Kim Jiyoong, Ogai Akiko, Nakatani Satoshi, Hashimura Kazuhiko, Kanzaki Hideaki, Komamura Kazuo, Asakura Masanori, Asanuma Hiroshi, Kitamura Soichiro, Tomoike Hitonobu, Kitakaze Masafumi
Cardiovascular Division, National Cardiovascular Center, Suita City, Osaka Pref, Japan.
J Am Coll Cardiol. 2006 Oct 3;48(7):1378-84. doi: 10.1016/j.jacc.2006.05.069. Epub 2006 Sep 14.
The goal of this work was to determine whether the blockade of histamine H2 receptors is beneficial for the pathophysiology of chronic heart failure (CHF).
Because CHF is one of the major life-threatening diseases, we need to find a novel effective therapy. Intriguingly, our previous study, which predicts the involvement of histamine in CHF, suggests that we should test this hypothesis in patients with CHF.
We selected 159 patients who received famotidine among symptomatic CHF patients for the retrospective study. We blindly selected age- and gender-matched CHF patients receiving drugs for gastritis other than histamine H2 receptor blockers as a control group. For the prospective study, 50 symptomatic CHF patients were randomly divided into 2 groups. One group received famotidine of 30 mg/day for 6 months, and the other group received teprenone.
In the retrospective study, famotidine of 20 to 40 mg decreased both left ventricular end-diastolic and end-systolic lengths (LVDd and LVDs, respectively) and the plasma B-type natriuretic peptide (BNP) levels (182 +/- 21 vs. 259 +/- 25 pg/ml, p < 0.05) with unaltered fractional shortening (FS). In a randomized, open-label study, compared with teprenone, famotidine of 30 mg prospectively decreased both New York Heart Association functional class (p < 0.05) and plasma BNP levels (183 +/- 26 pg/ml vs. 285 +/- 41 pg/ml, p < 0.05); this corresponded to decreasing both LVDd (57 +/- 2 mm vs. 64 +/- 2 mm, p < 0.05) and LVDs (47 +/- 2 mm vs. 55 +/- 2 mm, p < 0.05) with unaltered FS (15 +/- 1% vs. 17 +/- 1%). The frequency of readmission because of worsening of CHF was lower in the famotidine group (4% and 24%, p < 0.05). On the other hand, teprenone had no effects on CHF.
Famotidine improved both cardiac symptoms and ventricular remodeling associated with CHF. Histamine H2 receptor blockers may have therapeutic benefits for CHF.
本研究旨在确定组胺H2受体阻断对慢性心力衰竭(CHF)病理生理过程是否有益。
由于CHF是主要的危及生命的疾病之一,我们需要找到一种新的有效治疗方法。有趣的是,我们之前的研究预测组胺参与CHF,提示我们应在CHF患者中验证这一假设。
我们选择159例有症状的CHF患者中接受法莫替丁治疗的患者进行回顾性研究。我们随机选择年龄和性别匹配的接受除组胺H2受体阻滞剂以外的胃炎治疗药物的CHF患者作为对照组。在前瞻性研究中,50例有症状的CHF患者被随机分为2组。一组接受30mg/天的法莫替丁治疗6个月,另一组接受替普瑞酮治疗。
在回顾性研究中,20至40mg的法莫替丁可降低左心室舒张末期和收缩末期长度(分别为LVDd和LVDs)以及血浆B型利钠肽(BNP)水平(182±21对259±25pg/ml,p<0.05),而缩短分数(FS)未改变。在一项随机、开放标签研究中,与替普瑞酮相比,30mg的法莫替丁前瞻性地降低了纽约心脏协会心功能分级(p<0.05)和血浆BNP水平(183±26pg/ml对285±41pg/ml,p<0.05);这对应于LVDd(57±2mm对64±2mm,p<0.05)和LVDs(47±2mm对55±2mm,p<0.05)的降低,而FS未改变(15±1%对17±1%)。法莫替丁组因CHF恶化再次入院的频率较低(4%和24%,p<0.05)。另一方面,替普瑞酮对CHF无影响。
法莫替丁改善了与CHF相关的心脏症状和心室重构。组胺H2受体阻滞剂可能对CHF有治疗益处。