Insulin Glargine U100 Improved Glycemic Control and Reduced Nocturnal Hypoglycemia in Patients with Type 2 Diabetes Mellitus and Chronic Kidney Disease Stages 3 and 4.
basal insulin analogue
chronic kidney disease
hypoglycemia
insulin therapy
type 2 diabetes mellitus
Journal
Clinical therapeutics
ISSN: 1879-114X
Titre abrégé: Clin Ther
Pays: United States
ID NLM: 7706726
Informations de publication
Date de publication:
10 2019
10 2019
Historique:
received:
24
02
2019
revised:
10
07
2019
accepted:
12
07
2019
pubmed:
7
8
2019
medline:
24
6
2020
entrez:
7
8
2019
Statut:
ppublish
Résumé
Glycemic control in patients with chronic kidney disease (CKD) is particularly hard to achieve because of a slower insulin degradation by the kidney. It might modify the long-acting insulin analogue pharmacokinetics, increasing its time-action and the risk of hypoglycemia. However, because this insulin has no peak action, it might be a more tolerable approach to patients with CKD. This hypothesis remains to be tested, because no study has thus far examined the efficacy and safety profile of long-acting basal analogues in patients with significant loss of renal function. The purpose of this study was to compare the glycemic response to treatment with glargine U100 or neutral protamine Hagedorn (NPH) insulin in patients with type 2 diabetes mellitus (T2DM) and CKD stages 3 and 4. Thirty-four patients were randomly assigned to glargine U100 or NPH insulin after a 2-way crossover open-label design. The primary end point was the difference in glycosylated hemoglobin (HbA After 24 weeks, mean HbA Our results found that insulin glargine U100 could be effective, once it improved glycemic control, reducing HbA
Identifiants
pubmed: 31383366
pii: S0149-2918(19)30354-6
doi: 10.1016/j.clinthera.2019.07.011
pii:
doi:
Substances chimiques
Blood Glucose
0
Glycated Hemoglobin A
0
Hypoglycemic Agents
0
Insulin Glargine
2ZM8CX04RZ
Banques de données
ClinicalTrials.gov
['NCT02451917']
Types de publication
Journal Article
Randomized Controlled Trial
Langues
eng
Sous-ensembles de citation
IM
Pagination
2008-2020.e3Informations de copyright
Copyright © 2019. Published by Elsevier Inc.