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Efficacy and safety of dapagliflozin in patients with type 2 diabetes and moderate renal impairment (chronic kidney disease stage 3A) : The DERIVE Study

Fioretto, Paola (författare)
Department of Medicine, University of Padova, Padova, Italy
Del Prato, Stefano (författare)
Department of Clinical & Experimental Medicine, University of Pisa, Pisa, Italy
Buse, John B. (författare)
Department of Medicine, University of North Carolina School of Medicine, Chapel Hill, North Carolina, USA
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Goldenberg, Ronald (författare)
LMC Diabetes & Endocrinology, Thornhill, Canada
Giorgino, Francesco (författare)
Department of Emergency and Organ Transplantation, University of Bari Aldo Moro, Bari, Italy
Reyner, Daniel (författare)
AstraZeneca, Gaithersburg, Maryland, USA
Langkilde, Anna Maria (författare)
AstraZeneca, Gothenburg, Sweden
Sjöstrom, C. David (författare)
AstraZeneca, Gothenburg, Sweden
Sartipy, Peter (författare)
Högskolan i Skövde,Institutionen för biovetenskap,Forskningscentrum för Systembiologi,AstraZeneca, Gothenburg, Sweden,Bioinformatik, Bioinformatics
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 (creator_code:org_t)
2018-07-10
2018
Engelska.
Ingår i: Diabetes, obesity and metabolism. - : Wiley-Blackwell Publishing Inc.. - 1462-8902 .- 1463-1326. ; 20:11, s. 2532-2540
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Aims: Dapagliflozin is a selective inhibitor of sodium glucose co-transporter 2 (SGLT2). This study assessed the efficacy and safety of dapagliflozin 10 mg vs placebo in patients with type 2 diabetes (T2D) and moderate renal impairment (estimated glomerular filtration rate [eGFR], 45-59 mL/min/1.73 m(2); chronic kidney disease [CKD] stage 3A). Materials and methods: In this double-blind, parallel group, Phase 3 study (NCT02413398, ) patients with inadequately controlled T2D (HbA1c 7.0%-11.0%) were randomized (1:1) to dapagliflozin 10 mg once daily (N = 160) or matching placebo (N = 161) for 24 weeks. Randomization was stratified by pre-enrolment glucose-lowering therapy. The primary endpoint was change from baseline in HbA1c at Week 24. Results: At Week 24, compared with placebo, dapagliflozin significantly decreased HbA1c (difference [95% CI], -0.34% [-0.53, -0.15]; P < 0.001), body weight (difference [95% CI], -1.25 kg [-1.90, -0.59]; P < 0.001), fasting plasma glucose (difference [95% CI], -0.9 mmol/L [-1.5, -0.4]; P = 0.001) and systolic blood pressure (difference [95% CI], -3.1 mmHg [-6.3, 0.0]; P < 0.05). Decreases from baseline in eGFR were greater with dapagliflozin than placebo at Week 24 (-2.49 mL/min/1.73 m(2) [-4.96, -0.02]), however, eGFR returned to baseline levels at Week 27 (3 weeks post-treatment) (0.61 mL/min/1.73 m(2) [-1.59, 2.81]). No increase in adverse events (AEs; 41.9% vs 47.8%) or serious AEs (5.6% vs 8.7%) were reported with dapagliflozin versus placebo. No AEs of bone fractures, amputations or DKA were reported. Conclusions: The findings of this study (NCT02413398, ) support the positive benefit/risk profile of dapagliflozin for the treatment of patients with T2D and CKD 3A.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Endokrinologi och diabetes (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Endocrinology and Diabetes (hsv//eng)

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Bioinformatik
Bioinformatics
INF502 Biomarkers
INF502 Biomarkörer

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