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Silent myocardial dysfunction in vitamin D deficiency

INTRODUCTION: Vitamin D (VD) deficiency is a common disease that occurs in all stages of life. A growing number of studies call attention to the relationship between VD deficiency and cardiovascular disease. The aim of this study was to investigate the effect of VD on subclinical left ventricular (L...

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Autores principales: Ozer, Pelin Karaca, Emet, Samim, Karaayvaz, Ekrem Bilal, Elitok, Ali, Bilge, Ahmet Kaya, Adalet, Kamil, Oncul, Aytac
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7433788/
https://www.ncbi.nlm.nih.gov/pubmed/32832715
http://dx.doi.org/10.5114/amsad.2020.97110
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author Ozer, Pelin Karaca
Emet, Samim
Karaayvaz, Ekrem Bilal
Elitok, Ali
Bilge, Ahmet Kaya
Adalet, Kamil
Oncul, Aytac
author_facet Ozer, Pelin Karaca
Emet, Samim
Karaayvaz, Ekrem Bilal
Elitok, Ali
Bilge, Ahmet Kaya
Adalet, Kamil
Oncul, Aytac
author_sort Ozer, Pelin Karaca
collection PubMed
description INTRODUCTION: Vitamin D (VD) deficiency is a common disease that occurs in all stages of life. A growing number of studies call attention to the relationship between VD deficiency and cardiovascular disease. The aim of this study was to investigate the effect of VD on subclinical left ventricular (LV) function in diabetic and non-diabetic patients with no significant coronary artery disease. MATERIAL AND METHODS: We recruited 140 patients (80 diabetics and 60 non-diabetics) with symptoms of stable ischemic heart disease who underwent coronary angiography and who had no significant coronary artery disease in our clinic. The 25(OH)D(3) levels were measured and patients who had 25-(OH)D(3) levels below 20 ng/dl were defined as the VD deficient group. In addition to conventional echocardiographic parameters, tissue Doppler echocardiography was used for LV diastolic functions and 2D speckle tracking strain echocardiography (2D STE) for evaluating the longitudinal deformation indices of the LV myocardium. RESULTS: In all groups, LV global longitudinal strain (GLS) was significantly impaired in patients with VD deficiency (p < 0.001) compared to patients without VD deficiency. LV global longitudinal strain rate (GLSR) was significantly impaired in patients with VD deficiency (p = 0.003). The GLS was negatively associated with 25-(OH)D(3) in the VD deficiency group (r = –0.52623, p < 0.001). Conversely, GLS was positively associated with 25-(OH)D(3) levels in the normal VD group (r = 0.28, p = 0.048). CONCLUSIONS: VD deficiency is associated with impaired myocardial GLS. The present study demonstrated that VD deficiency may be the cause of subclinical myocardial dysfunction in patients with or without diabetes mellitus and no history of significant coronary artery disease.
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spelling pubmed-74337882020-08-21 Silent myocardial dysfunction in vitamin D deficiency Ozer, Pelin Karaca Emet, Samim Karaayvaz, Ekrem Bilal Elitok, Ali Bilge, Ahmet Kaya Adalet, Kamil Oncul, Aytac Arch Med Sci Atheroscler Dis Clinical Research INTRODUCTION: Vitamin D (VD) deficiency is a common disease that occurs in all stages of life. A growing number of studies call attention to the relationship between VD deficiency and cardiovascular disease. The aim of this study was to investigate the effect of VD on subclinical left ventricular (LV) function in diabetic and non-diabetic patients with no significant coronary artery disease. MATERIAL AND METHODS: We recruited 140 patients (80 diabetics and 60 non-diabetics) with symptoms of stable ischemic heart disease who underwent coronary angiography and who had no significant coronary artery disease in our clinic. The 25(OH)D(3) levels were measured and patients who had 25-(OH)D(3) levels below 20 ng/dl were defined as the VD deficient group. In addition to conventional echocardiographic parameters, tissue Doppler echocardiography was used for LV diastolic functions and 2D speckle tracking strain echocardiography (2D STE) for evaluating the longitudinal deformation indices of the LV myocardium. RESULTS: In all groups, LV global longitudinal strain (GLS) was significantly impaired in patients with VD deficiency (p < 0.001) compared to patients without VD deficiency. LV global longitudinal strain rate (GLSR) was significantly impaired in patients with VD deficiency (p = 0.003). The GLS was negatively associated with 25-(OH)D(3) in the VD deficiency group (r = –0.52623, p < 0.001). Conversely, GLS was positively associated with 25-(OH)D(3) levels in the normal VD group (r = 0.28, p = 0.048). CONCLUSIONS: VD deficiency is associated with impaired myocardial GLS. The present study demonstrated that VD deficiency may be the cause of subclinical myocardial dysfunction in patients with or without diabetes mellitus and no history of significant coronary artery disease. Termedia Publishing House 2020-07-11 /pmc/articles/PMC7433788/ /pubmed/32832715 http://dx.doi.org/10.5114/amsad.2020.97110 Text en Copyright: © 2020 Termedia & Banach http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Clinical Research
Ozer, Pelin Karaca
Emet, Samim
Karaayvaz, Ekrem Bilal
Elitok, Ali
Bilge, Ahmet Kaya
Adalet, Kamil
Oncul, Aytac
Silent myocardial dysfunction in vitamin D deficiency
title Silent myocardial dysfunction in vitamin D deficiency
title_full Silent myocardial dysfunction in vitamin D deficiency
title_fullStr Silent myocardial dysfunction in vitamin D deficiency
title_full_unstemmed Silent myocardial dysfunction in vitamin D deficiency
title_short Silent myocardial dysfunction in vitamin D deficiency
title_sort silent myocardial dysfunction in vitamin d deficiency
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7433788/
https://www.ncbi.nlm.nih.gov/pubmed/32832715
http://dx.doi.org/10.5114/amsad.2020.97110
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