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Effects of Linagliptin on Cardiovascular and Kidney Outcomes in People With Normal and Reduced Kidney Function: Secondary Analysis of the CARMELINA Randomized Trial
OBJECTIVE: Type 2 diabetes is a leading cause of kidney failure, but few outcome trials proactively enrolled individuals with chronic kidney disease (CKD). We performed secondary analyses of cardiovascular (CV) and kidney outcomes across baseline estimated glomerular filtration rate (eGFR) categorie...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Diabetes Association
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7372065/ https://www.ncbi.nlm.nih.gov/pubmed/32444457 http://dx.doi.org/10.2337/dc20-0279 |
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author | Perkovic, Vlado Toto, Robert Cooper, Mark E. Mann, Johannes F.E. Rosenstock, Julio McGuire, Darren K. Kahn, Steven E. Marx, Nikolaus Alexander, John H. Zinman, Bernard Pfarr, Egon Schnaidt, Sven Meinicke, Thomas von Eynatten, Maximillian George, Jyothis T. Johansen, Odd Erik Wanner, Christoph |
author_facet | Perkovic, Vlado Toto, Robert Cooper, Mark E. Mann, Johannes F.E. Rosenstock, Julio McGuire, Darren K. Kahn, Steven E. Marx, Nikolaus Alexander, John H. Zinman, Bernard Pfarr, Egon Schnaidt, Sven Meinicke, Thomas von Eynatten, Maximillian George, Jyothis T. Johansen, Odd Erik Wanner, Christoph |
author_sort | Perkovic, Vlado |
collection | PubMed |
description | OBJECTIVE: Type 2 diabetes is a leading cause of kidney failure, but few outcome trials proactively enrolled individuals with chronic kidney disease (CKD). We performed secondary analyses of cardiovascular (CV) and kidney outcomes across baseline estimated glomerular filtration rate (eGFR) categories (≥60, 45 to <60, 30 to <45, and <30 mL/min/1.73 m(2)) in Cardiovascular and Renal Microvascular Outcome Study With Linagliptin (CARMELINA), a cardiorenal placebo-controlled outcome trial of the dipeptidyl peptidase 4 inhibitor linagliptin (NCT01897532). RESEARCH DESIGN AND METHODS: Participants with CV disease and/or CKD were included. The primary outcome was time to first occurrence of CV death, nonfatal myocardial infarction, or nonfatal stroke (three-point major adverse CV event [3P-MACE]), with a secondary outcome of renal death, end-stage kidney disease, or sustained ≥40% decrease in eGFR from baseline. Other end points included progression of albuminuria, change in HbA(1c), and adverse events (AEs) including hypoglycemia. RESULTS: A total of 6,979 subjects (mean age 65.9 years; eGFR 54.6 mL/min/1.73 m(2); 80.1% albuminuria) were followed for 2.2 years. Across eGFR categories, linagliptin as compared with placebo did not affect the risk for 3P-MACE (hazard ratio 1.02 [95% CI 0.89, 1.17]) or the secondary kidney outcome (1.04 [0.89, 1.22]) (interaction P values >0.05). Regardless of eGFR, albuminuria progression was reduced with linagliptin, as was HbA(1c), without increasing risk for hypoglycemia. AEs were balanced among groups overall and across eGFR categories. CONCLUSIONS: Across all GFR categories, in participants with type 2 diabetes and CKD and/or CV disease, there was no difference in risk for linagliptin versus placebo on CV and kidney events. Significant reductions in risk for albuminuria progression and HbA(1c) and no difference in AEs were observed. |
format | Online Article Text |
