Impact of Empagliflozin on Blood Pressure in Patients With Type 2 Diabetes Mellitus and Hypertension by Background Antihypertensive Medication

被引:96
|
作者
Mancia, Giuseppe [1 ]
Cannon, Christopher P. [2 ,3 ]
Tikkanen, Ilkka [4 ,5 ]
Zeller, Cordula [6 ]
Ley, Ludwin [7 ]
Woerle, Hans J. [8 ]
Broedl, Uli C. [8 ]
Johansen, Odd Erik [9 ]
机构
[1] Univ Milano Bicocca, Milan, Italy
[2] Harvard Med Sch, Cardiovasc Div, Brigham & Womens Hosp, Boston, MA 02115 USA
[3] Harvard Clin Res Inst, Boston, MA USA
[4] Univ Helsinki, Abdominal Ctr, Helsinki Univ Hosp, Nephrol, Helsinki, Finland
[5] Minerva Fdn, Helsinki, Finland
[6] Boehringer Ingelheim Pharma GmbH & Co KG, Biostat & Data Sci, Biberach, Germany
[7] Boehringer Ingelheim Pharma GmbH & Co KG, Med Med Affairs Germany, Biberach, Germany
[8] Boehringer Ingelheim Pharma GmbH & Co KG, Med Therapeut Area Metab, Biberach, Germany
[9] Med Human Pharma Boehringer Ingelheim Norway KS, Asker, Norway
关键词
antihypertensive; blood pressure; diuretic; empagliflozin; hypertension; SGLT2; inhibitor; type 2 diabetes mellitus; DOUBLE-BLIND; ADD-ON; RENAL EVENTS; GUIDELINES; MANAGEMENT; INHIBITORS; METFORMIN; 24-WEEK; DISEASE; SAFETY;
D O I
10.1161/HYPERTENSIONAHA.116.07703
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
In the EMPA-REG BP trial, empagliflozin 10 mg and 25 mg once daily reduced glycohemoglobin, blood pressure (BP), and weight versus placebo in patients with type 2 diabetes mellitus and hypertension. Patients received placebo (n=271), empagliflozin 10 mg (n=276), or empagliflozin 25 mg (n=276) for 12 weeks (n=full analysis set). This present analysis investigated changes from baseline to week 12 in mean 24-hour systolic BP (SBP) and diastolic BP (DBP) in patients receiving 0, 1, or 2 antihypertensive medications and patients receiving/not receiving diuretics or angiotensin-converting enzyme inhibitors/angiotensin receptor blockers. Compared with placebo, empagliflozin 10 mg and 25 mg reduced mean 24-hour SBP/DBP in patients receiving 0 (10 mg: -3.89/-2.58 mmHg; 25 mg: -3.77/-2.45 mmHg), 1 (10 mg: -4.74/-1.97 mmHg; 25 mg: -4.27/-1.81 mmHg), or 2 (10 mg: -2.36/-0.68 mmHg; 25 mg: -4.17/-1.54 mmHg) antihypertensives. The effect of empagliflozin was not significantly different between subgroups by number of antihypertensives for changes in SBP (interaction P value 0.448) or DBP (interaction P value 0.498). Empagliflozin reduced 24-hour mean SBP/DBP irrespective of diuretic or angiotensin-converting enzyme inhibitor/angiotensin receptor blocker use, with no significant difference between subgroups by use/no use of diuretics (interaction P values 0.380 [systolic]; 0.240 [diastolic]) or angiotensin-converting enzyme inhibitors/angiotensin receptor blockers (interaction P values 0.900 [systolic]; 0.359 [diastolic]). In conclusion, in patients with type 2 diabetes mellitus and hypertension, empagliflozin for 12 weeks reduced SBP and DBP versus placebo, irrespective of the number of antihypertensives and use of diuretics or angiotensin-converting enzyme inhibitors/angiotensin receptor blockers. Clinical Trial Registration URL: https://clinicaltrials.gov. Unique identifier: NCT01370005.
引用
收藏
页码:1355 / 1364
页数:10
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