Hypoglycemia and Cardiovascular Outcomes in the CARMELINA and CAROLINA Trials of Linagliptin

Author:

Marx Nikolaus1,Kolkailah Ahmed A.2,Rosenstock Julio3,Johansen Odd Erik4,Cooper Mark E.5,Alexander John H.6,Toto Robert D.7,Wanner Christoph8,Espeland Mark A.9,Mattheus Michaela10,Schnaidt Sven11,Perkovic Vlado12,Gollop Nicholas D.13,McGuire Darren K.214

Affiliation:

1. Department of Internal Medicine I, University Hospital Aachen, RWTH Aachen University, Aachen, Germany

2. Division of Cardiology, Department of Internal Medicine, The University of Texas Southwestern Medical Center, Dallas

3. Dallas Diabetes Research Center at Medical City, Dallas, Texas

4. Therapeutic Area Cardiometabolism, Boehringer Ingelheim KS, Asker, Norway

5. Department of Diabetes, Central Clinical School, Monash University, Melbourne, Victoria, Australia

6. Duke Clinical Research Institute, Duke Health, Durham, North Carolina

7. Department of Internal Medicine, Division of Nephrology, The University of Texas Southwestern Medical Center, Dallas

8. Division of Nephrology, Department of Medicine, University Hospital Würzburg, Würzburg, Germany

9. Division of Gerontology and Geriatric Medicine, Wake Forest School of Medicine, Winston-Salem, North Carolina

10. Biostatistics and Data Sciences, Boehringer Ingelheim Pharma GmbH & Co KG, Ingelheim am Rhein, Germany

11. Biostatistics and Data Sciences, Boehringer Ingelheim Pharma GmbH & Co KG, Biberach an der Riß, Germany

12. Renal and Metabolic Division, The George Institute for Global Health, University of New South Wales Sydney, Newtown, New South Wales, Australia

13. Therapeutic Area Cardiometabolism, Boehringer Ingelheim International GmbH, Ingelheim am Rhein, Germany

14. Parkland Health, Dallas, Texas

Abstract

ImportancePrevious studies have reported an association between hypoglycemia and cardiovascular (CV) events in people with type 2 diabetes (T2D), but it is unclear if this association is causal or identifies a high-risk patient phenotype.ObjectiveTo evaluate the associations between hypoglycemia and CV outcomes.Design, Setting, and ParticipantsThis secondary analysis was a post hoc assessment of the multinational, double-blind CARMELINA (Cardiovascular and Renal Microvascular Outcome Study With Linagliptin; 2013-2016) and CAROLINA (Cardiovascular Outcome Trial of Linagliptin vs Glimepiride in Type 2 Diabetes; 2010-2018) randomized clinical trials of the antihyperglycemic drug, linagliptin, a dipeptidyl peptidase 4 inhibitor. Participants were adults with T2D at high CV risk with or without high kidney risk. By design, participants in the CARMELINA trial had longer duration of T2D and had a higher CV risk than participants in the CAROLINA trial. Data analyses were conducted between June 2021 and June 2023.InterventionLinagliptin or placebo in the CARMELINA trial, and linagliptin or glimepiride in the CAROLINA trial.Main Outcomes and MeasuresThe primary outcome for both trials was CV death, myocardial infarction (MI), or stroke (3-point major adverse CV events [3P-MACE]). For the present analyses, hospitalization for heart failure (HF) was added. Hypoglycemia was defined as plasma glucose less than 54 mg/dL or severe hypoglycemia (episodes requiring the assistance of another person). Associations between the first hypoglycemic episode and subsequent CV events and between nonfatal CV events (MI, stroke, hospitalization for HF) and subsequent hypoglycemic episodes were assessed using multivariable Cox proportional hazards regression models. Sensitivity analyses explored the risk of CV events within 60 days after each hypoglycemic episode.ResultsIn the CARMELINA trial (6979 patients; 4390 males [62.9%]; mean [SD] age, 65.9 [9.1] years), there was an association between hypoglycemia and subsequent 3P-MACE plus hospitalization for HF (hazard ratio [HR], 1.23; 95% CI, 1.04-1.46) as well as between nonfatal CV events and subsequent hypoglycemia (HR, 1.39; 95% CI, 1.06-1.83). In the CAROLINA trial (6033 patients; 3619 males (60.0%); mean [SD] age, 64.0 [9.5] years), there was no association between hypoglycemia and subsequent 3P-MACE plus hospitalization for HF (HR, 1.00; 95% CI, 0.76-1.32) and between nonfatal CV events and subsequent hypoglycemia (HR, 1.44; 95% CI, 0.96-2.16). In analyses of CV events occurring within 60 days after hypoglycemia, there was either no association or too few events to analyze.Conclusions and RelevanceThis study found bidirectional associations between hypoglycemia and CV outcomes in the CARMELINA trial but no associations in either direction in the CAROLINA trial, challenging the notion that hypoglycemia causes adverse CV events. The findings from the CARMELINA trial suggest that both hypoglycemia and CV events more likely identify patients at high risk for both.Trial RegistrationClinicalTrials.gov Identifier: NCT01897532 (CARMELINA) and NCT01243424 (CAROLINA)

Publisher

American Medical Association (AMA)

Subject

Cardiology and Cardiovascular Medicine

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