阿米洛利改善红细胞K转运和血红蛋白- o2结合:逆转冠心病心绞痛和心肌缺血的新治疗方法

Antonio R Delgado-Almeida, Carlos L Delgado, Antonio J Delgado-Leon
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引用次数: 3

摘要

未标记:冠心病(冠心病)是全世界发病率和死亡率的主要原因,其中心绞痛的逆转或心电图的改善对大多数患者来说仍然是一种不切实际的治疗选择,这表明微血管功能障碍或氧气输送受损可能是冠心病的关键因素。本文从临床和实验两方面阐述了首个探讨红细胞H/K和O2/CO2交换在冠心病中的作用的治疗创新的理论基础。随后是一项随机单盲试验,在心绞痛、ST-T改变和红细胞- k转运缺陷的患者中,阿米洛利和最佳药物治疗(OMT, n=35例)vs单独使用OMT (n=35例)。所有患者均进行了一系列临床评估、离子转运研究、心电图、无创主动脉波形和心血管血流动力学记录。采用SAS软件进行统计分析。结果:阿米洛利迅速改善了RBC-K(93.5±4 vs 84.5±4 mmol/lc, p= < 0.001),心绞痛(80%的病例,1.5±0.3周,CI:1.72 ~ 1.45), CCS级(1.3±0.5 vs 3.1±0.8,p < 0.001),而单独使用OMT的患者CCS级(3.2±0.4 vs 3.3±0.5,p= 0.21)。心绞痛的恢复持续了6个月(87% vs 26%, RR 2.1,优势比6.31,Pearson x2 34.6, 95% CI p < 0.0001)和1年(85% vs 37% OMT)。在阿米洛利6个月时,心电图恢复正常(29% vs 0%, RR∞未计算时间,优势比∞,Pearson x2 42.4, 95% CI, p < 0.0001),改善(55% vs 29%;RR2.1,优势比3.16,95% CI, p < 0.0001)或不变(15% vs 67% OMT)。1年后,7名服用阿米洛利的患者(18%)表现出心脏电再生的证据,而安慰剂组没有观察到。结论:在接受最佳心绞痛药物治疗的患者中,阿米洛利的这种治疗创新改善了RBC H/K和O2/CO2功能,并在诱导心脏电再生的同时逆转心绞痛ST-T改变。本文对该主题的相关专利进行了简要的讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Improving RBC K transport and hemoglobin-O2 binding by amiloride: A novel therapeutic approach for reversion of angina and myocardial ischemia in coronary heart diseases.

Unlabelled: Coronary heart disease (CHD) is the leading cause of morbidity and mortality across the entire world, in which reversion of angina or improvement of ECG remains an unrealistic therapeutic option for most patients, suggesting that microvascular dysfunction or impaired oxygen delivery might be critical factors in CHD. This research article, thus presents the rationale basis, clinical and experimental, for the first therapeutic innovation addressing the role of red blood cell (RBC) H/K and O2/CO2 exchanges in CHD. It is followed by a randomized single-blind trial of Amiloride and Optimal Medical Therapy (OMT, n=35 cases) vs OMT alone (n=35 cases) in patients having angina, ST-T alteration and a defective RBC-K transport. All patients had serial clinical evaluation, Ion Transport Studies, ECGs and non-invasive aortic waveform and cardiovascular hemodynamic recordings. Statistical analysis was performed by SAS.

Results: Amiloride rapidly improved RBC-K (93.5 ±4 vs 84.5 ±4 mmol/lc, p= < 0.001), angina (80% of cases, 1.5 ±0.3 weeks, CI:1.72 to 1.45), CCS Class (1.3 ±0.5 vs 3.1 ±0.8, p < 0.001) vs patients with OMT alone CCS Class (3.2 ± 0.4 vs 3.3 ± 0.5, p =0.21). Reversion of angina was sustained through the next 6-months (87% vs 26 % in OMT, RR 2.1, odds ratio 6.31, Pearson x2 34.6,p < 0.0001 at 95% CI) and 1-year (85% vs 37% OMT). At 6-months of amiloride, ECG became normal (29% vs 0%, RR ∞ uncalculated-time, odds ratio ∞, Pearson x2 42.4 at 95% CI, p < 0.0001), improved (55% vs 29%; RR2.1, odds ratio 3.16, 95% CI, p < 0.0001) or unchanged (15% vs 67% OMT). At 1-year, seven patients on amiloride (18%) exhibited evidence of electrical regeneration of the heart, not observed with placebo.

In conclusion: This therapeutical innovation of amiloride improves RBC H/K and O2/CO2 function, and reverses angina, ST-T alterations while inducing electrical regeneration of the heart, in patients receiving optimal medical treatment for angina. The article has short discussion on the relevant patents to the topic.

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