Discoordinate modulation of natriuretic peptides during acute cardiac allograft rejection in humans
Increased circulating levels of the cardiac polypeptide hormones atrial natriuretic factor (ANF) and brain natriuretic peptide (BNP) may be observed after orthotopic cardiac transplantation. Both the hypertrophic and inflammatory processes in the allograft may contribute to this increase, but no mec...
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Veröffentlicht in: | Circulation (New York, N.Y.) N.Y.), 1999-07, Vol.100 (3), p.287-291 |
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description | Increased circulating levels of the cardiac polypeptide hormones atrial natriuretic factor (ANF) and brain natriuretic peptide (BNP) may be observed after orthotopic cardiac transplantation. Both the hypertrophic and inflammatory processes in the allograft may contribute to this increase, but no mechanistic explanation has been suggested for this observation.
Plasma immunoreactive ANF and BNP determinations were performed in 10 consecutive transplant patients. These were correlated with degree of rejection as reflected by histopathological findings at serial endomyocardial biopsies. Three patients had associated hemodynamic measurements and blood samples 24 hours before and after transplantation. All rejection episodes that received treatment were accompanied by a marked increase in BNP plasma levels to > approximately 400 pg/mL. Steadily increasing BNP levels preceded overt rejection as assessed by histopathological criteria. The increase in plasma BNP was not always accompanied by an increase in ANF, which suggests the specific upregulation of BNP gene expression during acute rejection episodes. Treatment of the acute rejection episodes led to a substantial decrease of BNP plasma levels.
The significant selective increase in plasma BNP levels found in the present study has not been previously described. This finding provides a new insight into the mechanism of allograft rejection and the modulation of natriuretic peptide synthesis and release. Furthermore, although preliminary, the data suggest that BNP plasma levels could form the basis for a new, noninvasive screening test to predict acute cardiac allograft rejection. Because treatment with the antilymphocyte monoclonal antibody OKT3 (murine monoclonal antibody to the CD3 antigen of the human T-cell) decreased BNP plasma levels, cytokine production by T-cells may mediate the selective increase in circulating BNP. |
doi_str_mv | 10.1161/01.CIR.100.3.287 |
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Plasma immunoreactive ANF and BNP determinations were performed in 10 consecutive transplant patients. These were correlated with degree of rejection as reflected by histopathological findings at serial endomyocardial biopsies. Three patients had associated hemodynamic measurements and blood samples 24 hours before and after transplantation. All rejection episodes that received treatment were accompanied by a marked increase in BNP plasma levels to > approximately 400 pg/mL. Steadily increasing BNP levels preceded overt rejection as assessed by histopathological criteria. The increase in plasma BNP was not always accompanied by an increase in ANF, which suggests the specific upregulation of BNP gene expression during acute rejection episodes. Treatment of the acute rejection episodes led to a substantial decrease of BNP plasma levels.
The significant selective increase in plasma BNP levels found in the present study has not been previously described. This finding provides a new insight into the mechanism of allograft rejection and the modulation of natriuretic peptide synthesis and release. Furthermore, although preliminary, the data suggest that BNP plasma levels could form the basis for a new, noninvasive screening test to predict acute cardiac allograft rejection. Because treatment with the antilymphocyte monoclonal antibody OKT3 (murine monoclonal antibody to the CD3 antigen of the human T-cell) decreased BNP plasma levels, cytokine production by T-cells may mediate the selective increase in circulating BNP.</description><identifier>ISSN: 0009-7322</identifier><identifier>EISSN: 1524-4539</identifier><identifier>DOI: 10.1161/01.CIR.100.3.287</identifier><identifier>PMID: 10411854</identifier><identifier>CODEN: CIRCAZ</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams & Wilkins</publisher><subject>Adult ; Aged ; Atrial Natriuretic Factor - blood ; Atrial Natriuretic Factor - metabolism ; Biological and medical sciences ; Biomarkers - blood ; Cardiac Catheterization ; Endocardium - metabolism ; Endocardium - pathology ; Female ; Gene Expression Regulation ; Graft Rejection - blood ; Graft Rejection - metabolism ; Graft Rejection - pathology ; Heart Transplantation ; Humans ; Male ; Medical sciences ; Middle Aged ; Natriuretic Peptide, Brain - blood ; Natriuretic Peptide, Brain - metabolism ; Prospective Studies ; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases ; Surgery of the heart ; Transplantation, Homologous</subject><ispartof>Circulation (New York, N.Y.), 1999-07, Vol.100 (3), p.287-291</ispartof><rights>1999 INIST-CNRS</rights><rights>Copyright American Heart Association, Inc. Jul 20, 1999</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c434t-8bf685e21107ada9afe86350bd93e87165059549f5f45323dbea9f6af72a356c3</citedby><cites>FETCH-LOGICAL-c434t-8bf685e21107ada9afe86350bd93e87165059549f5f45323dbea9f6af72a356c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3674,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1890526$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10411854$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>MASTERS, R. G</creatorcontrib><creatorcontrib>DAVIES, R. A</creatorcontrib><creatorcontrib>VEINOT, J. P</creatorcontrib><creatorcontrib>HENDRY, P. J</creatorcontrib><creatorcontrib>SMITH, S. J</creatorcontrib><creatorcontrib>DE BOLD, A. J</creatorcontrib><title>Discoordinate modulation of natriuretic peptides during acute cardiac allograft rejection in humans</title><title>Circulation (New York, N.Y.)</title><addtitle>Circulation</addtitle><description>Increased circulating levels of the cardiac polypeptide hormones atrial natriuretic factor (ANF) and brain natriuretic peptide (BNP) may be observed after orthotopic cardiac transplantation. Both the hypertrophic and inflammatory processes in the allograft may contribute to this increase, but no mechanistic explanation has been suggested for this observation.
