Meta-analysis on the immunohistological detection of inflammatory cardiomyopathy in endomyocardial biopsies
Meta-analysis on immunohistological (IHC) concepts for the detection of inflammatory cardiomyopathy (InfCM) in endomyocardial biopsies (EMB). We included 61 publications, with 10,491 patients (mean age 47.1 years; men 66%) who underwent EMB and IHC evaluation. The 460 control patients were devoid of...
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description | Meta-analysis on immunohistological (IHC) concepts for the detection of inflammatory cardiomyopathy (InfCM) in endomyocardial biopsies (EMB). We included 61 publications, with 10,491 patients (mean age 47.1 years; men 66%) who underwent EMB and IHC evaluation. The 460 control patients were devoid of IHC proof of InfCM. The mean IHC detection rate of InfCM was 50.8% (95% CI 47.7–53.8%; range 18.4–91.7%). A publication bias was excluded (Funnel Plot
p
= 0.4264). This IHC detection rate was significantly (
p
|
doi_str_mv | 10.1007/s10741-019-09835-9 |
format | Article |
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p
= 0.4264). This IHC detection rate was significantly (
p
< 0.0001) higher compared to the histological detection of myocarditis according to the Dallas criteria (mean 8.04%; 95% CI 5.08–12.5%; subset of 3274 patients in 30 publications). However, 13 different diagnostic IHC criteria were described in the publications, with various thresholds of diverse phenotypes of quantified infiltrates, and endothelial expression of diverse cell adhesion molecules (CAM), quantified either visually or by digital image analysis (DIA). The comparison of IHC with cardiac magnetic resonance (CMR) data available in a subset of 13 publications with 1185 patients revealed a sensitivity for CMR of 69% (95% CI 58–79%), a specificity of 73% (95% CI 59–84%), and a ROC-AUC of 0.77 (95% CI 0.73–0.81). This meta-analysis encompassing 10,491 patients confirms a mean detection rate of InfCM in 50.8% of EMB, being significantly more sensitive compared to the histological Dallas criteria. IHC cannot be fully substituted by CMR. However, standardization of the diverse IHC markers and protocols seems pertinent, especially considering the published adverse prognostic impact of IHC-confirmed InfCM and its published suitability for the selection of candidates responding favorably to immunosuppression.</description><identifier>ISSN: 1382-4147</identifier><identifier>EISSN: 1573-7322</identifier><identifier>DOI: 10.1007/s10741-019-09835-9</identifier><identifier>PMID: 31396762</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Biopsy - methods ; Cardiology ; Cardiomyopathies - diagnosis ; Cardiomyopathy ; Cell adhesion & migration ; Cell adhesion molecules ; Heart diseases ; Humans ; Image processing ; Immunohistochemistry - methods ; Immunosuppression ; Inflammation ; Medicine ; Medicine & Public Health ; Meta-analysis ; Myocarditis ; Myocardium - pathology ; Phenotypes ; Standardization</subject><ispartof>Heart failure reviews, 2020-03, Vol.25 (2), p.277-294</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2019</rights><rights>Heart Failure Reviews is a copyright of Springer, (2019). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c441t-3359256bba90972bb7c9378e45f5ee6e3ecefd142a9b14648fb5df513a19252d3</citedby><cites>FETCH-LOGICAL-c441t-3359256bba90972bb7c9378e45f5ee6e3ecefd142a9b14648fb5df513a19252d3</cites><orcidid>0000-0002-9066-5262</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10741-019-09835-9$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10741-019-09835-9$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27923,27924,41487,42556,51318</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31396762$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Katzmann, Julius L.