukin-8 - blood</subject><subject>Male</subject><subject>Membrane Cofactor Protein - blood</subject><subject>Middle Aged</subject><subject>Natriuretic Peptide, Brain - blood</subject><subject>pacing</subject><subject>Statistics, Nonparametric</subject><issn>0147-8389</issn><issn>1540-8159</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkE1PwjAYgBujEUT_gtnJ22Y_t3LgQBCBBJUoRm9N17VhuA9sR2T-ejcheLVJ0yZ9nrfJA4CHYICadbsOEKPQ54j1AwxhGEBICQx2J6B7fDgFXYho5HPC-x1w4dwaNiSk7Bx0UMg5ZQh3wWBYVKk_K0wm81xWpa29sTFaVV5pvJG0SSqV96xdXaiVLYv0W1ZpWXjLlbZyU1-CMyMzp68OZw-83o-Xo6k_f5rMRsO5ryhk0KexDhlPeCzDJCamz3C7CWVM0yRBBlNkWD-OcKg1RojEFCqDjWIQ41gxTnrgZj93Y8vPrXaVyFOndJbJQpdbJ0IeIQYJaUC-B5UtnbPaiI1Nc2lrgaBo04m1aAuJtpBo04nfdGLXqNeHP7ZxrpM_8dCqAQZ74CvNdP3vwWIxHI2bW-P7ez91ld4dfWk_RBiRiIm3x4mYLuj74uGOihfyA8Z_i1g</recordid><startdate>200607</startdate><enddate>200607</enddate><creator>LAPPEGÅRD, KNUT T.</creator><creator>BJØRNSTAD, HANNE</creator><general>Blackwell Publishing Inc</general><scope>BSCLL</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>200607</creationdate><title>Anti-Inflammatory Effect of Cardiac Resynchronization Therapy</title><author>LAPPEGÅRD, KNUT T. ; BJØRNSTAD, HANNE</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4050-4be658d8ba6db3f952f9523455e4dd1f241f59b726ee2113b40cf2fc5022bc583</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Cardiac Pacing, Artificial</topic><topic>congestive heart failure</topic><topic>Female</topic><topic>Heart Failure - immunology</topic><topic>Heart Failure - therapy</topic><topic>Humans</topic><topic>immunology</topic><topic>Inflammation - blood</topic><topic>Interleukin-6 - blood</topic><topic>Interleukin-8 - blood</topic><topic>Male</topic><topic>Membrane Cofactor Protein - blood</topic><topic>Middle Aged</topic><topic>Natriuretic Peptide, Brain - blood</topic><topic>pacing</topic><topic>Statistics, Nonparametric</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>LAPPEGÅRD, KNUT T.</creatorcontrib><creatorcontrib>BJØRNSTAD, HANNE</creatorcontrib><collection>Istex</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>Pacing and clinical electrophysiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>LAPPEGÅRD, KNUT T.</au><au>BJØRNSTAD, HANNE</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Anti-Inflammatory Effect of Cardiac Resynchronization Therapy</atitle><jtitle>Pacing and clinical electrophysiology</jtitle><addtitle>Pacing Clin Electrophysiol</addtitle><date>2006-07</date><risdate>2006</risdate><volume>29</volume><issue>7</issue><spage>753</spage><epage>758</epage><pages>753-758</pages><issn>0147-8389</issn><eissn>1540-8159</eissn><abstract>Background: Congestive heart failure (CHF) is associated with persistent immune activation. Medical therapy has been shown to exert only limited anti‐inflammatory effects. Cardiac resynchronization therapy (CRT) reduces morbidity and mortality in a subset of patients with heart failure, but it is not known whether this treatment affects the immune system as well. To test this hypothesis, eight patients with heart failure scheduled for CRT were investigated for immune activation before and 6 months after CRT treatment.
Methods and Results: After 6 months, all patients had improved in NYHA‐class and LVEF, and there was a statistically significant reduction in serum N‐terminal pro brain natriuretic peptide (BNP). Furthermore, there was a statistically significant reduction in plasma levels of the chemokines monocyte chemoattractant protein 1 (MCP‐1) and interleukin 8 (IL‐8) and the cytokine interleukin 6 (IL‐6). We observed no changes in the levels of interleukin 1β (IL‐1β), tumor necrosis factor α (TNF‐α), interleukin 10 (IL‐10), or complement activation products. There was a significant correlation between changes in BNP and IL‐6 (r = 0.74, P = 0.037).
Conclusion: Although based upon a limited number of patients, this report indicates that CRT reduces peripheral markers of immune activation in patients with CHF. Further large scale studies are warranted to verify these findings.</abstract><cop>Malden, USA</cop><pub>Blackwell Publishing Inc</pub><pmid>16884512</pmid><doi>10.1111/j.1540-8159.2006.00430.x</doi><tpages>6</tpages></addata></record> |
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subjects | Aged Aged, 80 and over Cardiac Pacing, Artificial congestive heart failure Female Heart Failure - immunology Heart Failure - therapy Humans immunology Inflammation - blood Interleukin-6 - blood Interleukin-8 - blood Male Membrane Cofactor Protein - blood Middle Aged Natriuretic Peptide, Brain - blood pacing Statistics, Nonparametric |
title | Anti-Inflammatory Effect of Cardiac Resynchronization Therapy |
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