Effects of DPP‐4 inhibitor linagliptin and GLP‐1 receptor agonist liraglutide on physiological response to hypoglycaemia in Japanese subjects with type 2 diabetes: A randomized, open‐label, 2‐arm parallel comparative, exploratory trial
Dipeptidyl peptidase‐4 (DPP‐4) inhibitors reduce the risk of hypoglycaemia, possibly through augmentation of glucose‐dependent insulinotropic polypeptide (GIP) action, but not that of glucagon‐like peptide‐1 (GLP‐1) on glucagon secretion. To examine this model in Japanese individuals with type 2 dia...
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Published in | Diabetes, obesity & metabolism Vol. 19; no. 3; pp. 442 - 447 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Oxford, UK
Blackwell Publishing Ltd
01.03.2017
Wiley Subscription Services, Inc |
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Abstract | Dipeptidyl peptidase‐4 (DPP‐4) inhibitors reduce the risk of hypoglycaemia, possibly through augmentation of glucose‐dependent insulinotropic polypeptide (GIP) action, but not that of glucagon‐like peptide‐1 (GLP‐1) on glucagon secretion. To examine this model in Japanese individuals with type 2 diabetes (T2D), the effects of the DPP‐4 inhibitor linagliptin on glucagon and other counter‐regulatory hormone responses to hypoglycaemia were evaluated and compared with those of the GLP‐1 receptor agonist liraglutide in a multi‐centre, randomized, open‐label, 2‐arm parallel comparative, exploratory trial. Three‐step hypoglycaemic clamp glucose tests preceded by meal tolerance tests were performed before and after 2‐week treatment with the drugs. Glucagon levels were increased during the hypoglycaemic clamp test at 2.5 mmol/L. This increase was similar in the linagliptin and liraglutide groups, both before and after the 2‐week treatment. Changes in other counter‐regulatory hormones (ie, growth hormone, cortisol, epinephrine and norepinephrine) were also similar between the groups, but were suppressed substantially after 2‐week treatment compared to baseline. In conclusion, we confirmed that the glucagon response to hypoglycaemia was not affected by linagliptin or liraglutide treatment in Japanese individuals with T2D. |
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AbstractList | Dipeptidyl peptidase-4 (DPP-4) inhibitors reduce the risk of hypoglycaemia, possibly through augmentation of glucose-dependent insulinotropic polypeptide (GIP) action, but not that of glucagon-like peptide-1 (GLP-1) on glucagon secretion. To examine this model in Japanese individuals with type 2 diabetes (T2D), the effects of the DPP-4 inhibitor linagliptin on glucagon and other counter-regulatory hormone responses to hypoglycaemia were evaluated and compared with those of the GLP-1 receptor agonist liraglutide in a multi-centre, randomized, open-label, 2-arm parallel comparative, exploratory trial. Three-step hypoglycaemic clamp glucose tests preceded by meal tolerance tests were performed before and after 2-week treatment with the drugs. Glucagon levels were increased during the hypoglycaemic clamp test at 2.5mmol/L. This increase was similar in the linagliptin and liraglutide groups, both before and after the 2-week treatment. Changes in other counter-regulatory hormones (ie, growth hormone, cortisol, epinephrine and norepinephrine) were also similar between the groups, but were suppressed substantially after 2-week treatment compared to baseline. In conclusion, we confirmed that the glucagon response to hypoglycaemia was not affected by linagliptin or liraglutide treatment in Japanese individuals with T2D. Dipeptidyl peptidase‐4 (DPP‐4) inhibitors reduce the risk of hypoglycaemia, possibly through augmentation of glucose‐dependent insulinotropic polypeptide (GIP) action, but not that of glucagon‐like peptide‐1 (GLP‐1) on glucagon secretion. To examine this model in Japanese individuals with type 2 diabetes (T2D), the effects of the DPP‐4 inhibitor linagliptin on glucagon and other counter‐regulatory hormone responses to hypoglycaemia were evaluated and compared with those of the GLP‐1 receptor agonist liraglutide in a multi‐centre, randomized, open‐label, 