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The Beneficial Effects of Earlier Versus Later Implementation of Intensive Therapy in Type 1 Diabetes
OBJECTIVE: The principal aim is to estimate the benefits of earlier versus later implementation of intensive therapy in type 1 diabetes with respect to the long-term risks of progression of a renal (microvascular) and cardiovascular (macrovascular) complication in the Epidemiology of Diabetes Interv...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Diabetes Association
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8929189/ https://www.ncbi.nlm.nih.gov/pubmed/34380706 http://dx.doi.org/10.2337/dc21-1331 |
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author | Lachin, John M. Bebu, Ionut Nathan, David M. |
author_facet | Lachin, John M. Bebu, Ionut Nathan, David M. |
author_sort | Lachin, John M. |
collection | PubMed |
description | OBJECTIVE: The principal aim is to estimate the benefits of earlier versus later implementation of intensive therapy in type 1 diabetes with respect to the long-term risks of progression of a renal (microvascular) and cardiovascular (macrovascular) complication in the Epidemiology of Diabetes Interventions and Complications (EDIC) study. RESEARCH DESIGN AND METHODS: Cox proportional hazards regression models estimated the 20-year cumulative incidence (absolute risk) and the 20-year relative risk of cardiovascular disease (CVD) and reduced estimated glomerular filtration rate (eGFR) over the first 20 years of EDIC follow-up as a function of the mean HbA(1c). RESULTS: A hypothetical patient treated earlier with 10 years of intensive therapy and a mean HbA(1c) of 7% (53 mmol/mol) followed by 10 years with a mean of 9% (75 mmol/mol) would have a 33% reduction in the risk of CVD and a 52% reduction in reduced eGFR compared with a patient with a mean HbA(1c) of 9% (75 mmol/mol) over the first 10 years followed by later intensive therapy over 10 years with an HbA(1c) of 7% (53 mmol/mol). Despite both patients having the same average glycemic exposure over the 20 years, the patient with the lower HbA(1c) over the first 10 years had a lower risk of progression of complications over the 20 years than the patient who had the higher value initially. CONCLUSIONS: While implementation of intensive therapy at any time in type 1 diabetes will be beneficial, within the 20-year period modeled, earlier relative to later implementation is associated with a greater reduction in the risks of kidney and cardiovascular complications. |
format | Online Article Text |
id | pubmed-8929189 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Diabetes Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-89291892022-10-01 The Beneficial Effects of Earlier Versus Later Implementation of Intensive Therapy in Type 1 Diabetes Lachin, John M. Bebu, Ionut Nathan, David M. Diabetes Care Long-term Effects of Earlier Glycemic Control OBJECTIVE: The principal aim is to estimate the benefits of earlier versus later implementation of intensive therapy in type 1 diabetes with respect to the long-term risks of progression of a renal (microvascular) and cardiovascular (macrovascular) complication in the Epidemiology of Diabetes Interventions and Complications (EDIC) study. RESEARCH DESIGN AND METHODS: Cox proportional hazards regression models estimated the 20-year cumulative incidence (absolute risk) and the 20-year relative risk of cardiovascular disease (CVD) and reduced estimated glomerular filtration rate (eGFR) over the first 20 years of EDIC follow-up as a function of the mean HbA(1c). RESULTS: A hypothetical patient treated earlier with 10 years of intensive therapy and a mean HbA(1c) of 7% (53 mmol/mol) followed by 10 years with a mean of 9% (75 mmol/mol) would have a 33% reduction in the risk of CVD and a 52% reduction in reduced eGFR compared with a patient with a mean HbA(1c) of 9% (75 mmol/mol) over the first 10 years followed by later intensive therapy over 10 years with an HbA(1c) of 7% (53 mmol/mol). Despite both patients having the same average glycemic exposure over the 20 years, the patient with the lower HbA(1c) over the first 10 years had a lower risk of progression of complications over the 20 years than the patient who had the higher value initially. CONCLUSIONS: While implementation of intensive therapy at any time in type 1 diabetes will be beneficial, within the 20-year period modeled, earlier relative to later implementation is associated with a greater reduction in the risks of kidney and cardiovascular complications. American Diabetes Association 2021-10 2021-08-11 /pmc/articles/PMC8929189/ /pubmed/34380706 http://dx.doi.org/10.2337/dc21-1331 Text en © 2021 by the American Diabetes Association https://www.diabetesjournals.org/content/licenseReaders may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. More information is available at https://www.diabetesjournals.org/content/license. |
spellingShingle | Long-term Effects of Earlier Glycemic Control Lachin, John M. Bebu, Ionut Nathan, David M. The Beneficial Effects of Earlier Versus Later Implementation of Intensive Therapy in Type 1 Diabetes |
title | The Beneficial Effects of Earlier Versus Later Implementation of Intensive Therapy in Type 1 Diabetes |
title_full | The Beneficial Effects of Earlier Versus Later Implementation of Intensive Therapy in Type 1 Diabetes |
title_fullStr | The Beneficial Effects of Earlier Versus Later Implementation of Intensive Therapy in Type 1 Diabetes |
title_full_unstemmed | The Beneficial Effects of Earlier Versus Later Implementation of Intensive Therapy in Type 1 Diabetes |
title_short | The Beneficial Effects of Earlier Versus Later Implementation of Intensive Therapy in Type 1 Diabetes |
title_sort | beneficial effects of earlier versus later implementation of intensive therapy in type 1 diabetes |
topic | Long-term Effects of Earlier Glycemic Control |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8929189/ https://www.ncbi.nlm.nih.gov/pubmed/34380706 http://dx.doi.org/10.2337/dc21-1331 |
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