4.7 Review

New dual peroxisome proliferator activated receptor agonistSaroglitazar in diabetic dyslipidemia and non-alcoholic fatty liver disease: integrated analysis of the real world evidence

期刊

CARDIOVASCULAR DIABETOLOGY
卷 18, 期 -, 页码 -

出版社

BMC
DOI: 10.1186/s12933-019-0884-3

关键词

Saroglitazar; Dual PPAR agonist; Diabetic dyslipidemia; Triglyceride; Glycosylated hemoglobin; Alanine aminotransferase; Non-alcoholic fatty liver disease

向作者/读者索取更多资源

BackgroundSaroglitazar, a novel dual peroxisome proliferator activated receptor (PPAR) agonist, in clinical trials, has shown an improvement in lipid and glycemic parameters through the PPAR- and agonist actions, respectively. It was granted marketing authorization in India in 2013 for diabetic dyslipidemia. This review was conducted to summarize the effects of Saroglitazar in patients with diabetic dyslipidemia in real world clinical studies conducted after marketing authorization in India.MethodsIn this review, we selected real world clinical studies of Saroglitazar published as manuscripts and abstracts presented at scientific conferences. In all these studies, patients with diabetic dyslipidemia were treated with Saroglitazar 4mg once daily for at least 12weeks and different lipid and glycemic parameters were measured at the baseline and end of the study.ResultsIn 18 selected studies (5 published manuscripts and 13 abstracts), a total of 5824 patients with diabetic dyslipidemia were prescribed Saroglitazar 4mg for a duration ranging from 12 to 58weeks. Across all the studies, mean age of patients ranged from 49.6 to 59.1years and the proportion of female patients ranged from 22% to 42%. Across all the studies, there was a consistent mean reduction in triglyceride levels (45% to 62%), total cholesterol levels (17% to 26%), non-high-density lipoprotein cholesterol levels (21% to 36%), low-density lipoprotein cholesterol levels (11% to 27%), and glycosylated hemoglobin levels (0.7% to 1.6%) with an increase in mean high-density lipoprotein cholesterol levels (up to 9%) from baseline to end of the study. Saroglitazar also improved alanine aminotransferase levels and fatty liver (evaluated by FibroScan) in non-alcoholic fatty liver disease patients with diabetic dyslipidemia. Body weight remained unchanged and no significant adverse events (AEs) were reported in the studies.ConclusionSaroglitazar effectively improved lipid and glycemic parameters without significant AEs in patients with diabetic dyslipidemia in real-world clinical studies of up to 58weeks duration.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据