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Hemostatic state of children with type 1 diabetes

PURPOSE: Hyperglycemia is one of the factors responsible for the molecular alterations that modify hemostasis. The aim of this study was to determine the levels of circulating molecules that have a prothrombotic impact on the child and adolescent population with type 1 diabetes mellitus. METHODS: Th...

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Autores principales: Aleman, Mariano Nicolás, Díaz, Elba Irma, Luciardi, Maria Constanza, Mariani, Ana Carolina, Bazán, Maria Cristina, Abregu, Adela Victoria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Pediatric Endocrinology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8255861/
https://www.ncbi.nlm.nih.gov/pubmed/34218631
http://dx.doi.org/10.6065/apem.2040142.071
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author Aleman, Mariano Nicolás
Díaz, Elba Irma
Luciardi, Maria Constanza
Mariani, Ana Carolina
Bazán, Maria Cristina
Abregu, Adela Victoria
author_facet Aleman, Mariano Nicolás
Díaz, Elba Irma
Luciardi, Maria Constanza
Mariani, Ana Carolina
Bazán, Maria Cristina
Abregu, Adela Victoria
author_sort Aleman, Mariano Nicolás
collection PubMed
description PURPOSE: Hyperglycemia is one of the factors responsible for the molecular alterations that modify hemostasis. The aim of this study was to determine the levels of circulating molecules that have a prothrombotic impact on the child and adolescent population with type 1 diabetes mellitus. METHODS: There were 35 patients with type 1 diabetes mellitus (11.0±2.5 years of age and a median 3.7±2.0 years of the disease) with no vascular complications and 20 healthy controls with similar age, sex, and body mass index included in the study. The evaluated parameters were fibrinogen, plasminogen activator inhibitor-1 (PAI-1), von Willebrand factor antigen, and standard coagulation tests (platelet count, prothrombin time, and activated partial thromboplastin time). Glycemic control was evaluated by hemoglobin A1c and fasting blood glucose tests, and the presence of retinopathy and nephropathy was ruled out. The data obtained were analyzed by IBM SPSS Statistics ver. 20.0 and expressed as mean±standard deviation. The Pearson correlation coefficient was applied to investigate correlations between variables. RESULTS: Diabetic patients showed significantly higher levels of fibrinogen (308±66 mg/dL vs. 246±18 mg/dL, P=0.0001), PAI-1 (41.6±12 ng/mL vs. 11.7±1.0 ng/mL, P=0.0001), and von Willebrand factor antigen (284%±55% vs. 121%±19%, P=0.0001). However, standard coagulation tests did not show differences between the 2 groups. PAI-1 was correlated with glycemia, hemoglobin A1c, fibrinogen, and von Willebrand factor antigen. CONCLUSIONS: Elevated levels of fibrinogen, PAI-1, and von Willebrand factor antigen were found in the pediatric and adolescent population with type 1 diabetes mellitus, which suggests a prothrombotic state.
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spelling pubmed-82558612021-07-15 Hemostatic state of children with type 1 diabetes Aleman, Mariano Nicolás Díaz, Elba Irma Luciardi, Maria Constanza Mariani, Ana Carolina Bazán, Maria Cristina Abregu, Adela Victoria Ann Pediatr Endocrinol Metab Original Article PURPOSE: Hyperglycemia is one of the factors responsible for the molecular alterations that modify hemostasis. The aim of this study was to determine the levels of circulating molecules that have a prothrombotic impact on the child and adolescent population with type 1 diabetes mellitus. METHODS: There were 35 patients with type 1 diabetes mellitus (11.0±2.5 years of age and a median 3.7±2.0 years of the disease) with no vascular complications and 20 healthy controls with similar age, sex, and body mass index included in the study. The evaluated parameters were fibrinogen, plasminogen activator inhibitor-1 (PAI-1), von Willebrand factor antigen, and standard coagulation tests (platelet count, prothrombin time, and activated partial thromboplastin time). Glycemic control was evaluated by hemoglobin A1c and fasting blood glucose tests, and the presence of retinopathy and nephropathy was ruled out. The data obtained were analyzed by IBM SPSS Statistics ver. 20.0 and expressed as mean±standard deviation. The Pearson correlation coefficient was applied to investigate correlations between variables. RESULTS: Diabetic patients showed significantly higher levels of fibrinogen (308±66 mg/dL vs. 246±18 mg/dL, P=0.0001), PAI-1 (41.6±12 ng/mL vs. 11.7±1.0 ng/mL, P=0.0001), and von Willebrand factor antigen (284%±55% vs. 121%±19%, P=0.0001). However, standard coagulation tests did not show differences between the 2 groups. PAI-1 was correlated with glycemia, hemoglobin A1c, fibrinogen, and von Willebrand factor antigen. CONCLUSIONS: Elevated levels of fibrinogen, PAI-1, and von Willebrand factor antigen were found in the pediatric and adolescent population with type 1 diabetes mellitus, which suggests a prothrombotic state. Korean Society of Pediatric Endocrinology 2021-06 2021-06-30 /pmc/articles/PMC8255861/ /pubmed/34218631 http://dx.doi.org/10.6065/apem.2040142.071 Text en © 2021 Annals of Pediatric Endocrinology & Metabolism https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Aleman, Mariano Nicolás
Díaz, Elba Irma
Luciardi, Maria Constanza
Mariani, Ana Carolina
Bazán, Maria Cristina
Abregu, Adela Victoria
Hemostatic state of children with type 1 diabetes
title Hemostatic state of children with type 1 diabetes
title_full Hemostatic state of children with type 1 diabetes
title_fullStr Hemostatic state of children with type 1 diabetes
title_full_unstemmed Hemostatic state of children with type 1 diabetes
title_short Hemostatic state of children with type 1 diabetes
title_sort hemostatic state of children with type 1 diabetes
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8255861/
https://www.ncbi.nlm.nih.gov/pubmed/34218631
http://dx.doi.org/10.6065/apem.2040142.071
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