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Increased Derived Time in Range Is Associated with Reduced Risk of Major Adverse Cardiovascular Events, Severe Hypoglycemia, and Microvascular Events in Type 2 Diabetes: A Post Hoc Analysis of DEVOTE
Time spent in glycemic target range (time in range [TIR]; plasma glucose 70–180 mg/dL [3.9–10.0 mmol/L]) as a surrogate endpoint for long-term diabetes-related outcomes requires validation. This post hoc analysis investigated the association between TIR, derived from 8-point glucose profiles (derive...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mary Ann Liebert, Inc., publishers
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10398723/ https://www.ncbi.nlm.nih.gov/pubmed/37017470 http://dx.doi.org/10.1089/dia.2022.0447 |
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author | Bergenstal, Richard M. Hachmann-Nielsen, Elise Kvist, Kajsa Peters, Anne L. Tarp, Jens Magelund Buse, John B. |
author_facet | Bergenstal, Richard M. Hachmann-Nielsen, Elise Kvist, Kajsa Peters, Anne L. Tarp, Jens Magelund Buse, John B. |
author_sort | Bergenstal, Richard M. |
collection | PubMed |
description | Time spent in glycemic target range (time in range [TIR]; plasma glucose 70–180 mg/dL [3.9–10.0 mmol/L]) as a surrogate endpoint for long-term diabetes-related outcomes requires validation. This post hoc analysis investigated the association between TIR, derived from 8-point glucose profiles (derived TIR [dTIR]) at 12 months, and time to cardiovascular or severe hypoglycemic episodes in people with type 2 diabetes in the DEVOTE trial. At 12 months, dTIR was significantly negatively associated with time to first major adverse cardiovascular event (P = 0.0087), severe hypoglycemic episode (P < 0.0001), or microvascular event (P = 0.024). A nonsignificant trend was seen toward association between 12-month hemoglobin A1c (HbA1c) and these outcomes, but this was no longer seen after addition of dTIR to the model. The results support targeting TIR >70% and suggest dTIR could be used in addition to, or in some instances in place of, HbA1c as a clinical biomarker. TRIAL REGISTRATION DETAILS: ClinicalTrials.gov, NCT01959529 |
format | Online Article Text |
id | pubmed-10398723 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Mary Ann Liebert, Inc., publishers |
record_format | MEDLINE/PubMed |
spelling | pubmed-103987232023-08-04 Increased Derived Time in Range Is Associated with Reduced Risk of Major Adverse Cardiovascular Events, Severe Hypoglycemia, and Microvascular Events in Type 2 Diabetes: A Post Hoc Analysis of DEVOTE Bergenstal, Richard M. Hachmann-Nielsen, Elise Kvist, Kajsa Peters, Anne L. Tarp, Jens Magelund Buse, John B. Diabetes Technol Ther Original Articles Time spent in glycemic target range (time in range [TIR]; plasma glucose 70–180 mg/dL [3.9–10.0 mmol/L]) as a surrogate endpoint for long-term diabetes-related outcomes requires validation. This post hoc analysis investigated the association between TIR, derived from 8-point glucose profiles (derived TIR [dTIR]) at 12 months, and time to cardiovascular or severe hypoglycemic episodes in people with type 2 diabetes in the DEVOTE trial. At 12 months, dTIR was significantly negatively associated with time to first major adverse cardiovascular event (P = 0.0087), severe hypoglycemic episode (P < 0.0001), or microvascular event (P = 0.024). A nonsignificant trend was seen toward association between 12-month hemoglobin A1c (HbA1c) and these outcomes, but this was no longer seen after addition of dTIR to the model. The results support targeting TIR >70% and suggest dTIR could be used in addition to, or in some instances in place of, HbA1c as a clinical biomarker. TRIAL REGISTRATION DETAILS: ClinicalTrials.gov, NCT01959529 Mary Ann Liebert, Inc., publishers 2023-06-01 2023-05-29 /pmc/articles/PMC10398723/ /pubmed/37017470 http://dx.doi.org/10.1089/dia.2022.0447 Text en © Richard M. Bergenstal, et al., 2023; Published by Mary Ann Liebert, Inc. https://creativecommons.org/licenses/by/4.0/This Open Access article is distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. |
spellingShingle | Original Articles Bergenstal, Richard M. Hachmann-Nielsen, Elise Kvist, Kajsa Peters, Anne L. Tarp, Jens Magelund Buse, John B. Increased Derived Time in Range Is Associated with Reduced Risk of Major Adverse Cardiovascular Events, Severe Hypoglycemia, and Microvascular Events in Type 2 Diabetes: A Post Hoc Analysis of DEVOTE |
title | Increased Derived Time in Range Is Associated with Reduced Risk of Major Adverse Cardiovascular Events, Severe Hypoglycemia, and Microvascular Events in Type 2 Diabetes: A Post Hoc Analysis of DEVOTE |
title_full | Increased Derived Time in Range Is Associated with Reduced Risk of Major Adverse Cardiovascular Events, Severe Hypoglycemia, and Microvascular Events in Type 2 Diabetes: A Post Hoc Analysis of DEVOTE |
title_fullStr | Increased Derived Time in Range Is Associated with Reduced Risk of Major Adverse Cardiovascular Events, Severe Hypoglycemia, and Microvascular Events in Type 2 Diabetes: A Post Hoc Analysis of DEVOTE |
title_full_unstemmed | Increased Derived Time in Range Is Associated with Reduced Risk of Major Adverse Cardiovascular Events, Severe Hypoglycemia, and Microvascular Events in Type 2 Diabetes: A Post Hoc Analysis of DEVOTE |
title_short | Increased Derived Time in Range Is Associated with Reduced Risk of Major Adverse Cardiovascular Events, Severe Hypoglycemia, and Microvascular Events in Type 2 Diabetes: A Post Hoc Analysis of DEVOTE |
title_sort | increased derived time in range is associated with reduced risk of major adverse cardiovascular events, severe hypoglycemia, and microvascular events in type 2 diabetes: a post hoc analysis of devote |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10398723/ https://www.ncbi.nlm.nih.gov/pubmed/37017470 http://dx.doi.org/10.1089/dia.2022.0447 |
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