Brown Alexander J M, Lang Chim, McCrimmon Rory, Struthers Allan
Cardiovascular Medicine, Division of Molecular and Clinical Medicine, Medical Research Institute, Ninewells Hospital and Medical School, Mailbox 2, Dundee, DD1 9SY, UK.
Cardiology, Division of Molecular and Clinical Medicine, Medical Research Institute, Ninewells Hospital and Medical School, Mailbox 2, Dundee, DD1 9SY, UK.
BMC Cardiovasc Disord. 2017 Aug 23;17(1):229. doi: 10.1186/s12872-017-0663-6.
Patients with diabetes have a two to fourfold increased risk for development of and death from cardiovascular disease [CVD]. The current oral hypoglycaemic agents result in limited reduction in this cardiovascular risk. Sodium glucose linked co-transporter type 2 [SGLT2] inhibitors are a relatively new class of antidiabetic agent that have been shown to have potential cardiovascular benefits. In support of this, the EMPA-REG trial showed a striking 38% and 35% reduction in cardiovascular mortality and heart failure [HF] hospitalisation respectively. The exact mechanism (s) responsible for these effects remain (s) unclear. One potential mechanism is regression of Left ventricular hypertrophy (LVH).
The DAPA-LVH trial is a prospective, double-blind, randomised, placebo-controlled 'proof of concept' single-centre study that has been ongoing since January 2017. It is designed specifically to assess whether the SGLT2 inhibitor dapagliflozin regresses left ventricular [LV] mass in patients with diabetes and left ventricular hypertrophy [LVH]. We are utilising cardiac and abdominal magnetic resonance imaging [MRI] and ambulatory blood pressure monitoring to quantify the cardiovascular and systemic effects of dapagliflozin 10 mg once daily against standard care over a 1 year observation period. The primary endpoint is to detect the changes in LV mass. The secondary outcomes are to assess the changes in, LV volumes, blood pressure, weight, visceral and subcutaneous fat.
This trial will be able to determine if SGLT2 inhibitor therapy reduces LV mass in patient with diabetes and LVH thereby strengthening their position as oral hypoglycaemic agents with cardioprotective benefits.
Clinical Trials.gov: NCT02956811 . Registered November 2016.
糖尿病患者发生心血管疾病(CVD)及死于心血管疾病的风险增加两至四倍。目前的口服降糖药对这种心血管风险的降低作用有限。钠-葡萄糖协同转运蛋白2(SGLT2)抑制剂是一类相对较新的抗糖尿病药物,已显示出潜在的心血管益处。支持这一点的是,EMPA-REG试验显示心血管死亡率和心力衰竭(HF)住院率分别显著降低了38%和35%。导致这些效应的确切机制仍不清楚。一种潜在机制是左心室肥厚(LVH)的消退。
DAPA-LVH试验是一项前瞻性、双盲、随机、安慰剂对照的单中心“概念验证”研究,自2017年1月起进行。该研究专门设计用于评估SGLT2抑制剂达格列净是否能使糖尿病和左心室肥厚(LVH)患者的左心室(LV)质量消退。我们正在利用心脏和腹部磁共振成像(MRI)以及动态血压监测,在1年的观察期内,对每日一次服用10mg达格列净与标准治疗相比的心血管和全身效应进行量化。主要终点是检测LV质量的变化。次要结局是评估LV容积、血压、体重、内脏和皮下脂肪的变化。
该试验将能够确定SGLT2抑制剂治疗是否能降低糖尿病和LVH患者的LV质量,从而巩固其作为具有心脏保护益处的口服降糖药的地位。
ClinicalTrials.gov:NCT02956811。2016年11月注册。