Effects of Linagliptin on Cardiovascular and Kidney Outcomes in People With Normal and Reduced Kidney Function: Secondary Analysis of the CARMELINA Randomized Trial.

dc.contributor.author

Perkovic, Vlado

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Toto, Robert

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Cooper, Mark E

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Mann, Johannes FE

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Rosenstock, Julio

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McGuire, Darren K

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Kahn, Steven E

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Marx, Nikolaus

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Alexander, John H

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Zinman, Bernard

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Pfarr, Egon

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Schnaidt, Sven

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Meinicke, Thomas

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von Eynatten, Maximillian

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George, Jyothis T

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Johansen, Odd Erik

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Wanner, Christoph

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CARMELINA investigators

dc.date.accessioned

2021-05-10T18:09:16Z

dc.date.available

2021-05-10T18:09:16Z

dc.date.issued

2020-08

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2021-05-10T18:09:14Z

dc.description.abstract

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 m2) 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 HbA1c, 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 m2; 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 HbA1c, 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 HbA1c and no difference in AEs were observed.
dc.identifier

dc20-0279

dc.identifier.issn

0149-5992

dc.identifier.issn

1935-5548

dc.identifier.uri

https://hdl.handle.net/10161/22866

dc.language

eng

dc.publisher

American Diabetes Association

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Diabetes care

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10.2337/dc20-0279

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CARMELINA investigators

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Kidney

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Cardiovascular System

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Humans

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Diabetic Nephropathies

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Kidney Failure, Chronic

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Cardiovascular Diseases

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Diabetes Mellitus, Type 2

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Hypoglycemic Agents

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Glomerular Filtration Rate

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Prognosis

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Treatment Outcome

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Incidence

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Mortality

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Retrospective Studies

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Aged

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Middle Aged

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Female

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Male

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Renal Insufficiency, Chronic

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Dipeptidyl-Peptidase IV Inhibitors

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Linagliptin

dc.title

Effects of Linagliptin on Cardiovascular and Kidney Outcomes in People With Normal and Reduced Kidney Function: Secondary Analysis of the CARMELINA Randomized Trial.

dc.type

Journal article

duke.contributor.orcid

Alexander, John H|0000-0002-1444-2462

pubs.begin-page

1803

pubs.end-page

1812

pubs.issue

8

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School of Medicine

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Duke Clinical Research Institute

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Medicine, Cardiology

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Duke

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Institutes and Centers

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Medicine

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Clinical Science Departments

pubs.publication-status

Published

pubs.volume

43

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