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Sökning: id:"swepub:oai:lup.lub.lu.se:991ff9cc-bb35-467e-96e0-a9d6601c78f7" > Postprandial Glucag...

Postprandial Glucagon Reductions Correlate to Reductions in Postprandial Glucose and Glycated Hemoglobin with Lixisenatide Treatment in Type 2 Diabetes Mellitus : A Post Hoc Analysis

Ahrén, Bo (författare)
Lund University,Lunds universitet,Diabetes,Forskargrupper vid Lunds universitet,Lund University Research Groups
Galstyan, Gagik (författare)
National Centre of Endocrinology, Moscow
Gautier, Jean Francois (författare)
Lariboisière Hospital
visa fler...
Giorgino, Francesco (författare)
University of Bari Aldo Moro
Gomez-Peralta, Fernando (författare)
Hospital General de Segovia
Krebs, Michael (författare)
Medical University of Vienna
Nikonova, Elena (författare)
Artech Information Systems, LLC
Stager, William (författare)
Sanofi S.A., France
Vargas-Uricoechea, Hernando (författare)
Hospital Universitario San José
visa färre...
 (creator_code:org_t)
2016-06-18
2016
Engelska 8 s.
Ingår i: Diabetes Therapy. - : Springer Science and Business Media LLC. - 1869-6953 .- 1869-6961. ; 7:3, s. 583-590
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Introduction: The extent to which postprandial glucagon reductions contribute to lowering of postprandial glucose in patients with type 2 diabetes mellitus (T2DM) is currently unknown. The aim of this analysis was to determine whether a reduction in postprandial glucagon following treatment with the glucagon-like peptide-1 receptor agonist lixisenatide correlates with a reduction in postprandial glucose and glycated hemoglobin (HbA1c) in patients with T2DM. Methods: A post hoc analysis was performed on pooled data from the modified intent-to-treat populations of two lixisenatide Phase 3 trials: GetGoal-M (lixisenatide versus placebo as add-on to metformin) and GetGoal-S (lixisenatide versus placebo as add-on to sulfonylurea [SU] ± metformin). Glucagon levels were assessed 2 h after a standardized meal test performed at baseline and Week 24 and were examined for correlation with changes in 2-h postprandial glucose and HbA1c. Results: Lixisenatide reduced 2-h postprandial glucagon at Week 24 compared with placebo (P < 0.00001). The mean change in postprandial glucagon significantly correlated with reductions in postprandial glucose (P < 0.00001) and HbA1c (P < 0.00001). Conclusion: A reduction in postprandial glucagon following lixisenatide administration correlated with a decrease in postprandial glucose and HbA1c in patients with T2DM insufficiently controlled on metformin and/or SU. This suggests that lowering of postprandial glucagon contributes to the overall glycemic improvement observed with lixisenatide. Funding: Sanofi. Clinical Trial Numbers: NCT00712673 (GetGoal-M) and NCT00713830 (GetGoal-S).

Ämnesord

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

Nyckelord

Glucagon
Glucagon-like peptide-1 receptor agonist
Glycemic control
Lixisenatide
Prandial
Type 2 diabetes mellitus

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