Effects of Sodium‐Glucose Cotransporter 2 Inhibitors on 24‐Hour Ambulatory Blood Pressure: A Systematic Review and Meta‐Analysis
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- William L. Baker
- Department of Pharmacy Practice, University of Connecticut School of Pharmacy, Storrs, CT
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- Leo F. Buckley
- Department of Pharmacotherapy & Outcomes Science, Virginia Commonwealth University School of Pharmacy, Richmond, VA
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- Michael S. Kelly
- Department of Pharmacy Practice, Chapman University School of Pharmacy, Irvine, CA
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- John D. Bucheit
- Department of Pharmacotherapy & Outcomes Science, Virginia Commonwealth University School of Pharmacy, Richmond, VA
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- Eric D. Parod
- Department of Pharmacotherapy & Outcomes Science, Virginia Commonwealth University School of Pharmacy, Richmond, VA
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- Roy Brown
- School of Nursing, Virginia Commonwealth University, Richmond, VA
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- Salvatore Carbone
- VCU Pauley Heart Center, Virginia Commonwealth University, Richmond, VA
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- Antonio Abbate
- VCU Pauley Heart Center, Virginia Commonwealth University, Richmond, VA
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- Dave L. Dixon
- Department of Pharmacotherapy & Outcomes Science, Virginia Commonwealth University School of Pharmacy, Richmond, VA
Description
<jats:sec xml:lang="en"> <jats:title>Background</jats:title> <jats:p xml:lang="en">Sodium‐glucose cotransporter 2 (SGLT2) inhibitors are a novel class of antihyperglycemic agents that improve glycemic control by increasing glycosuria. Additional benefits beyond glucose lowering include significant improvements in seated clinic blood pressure (BP), partly attributed to their diuretic‐like actions. Less known are the effects of this class on 24‐hour ambulatory BP, which is a better predictor of cardiovascular risk than seated clinic BP.</jats:p> </jats:sec> <jats:sec xml:lang="en"> <jats:title>Methods and Results</jats:title> <jats:p xml:lang="en"> We performed a meta‐analysis of randomized, double‐blind, placebo‐controlled trials to investigate the effects of SGLT2 inhibitors on 24‐hour ambulatory BP. We searched all studies published before August 17, 2016, which reported 24‐hour ambulatory BP data. Mean differences in 24‐hour BP, daytime BP, and nighttime BP were calculated by a random‐effects model. SGLT2 inhibitors significantly reduce 24‐hour ambulatory systolic and diastolic BP by −3.76 mm Hg (95% CI, −4.23 to −2.34; I <jats:sup>2</jats:sup> =0.99) and −1.83 mm Hg (95% CI, −2.35 to −1.31; I <jats:sup>2</jats:sup> =0.76), respectively. Significant reductions in daytime and nighttime systolic and diastolic BP were also found. No association between baseline BP or change in body weight were observed. </jats:p> </jats:sec> <jats:sec xml:lang="en"> <jats:title>Conclusions</jats:title> <jats:p xml:lang="en">This meta‐analysis shows that the reduction in 24‐hour ambulatory BP observed with SGLT2 inhibitors is a class effect. The diurnal effect of SGLT2 inhibitors on 24‐hour ambulatory BP may contribute to their favorable effects on cardiovascular outcomes.</jats:p> </jats:sec>
Journal
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- Journal of the American Heart Association
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Journal of the American Heart Association 6 (5), e005686-, 2017-05-05
Ovid Technologies (Wolters Kluwer Health)
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Details 詳細情報について
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- CRID
- 1361418520039675008
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- ISSN
- 20479980
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- Data Source
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- Crossref