2‐arm parallel comparative, exploratory trial. Three‐step hypoglycaemic clamp glucose tests preceded by meal tolerance tests were performed before and after 2‐week treatment with the drugs. Glucagon levels were increased during the hypoglycaemic clamp test at 2.5 mmol/L. This increase was similar in the linagliptin and liraglutide groups, both before and after the 2‐week treatment. Changes in other counter‐regulatory hormones (ie, growth hormone, cortisol, epinephrine and norepinephrine) were also similar between the groups, but were suppressed substantially after 2‐week treatment compared to baseline. In conclusion, we confirmed that the glucagon response to hypoglycaemia was not affected by linagliptin or liraglutide treatment in Japanese individuals with T2D. Dipeptidyl peptidase-4 (DPP-4) inhibitors reduce the risk of hypoglycaemia, possibly through augmentation of glucose-dependent insulinotropic polypeptide (GIP) action, but not that of glucagon-like peptide-1 (GLP-1) on glucagon secretion. To examine this model in Japanese individuals with type 2 diabetes (T2D), the effects of the DPP-4 inhibitor linagliptin on glucagon and other counter-regulatory hormone responses to hypoglycaemia were evaluated and compared with those of the GLP-1 receptor agonist liraglutide in a multi-centre, randomized, open-label, 2-arm parallel comparative, exploratory trial. Three-step hypoglycaemic clamp glucose tests preceded by meal tolerance tests were performed before and after 2-week treatment with the drugs. Glucagon levels were increased during the hypoglycaemic clamp test at 2.5 mmol/L. This increase was similar in the linagliptin and liraglutide groups, both before and after the 2-week treatment. Changes in other counter-regulatory hormones (ie, growth hormone, cortisol, epinephrine and norepinephrine) were also similar between the groups, but were suppressed substantially after 2-week treatment compared to baseline. In conclusion, we confirmed that the glucagon response to hypoglycaemia was not affected by linagliptin or liraglutide treatment in Japanese individuals with T2D.Dipeptidyl peptidase-4 (DPP-4) inhibitors reduce the risk of hypoglycaemia, possibly through augmentation of glucose-dependent insulinotropic polypeptide (GIP) action, but not that of glucagon-like peptide-1 (GLP-1) on glucagon secretion. To examine this model in Japanese individuals with type 2 diabetes (T2D), the effects of the DPP-4 inhibitor linagliptin on glucagon and other counter-regulatory hormone responses to hypoglycaemia were evaluated and compared with those of the GLP-1 receptor agonist liraglutide in a multi-centre, randomized, open-label, 2-arm parallel comparative, exploratory trial. Three-step hypoglycaemic clamp glucose tests preceded by meal tolerance tests were performed before and after 2-week treatment with the drugs. Glucagon levels were increased during the hypoglycaemic clamp test at 2.5 mmol/L. This increase was similar in the linagliptin and liraglutide groups, both before and after the 2-week treatment. Changes in other counter-regulatory hormones (ie, growth hormone, cortisol, epinephrine and norepinephrine) were also similar between the groups, but were suppressed substantially after 2-week treatment compared to baseline. In conclusion, we confirmed that the glucagon response to hypoglycaemia was not affected by linagliptin or liraglutide treatment in Japanese individuals with T2D. Dipeptidyl peptidase‐4 ( DPP ‐4) inhibitors reduce the risk of hypoglycaemia, possibly through augmentation of glucose‐dependent insulinotropic polypeptide ( GIP ) action, but not that of glucagon‐like peptide‐1 ( GLP ‐1) on glucagon secretion. To examine this model in Japanese individuals with type 2 diabetes ( T2D ), the effects of the DPP ‐4 inhibitor linagliptin on glucagon and other counter‐regulatory hormone responses to hypoglycaemia were evaluated and compared with those of the GLP ‐1 receptor agonist liraglutide in a multi‐centre, randomized, open‐label, 2‐arm parallel comparative, exploratory trial. Three‐step hypoglycaemic clamp glucose tests preceded by meal tolerance tests were performed