Department of Cardiology, Bispebjerg Hospital, University of Copenhagen, Copenhagen, Denmark.
PLoS One. 2018 Jun 8;13(6):e0196962. doi: 10.1371/journal.pone.0196962. eCollection 2018.
Studies have suggested a beneficial effect of angiotensin-converting enzyme (ACE) inhibition. To explore whether the ACE inhibitor ramipril has a direct effect on the microvasculature beyond the blood pressure (BP) lowering effect, we investigated whether ramipril improved coronary microvascular function in normotensive women with coronary microvascular dysfunction (CMD).
We included 63 normotensive women with angina, no epicardial stenosis>50% and CMD defined as a coronary flow velocity reserve (CFVR)<2.2 assessed by adenosine stress-echocardiography in a randomized double-blinded, superiority trial with 1:1 allocation to placebo or ramipril (maximum dose 10 mg depending on blood pressure) for 24±6 weeks. Primary outcome was CFVR. Secondary outcomes were left ventricular systolic and diastolic function and symptoms evaluated by Seattle Angina Questionnaire (clinicaltrials.gov, NCT02525081).
Follow-up was available on 55 patients. BP remained unchanged during treatment in both groups. CFVR improved in both the ramipril (p = 0.004) and placebo group (p = 0.026) with no difference between groups (p = 0.63). Symptoms improved in both groups with no significant between-group differences. No changes were detected in parameters of systolic and diastolic function. No serious adverse reactions were reported.
In normotensive women with angina and CMD, treatment with ramipril had no significant effect on CFVR or symptoms compared with placebo. The effect of ACE inhibition previously reported may be mediated by blood pressure reduction.
研究表明血管紧张素转换酶(ACE)抑制剂具有有益作用。为了探究 ACE 抑制剂雷米普利是否除降压作用之外对微血管具有直接作用,我们研究了雷米普利是否能改善冠状动脉微血管功能障碍(CMD)的正常血压女性的冠状动脉微血管功能。
我们纳入了 63 名患有心绞痛、无 50%以上心外膜狭窄且 CMD 定义为腺苷应激超声心动图评估的冠状动脉血流储备(CFVR)<2.2 的正常血压女性,进行了一项随机、双盲、优效性试验,以 1:1 比例分配至安慰剂或雷米普利(最大剂量 10 毫克,取决于血压)治疗 24±6 周。主要结局为 CFVR。次要结局为左心室收缩和舒张功能以及西雅图心绞痛问卷(clinicaltrials.gov,NCT02525081)评估的症状。
55 名患者可进行随访。两组治疗期间血压均无变化。雷米普利组(p=0.004)和安慰剂组(p=0.026)的 CFVR 均有所改善,两组之间无差异(p=0.63)。两组症状均有所改善,两组之间无显著差异。收缩和舒张功能的参数均未发生变化。未报告严重不良反应。
在患有心绞痛和 CMD 的正常血压女性中,与安慰剂相比,雷米普利治疗对 CFVR 或症状无显著影响。先前报道的 ACE 抑制作用可能通过血压降低介导。