Literature DB >> 32275926

Control of 24-hour blood pressure with SGLT2 inhibitors to prevent cardiovascular disease.

Kazuomi Kario1, Keith C Ferdinand2, James H O'Keefe3.   

Abstract

The presence of hypertension (HTN) in patients with diabetes mellitus (DM) further worsens cardiovascular disease (CVD) prognosis. In addition, masked HTN and abnormal circadian blood pressure (BP) variability are common among patients with DM. Clinical trial data show that sodium-glucose cotransporter 2 inhibitors (SGLT2i) improve CVD prognosis and prevent progression of renal dysfunction in high-risk patients with type 2 DM (T2DM). Consistent reductions in 24-hour, daytime and nocturnal BP have been documented during treatment with SGLT2i in patients with DM and HTN, and these reductions are of a magnitude that is likely to be clinically significant. SGLT2i agents also appear to have beneficial effects on morning, evening and nocturnal home BP. Greater reductions in BP during treatment with SGLT2i have been reported in patient subgroups with higher body mass index, and in those with higher baseline BP. Other documented beneficial effects of SGLT2i include reductions in arterial stiffness and the potential to decrease the apnea-hypopnea index in patients with DM and obstructive sleep apnea. Recent guidelines highlight the important role of SGLT2i as part of the pharmacological management of patients with DM and HTN, and recommend consideration of SGLT2i early in the clinical course to reduce all-cause and CVD mortality in patients with T2DM and CVD. Overall, available data support a role for SGLT2i as effective BP-lowering agents in patients with T2DM and poorly controlled HTN, irrespective of baseline glucose control status. Sustained improvements in 24-hour BP and the 24-hour BP profile are likely to contribute to the CVD benefits of SGLT2i treatment.
Copyright © 2020. Published by Elsevier Inc.

Entities:  

Keywords:  24-hour blood pressure; Ambulatory blood pressure monitoring; Cardiovascular risk; Diabetes; Hypertension; Sodium glucose cotransport 2 inhibitors

Year:  2020        PMID: 32275926     DOI: 10.1016/j.pcad.2020.04.003

Source DB:  PubMed          Journal:  Prog Cardiovasc Dis        ISSN: 0033-0620            Impact factor:   8.194


  17 in total

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Authors:  Jan M Williams; Sydney R Murphy; Wenjie Wu; Jane J Border; Fan Fan; Richard J Roman
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Authors:  Kazuomi Kario; Masaki Mogi; Satoshi Hoshide
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7.  Randomized, "head-to-head" studies comparing different SGLT2 inhibitors are definitely needed.

Authors:  Kazuomi Kario; Noriko Harada; Satoshi Hoshide
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Review 8.  SGLT2is and Renal Protection: From Biological Mechanisms to Real-World Clinical Benefits.

Authors:  Giovanna Leoncini; Elisa Russo; Elisabetta Bussalino; Cecilia Barnini; Francesca Viazzi; Roberto Pontremoli
Journal:  Int J Mol Sci       Date:  2021-04-23       Impact factor: 5.923

Review 9.  Variability of risk factors and diabetes complications.

Authors:  Antonio Ceriello; Francesco Prattichizzo
Journal:  Cardiovasc Diabetol       Date:  2021-05-07       Impact factor: 9.951

10.  SGLT2i versus ARNI in heart failure with reduced ejection fraction: a systematic review and meta-analysis.

Authors:  Yuling Yan; Bin Liu; Jun Du; Jing Wang; Xiaodong Jing; Yajie Liu; Songbai Deng; Jianlin Du; Qiang She
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