before and after 2‐week treatment with the drugs. Glucagon levels were increased during the hypoglycaemic clamp test at 2.5 mmol/L. This increase was similar in the linagliptin and liraglutide groups, both before and after the 2‐week treatment. Changes in other counter‐regulatory hormones (ie, growth hormone, cortisol, epinephrine and norepinephrine) were also similar between the groups, but were suppressed substantially after 2‐week treatment compared to baseline. In conclusion, we confirmed that the glucagon response to hypoglycaemia was not affected by linagliptin or liraglutide treatment in Japanese individuals with T2D . |
Author | Murotani, Kenta Seino, Yutaka Seino, Susumu Shiramoto, Masanari Kurose, Takeshi Irie, Shin Eto, Takashi Kuwata, Hitoshi Ahrén, Bo Yabe, Daisuke Seino, Yusuke |
AuthorAffiliation | 1 Yutaka Seino Distinguished Center for Diabetes Research Kansai Electric Power Medical Research Institute Kobe Japan 2 Center for Diabetes, Endocrinology and Metabolism Kansai Electric Power Hospital Osaka Japan 7 Departments of Endocrinology and Diabetes Metabolic Medicine Nagoya University Graduate School of Medicine Nagoya Japan 8 Department of Clinical Sciences Lund University Lund Sweden 3 Center for Metabolism and Clinical Nutrition Kansai Electric Power Hospital Osaka Japan 4 Division of Molecular and Metabolic Medicine Kobe University Graduate School of Medicine Kobe Japan 5 Hakata Clinic SOUSEIKAI Fukuoka Japan 6 Division of Biostatistics, Clinical Research Center Aichi Medical University Hospital Nagakute Japan |
AuthorAffiliation_xml | – name: 3 Center for Metabolism and Clinical Nutrition Kansai Electric Power Hospital Osaka Japan – name: 4 Division of Molecular and Metabolic Medicine Kobe University Graduate School of Medicine Kobe Japan – name: 5 Hakata Clinic SOUSEIKAI Fukuoka Japan – name: 7 Departments of Endocrinology and Diabetes Metabolic Medicine Nagoya University Graduate School of Medicine Nagoya Japan – name: 1 Yutaka Seino Distinguished Center for Diabetes Research Kansai Electric Power Medical Research Institute Kobe Japan – name: 6 Division of Biostatistics, Clinical Research Center Aichi Medical University Hospital Nagakute Japan – name: 8 Department of Clinical Sciences Lund University Lund Sweden – name: 2 Center for Diabetes, Endocrinology and Metabolism Kansai Electric Power Hospital Osaka Japan |
Author_xml | – sequence: 1 givenname: Daisuke surname: Yabe fullname: Yabe, Daisuke email: ydaisuke-kyoto@umin.ac.jp organization: Kobe University Graduate School of Medicine – sequence: 2 givenname: Takashi surname: Eto fullname: Eto, Takashi organization: SOUSEIKAI – sequence: 3 givenname: Masanari surname: Shiramoto fullname: Shiramoto, Masanari organization: SOUSEIKAI – sequence: 4 givenname: Shin surname: Irie fullname: Irie, Shin organization: SOUSEIKAI – sequence: 5 givenname: Kenta surname: Murotani fullname: Murotani, Kenta organization: Aichi Medical University Hospital – sequence: 6 givenname: Yusuke surname: Seino fullname: Seino, Yusuke organization: Nagoya University Graduate School of Medicine – sequence: 7 givenname: Hitoshi surname: Kuwata fullname: Kuwata, Hitoshi organization: Kansai Electric Power Hospital – sequence: 8 givenname: Takeshi surname: Kurose fullname: Kurose, Takeshi organization: Kansai Electric Power Hospital – sequence: 9 givenname: Susumu surname: Seino fullname: Seino, Susumu organization: Kobe University Graduate School of Medicine – sequence: 10 givenname: Bo surname: Ahrén fullname: Ahrén, Bo organization: Lund University – sequence: 11 givenname: Yutaka surname: Seino fullname: Seino, Yutaka email: seino.yutaka@e2.kepco.co.jp organization: Kansai Electric Power Hospital |
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Cites_doi | 10.1210/jc.2013-3644 10.1210/jc.2012-2332 10.1111/j.2040-1124.2010.00022.x 10.1172/JCI116186 10.1111/dom.12395 10.1210/jc.2008-2152 10.1111/dom.12293 10.2337/diab.26.5.480 10.1111/dom.12398 10.2337/db13-0822 10.2337/db11-0979 10.1007/s11892-015-0602-9 10.1210/jcem.87.3.8355 10.2337/dc15-1274 10.1517/14656566.2013.824966 10.1007/s00125-015-3518-7 10.1111/jdi.12490 10.1111/dom.12284 10.1111/dom.12473 10.1007/s00125-012-2827-3 |
