Clinical Impact of Circulating Galectin-3 on Ventricular Arrhythmias and Heart Failure Hospitalization Independent of Prior Ventricular Arrhythmic Events in Patients with Implantable Cardioverter-defibrillators

Objective For risk stratification of sudden cardiac death in patients with structural heart disease, more precise predictors in addition to left ventricular ejection fraction (LVEF) are clinically needed. The present study assessed the utility of galectin-3 as an independent indicator for the progno...

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Veröffentlicht in:Internal Medicine 2022/04/01, Vol.61(7), pp.969-977
Hauptverfasser: Makimoto, Hisaki, Müller, Patrick, Denise, Kullmann, Clasen, Lukas, Lin, Tina, Angendohr, Stephan, Schmidt, Jan, Brinkmeyer, Christoph, Kelm, Malte, Bejinariu, Alexandru
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container_end_page 977
container_issue 7
container_start_page 969
container_title Internal Medicine
container_volume 61
creator Makimoto, Hisaki
Müller, Patrick
Denise, Kullmann
Clasen, Lukas
Lin, Tina
Angendohr, Stephan
Schmidt, Jan
Brinkmeyer, Christoph
Kelm, Malte
Bejinariu, Alexandru
description Objective For risk stratification of sudden cardiac death in patients with structural heart disease, more precise predictors in addition to left ventricular ejection fraction (LVEF) are clinically needed. The present study assessed the utility of galectin-3 as an independent indicator for the prognosis of heart failure patients with implantable cardioverter-defibrillators (ICD). Methods The study population consisted of 91 consecutive patients who underwent a routine ICD checkup in our ICD outpatient clinic. Circulating galectin-3 was assessed using a commercially available enzyme-linked immunosorbent assay kit. The enrolled patients were prospectively followed. The primary endpoint was defined as the occurrence of appropriate ICD therapy (AIT), and the secondary endpoint was defined as the occurrence of unplanned overnight hospitalization due to decompensated heart failure (dHF). Results During a mean follow-up of 472±107 days, AIT occurred in 18 patients (20%). Unplanned hospitalizations due to dHF were noted in 12 patients (13%). A receiver-operative characteristics analysis demonstrated a sensitivity of 83% and specificity of 68% for AIT occurrences with a galectin-3 cut-off value of 13.1 ng/mL (area under the curve =0.82). A Kaplan-Meier analysis demonstrated that patients with galectin-3 >13.1 ng/mL had significantly higher incidences of AIT as compared to those with lower galectin-3 (log-rank, p
doi_str_mv 10.2169/internalmedicine.7886-21
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The present study assessed the utility of galectin-3 as an independent indicator for the prognosis of heart failure patients with implantable cardioverter-defibrillators (ICD). Methods The study population consisted of 91 consecutive patients who underwent a routine ICD checkup in our ICD outpatient clinic. Circulating galectin-3 was assessed using a commercially available enzyme-linked immunosorbent assay kit. The enrolled patients were prospectively followed. The primary endpoint was defined as the occurrence of appropriate ICD therapy (AIT), and the secondary endpoint was defined as the occurrence of unplanned overnight hospitalization due to decompensated heart failure (dHF). Results During a mean follow-up of 472±107 days, AIT occurred in 18 patients (20%). Unplanned hospitalizations due to dHF were noted in 12 patients (13%). A receiver-operative characteristics analysis demonstrated a sensitivity of 83% and specificity of 68% for AIT occurrences with a galectin-3 cut-off value of 13.1 ng/mL (area under the curve =0.82). A Kaplan-Meier analysis demonstrated that patients with galectin-3 &gt;13.1 ng/mL had significantly higher incidences of AIT as compared to those with lower galectin-3 (log-rank, p&lt;0.001). This significance was also observed in both subgroup analyses with ischemic and non-ischemic etiology. Cox regression demonstrated that higher galectin-3 was an independent predictor of AIT and dHF, even after adjusting for previous arrhythmic events. Conclusion The circulating galectin-3 level can be used as a clinical indicator of subsequent occurrence of ventricular arrhythmic events and decompensated heart failure, regardless of a history of ventricular arrhythmias.