</creatorcontrib><creatorcontrib>Schlattmann, Peter</creatorcontrib><creatorcontrib>Rigopoulos, Angelos G.</creatorcontrib><creatorcontrib>Noutsias, Ewa</creatorcontrib><creatorcontrib>Bigalke, Boris</creatorcontrib><creatorcontrib>Pauschinger, Matthias</creatorcontrib><creatorcontrib>Tschope, Carsten</creatorcontrib><creatorcontrib>Sedding, Daniel</creatorcontrib><creatorcontrib>Schulze, P. Christian</creatorcontrib><creatorcontrib>Noutsias, Michel</creatorcontrib><title>Meta-analysis on the immunohistological detection of inflammatory cardiomyopathy in endomyocardial biopsies</title><title>Heart failure reviews</title><addtitle>Heart Fail Rev</addtitle><addtitle>Heart Fail Rev</addtitle><description>Meta-analysis on immunohistological (IHC) concepts for the detection of inflammatory cardiomyopathy (InfCM) in endomyocardial biopsies (EMB). We included 61 publications, with 10,491 patients (mean age 47.1 years; men 66%) who underwent EMB and IHC evaluation. The 460 control patients were devoid of IHC proof of InfCM. The mean IHC detection rate of InfCM was 50.8% (95% CI 47.7–53.8%; range 18.4–91.7%). A publication bias was excluded (Funnel Plot
p
= 0.4264). This IHC detection rate was significantly (
p
< 0.0001) higher compared to the histological detection of myocarditis according to the Dallas criteria (mean 8.04%; 95% CI 5.08–12.5%; subset of 3274 patients in 30 publications). However, 13 different diagnostic IHC criteria were described in the publications, with various thresholds of diverse phenotypes of quantified infiltrates, and endothelial expression of diverse cell adhesion molecules (CAM), quantified either visually or by digital image analysis (DIA). The comparison of IHC with cardiac magnetic resonance (CMR) data available in a subset of 13 publications with 1185 patients revealed a sensitivity for CMR of 69% (95% CI 58–79%), a specificity of 73% (95% CI 59–84%), and a ROC-AUC of 0.77 (95% CI 0.73–0.81). This meta-analysis encompassing 10,491 patients confirms a mean detection rate of InfCM in 50.8% of EMB, being significantly more sensitive compared to the histological Dallas criteria. IHC cannot be fully substituted by CMR. However, standardization of the diverse IHC markers and protocols seems pertinent, especially considering the published adverse prognostic impact of IHC-confirmed InfCM and its published suitability for the selection of candidates responding favorably to immunosuppression.</description><subject>Biopsy - methods</subject><subject>Cardiology</subject><subject>Cardiomyopathies - diagnosis</subject><subject>Cardiomyopathy</subject><subject>Cell adhesion & migration</subject><subject>Cell adhesion molecules</subject><subject>Heart diseases</subject><subject>Humans</subject><subject>Image processing</subject><subject>Immunohistochemistry - methods</subject><subject>Immunosuppression</subject><subject>Inflammation</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Meta-analysis</subject><subject>Myocarditis</subject><subject>Myocardium - pathology</subject><subject>Phenotypes</subject><subject>Standardization</subject><issn>1382-4147</issn><issn>1573-7322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp9kUtLxDAUhYMoOo7-ARdScOMmmlebyVLEF4y40XVI29uZaNuMSbrovzfzUMGFEEjC-c69cA5CZ5RcUULkdaBECooJVZioGc-x2kMTmkuOJWdsP735jGFBhTxCxyG8E0KEEuQQHXHKVSELNkEfzxANNr1px2BD5vosLiGzXTf0bmlDdK1b2Mq0WQ0RqmgT4JrM9k1rus5E58esMr62rhvdysTlmLQM-nr93wjJWlq3ChbCCTpoTBvgdHdP0dv93evtI56_PDzd3sxxJQSNmPNcsbwoS6OIkqwsZaW4nIHImxygAA4VNDUVzKiSikLMmjKvm5xyQ5OP1XyKLrdzV959DhCi7myooG1ND24ImjGZouBEyoRe_EHf3eBTGmuqUFIJns4UsS1VeReCh0avvO2MHzUlel2F3lahUxV6U4VWyXS-Gz2UHdQ_lu_sE8C3QEhSvwD_u_ufsV-CQZYb</recordid><startdate>20200301</startdate><enddate>20200301</enddate><creator>Katzmann, Julius L.</creator><creator>Schlattmann, Peter</creator><creator>Rigopoulos, Angelos G.