Model-based meta-analysis of HbA1c reduction across SGLT2 inhibitors using dose adjusted by urinary glucose excretion.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
21 Oct 2024
Historique:
received: 27 06 2024
accepted: 11 10 2024
medline: 22 10 2024
pubmed: 22 10 2024
entrez: 21 10 2024
Statut: epublish

Résumé

This study was aimed to evaluate whether the dose-response relationship of the sodium glucose co-transporter-2 inhibitors (SGLT2is) in patients with type 2 diabetes mellitus (T2DM)-canagliflozin, dapagliflozin, empagliflozin, ipragliflozin, luseogliflozin, and tofogliflozin-can be explained in a unified manner based on their ability to promote urinary glucose excretion (UGE). Information on HbA1c reduction at various doses of each SGLT2i was collected from literatures on randomized controlled trials and was normalized based on the daily UGE data from phase I studies. After normalizing doses, the dose-response relationship of HbA1c reduction of most of SGLT2is was represented by a unified nonlinear mixed-effect model, with the estimated maximum HbA1c (%) reduction (E

Identifiants

pubmed: 39433865
doi: 10.1038/s41598-024-76256-6
pii: 10.1038/s41598-024-76256-6
doi:

Substances chimiques

Sodium-Glucose Transporter 2 Inhibitors 0
Glycated Hemoglobin 0
Canagliflozin 0SAC974Z85
Glucosides 0
dapagliflozin 1ULL0QJ8UC
Benzhydryl Compounds 0
empagliflozin HDC1R2M35U
hemoglobin A1c protein, human 0
ipragliflozin 3N2N8OOR7X
Thiophenes 0
Glucose IY9XDZ35W2

Types de publication

Journal Article Meta-Analysis

Langues

eng

Sous-ensembles de citation

IM

Pagination

24695

Subventions

Organisme : Japan Society for the Promotion of Science
ID : 21K06797
Organisme : Japan Society for the Promotion of Science
ID : 21K06797

Informations de copyright

© 2024. The Author(s).

Références

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Auteurs

Hiromi Sato (H)

Laboratory of Clinical Pharmacology and Pharmacometrics, Graduate School of Pharmaceutical Sciences, Chiba University, 1-8-1 Inohana, Chuou-ku, Chiba-shi, Chiba, 260-8679, Japan. hiromi-s@chiba-u.jp.

Ayana Ishikawa (A)

Laboratory of Clinical Pharmacology and Pharmacometrics, Graduate School of Pharmaceutical Sciences, Chiba University, 1-8-1 Inohana, Chuou-ku, Chiba-shi, Chiba, 260-8679, Japan.

Hideki Yoshioka (H)

Laboratory of Clinical Pharmacology and Pharmacometrics, Graduate School of Pharmaceutical Sciences, Chiba University, 1-8-1 Inohana, Chuou-ku, Chiba-shi, Chiba, 260-8679, Japan.
Pharmaceuticals and Medical Devices Agency, Tokyo, Japan.

Ryota Jin (R)

Laboratory of Clinical Pharmacology and Pharmacometrics, Graduate School of Pharmaceutical Sciences, Chiba University, 1-8-1 Inohana, Chuou-ku, Chiba-shi, Chiba, 260-8679, Japan.

Yamato Sano (Y)

Laboratory of Clinical Pharmacology and Pharmacometrics, Graduate School of Pharmaceutical Sciences, Chiba University, 1-8-1 Inohana, Chuou-ku, Chiba-shi, Chiba, 260-8679, Japan.
Clinical Pharmacology, Pfizer R&D Japan, Tokyo, Japan.

Akihiro Hisaka (A)

Laboratory of Clinical Pharmacology and Pharmacometrics, Graduate School of Pharmaceutical Sciences, Chiba University, 1-8-1 Inohana, Chuou-ku, Chiba-shi, Chiba, 260-8679, Japan.

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