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Continuous subcutaneous insulin infusion alters microRNA expression and glycaemic variability in children with type 1 diabetes

To determine whether continuous subcutaneous insulin infusion (CSII) vs. multiple daily injections (MDI) therapy from near-diagnosis of type 1 diabetes is associated with reduced glycaemic variability (GV) and altered microRNA (miRNAs) expression. Adolescents (74% male) within 3-months of diabetes d...

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Autores principales: Scott, Emma S., Januszewski, Andrzej S., Carroll, Luke M., Fulcher, Gregory R., Joglekar, Mugdha V., Hardikar, Anandwardhan A., Jones, Timothy W., Davis, Elizabeth A., Jenkins, Alicia J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8370996/
https://www.ncbi.nlm.nih.gov/pubmed/34404828
http://dx.doi.org/10.1038/s41598-021-95824-8
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author Scott, Emma S.
Januszewski, Andrzej S.
Carroll, Luke M.
Fulcher, Gregory R.
Joglekar, Mugdha V.
Hardikar, Anandwardhan A.
Jones, Timothy W.
Davis, Elizabeth A.
Jenkins, Alicia J.
author_facet Scott, Emma S.
Januszewski, Andrzej S.
Carroll, Luke M.
Fulcher, Gregory R.
Joglekar, Mugdha V.
Hardikar, Anandwardhan A.
Jones, Timothy W.
Davis, Elizabeth A.
Jenkins, Alicia J.
author_sort Scott, Emma S.
collection PubMed
description To determine whether continuous subcutaneous insulin infusion (CSII) vs. multiple daily injections (MDI) therapy from near-diagnosis of type 1 diabetes is associated with reduced glycaemic variability (GV) and altered microRNA (miRNAs) expression. Adolescents (74% male) within 3-months of diabetes diagnosis (n = 27) were randomized to CSII (n = 12) or MDI. HbA1c, 1-5-Anhydroglucitol (1,5-AG), high sensitivity C-peptide and a custom TaqMan qPCR panel of 52 miRNAs were measured at baseline and follow-up (median (LQ-UQ); 535 (519–563) days). There were no significant differences between groups in baseline or follow-up HbA1c or C-peptide, nor baseline miRNAs. Mean ± SD 1,5-AG improved with CSII vs. MDI (3.1 ± 4.1 vs. − 2.2 ± − 7.0 mg/ml respectively, P = 0.029). On follow-up 11 miRNAs associated with diabetes vascular complications had altered expression in CSII-users. Early CSII vs. MDI use is associated with lower GV and less adverse vascular-related miRNAs. Relationships with future complications are of interest.
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spelling pubmed-83709962021-08-19 Continuous subcutaneous insulin infusion alters microRNA expression and glycaemic variability in children with type 1 diabetes Scott, Emma S. Januszewski, Andrzej S. Carroll, Luke M. Fulcher, Gregory R. Joglekar, Mugdha V. Hardikar, Anandwardhan A. Jones, Timothy W. Davis, Elizabeth A. Jenkins, Alicia J. Sci Rep Article To determine whether continuous subcutaneous insulin infusion (CSII) vs. multiple daily injections (MDI) therapy from near-diagnosis of type 1 diabetes is associated with reduced glycaemic variability (GV) and altered microRNA (miRNAs) expression. Adolescents (74% male) within 3-months of diabetes diagnosis (n = 27) were randomized to CSII (n = 12) or MDI. HbA1c, 1-5-Anhydroglucitol (1,5-AG), high sensitivity C-peptide and a custom TaqMan qPCR panel of 52 miRNAs were measured at baseline and follow-up (median (LQ-UQ); 535 (519–563) days). There were no significant differences between groups in baseline or follow-up HbA1c or C-peptide, nor baseline miRNAs. Mean ± SD 1,5-AG improved with CSII vs. MDI (3.1 ± 4.1 vs. − 2.2 ± − 7.0 mg/ml respectively, P = 0.029). On follow-up 11 miRNAs associated with diabetes vascular complications had altered expression in CSII-users. Early CSII vs. MDI use is associated with lower GV and less adverse vascular-related miRNAs. Relationships with future complications are of interest. Nature Publishing Group UK 2021-08-17 /pmc/articles/PMC8370996/ /pubmed/34404828 http://dx.doi.org/10.1038/s41598-021-95824-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Scott, Emma S.
Januszewski, Andrzej S.
Carroll, Luke M.
Fulcher, Gregory R.
Joglekar, Mugdha V.
Hardikar, Anandwardhan A.
Jones, Timothy W.
Davis, Elizabeth A.
Jenkins, Alicia J.
Continuous subcutaneous insulin infusion alters microRNA expression and glycaemic variability in children with type 1 diabetes
title Continuous subcutaneous insulin infusion alters microRNA expression and glycaemic variability in children with type 1 diabetes
title_full Continuous subcutaneous insulin infusion alters microRNA expression and glycaemic variability in children with type 1 diabetes
title_fullStr Continuous subcutaneous insulin infusion alters microRNA expression and glycaemic variability in children with type 1 diabetes
title_full_unstemmed Continuous subcutaneous insulin infusion alters microRNA expression and glycaemic variability in children with type 1 diabetes
title_short Continuous subcutaneous insulin infusion alters microRNA expression and glycaemic variability in children with type 1 diabetes
title_sort continuous subcutaneous insulin infusion alters microrna expression and glycaemic variability in children with type 1 diabetes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8370996/
https://www.ncbi.nlm.nih.gov/pubmed/34404828
http://dx.doi.org/10.1038/s41598-021-95824-8
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