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Efficacy and Safety of Ranolazine in Diabetic Patients: A Systematic Review and Meta-analysis
Background:Recent studies have discovered that the antiangina agent ranolazine exerts a glucometabolic effect. Objective: This systematic review and meta-analysis aimed to further understand the efficacy and safety profile of ranolazine in patients with diabetes. Methods: Randomized controlled trial...
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Published in: | The Annals of pharmacotherapy 2018-05, Vol.52 (5), p.415-424 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Background:Recent studies have discovered that the antiangina agent ranolazine exerts a glucometabolic effect. Objective: This systematic review and meta-analysis aimed to further understand the efficacy and safety profile of ranolazine in patients with diabetes. Methods: Randomized controlled trials (RCTs) were searched in PubMed, Cochrane, and EMBASE databases and in ClinicalTrials.gov up to July 2017. Efficacy end points were defined as the change in hemoglobin A1C (A1C) and fasting serum glucose (FSG) levels. Safety end points included the incidence of hypoglycemia, persistent hyperglycemia, and major adverse cardiovascular events (MACE). Sensitive and subgroup analyses were also conducted. Results: Seven RCTs with 4461 diabetic patients were selected. Compared with placebo, the use of ranolazine significantly reduced the levels of A1C (weighted mean difference [WMD] = −0.49%; 95% CI = −0.58 to −0.40; P < 0.00001) and FSG (WMD = −6.70 mg/dL; 95% CI = −11.87 to −1.52; P = 0.01). No significant differences were observed in the rates of hypoglycemia (relative risk [RR] = 1.17; 95% CI = 0.76 to 1.80; P = 0.47), persistent hyperglycemia (RR = 0.78; 95% CI = 0.47 to 1.31; P = 0.35), and MACE (RR = 0.65; 95% CI = 0.32 to 1.32; P = 0.23). Conclusion: Ranolazine exerts a positive effect on glucose control and is a well-tolerated agent for patients with diabetes. |
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ISSN: | 1060-0280 1542-6270 |
DOI: | 10.1177/1060028017747901 |