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Impact of Being Eligible for Type 2 Diabetes Treatment on All-Cause Mortality and Cardiovascular Events: Regression Discontinuity Design Study

BACKGROUND: Individuals with type 2 diabetes (T2D) have a twofold increased risk for cardiovascular events (CVE), and CVE is responsible for nearly 80% of the mortality. Current treatment guidelines state that individuals should immediately initiate antidiabetic treatment and cardiovascular risk-fac...

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Autores principales: Petersen, Irene, Nicolaisen, Sia Kromann, Ricciardi, Federico, Sharma, Manuj, Thomsen, Reimar W, Baio, Gianluca, Pedersen, Lars
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7294562/
https://www.ncbi.nlm.nih.gov/pubmed/32606982
http://dx.doi.org/10.2147/CLEP.S251704
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author Petersen, Irene
Nicolaisen, Sia Kromann
Ricciardi, Federico
Sharma, Manuj
Thomsen, Reimar W
Baio, Gianluca
Pedersen, Lars
author_facet Petersen, Irene
Nicolaisen, Sia Kromann
Ricciardi, Federico
Sharma, Manuj
Thomsen, Reimar W
Baio, Gianluca
Pedersen, Lars
author_sort Petersen, Irene
collection PubMed
description BACKGROUND: Individuals with type 2 diabetes (T2D) have a twofold increased risk for cardiovascular events (CVE), and CVE is responsible for nearly 80% of the mortality. Current treatment guidelines state that individuals should immediately initiate antidiabetic treatment and cardiovascular risk-factor management from T2D diagnosis. However, the evidence base is sparse, and randomized trials are unlikely to be conducted. We examined the impact of being eligible for T2D treatment, as determined by the threshold of HbA(1c) ≥6.5% (≥48 mmol/mol), on all-cause mortality and CVE. We hypothesised that individuals who were just above this threshold had a lower risk of CVE and all-cause mortality than individuals just below. METHODS AND FINDINGS: We used the regression discontinuity design (RDD), a quasi-experimental design, comparing rates of all-cause mortality and CVE in people just below and just above the eligibility for treatment threshold. We included Danish healthcare records from 43,070 individuals aged 40–80 years with no previous T2D record and the first record of HbA(1c )in the range of 6.0–7.0% (42–53 mmol/mol) between 2006 and 2014. In total, 36,360 individuals had the first record of HbA(1c) between 6.0% and 6.4% (42–47 mmol/mol), and 6710 individuals had a first record between 6.5% and 7.0% (48–53 mmol/mol). Individuals with a measurement just above 6.5% (48 mmol/mol) had a 21% lower rate of death or CVE, compared to those just below (hazard ratio: 0.79 (95% CI 0.69–0.90)). Few individuals received early metformin treatment. However, the chance of metformin treatment initiation within 3 months was substantially higher for individuals with an HbA(1c) measurement above (14%) than below (1%) the threshold. CONCLUSION: Individuals with first record of HbA(1c) measure just above treatment threshold experienced a 21% lower rate of death or CVE than those just below. Lifestyle modifications and cardiovascular risk-factor management may contribute to this reduced rate.
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spelling pubmed-72945622020-06-29 Impact of Being Eligible for Type 2 Diabetes Treatment on All-Cause Mortality and Cardiovascular Events: Regression Discontinuity Design Study Petersen, Irene Nicolaisen, Sia Kromann Ricciardi, Federico Sharma, Manuj Thomsen, Reimar W Baio, Gianluca Pedersen, Lars Clin Epidemiol Original Research BACKGROUND: Individuals with type 2 diabetes (T2D) have a twofold increased risk for cardiovascular events (CVE), and CVE is responsible for nearly 80% of the mortality. Current treatment guidelines state that individuals should immediately initiate antidiabetic treatment and cardiovascular risk-factor management from T2D diagnosis. However, the evidence base is sparse, and randomized trials are unlikely to be conducted. We examined the impact of being eligible for T2D treatment, as determined by the threshold of HbA(1c) ≥6.5% (≥48 mmol/mol), on all-cause mortality and CVE. We hypothesised that individuals who were just above this threshold had a lower risk of CVE and all-cause mortality than individuals just below. METHODS AND FINDINGS: We used the regression discontinuity design (RDD), a quasi-experimental design, comparing rates of all-cause mortality and CVE in people just below and just above the eligibility for treatment threshold. We included Danish healthcare records from 43,070 individuals aged 40–80 years with no previous T2D record and the first record of HbA(1c )in the range of 6.0–7.0% (42–53 mmol/mol) between 2006 and 2014. In total, 36,360 individuals had the first record of HbA(1c) between 6.0% and 6.4% (42–47 mmol/mol), and 6710 individuals had a first record between 6.5% and 7.0% (48–53 mmol/mol). Individuals with a measurement just above 6.5% (48 mmol/mol) had a 21% lower rate of death or CVE, compared to those just below (hazard ratio: 0.79 (95% CI 0.69–0.90)). Few individuals received early metformin treatment. However, the chance of metformin treatment initiation within 3 months was substantially higher for individuals with an HbA(1c) measurement above (14%) than below (1%) the threshold. CONCLUSION: Individuals with first record of HbA(1c) measure just above treatment threshold experienced a 21% lower rate of death or CVE than those just below. Lifestyle modifications and cardiovascular risk-factor management may contribute to this reduced rate. Dove 2020-06-03 /pmc/articles/PMC7294562/ /pubmed/32606982 http://dx.doi.org/10.2147/CLEP.S251704 Text en © 2020 Petersen et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Petersen, Irene
Nicolaisen, Sia Kromann
Ricciardi, Federico
Sharma, Manuj
Thomsen, Reimar W
Baio, Gianluca
Pedersen, Lars
Impact of Being Eligible for Type 2 Diabetes Treatment on All-Cause Mortality and Cardiovascular Events: Regression Discontinuity Design Study
title Impact of Being Eligible for Type 2 Diabetes Treatment on All-Cause Mortality and Cardiovascular Events: Regression Discontinuity Design Study
title_full Impact of Being Eligible for Type 2 Diabetes Treatment on All-Cause Mortality and Cardiovascular Events: Regression Discontinuity Design Study
title_fullStr Impact of Being Eligible for Type 2 Diabetes Treatment on All-Cause Mortality and Cardiovascular Events: Regression Discontinuity Design Study
title_full_unstemmed Impact of Being Eligible for Type 2 Diabetes Treatment on All-Cause Mortality and Cardiovascular Events: Regression Discontinuity Design Study
title_short Impact of Being Eligible for Type 2 Diabetes Treatment on All-Cause Mortality and Cardiovascular Events: Regression Discontinuity Design Study
title_sort impact of being eligible for type 2 diabetes treatment on all-cause mortality and cardiovascular events: regression discontinuity design study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7294562/
https://www.ncbi.nlm.nih.gov/pubmed/32606982
http://dx.doi.org/10.2147/CLEP.S251704
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