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Wolfgang E. Schmidt

Researcher at Ruhr University Bochum

Publications -  126
Citations -  7030

Wolfgang E. Schmidt is an academic researcher from Ruhr University Bochum. The author has contributed to research in topics: Insulin & Type 2 diabetes. The author has an hindex of 41, co-authored 117 publications receiving 6557 citations.

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Liraglutide once a day versus exenatide twice a day for type 2 diabetes: a 26-week randomised, parallel-group, multinational, open-label trial (LEAD-6).

TL;DR: Liraglutide once a day provided significantly greater improvements in glycaemic control than did exenatide twice a day, and was generally better tolerated, suggesting that liragLutide might be a treatment option for type 2 diabetes, especially when weight loss and risk of hypoglycaemia are major considerations.
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Predictors of incretin concentrations in subjects with normal, impaired, and diabetic glucose tolerance

TL;DR: Deteriorations in glucose homeostasis can develop in the absence of any impairment in GIP or GLP-1 levels, which suggests that the defects in GLP1 concentrations previously described in patients with long-standing type 2 diabetes are likely secondary to other hormonal and metabolic alterations, such as hyperglucagonemia.
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Gastric inhibitory polypeptide (GIP) dose-dependently stimulates glucagon secretion in healthy human subjects at euglycaemia

TL;DR: Glucagon secretion is dose-dependently stimulated by GIP at basal glucose concentrations, and this results underline differences between GIP and the glucagonostatic incretin GLP-1.
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Glucagon-like peptide 1 abolishes the postprandial rise in triglyceride concentrations and lowers levels of non-esterified fatty acids in humans

TL;DR: GLP-1 improves postprandial lipidaemia, presumably as a result of delayed gastric emptying and insulin-mediated inhibition of lipolysis, and may reduce the cardiovascular risk in patients with type 2 diabetes.
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Glucagon-like peptide 2 stimulates glucagon secretion, enhances lipid absorption, and inhibits gastric acid secretion in humans.

TL;DR: GLP-2 reduces gastric acid secretion but does not seem to have an influence on gastric emptying, and changes in postprandial lipid excursions seem to reflect enhanced intestinal nutrient absorption during GLp-2 administration.