</description><identifier>ISSN: 0918-2918</identifier><identifier>ISSN: 1349-7235</identifier><identifier>EISSN: 1349-7235</identifier><identifier>DOI: 10.2169/internalmedicine.7886-21</identifier><identifier>PMID: 35370254</identifier><language>eng</language><publisher>Japan: The Japanese Society of Internal Medicine</publisher><subject>Arrhythmia ; Arrhythmias, Cardiac - etiology ; Cardiac arrhythmia ; Congestive heart failure ; Coronary artery disease ; Defibrillators ; Defibrillators, Implantable - adverse effects ; Enzyme-linked immunosorbent assay ; Etiology ; Galectin 3 ; Heart failure ; Heart Failure - complications ; Heart Failure - therapy ; Hospitalization ; Humans ; implantable cardioverter-defibrillator ; Internal medicine ; Ischemia ; ischemic cardiomyopathy ; non-ischemic cardiomyopathy ; Original ; Patients ; Population studies ; Stroke Volume ; Ventricle ; Ventricular Function, Left ; ventricular tachycardia</subject><ispartof>Internal Medicine, 2022/04/01, Vol.61(7), pp.969-977</ispartof><rights>2022 by The Japanese Society of Internal Medicine</rights><rights>Copyright Japan Science and Technology Agency 2022</rights><rights>Copyright © 2022 by The Japanese Society of Internal Medicine</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c609t-98765fdf5ced1d9c274f9b103e575cb92e53fb986163324102986e0c9182cea53</citedby><cites>FETCH-LOGICAL-c609t-98765fdf5ced1d9c274f9b103e575cb92e53fb986163324102986e0c9182cea53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9038450/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9038450/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,882,1877,27905,27906,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35370254$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Makimoto, Hisaki</creatorcontrib><creatorcontrib>Müller, Patrick</creatorcontrib><creatorcontrib>Denise, Kullmann</creatorcontrib><creatorcontrib>Clasen, Lukas</creatorcontrib><creatorcontrib>Lin, Tina</creatorcontrib><creatorcontrib>Angendohr, Stephan</creatorcontrib><creatorcontrib>Schmidt, Jan</creatorcontrib><creatorcontrib>Brinkmeyer, Christoph</creatorcontrib><creatorcontrib>Kelm, Malte</creatorcontrib><creatorcontrib>Bejinariu, Alexandru</creatorcontrib><title>Clinical Impact of Circulating Galectin-3 on Ventricular Arrhythmias and Heart Failure Hospitalization Independent of Prior Ventricular Arrhythmic Events in Patients with Implantable Cardioverter-defibrillators</title><title>Internal Medicine</title><addtitle>Intern. Med.</addtitle><description>Objective For risk stratification of sudden cardiac death in patients with structural heart disease, more precise predictors in addition to left ventricular ejection fraction (LVEF) are clinically needed. The present study assessed the utility of galectin-3 as an independent indicator for the prognosis of heart failure patients with implantable cardioverter-defibrillators (ICD). Methods The study population consisted of 91 consecutive patients who underwent a routine ICD checkup in our ICD outpatient clinic. Circulating galectin-3 was assessed using a commercially available enzyme-linked immunosorbent assay kit. The enrolled patients were prospectively followed. The primary endpoint was defined as the occurrence of appropriate ICD therapy (AIT), and the secondary endpoint was defined as the occurrence of unplanned overnight hospitalization due to decompensated heart failure (dHF). Results During a mean follow-up of 472±107 days, AIT occurred in 18 patients (20%). Unplanned hospitalizations due to dHF were noted in 12 patients (13%). A receiver-operative characteristics analysis demonstrated a sensitivity of 83% and specificity of 68% for AIT occurrences with a galectin-3 cut-off value of 13.1 ng/mL (area under the curve =0.82). A Kaplan-Meier analysis demonstrated that patients with galectin-3 &gt;13.1 ng/mL had significantly higher incidences of AIT as compared to those with lower galectin-3 (log-rank, p&lt;0.001). This significance was also observed in both subgroup analyses with ischemic and non-ischemic etiology. Cox regression demonstrated that higher galectin-3 was an independent predictor of AIT and dHF, even after adjusting for previous arrhythmic events. Conclusion The circulating galectin-3 level can be used as a clinical indicator of subsequent occurrence of ventricular arrhythmic events and decompensated heart failure, regardless of a history of ventricular arrhythmias.