Circulating Angiokines Are Associated With Reverse Remodeling and Outcomes in Chronic Heart Failure

We sought to determine whether circulating modifiers of endothelial function are associated with cardiac structure and clinical outcomes in patients with heart failure with reduced ejection fraction (HFrEF). We measured 25 proteins related to endothelial function in 99 patients from the GUIDE-IT stu...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of cardiac failure 2023-06, Vol.29 (6), p.896-906
Hauptverfasser: Harrington, JOSEPHINE, NIXON, ANDREW B., DAUBERT, MELISSA A., YOW, ERIC, JANUZZI, JAMES, FIUZAT, MONA, WHELLAN, DAVID J., O'CONNOR, CHRISTOPHER M., EZEKOWITZ, JUSTIN, PIÑA, ILEANA L., ADAMS, KIRKWOOD F., FELKER, G. MICHAEL, KARRA, RAVI
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 906
container_issue 6
container_start_page 896
container_title Journal of cardiac failure
container_volume 29
creator Harrington, JOSEPHINE
NIXON, ANDREW B.
DAUBERT, MELISSA A.
YOW, ERIC
JANUZZI, JAMES
FIUZAT, MONA
WHELLAN, DAVID J.
O'CONNOR, CHRISTOPHER M.
EZEKOWITZ, JUSTIN
PIÑA, ILEANA L.
ADAMS, KIRKWOOD F.
FELKER, G. MICHAEL
KARRA, RAVI
description We sought to determine whether circulating modifiers of endothelial function are associated with cardiac structure and clinical outcomes in patients with heart failure with reduced ejection fraction (HFrEF). We measured 25 proteins related to endothelial function in 99 patients from the GUIDE-IT study. Protein levels were evaluated for association with echocardiographic parameters and the incidence of all-cause death and hospitalization for heart failure (HHF). Higher concentrations of angiopoietin 2 (ANGPT2), vascular endothelial growth factor receptor 1 (VEGFR1) and hepatocyte growth factor (HGF) were significantly associated with worse function and larger ventricular volumes. Over time, decreases in ANGPT2 and, to a lesser extent, VEGFR1 and HGF, were associated with improvements in cardiac size and function. Individuals with higher concentrations of ANGPT2, VEGFR1 or HGF had increased risks for a composite of death and HHF in the following year (HR 2.76 (95% CI 1.73–4.40) per 2-fold change in ANGPT2; HR 1.76 (95% CI 1.11–2.79) for VEGFR1; and HR 4.04 (95% CI 2.19–7.44) for HGF). Proteins related to endothelial function associate with cardiac size, cardiac function and clinical outcomes in patients with HFrEF. These results support the concept that endothelial function may be an important contributor to the progression to and the recovery from HFrEF. Take-Home Visual Graphic: Changes in circulating angiokines are associated with reverse remodeling and outcomes in chronic heart failure. [Display omitted]
doi_str_mv 10.1016/j.cardfail.2022.12.011
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2765072768</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1071916423000039</els_id><sourcerecordid>2765072768</sourcerecordid><originalsourceid>FETCH-LOGICAL-c368t-ec57a4d8415ced37092dfdefb73aa2266289f0c84d234c664d32a78e1de750cd3</originalsourceid><addsrcrecordid>eNqFkMtOwzAQRS0EoqXwC8hLNgl-xU53VBUvqRISArG0jD0BlyQudoLE3-OqhS2bmVncO3PnIHROSUkJlZfr0proGuPbkhHGSspKQukBmtKKs6IWVBzmmShazKkUE3SS0poQUguijtGES8nZnIspsksf7diawfdveNG_-fDhe0h4EQEvUgrWmwEcfvHDO36EL4gJcu-Cg3brML3DD-NgQ5c9vsfL9xh6b_EdmDjgmxxvjHCKjhrTJjjb9xl6vrl-Wt4Vq4fb--ViVVgu66EAWykjXM5eWXBckTlzjYPmVXFjGJOS1fOG2Fo4xoWVUjjOjKqBOlAVsY7P0MVu7yaGzxHSoDufLLSt6SGMSTMlK6JyrbNU7qQ2hpQiNHoTfWfit6ZEbwHrtf4FrLeANWU6A87G8_2N8bUD92f7JZoFVzsB5E-_PESdrIc-f-Qj2EG74P-78QNzV5A7</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2765072768</pqid></control><display><type>article</type><title>Circulating Angiokines Are Associated With Reverse Remodeling and Outcomes in Chronic Heart Failure</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Harrington, JOSEPHINE ; NIXON, ANDREW B. ; DAUBERT, MELISSA A. ; YOW, ERIC ; JANUZZI, JAMES ; FIUZAT, MONA ; WHELLAN, DAVID J. ; O'CONNOR, CHRISTOPHER M. ; EZEKOWITZ, JUSTIN ; PIÑA, ILEANA L. ; ADAMS, KIRKWOOD F. ; FELKER, G. MICHAEL ; KARRA, RAVI</creator><creatorcontrib>Harrington, JOSEPHINE ; NIXON, ANDREW