دورية أكاديمية

Randomized, Double-Blind, Placebo-Controlled Crossover Trial of Once Daily Empagliflozin 25 mg for the Treatment of Postprandial Hypoglycemia After Roux-en-Y Gastric Bypass

التفاصيل البيبلوغرافية
العنوان: Randomized, Double-Blind, Placebo-Controlled Crossover Trial of Once Daily Empagliflozin 25 mg for the Treatment of Postprandial Hypoglycemia After Roux-en-Y Gastric Bypass
المؤلفون: Ferreira, Antonio, Schönenberger, Katja A, Potoczna, Natascha, Vogt, Andreas, Gerber, Philipp A, Zehetner, Jörg, Giachino, Daniel, Nett, Philipp, Gawinecka, Joanna, Cossu, Luca, Fuster, Daniel G, Dalla Man, Chiara, Facchinetti, Andrea, Melmer, Andreas, Nakas, Christos T, Hepprich, Matthias, Donath, Marc Y, Herzig, David, Bally, Lia
المصدر: Ferreira, Antonio; Schönenberger, Katja A; Potoczna, Natascha; Vogt, Andreas; Gerber, Philipp A; Zehetner, Jörg; Giachino, Daniel; Nett, Philipp; Gawinecka, Joanna; Cossu, Luca; Fuster, Daniel G; Dalla Man, Chiara; Facchinetti, Andrea; Melmer, Andreas; Nakas, Christos T; Hepprich, Matthias; Donath, Marc Y; Herzig, David; Bally, Lia (2023). Randomized, Double-Blind, Placebo-Controlled Crossover Trial of Once Daily Empagliflozin 25 mg for the Treatment of Postprandial Hypoglycemia After Roux-en-Y Gastric Bypass. Diabetes Technology & Therapeutics, 25(7):467-475.
بيانات النشر: Mary Ann Liebert
سنة النشر: 2023
المجموعة: University of Zurich (UZH): ZORA (Zurich Open Repository and Archive
مصطلحات موضوعية: Institute of Clinical Chemistry, Clinic for Endocrinology and Diabetology, 610 Medicine & health, 540 Chemistry, Medical Laboratory Technology, Endocrinology, Diabetes and Metabolism
الوصف: Aims: To investigate the effect of empagliflozin on glucose dynamics in individuals suffering from postbariatric hypoglycemia (PBH) after Roux-en-Y gastric bypass (RYGB). Methods: Twenty-two adults with PBH after RYGB were randomized to empagliflozin 25 mg or placebo once daily over 20 days in a randomized, double-blind, placebo-controlled, crossover trial. The primary efficacy outcome was the amplitude of plasma glucose excursion (peak to nadir) during a mixed-meal tolerance test (MMTT). Outcomes of the outpatient period were assessed using continuous glucose monitoring (CGM) and an event-tracking app. Results: The amplitude of glucose excursion during the MMTT was 8.1 ± 2.4 mmol/L with empagliflozin versus 8.1 ± 2.6 mmol/L with placebo (mean ± standard deviation, P = 0.807). CGM-based mean amplitude of glucose excursion during the 20-day period was lower with empagliflozin than placebo (4.8 ± 1.3 vs. 5.2 ± 1.6. P = 0.028). Empagliflozin reduced the time spent with CGM values >10.0 mmol/L (3.8 ± 3.5% vs. 4.7 ± 3.8%, P = 0.009), but not the time spent with CGM values <3.0 mmol/L (1.7 ± 1.6% vs. 1.5 ± 1.5%, P = 0.457). No significant difference was observed in the quantity and quality of recorded symptoms. Eleven adverse events occurred with empagliflozin (three drug-related) and six with placebo. Conclusions: Empagliflozin 25 mg reduces glucose excursions but not hypoglycemia in individuals with PBH.
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/pdf
اللغة: English
تدمد: 1520-9156
العلاقة: https://www.zora.uzh.ch/id/eprint/236243/1/Joanna3.pdfTest; info:pmid/37093196; urn:issn:1520-9156
DOI: 10.5167/uzh-236243
DOI: 10.1089/dia.2023.0036
الإتاحة: https://doi.org/10.5167/uzh-23624310.1089/dia.2023.0036Test
https://www.zora.uzh.ch/id/eprint/236243Test/
https://www.zora.uzh.ch/id/eprint/236243/1/Joanna3.pdfTest
حقوق: info:eu-repo/semantics/openAccess
رقم الانضمام: edsbas.E067A366
قاعدة البيانات: BASE
الوصف
تدمد:15209156
DOI:10.5167/uzh-236243