Plasma immunoreactive ANF and BNP determinations were performed in 10 consecutive transplant patients. These were correlated with degree of rejection as reflected by histopathological findings at serial endomyocardial biopsies. Three patients had associated hemodynamic measurements and blood samples 24 hours before and after transplantation. All rejection episodes that received treatment were accompanied by a marked increase in BNP plasma levels to > approximately 400 pg/mL. Steadily increasing BNP levels preceded overt rejection as assessed by histopathological criteria. The increase in plasma BNP was not always accompanied by an increase in ANF, which suggests the specific upregulation of BNP gene expression during acute rejection episodes. Treatment of the acute rejection episodes led to a substantial decrease of BNP plasma levels.
The significant selective increase in plasma BNP levels found in the present study has not been previously described. This finding provides a new insight into the mechanism of allograft rejection and the modulation of natriuretic peptide synthesis and release. Furthermore, although preliminary, the data suggest that BNP plasma levels could form the basis for a new, noninvasive screening test to predict acute cardiac allograft rejection. Because treatment with the antilymphocyte monoclonal antibody OKT3 (murine monoclonal antibody to the CD3 antigen of the human T-cell) decreased BNP plasma levels, cytokine production by T-cells may mediate the selective increase in circulating BNP.</description><subject>Adult</subject><subject>Aged</subject><subject>Atrial Natriuretic Factor - blood</subject><subject>Atrial Natriuretic Factor - metabolism</subject><subject>Biological and medical sciences</subject><subject>Biomarkers - blood</subject><subject>Cardiac Catheterization</subject><subject>Endocardium - metabolism</subject><subject>Endocardium - pathology</subject><subject>Female</subject><subject>Gene Expression Regulation</subject><subject>Graft Rejection - blood</subject><subject>Graft Rejection - metabolism</subject><subject>Graft Rejection - pathology</subject><subject>Heart Transplantation</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Natriuretic Peptide, Brain - blood</subject><subject>Natriuretic Peptide, Brain - metabolism</subject><subject>Prospective Studies</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</subject><subject>Surgery of the heart</subject><subject>Transplantation, Homologous</subject><issn>0009-7322</issn><issn>1524-4539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkM1r3DAQxUVpSTZp7z0VUUpudkeSJVvHsm0-IFAo6VnMylKqxba2knXofx81u9CS0zDD7z3mPULeM2gZU-wzsHZ796NlAK1o-dC_Ihsmedd0UujXZAMAuukF5-fkIud9XZXo5Rk5Z9AxNshuQ-zXkG2MaQwLro7OcSwTriEuNHpaTymU5NZg6cEd1jC6TMeSwvJI0ZbKW6xKtBSnKT4m9CtNbu_ss0FY6K8y45Lfkjcep-zeneYl-Xn97WF729x_v7nbfrlvbCe6tRl2Xg3SccagxxE1ejcoIWE3auGGnikJUstOe-lrPi7GnUPtFfqeo5DKiktydfQ9pPi7uLyauYZz04SLiyUbpTVwxbsKfnwB7mNJS_3NcMaVAimHCsERsinmnJw3hxRmTH8MA_O3fQPM1PbrCkaY2n6VfDj5lt3sxv8Ex7or8OkEYLY4-YSLDfkfN2iQXIknHuSNbQ</recordid><startdate>19990720</startdate><enddate>19990720</enddate><creator>MASTERS, R. G</creator><creator>DAVIES, R. A</creator><creator>VEINOT, J. P</creator><creator>HENDRY, P. J</creator><creator>SMITH, S. J</creator><creator>DE BOLD, A. J</creator><general>Lippincott Williams & Wilkins</general><general>American Heart Association, Inc</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>K9.</scope><scope>NAPCQ</scope><scope>U9A</scope><scope>7X8</scope></search><sort><creationdate>19990720</creationdate><title>Discoordinate modulation of natriuretic peptides during acute cardiac allograft rejection in humans</title><author>MASTERS, R. G ; DAVIES, R. A ; VEINOT, J. P ; HENDRY, P. J ; SMITH, S. J ; DE BOLD, A. J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c434t-8bf685e21107ada9afe86350bd93e87165059549f5f45323dbea9f6af72a356c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Atrial Natriuretic Factor - blood</topic><topic>Atrial Natriuretic Factor - metabolism</topic><topic>Biological and medical sciences</topic><topic>Biomarkers - blood</topic><topic>Cardiac Catheterization</topic><topic>Endocardium - metabolism</topic><topic>Endocardium - pathology</topic><topic>Female</topic><topic>Gene Expression Regulation</topic><topic>Graft Rejection - blood</topic><topic>Graft Rejection - metabolism</topic><topic>Graft Rejection - pathology</topic><topic>Heart Transplantation</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Natriuretic Peptide, Brain - blood</topic><topic>Natriuretic Peptide, Brain - metabolism</topic><topic>Prospective Studies</topic><topic>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</topic><topic>Surgery of the heart</topic><topic>Transplantation, Homologous</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>MASTERS, R. G</creatorcontrib><creatorcontrib>DAVIES, R. A</creatorcontrib><creatorcontrib>VEINOT, J. P</creatorcontrib><creatorcontrib>HENDRY, P. J</creatorcontrib><creatorcontrib>SMITH, S. J</creatorcontrib><creatorcontrib>DE BOLD, A. 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J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Discoordinate modulation of natriuretic peptides during acute cardiac allograft rejection in humans</atitle><jtitle>Circulation (New York, N.Y.)</jtitle><addtitle>Circulation</addtitle><date>1999-07-20</date><risdate>1999</risdate><volume>100</volume><issue>3</issue><spage>287</spage><epage>291</epage><pages>287-291</pages><issn>0009-7322</issn><eissn>1524-4539</eissn><coden>CIRCAZ</coden><abstract>Increased circulating levels of the cardiac polypeptide hormones atrial natriuretic factor (ANF) and brain natriuretic peptide (BNP) may be observed after orthotopic cardiac transplantation. Both the hypertrophic and inflammatory processes in the allograft may contribute to this increase, but no mechanistic explanation has been suggested for this observation.
Plasma immunoreactive ANF and BNP determinations were performed in 10 consecutive transplant patients. These were correlated with degree of rejection as reflected by histopathological findings at serial endomyocardial biopsies. Three patients had associated hemodynamic measurements and blood samples 24 hours before and after transplantation. All rejection episodes that received treatment were accompanied by a marked increase in BNP plasma levels to > approximately 400 pg/mL. Steadily increasing BNP levels preceded overt rejection as assessed by histopathological criteria. The increase in plasma BNP was not always accompanied by an increase in ANF, which suggests the specific upregulation of BNP gene expression during acute rejection episodes. Treatment of the acute rejection episodes led to a substantial decrease of BNP plasma levels.
The significant selective increase in plasma BNP levels found in the present study has not been previously described. This finding provides a new insight into the mechanism of allograft rejection and the modulation of natriuretic peptide synthesis and release. Furthermore, although preliminary, the data suggest that BNP plasma levels could form the basis for a new, noninvasive screening test to predict acute cardiac allograft rejection. Because treatment with the antilymphocyte monoclonal antibody OKT3 (murine monoclonal antibody to the CD3 antigen of the human T-cell) decreased BNP plasma levels, cytokine production by T-cells may mediate the selective increase in circulating BNP.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams & Wilkins</pub><pmid>10411854</pmid><doi>10.1161/01.CIR.100.3.287</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Atrial Natriuretic Factor - blood Atrial Natriuretic Factor - metabolism Biological and medical sciences Biomarkers - blood Cardiac Catheterization Endocardium - metabolism Endocardium - pathology Female Gene Expression Regulation Graft Rejection - blood Graft Rejection - metabolism Graft Rejection - pathology Heart Transplantation Humans Male Medical sciences Middle Aged Natriuretic Peptide, Brain - blood Natriuretic Peptide, Brain - metabolism Prospective Studies Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases Surgery of the heart Transplantation, Homologous |
title | Discoordinate modulation of natriuretic peptides during acute cardiac allograft rejection in humans |
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