B. ; DAUBERT, MELISSA A. ; YOW, ERIC ; JANUZZI, JAMES ; FIUZAT, MONA ; WHELLAN, DAVID J. ; O'CONNOR, CHRISTOPHER M. ; EZEKOWITZ, JUSTIN ; PIÑA, ILEANA L. ; ADAMS, KIRKWOOD F. ; FELKER, G. MICHAEL ; KARRA, RAVI</creatorcontrib><description>We sought to determine whether circulating modifiers of endothelial function are associated with cardiac structure and clinical outcomes in patients with heart failure with reduced ejection fraction (HFrEF). We measured 25 proteins related to endothelial function in 99 patients from the GUIDE-IT study. Protein levels were evaluated for association with echocardiographic parameters and the incidence of all-cause death and hospitalization for heart failure (HHF). Higher concentrations of angiopoietin 2 (ANGPT2), vascular endothelial growth factor receptor 1 (VEGFR1) and hepatocyte growth factor (HGF) were significantly associated with worse function and larger ventricular volumes. Over time, decreases in ANGPT2 and, to a lesser extent, VEGFR1 and HGF, were associated with improvements in cardiac size and function. Individuals with higher concentrations of ANGPT2, VEGFR1 or HGF had increased risks for a composite of death and HHF in the following year (HR 2.76 (95% CI 1.73–4.40) per 2-fold change in ANGPT2; HR 1.76 (95% CI 1.11–2.79) for VEGFR1; and HR 4.04 (95% CI 2.19–7.44) for HGF). Proteins related to endothelial function associate with cardiac size, cardiac function and clinical outcomes in patients with HFrEF. These results support the concept that endothelial function may be an important contributor to the progression to and the recovery from HFrEF. Take-Home Visual Graphic: Changes in circulating angiokines are associated with reverse remodeling and outcomes in chronic heart failure. [Display omitted]</description><identifier>ISSN: 1071-9164</identifier><identifier>EISSN: 1532-8414</identifier><identifier>DOI: 10.1016/j.cardfail.2022.12.011</identifier><identifier>PMID: 36632934</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Cause of Death ; Chronic Disease ; Heart Failure - epidemiology ; Humans ; Risk Factors ; Stroke Volume - physiology ; Vascular Endothelial Growth Factor A ; Ventricular Dysfunction, Left ; Ventricular Function, Left - physiology</subject><ispartof>Journal of cardiac failure, 2023-06, Vol.29 (6), p.896-906</ispartof><rights>2023 Elsevier Inc.</rights><rights>Copyright © 2023 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c368t-ec57a4d8415ced37092dfdefb73aa2266289f0c84d234c664d32a78e1de750cd3</citedby><cites>FETCH-LOGICAL-c368t-ec57a4d8415ced37092dfdefb73aa2266289f0c84d234c664d32a78e1de750cd3</cites><orcidid>0000-0001-6741-285X ; 0000-0001-5169-117X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1071916423000039$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36632934$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Harrington, JOSEPHINE</creatorcontrib><creatorcontrib>NIXON, ANDREW B.</creatorcontrib><creatorcontrib>DAUBERT, MELISSA A.</creatorcontrib><creatorcontrib>YOW, ERIC</creatorcontrib><creatorcontrib>JANUZZI, JAMES</creatorcontrib><creatorcontrib>FIUZAT, MONA</creatorcontrib><creatorcontrib>WHELLAN, DAVID J.</creatorcontrib><creatorcontrib>O'CONNOR, CHRISTOPHER M.</creatorcontrib><creatorcontrib>EZEKOWITZ, JUSTIN</creatorcontrib><creatorcontrib>PIÑA, ILEANA L.</creatorcontrib><creatorcontrib>ADAMS, KIRKWOOD F.</creatorcontrib><creatorcontrib>FELKER, G. MICHAEL</creatorcontrib><creatorcontrib>KARRA, RAVI</creatorcontrib><title>Circulating Angiokines Are Associated With Reverse Remodeling and Outcomes in Chronic Heart Failure</title><title>Journal of cardiac failure</title><addtitle>J Card Fail</addtitle><description>We sought to determine whether circulating modifiers of endothelial function are associated with cardiac structure and clinical outcomes in patients with heart failure with reduced ejection fraction (HFrEF). We measured 25 proteins related to endothelial function in 99 patients from the GUIDE-IT study. Protein levels were evaluated for association with echocardiographic parameters and the incidence of all-cause death and hospitalization for heart