Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Desirée Thielke"'
Autor:
Åsa Ericsson, Johan Jendle, Emelie Andersson, Nino Hallén, Katarina Steen Carlsson, Peter Lindgren, Desirée Thielke, Sofie Persson
Publikováno v:
Diabetologia
Aims/hypothesis The risk of complications and medical consequences of type 2 diabetes are well known. Hospital costs have been identified as a key driver of total costs in studies of the economic burden of type 2 diabetes. Less evidence has been gene
Autor:
Peter Lindgren, Emelie Andersson, Brian Larsen Thorsted, Pierre Johansen, Sofie Persson, Katarina Steen Carlsson, Desirée Thielke, Johan Jendle
Publikováno v:
Diabetes, Obesity and Metabolism. 22:1586-1597
Aims: To analyse days absent from work related to individual microvascular, macrovascular and other complications of type 2 diabetes (T2D) and to identify key drivers of absence. Materials and methods: National health and socio-economic individual-le
Autor:
Andrei Mircea Catarig, Carel W. le Roux, Ildiko Lingvay, Rory J. McCrimmon, Juan P. Frias, Desirée Thielke, Nanna L. Lausvig
Publikováno v:
Diabetologia
Aims/hypothesis Intra-abdominal or visceral obesity is associated with insulin resistance and an increased risk for cardiovascular disease. This study aimed to compare the effects of semaglutide 1.0 mg and canagliflozin 300 mg on body composition in
Publikováno v:
Diabetes, Obesity & Metabolism
Buse, J B, Holst, I, Knop, F K, Kvist, K, Thielke, D & Pratley, R 2021, ' Prototype of an evidence-based tool to aid individualized treatment for type 2 diabetes ', Diabetes, Obesity and Metabolism, vol. 23, no. 7, pp. 1666-1671 . https://doi.org/10.1111/dom.14381
Buse, J B, Holst, I, Knop, F K, Kvist, K, Thielke, D & Pratley, R 2021, ' Prototype of an evidence-based tool to aid individualized treatment for type 2 diabetes ', Diabetes, Obesity and Metabolism, vol. 23, no. 7, pp. 1666-1671 . https://doi.org/10.1111/dom.14381
Data‐driven tools are needed to inform individualized treatment decisions for people with type 2 diabetes (T2D). To show how treatment might be individualized, an interactive outline tool was developed to predict treatment outcomes. Individualized
Autor:
Peter Lindgren, Johan Jendle, Desirée Thielke, Katarina Steen Carlsson, Emelie Andersson, Sofie Persson, Åsa Ericsson, Nino Hallén
Publikováno v:
Diabetes. 69
Background: The prevalence of type 2 diabetes (T2D) has increased rapidly over the last decades. The risks of complications and the medical consequences are well known, where hospital costs have been identified as a key driver of total costs. Less ev
Autor:
Brian Larsen Thorsted, Peter Lindgren, Johan Jendle, Emelie Andersson, Pierre Johansen, Sofie Persson, Desirée Thielke, Katarina Steen Carlsson
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b07f3858a3a74b6a1317d552cac39fed
https://doi.org/10.1111/dom.14070/v2/response1
https://doi.org/10.1111/dom.14070/v2/response1
Publikováno v:
Diabetes, Obesity & Metabolism
Aims Semaglutide is a glucagon-like peptide-1 (GLP-1) analogue approved for the treatment of type 2 diabetes. The impact of switching treatment from another GLP-1 receptor agonist (GLP-1RA) to semaglutide was investigated by analyses of exposure-resp
Autor:
Andrei Mircea Catarig, Nanna L. Lausvig, Ildiko Lingvay, Harish Kumar, Carel W. le Roux, Desirée Thielke, Adie Viljoen, Juan P. Frias, Rory J. McCrimmon
Publikováno v:
The lancet. Diabetesendocrinology. 7(11)
Summary Background Existing guidelines for management of type 2 diabetes recommend a patient-centred approach to guide the choice of pharmacological agents. Although glucagon-like peptide-1 (GLP-1) receptor agonists and sodium–glucose cotransporter
Autor:
Bernard Zinman, Robert S. Busch, Athena Philis-Tsimikas, Desirée Thielke, Vaishali Bhosekar, Ingrid Holst, Bernhard Ludvik, Vincent Woo, James Thrasher
Publikováno v:
The lancet. Diabetesendocrinology. 7(5)
Summary Background Semaglutide is a once-weekly glucagon-like peptide-1 (GLP-1) analogue for type 2 diabetes. Few clinical trials have reported on the concomitant use of GLP-1 receptor agonists with sodium-glucose cotransporter-2 (SGLT-2) inhibitors.