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HbA1c and FIB-4 as serologic markers for the risk of progression of stage A heart failure

The use of glycosylated hemoglobin as a diabetic glycemic control and cardiovascular risk marker is well documented. It has also been suggested as a marker for early diastolic hemodynamic changes leading to clinical heart failure, but is less well characterized. This study explored the association b...

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Autores principales: Grigg, William, Mahfooz, Faisal, Chaudhary, Dharmista, Zapata, Isain, Duffee, Douglas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Magdi Yacoub Heart Foundation 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9491392/
https://www.ncbi.nlm.nih.gov/pubmed/36185157
http://dx.doi.org/10.21542/gcsp.2021.25
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author Grigg, William
Mahfooz, Faisal
Chaudhary, Dharmista
Zapata, Isain
Duffee, Douglas
author_facet Grigg, William
Mahfooz, Faisal
Chaudhary, Dharmista
Zapata, Isain
Duffee, Douglas
author_sort Grigg, William
collection PubMed
description The use of glycosylated hemoglobin as a diabetic glycemic control and cardiovascular risk marker is well documented. It has also been suggested as a marker for early diastolic hemodynamic changes leading to clinical heart failure, but is less well characterized. This study explored the association between elevated glycosylated hemoglobin and liver Fibrosis-4 values and worsening measures of diastolic cardiac function in order to assess their potential as early serologic markers in cardiovascular disease prevention. A retrospective cohort analysis was conducted in 102 patients presenting to the Parkview Medical Center health system who had received a full resting echo characterized by normal systolic ejection fraction and clinical risk factors associated with stage A heart failure in conjunction with glycosylated hemoglobin and Fibrosis-4 scores within a 3-month time window. Using regression analysis, measures of diastolic cardiac function were assessed in conjunction with rising glycosylated hemoglobin levels characterized as <6.5 and >6.5 and Fibrosis-4 scores after controlling for the presence of hypertension, coronary artery disease and valvular heart disease. Glycosylated hemoglobin levels >6.5 were significantly associated with a higher E/e’ ratio and closely associated with an elevated left atrial volume index both indicative of elevated left atrial pressure as a sensitive marker for diastolic cardiac dysfunction. Fibrosis-4 scores did not appear to be clinically associated with progression of diastolic dysfunction. Thus, glycosylated hemoglobin may act as an early marker for identifying patients at increased risk for the progression of stage A heart failure. Fibrosis-4 scores do not appear to be related.
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spelling pubmed-94913922022-09-29 HbA1c and FIB-4 as serologic markers for the risk of progression of stage A heart failure Grigg, William Mahfooz, Faisal Chaudhary, Dharmista Zapata, Isain Duffee, Douglas Glob Cardiol Sci Pract Research Article The use of glycosylated hemoglobin as a diabetic glycemic control and cardiovascular risk marker is well documented. It has also been suggested as a marker for early diastolic hemodynamic changes leading to clinical heart failure, but is less well characterized. This study explored the association between elevated glycosylated hemoglobin and liver Fibrosis-4 values and worsening measures of diastolic cardiac function in order to assess their potential as early serologic markers in cardiovascular disease prevention. A retrospective cohort analysis was conducted in 102 patients presenting to the Parkview Medical Center health system who had received a full resting echo characterized by normal systolic ejection fraction and clinical risk factors associated with stage A heart failure in conjunction with glycosylated hemoglobin and Fibrosis-4 scores within a 3-month time window. Using regression analysis, measures of diastolic cardiac function were assessed in conjunction with rising glycosylated hemoglobin levels characterized as <6.5 and >6.5 and Fibrosis-4 scores after controlling for the presence of hypertension, coronary artery disease and valvular heart disease. Glycosylated hemoglobin levels >6.5 were significantly associated with a higher E/e’ ratio and closely associated with an elevated left atrial volume index both indicative of elevated left atrial pressure as a sensitive marker for diastolic cardiac dysfunction. Fibrosis-4 scores did not appear to be clinically associated with progression of diastolic dysfunction. Thus, glycosylated hemoglobin may act as an early marker for identifying patients at increased risk for the progression of stage A heart failure. Fibrosis-4 scores do not appear to be related. Magdi Yacoub Heart Foundation 2021-12-31 /pmc/articles/PMC9491392/ /pubmed/36185157 http://dx.doi.org/10.21542/gcsp.2021.25 Text en Copyright ©2021 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution license CC BY 4.0, which permits unrestricted use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Grigg, William
Mahfooz, Faisal
Chaudhary, Dharmista
Zapata, Isain
Duffee, Douglas
HbA1c and FIB-4 as serologic markers for the risk of progression of stage A heart failure
title HbA1c and FIB-4 as serologic markers for the risk of progression of stage A heart failure
title_full HbA1c and FIB-4 as serologic markers for the risk of progression of stage A heart failure
title_fullStr HbA1c and FIB-4 as serologic markers for the risk of progression of stage A heart failure
title_full_unstemmed HbA1c and FIB-4 as serologic markers for the risk of progression of stage A heart failure
title_short HbA1c and FIB-4 as serologic markers for the risk of progression of stage A heart failure
title_sort hba1c and fib-4 as serologic markers for the risk of progression of stage a heart failure
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9491392/
https://www.ncbi.nlm.nih.gov/pubmed/36185157
http://dx.doi.org/10.21542/gcsp.2021.25
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