failure (HHF). Higher concentrations of angiopoietin 2 (ANGPT2), vascular endothelial growth factor receptor 1 (VEGFR1) and hepatocyte growth factor (HGF) were significantly associated with worse function and larger ventricular volumes. Over time, decreases in ANGPT2 and, to a lesser extent, VEGFR1 and HGF, were associated with improvements in cardiac size and function. Individuals with higher concentrations of ANGPT2, VEGFR1 or HGF had increased risks for a composite of death and HHF in the following year (HR 2.76 (95% CI 1.73–4.40) per 2-fold change in ANGPT2; HR 1.76 (95% CI 1.11–2.79) for VEGFR1; and HR 4.04 (95% CI 2.19–7.44) for HGF). Proteins related to endothelial function associate with cardiac size, cardiac function and clinical outcomes in patients with HFrEF. These results support the concept that endothelial function may be an important contributor to the progression to and the recovery from HFrEF. Take-Home Visual Graphic: Changes in circulating angiokines are associated with reverse remodeling and outcomes in chronic heart failure. [Display omitted]</description><subject>Cause of Death</subject><subject>Chronic Disease</subject><subject>Heart Failure - epidemiology</subject><subject>Humans</subject><subject>Risk Factors</subject><subject>Stroke Volume - physiology</subject><subject>Vascular Endothelial Growth Factor A</subject><subject>Ventricular Dysfunction, Left</subject><subject>Ventricular Function, Left - physiology</subject><issn>1071-9164</issn><issn>1532-8414</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMtOwzAQRS0EoqXwC8hLNgl-xU53VBUvqRISArG0jD0BlyQudoLE3-OqhS2bmVncO3PnIHROSUkJlZfr0proGuPbkhHGSspKQukBmtKKs6IWVBzmmShazKkUE3SS0poQUguijtGES8nZnIspsksf7diawfdveNG_-fDhe0h4EQEvUgrWmwEcfvHDO36EL4gJcu-Cg3brML3DD-NgQ5c9vsfL9xh6b_EdmDjgmxxvjHCKjhrTJjjb9xl6vrl-Wt4Vq4fb--ViVVgu66EAWykjXM5eWXBckTlzjYPmVXFjGJOS1fOG2Fo4xoWVUjjOjKqBOlAVsY7P0MVu7yaGzxHSoDufLLSt6SGMSTMlK6JyrbNU7qQ2hpQiNHoTfWfit6ZEbwHrtf4FrLeANWU6A87G8_2N8bUD92f7JZoFVzsB5E-_PESdrIc-f-Qj2EG74P-78QNzV5A7</recordid><startdate>202306</startdate><enddate>202306</enddate><creator>Harrington, JOSEPHINE</creator><creator>NIXON, ANDREW B.</creator><creator>DAUBERT, MELISSA A.</creator><creator>YOW, ERIC</creator><creator>JANUZZI, JAMES</creator><creator>FIUZAT, MONA</creator><creator>WHELLAN, DAVID J.</creator><creator>O'CONNOR, CHRISTOPHER M.</creator><creator>EZEKOWITZ, JUSTIN</creator><creator>PIÑA, ILEANA L.</creator><creator>ADAMS, KIRKWOOD F.</creator><creator>FELKER, G. MICHAEL</creator><creator>KARRA, RAVI</creator><general>Elsevier Inc</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>7X8</scope><orcidid>https://orcid.org/0000-0001-6741-285X</orcidid><orcidid>https://orcid.org/0000-0001-5169-117X</orcidid></search><sort><creationdate>202306</creationdate><title>Circulating Angiokines Are Associated With Reverse Remodeling and Outcomes in Chronic Heart Failure</title><author>Harrington, JOSEPHINE ; NIXON, ANDREW B. ; DAUBERT, MELISSA A. ; YOW, ERIC ; JANUZZI, JAMES ; FIUZAT, MONA ; WHELLAN, DAVID J. ; O'CONNOR, CHRISTOPHER M. ; EZEKOWITZ, JUSTIN ; PIÑA, ILEANA L. ; ADAMS, KIRKWOOD F. ; FELKER, G. MICHAEL ; KARRA, RAVI</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c368t-ec57a4d8415ced37092dfdefb73aa2266289f0c84d234c664d32a78e1de750cd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Cause of Death</topic><topic>Chronic Disease</topic><topic>Heart Failure - epidemiology</topic><topic>Humans</topic><topic>Risk Factors</topic><topic>Stroke Volume - physiology</topic><topic>Vascular Endothelial Growth Factor A</topic><topic>Ventricular Dysfunction, Left</topic><topic>Ventricular Function, Left - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Harrington, JOSEPHINE</creatorcontrib><creatorcontrib>NIXON, ANDREW B.</creatorcontrib><creatorcontrib>DAUBERT, MELISSA A.</creatorcontrib><creatorcontrib>YOW, ERIC</creatorcontrib><creatorcontrib>JANUZZI, JAMES</creatorcontrib><creatorcontrib>FIUZAT, MONA</creatorcontrib><creatorcontrib>WHELLAN, DAVID J.</creatorcontrib><creatorcontrib>O'CONNOR, CHRISTOPHER M.</creatorcontrib><creatorcontrib>EZEKOWITZ, JUSTIN</creatorcontrib><creatorcontrib>PIÑA, ILEANA L.