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In Acute Myocardial Infarction Liver Parameters Are Associated With Stenosis Diameter

Detection of high-risk subjects in acute myocardial infarction (AMI) by noninvasive means would reduce the need for intracardiac catheterization and associated complications. Liver enzymes are associated with cardiovascular disease risk. A potential predictive value for liver serum markers for the s...

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Autores principales: Baars, Theodor, Neumann, Ursula, Jinawy, Mona, Hendricks, Stefanie, Sowa, Jan-Peter, Kälsch, Julia, Riemenschneider, Mona, Gerken, Guido, Erbel, Raimund, Heider, Dominik, Canbay, Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4753945/
https://www.ncbi.nlm.nih.gov/pubmed/26871849
http://dx.doi.org/10.1097/MD.0000000000002807
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author Baars, Theodor
Neumann, Ursula
Jinawy, Mona
Hendricks, Stefanie
Sowa, Jan-Peter
Kälsch, Julia
Riemenschneider, Mona
Gerken, Guido
Erbel, Raimund
Heider, Dominik
Canbay, Ali
author_facet Baars, Theodor
Neumann, Ursula
Jinawy, Mona
Hendricks, Stefanie
Sowa, Jan-Peter
Kälsch, Julia
Riemenschneider, Mona
Gerken, Guido
Erbel, Raimund
Heider, Dominik
Canbay, Ali
author_sort Baars, Theodor
collection PubMed
description Detection of high-risk subjects in acute myocardial infarction (AMI) by noninvasive means would reduce the need for intracardiac catheterization and associated complications. Liver enzymes are associated with cardiovascular disease risk. A potential predictive value for liver serum markers for the severity of stenosis in AMI was analyzed. Patients with AMI undergoing percutaneous coronary intervention (PCI; n = 437) were retrospectively evaluated. Minimal lumen diameter (MLD) and percent stenosis diameter (SD) were determined from quantitative coronary angiography. Patients were classified according to the severity of stenosis (SD ≥ 50%, n = 357; SD < 50%, n = 80). Routine heart and liver parameters were associated with SD using random forests (RF). A prediction model (M10) was developed based on parameter importance analysis in RF. Age, alkaline phosphatase (AP), aspartate aminotransferase (AST), and MLD differed significantly between SD ≥ 50 and SD < 50. Age, AST, alanine aminotransferase (ALT), and troponin correlated significantly with SD, whereas MLD correlated inversely with SD. M10 (age, BMI, AP, AST, ALT, gamma-glutamyltransferase, creatinine, troponin) reached an AUC of 69.7% (CI 63.8–75.5%, P < 0.0001). Routine liver parameters are associated with SD in AMI. A small set of noninvasively determined parameters can identify SD in AMI, and might avoid unnecessary coronary angiography in patients with low risk. The model can be accessed via http://stenosis.heiderlab.de.
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spelling pubmed-47539452016-02-26 In Acute Myocardial Infarction Liver Parameters Are Associated With Stenosis Diameter Baars, Theodor Neumann, Ursula Jinawy, Mona Hendricks, Stefanie Sowa, Jan-Peter Kälsch, Julia Riemenschneider, Mona Gerken, Guido Erbel, Raimund Heider, Dominik Canbay, Ali Medicine (Baltimore) 3400 Detection of high-risk subjects in acute myocardial infarction (AMI) by noninvasive means would reduce the need for intracardiac catheterization and associated complications. Liver enzymes are associated with cardiovascular disease risk. A potential predictive value for liver serum markers for the severity of stenosis in AMI was analyzed. Patients with AMI undergoing percutaneous coronary intervention (PCI; n = 437) were retrospectively evaluated. Minimal lumen diameter (MLD) and percent stenosis diameter (SD) were determined from quantitative coronary angiography. Patients were classified according to the severity of stenosis (SD ≥ 50%, n = 357; SD < 50%, n = 80). Routine heart and liver parameters were associated with SD using random forests (RF). A prediction model (M10) was developed based on parameter importance analysis in RF. Age, alkaline phosphatase (AP), aspartate aminotransferase (AST), and MLD differed significantly between SD ≥ 50 and SD < 50. Age, AST, alanine aminotransferase (ALT), and troponin correlated significantly with SD, whereas MLD correlated inversely with SD. M10 (age, BMI, AP, AST, ALT, gamma-glutamyltransferase, creatinine, troponin) reached an AUC of 69.7% (CI 63.8–75.5%, P < 0.0001). Routine liver parameters are associated with SD in AMI. A small set of noninvasively determined parameters can identify SD in AMI, and might avoid unnecessary coronary angiography in patients with low risk. The model can be accessed via http://stenosis.heiderlab.de. Wolters Kluwer Health 2016-02-12 /pmc/articles/PMC4753945/ /pubmed/26871849 http://dx.doi.org/10.1097/MD.0000000000002807 Text en Copyright © 2016 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0, where it is permissible to download, share and reproduce the work in any medium, provided it is properly cited. The work cannot be changed in any way or used commercially. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle 3400
Baars, Theodor
Neumann, Ursula
Jinawy, Mona
Hendricks, Stefanie
Sowa, Jan-Peter
Kälsch, Julia
Riemenschneider, Mona
Gerken, Guido
Erbel, Raimund
Heider, Dominik
Canbay, Ali
In Acute Myocardial Infarction Liver Parameters Are Associated With Stenosis Diameter
title In Acute Myocardial Infarction Liver Parameters Are Associated With Stenosis Diameter
title_full In Acute Myocardial Infarction Liver Parameters Are Associated With Stenosis Diameter
title_fullStr In Acute Myocardial Infarction Liver Parameters Are Associated With Stenosis Diameter
title_full_unstemmed In Acute Myocardial Infarction Liver Parameters Are Associated With Stenosis Diameter
title_short In Acute Myocardial Infarction Liver Parameters Are Associated With Stenosis Diameter
title_sort in acute myocardial infarction liver parameters are associated with stenosis diameter
topic 3400
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4753945/
https://www.ncbi.nlm.nih.gov/pubmed/26871849
http://dx.doi.org/10.1097/MD.0000000000002807
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