MARRIAGE: A Randomized Trial of Moxonidine Versus Ramipril or in Combination With Ramipril in Overweight Patients With Hypertension and Impaired Fasting Glucose or Diabetes Mellitus. Impact on Blood Pressure, Heart Rate and Metabolic Parameters.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-01-01 DOI:10.1177/10742484241258381
Paul Valensi, Selim Jambart
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Abstract

Background: Moxonidine, an imidazoline I1 receptor agonist, is an effective antihypertensive drug that was shown to improve insulin sensitivity. RAAS-blockers are recommended as first-line therapy in patients with diabetes, alone or in combination with a calcium-channel antagonist or a diuretic.

Aims: This study compared the effects of moxonidine and ramipril on blood pressure (BP) and glucose metabolism in overweight patients with mild-to-moderate hypertension and impaired fasting glucose or type 2 diabetes.

Methods: Treatment-naïve patients for hypertension and dysglycemia were randomized to 12 weeks of double-blind moxonidine 0.4 mg or ramipril 5 mg once-daily treatment. At 12 weeks, for a further 12 weeks non-responders received combination of mox/ram, while responders continued blinded treatment.

Results: Moxonidine and ramipril were equivalent in lowering SiDBP and SiSBP at the end of the first 12 weeks. The responder rate was approximately 50% in both groups, with a mean SiDBP and SiSBP decrease of 10 and 15 mm Hg in the responders, respectively. The normalization rate (SiDBP < 85 mm Hg) was non significantly different between treatments groups. Moxonidine reduced heart rate (HR) (average -3.5 bpm, p = 0.017) during monotherapy, and when added to ramipril. HbA1c decreased significantly at Week 12 in both groups. Neither drug affected glucose or insulin response to the oral glucose tolerance test. In non-responders, moxonidine/ramipril combination further reduced BP without compromising metabolic parameters.

Conclusion: Moxonidine 0.4 mg and ramipril 5 mg were equally effective on BP lowering and were well tolerated and mostly metabolically neutral either as monotherapies or in combination. HR was lowered on moxonidine treatment.

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MARRIAGE:莫索尼定与雷米普利或与雷米普利联合治疗超重高血压、空腹血糖受损或糖尿病患者的随机试验。对血压、心率和代谢参数的影响。
背景:莫索尼定是一种咪唑啉 I1 受体激动剂,是一种有效的降压药,可改善胰岛素敏感性。目的:本研究比较了莫索尼定和雷米普利对轻中度高血压、空腹血糖受损或 2 型糖尿病超重患者血压和糖代谢的影响:方法:对未经治疗的高血压和血糖异常患者随机进行为期 12 周的双盲莫索尼丁 0.4 毫克或雷米普利 5 毫克治疗,每天一次。12周后,无应答者再接受12周的莫索尼定/雷米普利联合治疗,有反应者则继续接受盲法治疗:结果:在头 12 周结束时,莫索尼定和雷米普利在降低 SiDBP 和 SiSBP 方面效果相当。两组的应答率均约为 50%,应答者的 SiDBP 和 SiSBP 平均降幅分别为 10 毫米汞柱和 15 毫米汞柱。在单药治疗期间以及与雷米普利合用时,正常化率(SiDBP p = 0.017)均有所提高。第 12 周时,两组患者的 HbA1c 均明显下降。两种药物均不影响口服葡萄糖耐量试验的葡萄糖或胰岛素反应。对于无应答者,莫索尼定/雷米普利联合用药可进一步降低血压,但不会影响代谢指标:莫索尼定 0.4 毫克和雷米普利 5 毫克对降低血压同样有效,且耐受性良好,无论是作为单药还是联合用药,代谢指标大多呈中性。莫索尼定治疗可降低心率。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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