Key Laboratory of Diabetes Immunology, Central South University, Ministry of Education, National Clinical Research Center for Metabolic Diseases, Changsha, Hunan, China
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Key Laboratory of Diabetes Immunology, Central South University, Ministry of Education, National Clinical Research Center for Metabolic Diseases, Changsha, Hunan, China
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Key Laboratory of Diabetes Immunology, Central South University, Ministry of Education, National Clinical Research Center for Metabolic Diseases, Changsha, Hunan, China
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Key Laboratory of Diabetes Immunology, Central South University, Ministry of Education, National Clinical Research Center for Metabolic Diseases, Changsha, Hunan, China
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influence of incretin-based therapy added to insulin vs placebo or no drug added to insulin in subjects with type 1 diabetes on the key outcomes HbA1c, total insulin dose, body weight, severe hypoglycaemia and gastrointestinal side effects. Methods
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Faculty of Medicine, University of Latvia, Riga, Latvia
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perspectives in the combinatory use of incretin-based therapies in diabesity and physiological nature of hormonal crosstalk The primary objective of treating diabetes in particular novel pharmacological options leading to significant weight loss is to enhance
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Department of Medicine, Gentofte and Herlev Hospital, University of Copenhagen, Denmark
Steno Diabetes Center Copenhagen, Gentofte, Denmark
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Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark
Center for Cancer and Organ Diseases, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark
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Novartis Healthcare A/S, Copenhagen, Denmark
Department of Nephrology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark
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Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark
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Department of Medicine, Gentofte and Herlev Hospital, University of Copenhagen, Denmark
Novartis Healthcare A/S, Copenhagen, Denmark
Department of Nephrology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark
Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark
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to incretin-based treatments. Another strength of our study is the sample size of 104 individuals characterized by the OGTT and IIGI method, which is the largest cohort used to evaluate the impact of TCF7L2 genotype on the action of endogenous
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of cancer, especially pancreatic cancer, in patients on incretin therapies ( 25 ). However, randomized clinical trials showed that incretin-based drugs were not associated with an increased risk of pancreatic cancer ( 26 ). Overall, the scarce in
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glucose challenge in association with reduced insulin secretion. This is the base for the success of incretin therapy in type 2 diabetes (22) . In insulin-resistant mice, we have previously demonstrated that the β-cell response to intravenous GLP1 is
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440 T2DM patients with inadequate glycemic control. The incretin-based therapies like GLP-1 agonists and DPP-4 inhibitors are being reported to be particularly effective in Asian patients with T2DM ( 25 ). This could be due to genetic factors, possibly
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Department of Gastroenterology, Turku University Hospital, Turku, Finland
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Department of Endocrinology, Turku University Hospital, Turku, Finland
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. Both GLP-1 and GIP are insulinotropic at basal and postprandial glucose levels and contribute nearly equally to the incretin effect of a meal in healthy subjects . Regulatory Peptides 2003 114 115 – 121 . ( https://doi.org/10.1016/S0167
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verify it by stratifying the analyses and reassessing the risks based on the presence (or absence) of GLP-1 receptors on thyroid samples. Conclusion Further studies are urgently needed to provide more evidence on the role played by the incretin
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(mmHg) 77 ± 9 Heart rate (b.p.m) 75 ± 10 Drug therapy Antihypertensives ACE inhibitors (%) 14 (67) Calcium channel blockers (%) 9 (43) Diuretics (%) 7 (33) Statin (%) 6 (29
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metabolic shift is partly independent of weight loss, and the underlying mechanisms are not completely understood ( 3 , 4 , 5 , 6 ). Shortly after RYGB, a greater incretin response occurs post-prandially, which enhances insulin secretion, reduces food