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dc.contributor.authorRizzo, Manfredi
dc.date.accessioned2024-06-21T10:37:11Z
dc.date.available2024-06-21T10:37:11Z
dc.date.issued2023-11
dc.identifier.urihttps://repository.mbru.ac.ae/handle/1/1518
dc.description.abstractAbstract: In a recently published, post-hoc analysis of the hallmark EMPA-REG OUTCOME trial, Kramer ¨ et al.1 assessed whether changes in cardiac and haemodynamic markers achieved with empagliflozin in subjects with type 2 diabetes mellitus (T2DM) may mediate its significant benefits across a number of surrogate cardiovascular and kidney outcomes. They have demonstrated that empagliflozin treatment resulted in a significant decrease in pulse pressure (PP), mean arterial pressure (MAP) and cardiac workload, compared with placebo; at week 12, placebo-adjusted mean changes from baseline were − 2.5 mmHg for PP, − 2.2 mmHg for MAP and − 315 mmHg x beats per minute (bpm) for cardiac workload (p < 0.0001 for all). They have also found that such benefits were present for both empagliflozin groups (10 mg and 25 mg) combined, while treatment differences were maintained throughout to week 164.1en_US
dc.language.isoenen_US
dc.subjectEmpagliflozinen_US
dc.subjectSGLT-2 inhibitoren_US
dc.subjectType 2 diabetesen_US
dc.subjectCardiovscularen_US
dc.subjectRenalen_US
dc.subjectOutcomeen_US
dc.titleUnderstanding the mechanisms mediating cardi-renal benefit of empagliflozin in type 2 diabetes mellitusen_US
dc.typeArticleen_US


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