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Evidence for congruent impairment in micro and macrovascular function in type 1 diabetes

Diabetes affects large and small vessels through mechanisms only partially known. In the present study, we evaluated the function of capillaries and large arteries in subjects with type 1 diabetes mellitus (T1DM) to study the effect of chronic hyperglycemia in the absence of other cardiovascular ris...

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Autores principales: Irace, Concetta, Messiniti, Valentina, Tassone, Bruno, Cortese, Claudio, Barrett, Eugene J., Gnasso, Agostino
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5683560/
https://www.ncbi.nlm.nih.gov/pubmed/29131837
http://dx.doi.org/10.1371/journal.pone.0187525
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author Irace, Concetta
Messiniti, Valentina
Tassone, Bruno
Cortese, Claudio
Barrett, Eugene J.
Gnasso, Agostino
author_facet Irace, Concetta
Messiniti, Valentina
Tassone, Bruno
Cortese, Claudio
Barrett, Eugene J.
Gnasso, Agostino
author_sort Irace, Concetta
collection PubMed
description Diabetes affects large and small vessels through mechanisms only partially known. In the present study, we evaluated the function of capillaries and large arteries in subjects with type 1 diabetes mellitus (T1DM) to study the effect of chronic hyperglycemia in the absence of other cardiovascular risk factors. Twenty-five subjects with T1DM and 12 healthy age-matched controls were enrolled. Nine patients had mild or moderate retinopathy. Contrast enhanced ultrasound was used to measure perfusion of the deep forearm flexor muscle of the non-dominant arm at rest (baseline) and after an ischemic stimulus (reactive hyperemia). Perfusion was expressed as Video Intensity (VI) in arbitrary unit (a.u.)/mm(2). The time to reach peak VI after ischemia was also recorded. The function of large arteries was evaluated using flow-mediated vasodilation (FMD). VI was significantly lower in T1DM compared to control subjects both at baseline (0.22±0.16 vs 0.44±0.35 a.u./mm(2), p<0.05), and after ischemia (0.33±0.24 vs 0.68±0.46 a.u./mm(2), p<0.05). The time to reach peak VI after ischemia was markedly longer in T1DM (5.6±2.2 vs 4.0±1.7 seconds, p<0.02). These differences were more marked in T1DM subjects with retinopathy. FMD was lower in TIDM patients compared to controls (5.4±6.4 vs 10.7±4.5%, p<0.01). The present findings demonstrate that T1DM patients have defective peripheral skeletal muscle perfusion both at rest and after ischemia compared with control subjects. Low muscle perfusion associates with low FMD of the brachial artery. Furthermore, T1DM subjects with retinopathy have the least muscle perfusion and blunted response to hyperemia compared to T1DM without retinopathy.
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spelling pubmed-56835602017-11-30 Evidence for congruent impairment in micro and macrovascular function in type 1 diabetes Irace, Concetta Messiniti, Valentina Tassone, Bruno Cortese, Claudio Barrett, Eugene J. Gnasso, Agostino PLoS One Research Article Diabetes affects large and small vessels through mechanisms only partially known. In the present study, we evaluated the function of capillaries and large arteries in subjects with type 1 diabetes mellitus (T1DM) to study the effect of chronic hyperglycemia in the absence of other cardiovascular risk factors. Twenty-five subjects with T1DM and 12 healthy age-matched controls were enrolled. Nine patients had mild or moderate retinopathy. Contrast enhanced ultrasound was used to measure perfusion of the deep forearm flexor muscle of the non-dominant arm at rest (baseline) and after an ischemic stimulus (reactive hyperemia). Perfusion was expressed as Video Intensity (VI) in arbitrary unit (a.u.)/mm(2). The time to reach peak VI after ischemia was also recorded. The function of large arteries was evaluated using flow-mediated vasodilation (FMD). VI was significantly lower in T1DM compared to control subjects both at baseline (0.22±0.16 vs 0.44±0.35 a.u./mm(2), p<0.05), and after ischemia (0.33±0.24 vs 0.68±0.46 a.u./mm(2), p<0.05). The time to reach peak VI after ischemia was markedly longer in T1DM (5.6±2.2 vs 4.0±1.7 seconds, p<0.02). These differences were more marked in T1DM subjects with retinopathy. FMD was lower in TIDM patients compared to controls (5.4±6.4 vs 10.7±4.5%, p<0.01). The present findings demonstrate that T1DM patients have defective peripheral skeletal muscle perfusion both at rest and after ischemia compared with control subjects. Low muscle perfusion associates with low FMD of the brachial artery. Furthermore, T1DM subjects with retinopathy have the least muscle perfusion and blunted response to hyperemia compared to T1DM without retinopathy. Public Library of Science 2017-11-13 /pmc/articles/PMC5683560/ /pubmed/29131837 http://dx.doi.org/10.1371/journal.pone.0187525 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Irace, Concetta
Messiniti, Valentina
Tassone, Bruno
Cortese, Claudio
Barrett, Eugene J.
Gnasso, Agostino
Evidence for congruent impairment in micro and macrovascular function in type 1 diabetes
title Evidence for congruent impairment in micro and macrovascular function in type 1 diabetes
title_full Evidence for congruent impairment in micro and macrovascular function in type 1 diabetes
title_fullStr Evidence for congruent impairment in micro and macrovascular function in type 1 diabetes
title_full_unstemmed Evidence for congruent impairment in micro and macrovascular function in type 1 diabetes
title_short Evidence for congruent impairment in micro and macrovascular function in type 1 diabetes
title_sort evidence for congruent impairment in micro and macrovascular function in type 1 diabetes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5683560/
https://www.ncbi.nlm.nih.gov/pubmed/29131837
http://dx.doi.org/10.1371/journal.pone.0187525
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