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Dapagliflozin once daily plus exenatide once weekly in obese adults without diabetes : Sustained reductions in body weight, glycaemia and blood pressure over 1 year

Lundkvist, Per (författare)
Uppsala universitet,Klinisk diabetologi och metabolism
Pereira, Maria J, 1981- (författare)
Uppsala universitet,Klinisk diabetologi och metabolism
Katsogiannos, Petros (författare)
Uppsala universitet,Klinisk diabetologi och metabolism
visa fler...
Sjöström, C. David (författare)
AstraZeneca, Gothenburg
Johnsson, Eva (författare)
AstraZeneca, Gothenburg
Eriksson, Jan W. (författare)
Uppsala universitet,Klinisk diabetologi och metabolism
visa färre...
 (creator_code:org_t)
2017-05-31
2017
Engelska.
Ingår i: Diabetes, obesity and metabolism. - : Wiley. - 1462-8902 .- 1463-1326. ; 19:9, s. 1276-1288
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Aims: Dapagliflozin and exenatide reduce body weight by differing mechanisms. Dual therapy with these agents reduces body weight, adipose tissue volume, glycaemia and systolic blood pressure (SBP) over 24weeks. Here, we examined these effects over 1year in obese adults without diabetes.Materials and methods: Obese adults without diabetes (N=50; aged 18-70years; body mass index, 30-45kg/m(2)) were initially randomized to double-blind oral dapagliflozin 10mg once daily plus subcutaneous long-acting exenatide 2mg once weekly or to placebo. They entered an open-label extension from 24 to 52weeks during which all participants received active treatment.Results: Of the original 25 dapagliflozin+exenatide-treated and 25 placebo-treated participants, respectively, 21 (84%) and 17 (68%) entered the open-label period and 16 (64%) and 17 (68%) completed 52weeks of treatment. At baseline, mean body weight was 104.6kg, and 73.5% of participants had prediabetes (impaired fasting glucose or impaired glucose tolerance). Reductions with dapagliflozin+exenatide at 24weeks were sustained at 52weeks, respectively, for body weight (-4.5 and -5.7kg), total adipose tissue volume (-3.8 and -5.3L), proportion with prediabetes (34.8% and 35.3%), and SBP (-9.8 and -12.0mm Hg). Effects on body weight, SBP and glycaemia at 52weeks with placebodapagliflozin+exenatide were similar to those observed with continuation of dapagliflozin+exenatide. Nausea and injection-site reactions were more frequent with dapagliflozin+exenatide than with placebo and diminished over time. Safety and tolerability were similar to that in previous diabetes trials with these agents. No clear difference in adverse event-related withdrawals between placebo and active treatment periods was observed.Conclusions: Dapagliflozin+exenatide dual therapy produced sustained reductions in body weight, prediabetes and SBP over 52weeks and was well tolerated in obese adults without diabetes.

Ämnesord

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

Nyckelord

dapagliflozin
exenatide
obesity
prediabetes

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