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- W2155258805 abstract "This randomised, double-blind, parallel-group, mul-ticentre study investigated the effects of the dual peroxisome proliferator-activated receptor (PPAR) α/γ agonist, tesaglitazar (0.5 and 1 mg), as add-on treatment in 568 patients with type 2 diabetes that was poorly controlled with sulphonylurea therapy titrated to the highest tolerated dose. There was a significant placebo-corrected reduction in glycosylated haemoglobin (HbA 1C ) from baseline to week 24 with tesaglitazar 0.5 mg and 1 mg (mean [95% confidence interval]: −0.93% [-1.09, −0.77] and −1.3% [-1.46, −1.14]; p<0.0001). Significant reductions were observed in insulin, fasting plasma glucose (FPG), triglyceride (all p<0.001) and non-high-density lipoprotein (HDL) cholesterol (p<0.001). Tesaglitazar increased levels of HDL-cholesterol (p<0.0001), adiponectin (p<0.0001) and leptin (p<0.001), but was associated with dose-dependent increases in serum creatinine and decreases in haemoglobin. This study showed improvements in glycaemic control and dyslipidaemia in patients with type 2 diabetes poorly controlled with existing sulphonylurea therapy. Although tesaglitazar has now been discontinued from clinical development, these results remain relevant to future research into PPAR agonists." @default.
- W2155258805 created "2016-06-24" @default.
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- W2155258805 date "2007-09-01" @default.
- W2155258805 modified "2023-10-16" @default.
- W2155258805 title "Tesaglitazar, as add-on therapy to sulphonylurea, dose-dependently improves glucose and lipid abnormalities in patients with type 2 diabetes" @default.
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- W2155258805 doi "https://doi.org/10.3132/dvdr.2007.040" @default.
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