Effect of Linagliptin on Cognitive Performance in Patients With Type 2 Diabetes and Cardiorenal Comorbidities: The CARMELINA Randomized Trial.


Journal

Diabetes care
ISSN: 1935-5548
Titre abrégé: Diabetes Care
Pays: United States
ID NLM: 7805975

Informations de publication

Date de publication:
10 2019
Historique:
received: 20 04 2019
accepted: 15 07 2019
pubmed: 11 8 2019
medline: 26 6 2020
entrez: 11 8 2019
Statut: ppublish

Résumé

Type 2 diabetes is associated with cognitive dysfunction and an increased dementia risk, particularly in individuals with concomitant cardiovascular and/or kidney disease. Incretin therapies may modulate this risk via glycemic and nonglycemic pathways. We explored if the dipeptidyl peptidase 4 inhibitor linagliptin could prevent cognitive decline in people with type 2 diabetes with cardiorenal disease. The CArdiovascular and Renal Microvascular outcomE study with LINAgliptin (CARMELINA)-COG substudy was an integral part of CARMELINA (NCT01897532) that randomized participants with cardiorenal disease to linagliptin 5 mg or placebo once daily (1:1), in addition to standard of care. The primary cognitive outcome was the occurrence of accelerated cognitive decline at the end of treatment, defined as a regression-based index score ≤16th percentile on the Mini-Mental State Examination (MMSE) or a composite measure of attention and executive functioning and analyzed in participants with a baseline MMSE ≥24. Effects across subgroups by baseline factors, as well as absolute cognitive changes, were also assessed. Of the 6,979 participants in CARMELINA, CARMELINA-COG included 1,545 (mean ± SD age, 68 ± 8 years; MMSE, 28.3 ± 1.7; estimated glomerular filtration rate, 52 ± 23 mL/min/1.73 m In a large international cardiovascular outcome trial in people with type 2 diabetes and cardiorenal disease, linagliptin did not modulate cognitive decline over 2.5 years.

Identifiants

pubmed: 31399442
pii: dc19-0783
doi: 10.2337/dc19-0783
doi:

Substances chimiques

Blood Glucose 0
Dipeptidyl-Peptidase IV Inhibitors 0
Incretins 0
Linagliptin 3X29ZEJ4R2

Banques de données

ClinicalTrials.gov
['NCT01897532']

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1930-1938

Informations de copyright

© 2019 by the American Diabetes Association.

Auteurs

Geert Jan Biessels (GJ)

Department of Neurology, UMC Utrecht Brain Center, University Medical Center Utrecht, Utrecht, the Netherlands g.j.biessels@umcutrecht.nl.

Chloë Verhagen (C)

Department of Neurology, UMC Utrecht Brain Center, University Medical Center Utrecht, Utrecht, the Netherlands.

Jolien Janssen (J)

Department of Neurology, UMC Utrecht Brain Center, University Medical Center Utrecht, Utrecht, the Netherlands.
Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht, the Netherlands.

Esther van den Berg (E)

Department of Neurology, UMC Utrecht Brain Center, University Medical Center Utrecht, Utrecht, the Netherlands.
Department of Neurology, Erasmus MC-University Medical Center, Rotterdam, the Netherlands.

Bernard Zinman (B)

Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, University of Toronto, Toronto, Ontario, Canada.

Julio Rosenstock (J)

Dallas Diabetes Research Center, Dallas, TX.

Jyothis T George (JT)

Therapeutic Area Cardiometabolism, Boehringer Ingelheim Pharma GmbH & Co. KG, Ingelheim, Germany.

Anna Passera (A)

HMS Analytical Software GmbH, Sulzbach, Germany.

Sven Schnaidt (S)

Biostatistics and Data Sciences, Boehringer Ingelheim, Biberach, Germany.

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Classifications MeSH