Rosiglitazone evaluated for cardiovascular outcomes--an interim analysis.
By P. Home, Stuart J. Pocock, H. Beck-Nielsen, R. Gomis, M. Hanefeld, N. Jones, M. Komajda, J. McMurray, Theodora S Temelkova-Kurktschiev. New England Journal of Medicine, 2007
804 citations recorded by the source corpus.
Subfields: Endocrinology, Diabetes and Metabolism, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/22c8c809c4931e5ff834bfb0dfe8fe3b1d9d4fbd
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In Endocrinology, Diabetes and Metabolism
In Molecular Biology
Citations in the corpus
- AMPK in Health and Disease. (2009, background): “In light of recent studies demonstrating an increased incidence of myocardial ischemic events with rosiglitazone treatment (204, 417), it is interesting to speculate that this may be due to chronic 1058 GREGORY R.”
- Natural product agonists of peroxisome proliferator-activated receptor gamma (PPARγ): a review (2014, result): “However, some meta-analyses indicated that among patients with impaired glucose tolerance or type 2 diabetes the use of rosiglitazone for at least 12 months was associated with a significantly increased risk of myocardial infarction and heart failure, as well as with an elevated risk of cardiovascul”
- Canadian Diabetes Association Clinical Practice Guidelines Expert Committee (2013, neutral): “Although meta-analyses of smaller, underpowered studies suggested possible risk of MI with rosiglitazone (31,32), this has not been demonstrated in a larger randomized clinical trial (33,34).”
- Comparative determinants of 4-year cardiovascular event rates in stable outpatients at risk of or with atherothrombosis. (2010, background): “For example, the discrepancy between diabetes trials targeting cardiovascular events and the low event rates in those trials illustrates the potential utility of the simple risk enrichment strategies found in the current analysis.(6) Planned trials of diabetic patients specifically designed to asses”
- Systematic Review: Comparative Effectiveness and Safety of Oral Medications for Type 2 Diabetes Mellitus (2007, background): “31) for the primary end point of hospitalization or death from cardiovascular disease (29).”