</creator><creator>Noutsias, Ewa</creator><creator>Bigalke, Boris</creator><creator>Pauschinger, Matthias</creator><creator>Tschope, Carsten</creator><creator>Sedding, Daniel</creator><creator>Schulze, P. Christian</creator><creator>Noutsias, Michel</creator><general>Springer US</general><general>Springer Nature B.V</general><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>3V.</scope><scope>7QP</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-9066-5262</orcidid></search><sort><creationdate>20200301</creationdate><title>Meta-analysis on the immunohistological detection of inflammatory cardiomyopathy in endomyocardial biopsies</title><author>Katzmann, Julius L. ; Schlattmann, Peter ; Rigopoulos, Angelos G. ; Noutsias, Ewa ; Bigalke, Boris ; Pauschinger, Matthias ; Tschope, Carsten ; Sedding, Daniel ; Schulze, P. 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Christian</au><au>Noutsias, Michel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Meta-analysis on the immunohistological detection of inflammatory cardiomyopathy in endomyocardial biopsies</atitle><jtitle>Heart failure reviews</jtitle><stitle>Heart Fail Rev</stitle><addtitle>Heart Fail Rev</addtitle><date>2020-03-01</date><risdate>2020</risdate><volume>25</volume><issue>2</issue><spage>277</spage><epage>294</epage><pages>277-294</pages><issn>1382-4147</issn><eissn>1573-7322</eissn><abstract>Meta-analysis on immunohistological (IHC) concepts for the detection of inflammatory cardiomyopathy (InfCM) in endomyocardial biopsies (EMB). We included 61 publications, with 10,491 patients (mean age 47.1 years; men 66%) who underwent EMB and IHC evaluation. The 460 control patients were devoid of IHC proof of InfCM. The mean IHC detection rate of InfCM was 50.8% (95% CI 47.7–53.8%; range 18.4–91.7%). A publication bias was excluded (Funnel Plot
p
= 0.4264). This IHC detection rate was significantly (
p
< 0.0001) higher compared to the histological detection of myocarditis according to the Dallas criteria (mean 8.04%; 95% CI 5.08–12.5%; subset of 3274 patients in 30 publications). However, 13 different diagnostic IHC criteria were described in the publications, with various thresholds of diverse phenotypes of quantified infiltrates, and endothelial expression of diverse cell adhesion molecules (CAM), quantified either visually or by digital image analysis (DIA). The comparison of IHC with cardiac magnetic resonance (CMR) data available in a subset of 13 publications with 1185 patients revealed a sensitivity for CMR of 69% (95% CI 58–79%), a specificity of 73% (95% CI 59–84%), and a ROC-AUC of 0.77 (95% CI 0.73–0.81). This meta-analysis encompassing 10,491 patients confirms a mean detection rate of InfCM in 50.8% of EMB, being significantly more sensitive compared to the histological Dallas criteria. IHC cannot be fully substituted by CMR. However, standardization of the diverse IHC markers and protocols seems pertinent, especially considering the published adverse prognostic impact of IHC-confirmed InfCM and its published suitability for the selection of candidates responding favorably to immunosuppression.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>31396762</pmid><doi>10.1007/s10741-019-09835-9</doi><tpages>18</tpages><orcidid>https://orcid.org/0000-0002-9066-5262</orcidid></addata></record> |
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subjects | Biopsy - methods Cardiology Cardiomyopathies - diagnosis Cardiomyopathy Cell adhesion & migration Cell adhesion molecules Heart diseases Humans Image processing Immunohistochemistry - methods Immunosuppression Inflammation Medicine Medicine & Public Health Meta-analysis Myocarditis Myocardium - pathology Phenotypes Standardization |
title | Meta-analysis on the immunohistological detection of inflammatory cardiomyopathy in endomyocardial biopsies |
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