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Keywords | glucagon response sympatho-adrenal response GLP-1 receptor agonist hypoglycaemia DPP-4 inhibitor |
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License | Attribution-NonCommercial-NoDerivs http://creativecommons.org/licenses/by-nc-nd/4.0 2016 The Authors. Diabetes, Obesity and Metabolism published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
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References_xml | – volume: 7 start-page: 74 year: 2015 end-page: 81 article-title: Restoration of the insulinotropic effect of glucose‐dependent insulinotropic polypeptide contributes to the antidiabetic effect of dipeptidyl peptidase‐4 inhibitors publication-title: Diabetes Obes Metab – volume: 58 start-page: 1091 year: 2015 end-page: 1099 article-title: DPP‐4 inhibition contributes to the prevention of hypoglycaemia through a GIP‐glucagon counterregulatory axis in mice publication-title: Diabetologia – volume: 91 start-page: 301 year: 1993 end-page: 307 article-title: Preserved incretin activity of glucagon‐like peptide 1 [7–36 amide] but not of synthetic human gastric inhibitory polypeptide in patients with type‐2 diabetes mellitus publication-title: J Clin Invest – volume: 14 start-page: 2047 year: 2013 end-page: 2058 article-title: Dipeptidyl peptidase‐4 inhibitors for the treatment of type 2 diabetes: comparison, efficacy and safety publication-title: Expert Opin Pharmacother – volume: 1 start-page: 9 year: 2010 end-page: 23 article-title: GIP and GLP‐1, the two incretin hormones: silimarities and differences publication-title: J Diabetes Invest – volume: 56 start-page: 696 year: 2013 end-page: 708 article-title: Differences in the glucose‐lowering efficacy of dipeptidyl peptidase‐4 inhibitors between Asians and Non‐Asians: a systematic review and meta‐analysis publication-title: Diabetologia – volume: 94 start-page: 1236 year: 2009 end-page: 1243 article-title: Vildagliptin enhances islet responsiveness to both hyper‐ and hypoglycemia in patients with type 2 diabetes publication-title: J Clin Endocrinol Metab – volume: 17 start-page: 742 year: 2015 end-page: 750 article-title: Counter‐regulatory hormone responses to hypoglycaemia in people with type 1 diabetes after 4 weeks of treatment with liraglutide adjunct to insulin: a randomized, placebo‐controlled, double‐blind, crossover trial publication-title: Diabetes Obes Metab – volume: 97 start-page: 3799 year: 2012 end-page: 3806 article-title: Vildagliptin reduces glucagon during hyperglycemia and sustains glucagon counterregulation during hypoglycemia in type 1 diabetes publication-title: J Clin Endocrinol Metab – volume: 16 start-page: 812 year: 2014 end-page: 818 article-title: Glucagon dynamics during hypoglycaemia and food‐re‐challenge following treatment with vildagliptin in insulin‐treated patients with type 2 diabetes publication-title: Diabetes Obes Metab – volume: 16 start-page: 900 year: 2014 end-page: 909 article-title: Differences in the HbA1c‐lowering efficacy of glucagon‐like peptide‐1 analogues between Asians and non‐Asians: a systematic review and meta‐analysis publication-title: Diabetes Obes Metab – volume: 62 start-page: 3316 year: 2013 end-page: 3323 article-title: Incretin action in the pancreas: potential promise, possible perils, and pathological pitfalls publication-title: Diabetes – volume: 87 start-page: 1239 year: 2002 end-page: 1246 article-title: Effects of glucagon‐like peptide 1 on counterregulatory hormone responses, cognitive functions, and insulin secretion during hyperinsulinemic, stepped hypoglycemic clamp experiments in healthy volunteers publication-title: J Clin Endocrinol Metab – volume: 60 start-page: 3103 year: 2011 end-page: 3109 article-title: Glucose‐dependent insulinotropic polypeptide: a bifunctional glucose‐dependent regulator of glucagon and insulin secretion in humans publication-title: Diabetes – volume: 17 start-page: 82 year: 2015 end-page: 90 article-title: Albiglutide does not impair the counter‐regulatory hormone response to hypoglycaemia: a