id | pubmed-7372065 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Diabetes Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-73720652020-07-24 Effects of Linagliptin on Cardiovascular and Kidney Outcomes in People With Normal and Reduced Kidney Function: Secondary Analysis of the CARMELINA Randomized Trial Perkovic, Vlado Toto, Robert Cooper, Mark E. Mann, Johannes F.E. Rosenstock, Julio McGuire, Darren K. Kahn, Steven E. Marx, Nikolaus Alexander, John H. Zinman, Bernard Pfarr, Egon Schnaidt, Sven Meinicke, Thomas von Eynatten, Maximillian George, Jyothis T. Johansen, Odd Erik Wanner, Christoph Diabetes Care Emerging Therapies: Drugs and Regimens OBJECTIVE: Type 2 diabetes is a leading cause of kidney failure, but few outcome trials proactively enrolled individuals with chronic kidney disease (CKD). We performed secondary analyses of cardiovascular (CV) and kidney outcomes across baseline estimated glomerular filtration rate (eGFR) categories (≥60, 45 to <60, 30 to <45, and <30 mL/min/1.73 m(2)) in Cardiovascular and Renal Microvascular Outcome Study With Linagliptin (CARMELINA), a cardiorenal placebo-controlled outcome trial of the dipeptidyl peptidase 4 inhibitor linagliptin (NCT01897532). RESEARCH DESIGN AND METHODS: Participants with CV disease and/or CKD were included. The primary outcome was time to first occurrence of CV death, nonfatal myocardial infarction, or nonfatal stroke (three-point major adverse CV event [3P-MACE]), with a secondary outcome of renal death, end-stage kidney disease, or sustained ≥40% decrease in eGFR from baseline. Other end points included progression of albuminuria, change in HbA(1c), and adverse events (AEs) including hypoglycemia. RESULTS: A total of 6,979 subjects (mean age 65.9 years; eGFR 54.6 mL/min/1.73 m(2); 80.1% albuminuria) were followed for 2.2 years. Across eGFR categories, linagliptin as compared with placebo did not affect the risk for 3P-MACE (hazard ratio 1.02 [95% CI 0.89, 1.17]) or the secondary kidney outcome (1.04 [0.89, 1.22]) (interaction P values >0.05). Regardless of eGFR, albuminuria progression was reduced with linagliptin, as was HbA(1c), without increasing risk for hypoglycemia. AEs were balanced among groups overall and across eGFR categories. CONCLUSIONS: Across all GFR categories, in participants with type 2 diabetes and CKD and/or CV disease, there was no difference in risk for linagliptin versus placebo on CV and kidney events. Significant reductions in risk for albuminuria progression and HbA(1c) and no difference in AEs were observed. American Diabetes Association 2020-08 2020-05-22 /pmc/articles/PMC7372065/ /pubmed/32444457 http://dx.doi.org/10.2337/dc20-0279 Text en © 2020 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 | Emerging Therapies: Drugs and Regimens Perkovic, Vlado Toto, Robert Cooper, Mark E. Mann, Johannes F.E. Rosenstock, Julio McGuire, Darren K. Kahn, Steven E. Marx, Nikolaus Alexander, John H. Zinman, Bernard Pfarr, Egon Schnaidt, Sven Meinicke, Thomas von Eynatten, Maximillian George, Jyothis T. Johansen, Odd Erik Wanner, Christoph Effects of Linagliptin on Cardiovascular and Kidney Outcomes in People With Normal and Reduced Kidney Function: Secondary Analysis of the CARMELINA Randomized Trial |
title | Effects of Linagliptin on Cardiovascular and Kidney Outcomes in People With Normal and Reduced Kidney Function: Secondary Analysis of the CARMELINA Randomized Trial |
title_full | Effects of Linagliptin on Cardiovascular and Kidney Outcomes in People With Normal and Reduced Kidney Function: Secondary Analysis of the CARMELINA Randomized Trial |
title_fullStr | Effects of Linagliptin on Cardiovascular and Kidney Outcomes in People With Normal and Reduced Kidney Function: Secondary Analysis of the CARMELINA Randomized Trial |
title_full_unstemmed | Effects of Linagliptin on Cardiovascular and Kidney Outcomes in People With Normal and Reduced Kidney Function: Secondary Analysis of the CARMELINA Randomized Trial |
title_short | Effects of Linagliptin on Cardiovascular and Kidney Outcomes in People With Normal and Reduced Kidney Function: Secondary Analysis of the CARMELINA Randomized Trial |
title_sort | effects of linagliptin on cardiovascular and kidney outcomes in people with normal and reduced kidney function: secondary analysis of the carmelina randomized trial |
topic | Emerging Therapies: Drugs and Regimens |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7372065/ https://www.ncbi.nlm.nih.gov/pubmed/32444457 http://dx.doi.org/10.2337/dc20-0279 |
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