</creatorcontrib><creatorcontrib>ADAMS, KIRKWOOD F.</creatorcontrib><creatorcontrib>FELKER, G. MICHAEL</creatorcontrib><creatorcontrib>KARRA, RAVI</creatorcontrib><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>Journal of cardiac failure</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Harrington, JOSEPHINE</au><au>NIXON, ANDREW B.</au><au>DAUBERT, MELISSA A.</au><au>YOW, ERIC</au><au>JANUZZI, JAMES</au><au>FIUZAT, MONA</au><au>WHELLAN, DAVID J.</au><au>O'CONNOR, CHRISTOPHER M.</au><au>EZEKOWITZ, JUSTIN</au><au>PIÑA, ILEANA L.</au><au>ADAMS, KIRKWOOD F.</au><au>FELKER, G. MICHAEL</au><au>KARRA, RAVI</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Circulating Angiokines Are Associated With Reverse Remodeling and Outcomes in Chronic Heart Failure</atitle><jtitle>Journal of cardiac failure</jtitle><addtitle>J Card Fail</addtitle><date>2023-06</date><risdate>2023</risdate><volume>29</volume><issue>6</issue><spage>896</spage><epage>906</epage><pages>896-906</pages><issn>1071-9164</issn><eissn>1532-8414</eissn><abstract>We sought to determine whether circulating modifiers of endothelial function are associated with cardiac structure and clinical outcomes in patients with heart failure with reduced ejection fraction (HFrEF). We measured 25 proteins related to endothelial function in 99 patients from the GUIDE-IT study. Protein levels were evaluated for association with echocardiographic parameters and the incidence of all-cause death and hospitalization for heart failure (HHF). Higher concentrations of angiopoietin 2 (ANGPT2), vascular endothelial growth factor receptor 1 (VEGFR1) and hepatocyte growth factor (HGF) were significantly associated with worse function and larger ventricular volumes. Over time, decreases in ANGPT2 and, to a lesser extent, VEGFR1 and HGF, were associated with improvements in cardiac size and function. Individuals with higher concentrations of ANGPT2, VEGFR1 or HGF had increased risks for a composite of death and HHF in the following year (HR 2.76 (95% CI 1.73–4.40) per 2-fold change in ANGPT2; HR 1.76 (95% CI 1.11–2.79) for VEGFR1; and HR 4.04 (95% CI 2.19–7.44) for HGF). Proteins related to endothelial function associate with cardiac size, cardiac function and clinical outcomes in patients with HFrEF. These results support the concept that endothelial function may be an important contributor to the progression to and the recovery from HFrEF. Take-Home Visual Graphic: Changes in circulating angiokines are associated with reverse remodeling and outcomes in chronic heart failure. [Display omitted]</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>36632934</pmid><doi>10.1016/j.cardfail.2022.12.011</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0001-6741-285X</orcidid><orcidid>https://orcid.org/0000-0001-5169-117X</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 1071-9164
ispartof Journal of cardiac failure, 2023-06, Vol.29 (6), p.896-906
issn 1071-9164
1532-8414
language eng
recordid cdi_proquest_miscellaneous_2765072768
source MEDLINE; Elsevier ScienceDirect Journals
subjects Cause of Death
Chronic Disease
Heart Failure - epidemiology
Humans
Risk Factors
Stroke Volume - physiology
Vascular Endothelial Growth Factor A
Ventricular Dysfunction, Left
Ventricular Function, Left - physiology
title Circulating Angiokines Are Associated With Reverse Remodeling and Outcomes in Chronic Heart Failure
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-21T21%3A15%3A59IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Circulating%20Angiokines%20Are%20Associated%20With%20Reverse%20Remodeling%20and%20Outcomes%20in%20Chronic%20Heart%20Failure&rft.jtitle=Journal%20of%20cardiac%20failure&rft.au=Harrington,%20JOSEPHINE&rft.date=2023-06&rft.volume=29&rft.issue=6&rft.spage=896&rft.epage=906&rft.pages=896-906&rft.issn=1071-9164&rft.eissn=1532-8414&rft_id=info:doi/10.1016/j.cardfail.2022.12.011&rft_dat=%3Cproquest_cross%3E2765072768%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2765072768&rft_id=info:pmid/36632934&rft_els_id=S1071916423000039&rfr_iscdi=true