randomized, double‐blind, placebo‐controlled, stepped glucose clamp study in subjects with type 2 diabetes mellitus publication-title: Diabetes Obes Metab – volume: 7 start-page: 102 year: 2016 end-page: 109 article-title: Incretin‐based drugs for type 2 diabetes: focus on East Asian perspectives publication-title: J Diabetes Invest – volume: 99 start-page: E418 year: 2014 end-page: E426 article-title: Glucose‐dependent insulinotropic polypeptide: blood glucose stabilizing effects in patients with type 2 diabetes publication-title: J Clin Endocrinol Metab – volume: 26 start-page: 480 year: 1977 end-page: 484 article-title: Synthetic gastric inhibitory polypeptide. Stimulatory effect on insulin and glucagon secretion in the rat publication-title: Diabetes – volume: 15 start-page: 602 year: 2015 article-title: Beta cell dysfunction versus insulin resistance in the pathogenesis of type 2 diabetes in East Asians publication-title: Curr Diab Rep – volume: 39 start-page: 242 year: 2016 end-page: 249 article-title: Effect of the GLP‐1 receptor agonist lixisenatide on counterregulatory responses to hypoglycemia in subjects with insulin‐treated type 2 diabetes publication-title: Diabetes Care – ident: e_1_2_6_8_1 doi: 10.1210/jc.2013-3644 – ident: e_1_2_6_20_1 doi: 10.1210/jc.2012-2332 – ident: e_1_2_6_4_1 doi: 10.1111/j.2040-1124.2010.00022.x – ident: e_1_2_6_7_1 doi: 10.1172/JCI116186 – ident: e_1_2_6_19_1 doi: 10.1111/dom.12395 – ident: e_1_2_6_12_1 doi: 10.1210/jc.2008-2152 – ident: e_1_2_6_18_1 doi: 10.1111/dom.12293 – ident: e_1_2_6_9_1 doi: 10.2337/diab.26.5.480 – ident: e_1_2_6_13_1 doi: 10.1111/dom.12398 – ident: e_1_2_6_5_1 doi: 10.2337/db13-0822 – ident: e_1_2_6_10_1 doi: 10.2337/db11-0979 – ident: e_1_2_6_16_1 doi: 10.1007/s11892-015-0602-9 – ident: e_1_2_6_6_1 doi: 10.1210/jcem.87.3.8355 – volume: 39 start-page: 242 year: 2016 ident: e_1_2_6_14_1 article-title: Effect of the GLP‐1 receptor agonist lixisenatide on counterregulatory responses to hypoglycemia in subjects with insulin‐treated type 2 diabetes publication-title: Diabetes Care doi: 10.2337/dc15-1274 – ident: e_1_2_6_2_1 doi: 10.1517/14656566.2013.824966 – ident: e_1_2_6_11_1 doi: 10.1007/s00125-015-3518-7 – ident: e_1_2_6_3_1 doi: 10.1111/jdi.12490 – ident: e_1_2_6_15_1 doi: 10.1111/dom.12284 – ident: e_1_2_6_21_1 doi: 10.1111/dom.12473 – ident: e_1_2_6_17_1 doi: 10.1007/s00125-012-2827-3 |
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Snippet | Dipeptidyl peptidase‐4 (DPP‐4) inhibitors reduce the risk of hypoglycaemia, possibly through augmentation of glucose‐dependent insulinotropic polypeptide (GIP)... Dipeptidyl peptidase‐4 ( DPP ‐4) inhibitors reduce the risk of hypoglycaemia, possibly through augmentation of glucose‐dependent insulinotropic polypeptide (... Dipeptidyl peptidase-4 (DPP-4) inhibitors reduce the risk of hypoglycaemia, possibly through augmentation of glucose-dependent insulinotropic polypeptide (GIP)... |
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SubjectTerms | Aged Antidiabetics Brief Report Brief Reports Clinical Medicine Diabetes Diabetes Mellitus, Type 2 - drug therapy Dipeptidyl-peptidase IV Dipeptidyl-Peptidase IV Inhibitors - therapeutic use DPP-4 inhibitor Endocrinology and Diabetes Endokrinologi och diabetes Epinephrine - metabolism Evidence-based medicine Female GLP-1 receptor agonist GLP-1 receptor agonists Glucagon - metabolism Glucagon response Glucagon-Like Peptide-1 Receptor - agonists Glucose Glucose Clamp Technique Human Growth Hormone - metabolism Humans Hydrocortisone - metabolism Hypoglycaemia Hypoglycemia Hypoglycemia - metabolism Hypoglycemic Agents - therapeutic use Japan Klinisk medicin Linagliptin - therapeutic use Liraglutide - therapeutic use Male Medical and Health Sciences Medicin och hälsovetenskap Middle Aged Norepinephrine - metabolism Sympatho-adrenal response |
Title | Effects of DPP‐4 inhibitor linagliptin and GLP‐1 receptor agonist liraglutide on physiological response to hypoglycaemia in Japanese subjects with type 2 diabetes: A randomized, open‐label, 2‐arm parallel comparative, exploratory trial |
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