</description><subject>Arrhythmia</subject><subject>Arrhythmias, Cardiac - etiology</subject><subject>Cardiac arrhythmia</subject><subject>Congestive heart failure</subject><subject>Coronary artery disease</subject><subject>Defibrillators</subject><subject>Defibrillators, Implantable - adverse effects</subject><subject>Enzyme-linked immunosorbent assay</subject><subject>Etiology</subject><subject>Galectin 3</subject><subject>Heart failure</subject><subject>Heart Failure - complications</subject><subject>Heart Failure - therapy</subject><subject>Hospitalization</subject><subject>Humans</subject><subject>implantable cardioverter-defibrillator</subject><subject>Internal medicine</subject><subject>Ischemia</subject><subject>ischemic cardiomyopathy</subject><subject>non-ischemic cardiomyopathy</subject><subject>Original</subject><subject>Patients</subject><subject>Population studies</subject><subject>Stroke Volume</subject><subject>Ventricle</subject><subject>Ventricular Function, Left</subject><subject>ventricular tachycardia</subject><issn>0918-2918</issn><issn>1349-7235</issn><issn>1349-7235</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptUk1vEzEQXSEQDYW_gCxx4bLFH-vd9QWpitomUgU9AFfL651NHDl2sL2pys_kF-FNSgSFy3jkefPm6xUFIviCklp8MC5BcMpuoTfaOLho2rYuKXlWzAirRNlQxp8XMyxIW9JszopXMW4wZm0j6MvijHHWYMqrWfFzbo0zWlm03O6UTsgPaG6CHq1Kxq3QjbKgs1cy5B36Bi4FMwUDugxh_ZDWW6MiUq5HC1AhoWtl7BgALXzcmaSs-ZF5cubS9bCDbNyhxF0wPvyfTqOrff6PyDh0l5MP_r1J66lDq1xSnQU0V6E3fg8hL6LsYTBdMDb37EN8XbwYlI3w5vE9L75eX32ZL8rbzzfL-eVtqWssUinapuZDP3ANPemFpk01iI5gBrzhuhMUOBs60dakZoxWBNPsA9Z5nVSD4uy8-Hjk3Y1dPoSehlFW7oLZqvAgvTLy74gza7nyeynyHSqOM8H7R4Lgv48Qk9yaqCGP4cCPUdK6qkVFsagz9N0T6MaPkwKOKMJ5hUVGtUeUDj7GAMOpGYLlJBz5VDhyEk4O5dS3fw5zSvytlAz4dARsYlIrOAHy0Y228C9zTWRzMMcKJ6BeqyDBsV8PBOgu</recordid><startdate>20220401</startdate><enddate>20220401</enddate><creator>Makimoto, Hisaki</creator><creator>Müller, Patrick</creator><creator>Denise, Kullmann</creator><creator>Clasen, Lukas</creator><creator>Lin, Tina</creator><creator>Angendohr, Stephan</creator><creator>Schmidt, Jan</creator><creator>Brinkmeyer, Christoph</creator><creator>Kelm, Malte</creator><creator>Bejinariu, Alexandru</creator><general>The Japanese Society of Internal Medicine</general><general>Japan Science and Technology Agency</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>7T5</scope><scope>7TK</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20220401</creationdate><title>Clinical Impact of Circulating Galectin-3 on Ventricular Arrhythmias and Heart Failure Hospitalization Independent of Prior Ventricular Arrhythmic Events in Patients with Implantable Cardioverter-defibrillators</title><author>Makimoto, Hisaki ; Müller, Patrick ; Denise, Kullmann ; Clasen, Lukas ; Lin, Tina ; Angendohr, Stephan ; Schmidt, Jan ; Brinkmeyer, Christoph ; Kelm, Malte ; Bejinariu, Alexandru</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c609t-98765fdf5ced1d9c274f9b103e575cb92e53fb986163324102986e0c9182cea53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Arrhythmia</topic><topic>Arrhythmias, Cardiac - etiology</topic><topic>Cardiac arrhythmia</topic><topic>Congestive heart failure</topic><topic>Coronary artery disease</topic><topic>Defibrillators</topic><topic>Defibrillators, Implantable - adverse effects</topic><topic>Enzyme-linked immunosorbent assay</topic><topic>Etiology</topic><topic>Galectin 3</topic><topic>Heart failure</topic><topic>Heart Failure - complications</topic><topic>Heart Failure - therapy</topic><topic>Hospitalization</topic><topic>Humans</topic><topic>implantable cardioverter-defibrillator</topic><topic>Internal medicine</topic><topic>Ischemia</topic><topic>ischemic cardiomyopathy</topic><topic>non-ischemic cardiomyopathy</topic><topic>Original</topic><topic>Patients</topic><topic>Population studies</topic><topic>Stroke Volume</topic><topic>Ventricle</topic><topic>Ventricular Function, Left</topic><topic>ventricular