Plasma Galectin-3 predicts deleterious vascular dysfunction affecting post-myocardial infarction patients: An explanatory study

In a previous analysis of a post-myocardial infarction (MI) cohort, abnormally high systemic vascular resistances (SVR) were shown to be frequently revealed by MRI during the healing period, independently of MI severity, giving evidence of vascular dysfunction and limiting further recovery of cardia...

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Veröffentlicht in:PloS one 2020-05, Vol.15 (5), p.e0232572-e0232572
Hauptverfasser: Huttin, Olivier, Mandry, Damien, Popovic, Batric, Rossignol, Patrick, Odille, Freddy, Micard, Emilien, Lamiral, Zohra, Zannad, Faïez, Girerd, Nicolas, Marie, Pierre-Yves
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container_title PloS one
container_volume 15
creator Huttin, Olivier
Mandry, Damien
Popovic, Batric
Rossignol, Patrick
Odille, Freddy
Micard, Emilien
Lamiral, Zohra
Zannad, Faïez
Girerd, Nicolas
Marie, Pierre-Yves
description In a previous analysis of a post-myocardial infarction (MI) cohort, abnormally high systemic vascular resistances (SVR) were shown to be frequently revealed by MRI during the healing period, independently of MI severity, giving evidence of vascular dysfunction and limiting further recovery of cardiac function. The present ancillary and exploratory analysis of the same cohort was aimed at characterizing those patients suffering from high SVR remotely from MI with a large a panel of cardiovascular MRI parameters and blood biomarkers. MRI and blood sampling were performed 2-4 days after a reperfused MI and 6 months thereafter in 121 patients. SVR were monitored with a phase-contrast MRI sequence and patients with abnormally high SVR at 6-months were characterized through MRI parameters and blood biomarkers, including Galectin-3, an indicator of cardiovascular inflammation and fibrosis after MI. SVR were normal at 6-months in 90 patients (SVR-) and abnormally high in 31 among whom 21 already had high SVR at the acute phase (SVR++) while 10 did not (SVR+). When compared with SVR-, both SVR+ and SVR++ exhibited lower recovery in cardiac function from baseline to 6-months, while baseline levels of Galectin-3 were significantly different in both SVR+ (median: 14.4 (interquartile range: 12.3-16.7) ng.mL-1) and SVR++ (13.0 (11.7-19.4) ng.mL-1) compared to SVR- (11.7 (9.8-13.5) ng.mL-1, both p < 0.05). Plasma Galectin-3 was an independent baseline predictor of high SVR at 6-months (p = 0.002), together with the baseline levels of SVR and left ventricular end-diastolic volume, whereas indices of MI severity and left ventricular function were not. In conclusion, plasma Galectin-3 predicts a deleterious vascular dysfunction affecting post-MI patients, an observation that could lead to consider new therapeutic targets if confirmed through dedicated prospective studies.
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The present ancillary and exploratory analysis of the same cohort was aimed at characterizing those patients suffering from high SVR remotely from MI with a large a panel of cardiovascular MRI parameters and blood biomarkers. MRI and blood sampling were performed 2-4 days after a reperfused MI and 6 months thereafter in 121 patients. SVR were monitored with a phase-contrast MRI sequence and patients with abnormally high SVR at 6-months were characterized through MRI parameters and blood biomarkers, including Galectin-3, an indicator of cardiovascular inflammation and fibrosis after MI. SVR were normal at 6-months in 90 patients (SVR-) and abnormally high in 31 among whom 21 already had high SVR at the acute phase (SVR++) while 10 did not (SVR+). When compared with SVR-, both SVR+ and SVR++ exhibited lower recovery in cardiac function from baseline to 6-months, while baseline levels of Galectin-3 were significantly different in both SVR+ (median: 14.4 (interquartile range: 12.3-16.7) ng.mL-1) and SVR++ (13.0 (11.7-19.4) ng.mL-1) compared to SVR- (11.7 (9.8-13.5) ng.mL-1, both p &lt; 0.05). Plasma Galectin-3 was an independent baseline predictor of high SVR at 6-months (p = 0.002), together with the baseline levels of SVR and left ventricular end-diastolic volume, whereas indices of MI severity and left ventricular function were not. 