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Cardiac Autonomic Neuropathy Measured by Heart Rate Variability and Markers of Subclinical Atherosclerosis in Early Type 2 Diabetes

Cardiac autonomic neuropathy (CAN) is a critical complication of type 2 diabetes mellitus (T2DM). Heart rate variability (HRV) is a noninvasive tool to assess cardiac autonomic function. We aimed to evaluate whether CAN is associated with increased risk of atherosclerosis in T2DM. A total of 57 diab...

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Autores principales: Fakhrzadeh, Hossein, Yamini-Sharif, Ahmad, Sharifi, Farshad, Tajalizadekhoob, Yaser, Mirarefin, Mojde, Mohammadzadeh, Maryam, Sadeghian, Saeed, Badamchizadeh, Zohre, Larijani, Bagher
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scholarly Research Network 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3521488/
https://www.ncbi.nlm.nih.gov/pubmed/23259073
http://dx.doi.org/10.5402/2012/168264
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author Fakhrzadeh, Hossein
Yamini-Sharif, Ahmad
Sharifi, Farshad
Tajalizadekhoob, Yaser
Mirarefin, Mojde
Mohammadzadeh, Maryam
Sadeghian, Saeed
Badamchizadeh, Zohre
Larijani, Bagher
author_facet Fakhrzadeh, Hossein
Yamini-Sharif, Ahmad
Sharifi, Farshad
Tajalizadekhoob, Yaser
Mirarefin, Mojde
Mohammadzadeh, Maryam
Sadeghian, Saeed
Badamchizadeh, Zohre
Larijani, Bagher
author_sort Fakhrzadeh, Hossein
collection PubMed
description Cardiac autonomic neuropathy (CAN) is a critical complication of type 2 diabetes mellitus (T2DM). Heart rate variability (HRV) is a noninvasive tool to assess cardiac autonomic function. We aimed to evaluate whether CAN is associated with increased risk of atherosclerosis in T2DM. A total of 57 diabetic and 54 nondiabetic subjects, free of coronary heart disease, were recruited. Carotid intima media thickness (CIMT), coronary calcium score (CAC), and brachial Flow Mediated Dilation (FMD) were measured. Heart rate variability and vagal components of autonomic function were determined. Significant reduction of normalized HF power (P < 0.05) and total power (P < 0.01) was observed in T2DM. CIMT and CAC scores were significantly higher while FMD was significantly lower in diabetics (P < 0.01 for all). Median HbA(1c) levels were significantly higher in diabetics. CIMT was inversely and independently associated with total power both in diabetics and controls (P < 0.01 for both groups). There was also an inverse association between total power and median HbA(1c). Autonomic dysfunction, especially parasympathetic neuropathy, was present since early-stage T2DM. This was related to subclinical atherosclerosis. Early detection of cardiac autonomic neuropathy can help us detect the development of atherosclerosis earlier in T2DM to prevent unfavorable outcomes.
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spelling pubmed-35214882012-12-20 Cardiac Autonomic Neuropathy Measured by Heart Rate Variability and Markers of Subclinical Atherosclerosis in Early Type 2 Diabetes Fakhrzadeh, Hossein Yamini-Sharif, Ahmad Sharifi, Farshad Tajalizadekhoob, Yaser Mirarefin, Mojde Mohammadzadeh, Maryam Sadeghian, Saeed Badamchizadeh, Zohre Larijani, Bagher ISRN Endocrinol Clinical Study Cardiac autonomic neuropathy (CAN) is a critical complication of type 2 diabetes mellitus (T2DM). Heart rate variability (HRV) is a noninvasive tool to assess cardiac autonomic function. We aimed to evaluate whether CAN is associated with increased risk of atherosclerosis in T2DM. A total of 57 diabetic and 54 nondiabetic subjects, free of coronary heart disease, were recruited. Carotid intima media thickness (CIMT), coronary calcium score (CAC), and brachial Flow Mediated Dilation (FMD) were measured. Heart rate variability and vagal components of autonomic function were determined. Significant reduction of normalized HF power (P < 0.05) and total power (P < 0.01) was observed in T2DM. CIMT and CAC scores were significantly higher while FMD was significantly lower in diabetics (P < 0.01 for all). Median HbA(1c) levels were significantly higher in diabetics. CIMT was inversely and independently associated with total power both in diabetics and controls (P < 0.01 for both groups). There was also an inverse association between total power and median HbA(1c). Autonomic dysfunction, especially parasympathetic neuropathy, was present since early-stage T2DM. This was related to subclinical atherosclerosis. Early detection of cardiac autonomic neuropathy can help us detect the development of atherosclerosis earlier in T2DM to prevent unfavorable outcomes. International Scholarly Research Network 2012-12-04 /pmc/articles/PMC3521488/ /pubmed/23259073 http://dx.doi.org/10.5402/2012/168264 Text en Copyright © 2012 Hossein Fakhrzadeh et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
Fakhrzadeh, Hossein
Yamini-Sharif, Ahmad
Sharifi, Farshad
Tajalizadekhoob, Yaser
Mirarefin, Mojde
Mohammadzadeh, Maryam
Sadeghian, Saeed
Badamchizadeh, Zohre
Larijani, Bagher
Cardiac Autonomic Neuropathy Measured by Heart Rate Variability and Markers of Subclinical Atherosclerosis in Early Type 2 Diabetes
title Cardiac Autonomic Neuropathy Measured by Heart Rate Variability and Markers of Subclinical Atherosclerosis in Early Type 2 Diabetes
title_full Cardiac Autonomic Neuropathy Measured by Heart Rate Variability and Markers of Subclinical Atherosclerosis in Early Type 2 Diabetes
title_fullStr Cardiac Autonomic Neuropathy Measured by Heart Rate Variability and Markers of Subclinical Atherosclerosis in Early Type 2 Diabetes
title_full_unstemmed Cardiac Autonomic Neuropathy Measured by Heart Rate Variability and Markers of Subclinical Atherosclerosis in Early Type 2 Diabetes
title_short Cardiac Autonomic Neuropathy Measured by Heart Rate Variability and Markers of Subclinical Atherosclerosis in Early Type 2 Diabetes
title_sort cardiac autonomic neuropathy measured by heart rate variability and markers of subclinical atherosclerosis in early type 2 diabetes
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3521488/
https://www.ncbi.nlm.nih.gov/pubmed/23259073
http://dx.doi.org/10.5402/2012/168264
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