tachycardia</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Makimoto, Hisaki</creatorcontrib><creatorcontrib>Müller, Patrick</creatorcontrib><creatorcontrib>Denise, Kullmann</creatorcontrib><creatorcontrib>Clasen, Lukas</creatorcontrib><creatorcontrib>Lin, Tina</creatorcontrib><creatorcontrib>Angendohr, Stephan</creatorcontrib><creatorcontrib>Schmidt, Jan</creatorcontrib><creatorcontrib>Brinkmeyer, Christoph</creatorcontrib><creatorcontrib>Kelm, Malte</creatorcontrib><creatorcontrib>Bejinariu, Alexandru</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Internal Medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Makimoto, Hisaki</au><au>Müller, Patrick</au><au>Denise, Kullmann</au><au>Clasen, Lukas</au><au>Lin, Tina</au><au>Angendohr, Stephan</au><au>Schmidt, Jan</au><au>Brinkmeyer, Christoph</au><au>Kelm, Malte</au><au>Bejinariu, Alexandru</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical Impact of Circulating Galectin-3 on Ventricular Arrhythmias and Heart Failure Hospitalization Independent of Prior Ventricular Arrhythmic Events in Patients with Implantable Cardioverter-defibrillators</atitle><jtitle>Internal Medicine</jtitle><addtitle>Intern. Med.</addtitle><date>2022-04-01</date><risdate>2022</risdate><volume>61</volume><issue>7</issue><spage>969</spage><epage>977</epage><pages>969-977</pages><artnum>7886-21</artnum><issn>0918-2918</issn><issn>1349-7235</issn><eissn>1349-7235</eissn><abstract>Objective For risk stratification of sudden cardiac death in patients with structural heart disease, more precise predictors in addition to left ventricular ejection fraction (LVEF) are clinically needed. The present study assessed the utility of galectin-3 as an independent indicator for the prognosis of heart failure patients with implantable cardioverter-defibrillators (ICD). Methods The study population consisted of 91 consecutive patients who underwent a routine ICD checkup in our ICD outpatient clinic. Circulating galectin-3 was assessed using a commercially available enzyme-linked immunosorbent assay kit. The enrolled patients were prospectively followed. The primary endpoint was defined as the occurrence of appropriate ICD therapy (AIT), and the secondary endpoint was defined as the occurrence of unplanned overnight hospitalization due to decompensated heart failure (dHF). Results During a mean follow-up of 472±107 days, AIT occurred in 18 patients (20%). Unplanned hospitalizations due to dHF were noted in 12 patients (13%). A receiver-operative characteristics analysis demonstrated a sensitivity of 83% and specificity of 68% for AIT occurrences with a galectin-3 cut-off value of 13.1 ng/mL (area under the curve =0.82). A Kaplan-Meier analysis demonstrated that patients with galectin-3 &gt;13.1 ng/mL had significantly higher incidences of AIT as compared to those with lower galectin-3 (log-rank, p&lt;0.001). This significance was also observed in both subgroup analyses with ischemic and non-ischemic etiology. Cox regression demonstrated that higher galectin-3 was an independent predictor of AIT and dHF, even after adjusting for previous arrhythmic events. Conclusion The circulating galectin-3 level can be used as a clinical indicator of subsequent occurrence of ventricular arrhythmic events and decompensated heart failure, regardless of a history of ventricular arrhythmias.</abstract><cop>Japan</cop><pub>The Japanese Society of Internal Medicine</pub><pmid>35370254</pmid><doi>10.2169/internalmedicine.7886-21</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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1349-7235
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source J-STAGE Free; MEDLINE; PubMed Central Open Access; PubMed Central
subjects Arrhythmia
Arrhythmias, Cardiac - etiology
Cardiac arrhythmia
Congestive heart failure
Coronary artery disease
Defibrillators
Defibrillators, Implantable - adverse effects
Enzyme-linked immunosorbent assay
Etiology
Galectin 3
Heart failure
Heart Failure - complications
Heart Failure - therapy
Hospitalization
Humans
implantable cardioverter-defibrillator
Internal medicine
Ischemia
ischemic cardiomyopathy
non-ischemic cardiomyopathy
Original
Patients
Population studies
Stroke Volume
Ventricle
Ventricular Function, Left
ventricular tachycardia
title Clinical Impact of Circulating Galectin-3 on Ventricular Arrhythmias and Heart Failure Hospitalization Independent of Prior Ventricular Arrhythmic Events in Patients with Implantable Cardioverter-defibrillators
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