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Academic</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Advanced Technologies &amp; Aerospace Database</collection><collection>ProQuest Advanced Technologies &amp; Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Materials Science Collection</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Huttin, Olivier</au><au>Mandry, Damien</au><au>Popovic, Batric</au><au>Rossignol, Patrick</au><au>Odille, Freddy</au><au>Micard, Emilien</au><au>Lamiral, Zohra</au><au>Zannad, Faïez</au><au>Girerd, Nicolas</au><au>Marie, Pierre-Yves</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Plasma Galectin-3 predicts deleterious vascular dysfunction affecting post-myocardial infarction patients: An explanatory study</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2020-05-11</date><risdate>2020</risdate><volume>15</volume><issue>5</issue><spage>e0232572</spage><epage>e0232572</epage><pages>e0232572-e0232572</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>In a previous analysis of a post-myocardial infarction (MI) cohort, abnormally high systemic vascular resistances (SVR) were shown to be frequently revealed by MRI during the healing period, independently of MI severity, giving evidence of vascular dysfunction and limiting further recovery of cardiac function. The present ancillary and exploratory analysis of the same cohort was aimed at characterizing those patients suffering from high SVR remotely from MI with a large a panel of cardiovascular MRI parameters and blood biomarkers. MRI and blood sampling were performed 2-4 days after a reperfused MI and 6 months thereafter in 121 patients. SVR were monitored with a phase-contrast MRI sequence and patients with abnormally high SVR at 6-months were characterized through MRI parameters and blood biomarkers, including Galectin-3, an indicator of cardiovascular inflammation and fibrosis after MI. SVR were normal at 6-months in 90 patients (SVR-) and abnormally high in 31 among whom 21 already had high SVR at the acute phase (SVR++) while 10 did not (SVR+). When compared with SVR-, both SVR+ and SVR++ exhibited lower recovery in cardiac function from baseline to 6-months, while baseline levels of Galectin-3 were significantly different in both SVR+ (median: 14.4 (interquartile range: 12.3-16.7) ng.mL-1) and SVR++ (13.0 (11.7-19.4) ng.mL-1) compared to SVR- (11.7 (9.8-13.5) ng.mL-1, both p &lt; 0.05). Plasma Galectin-3 was an independent baseline predictor of high SVR at 6-months (p = 0.002), together with the baseline levels of SVR and left ventricular end-diastolic volume, whereas indices of MI severity and left ventricular function were not. In conclusion, plasma Galectin-3 predicts a deleterious vascular dysfunction affecting post-MI patients, an observation that could lead to consider new therapeutic targets if confirmed through dedicated prospective studies.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>32392260</pmid><doi>10.1371/journal.pone.0232572</doi><tpages>e0232572</tpages><orcidid>https://orcid.org/0000-0001-7319-3737</orcidid><orcidid>https://orcid.org/0000-0002-2454-6468</orcidid><orcidid>https://orcid.org/0000-0001-7456-1570</orcidid><orcidid>https://orcid.org/0000-0001-5260-8905</orcidid><orcidid>https://orcid.org/0000-0002-3278-2057</orcidid><oa>free_for_read</oa></addata></record>
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1932-6203
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subjects Aged
Analysis
Angioplasty
Biological markers
Biology and Life Sciences
Biomarkers
Biomarkers - blood
Blood
Blood tests
Cardiac function
Cardiac patients
Cardiology
Cardiology and cardiovascular system
Complications and side effects
Confidence intervals
Demographic aspects
Diagnostic imaging
Female
Fibrosis
Galectin 3 - blood
Galectin-3
Heart
Heart attack
Heart attacks
Heart failure
Human health and pathology
Humans
Inflammation
Life Sciences
Magnetic Resonance Imaging
Male
Medical imaging
Medical research
Medicine and Health Sciences
Middle Aged
Myocardial infarction
Myocardial Infarction - blood
Myocardial Infarction - complications
Parameters
Patient monitoring equipment
Recovery
Research and Analysis Methods
Risk Factors
Stroke
Suffering
Therapeutic applications
Variables
Vascular diseases
Vascular Diseases - blood
Vascular Diseases - diagnostic imaging
Vascular Diseases - etiology
Vascular Diseases - physiopathology
Vascular Resistance - physiology
Ventricle
title Plasma Galectin-3 predicts deleterious vascular dysfunction affecting post-myocardial infarction patients: An explanatory study
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