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美托洛尔联合标准治疗对Fas/Fas配体血浆浓度及左心室功能的影响

Plasma concentration of Fas/Fas ligand and left ventricular function in response to metoprolol in conjunction with standard treatment.

作者信息

Hou Yuan-ping, Wu Jin-ling, Fan Qian, Liu Miao-bing, Yin Bao-ling, Zhang Lin

机构信息

Department of Internal Medicine, Division of Cardiology, Beijing Chaoyang Hospital-Affiliate of Capital University Medical Sciences, 8 Baijiazhuang Road, 100020 Beijing, People's Republic of China.

出版信息

Clin Sci (Lond). 2007 Mar;112(5):299-304. doi: 10.1042/CS20060213.

Abstract

Recent studies suggest that cardiac myocyte apoptosis contributes to the progress of CHF (congestive heart failure). In the present study, we tested the hypothesis that metoprolol in conjunction with the standard treatment regime for CHF [an ACE (angiotensin-converting enzyme) inhibitor, diuretics and digoxin] may significantly reduce the plasma concentrations of the apoptotic mediators sFas (soluble Fas) and sFasL (soluble Fas ligand) in patients with CHF. An ELISA was used to determine the plasma concentrations of sFas and sFasL in 106 patients with stable CHF at recruitment. Echocardiography was performed at baseline and after 1 year of treatment with metoprolol in conjunction with the standard treatment regime for CHF (i.e. an ACE inhibitor, diuretics and digoxin). The dose of metoprolol was doubled on a biweekly basis up to 50 mg twice a day or maintained at the maximum tolerated dose. Data after 1 year were available for 92 patients and were analysed. The plasma concentrations of sFas and sFasL in patients with CHF decreased significantly (P<0.01) after 1 year of treatment with metoprolol in conjunction with the standard treatment regime compared with at baseline (5.4+/-0.2 compared with 3.2+/-0.1 ng/ml respectively for sFas, and 52.1+/-2.3 compared with 26.7+/-1.0 pg/ml respectively for sFasL). Compared with baseline, after 1 year of treatment with metoprolol in conjunction with the standard treatment regime there were significant improvements in LV (left ventricular) ejection fraction (from 32.6+/-0.9 to 51.5+/-0.8%; P<0.01), LV end-diastolic dimension (from 69.8+/-0.6 to 57.7+/-0.3 mm; P<0.01), LV end-systolic dimension (from 53.9+/-0.6 to 40.5+/-0.5 mm; P<0.01), LV end-diastolic volume (from 254.7+/-5.0 to 164.1+/-2.2 ml; P<0.01) and LV end-systolic volume (from 142.0+/-4.2 to 72.2+/-2.0 ml; P<0.01). In addition, the distance walked in a 6-min walk test increased markedly (P<0.01) from 260.3+/-5.2 m at baseline to 440.9+/-5.7 m after 1 year of treatment. In conclusion, we have demonstrated that metoprolol in conjunction with an ACE inhibitor, diuretics and digoxin in patients with CHF can lead to a reverse in LV remodelling potentially through its anti-apoptotic effects.

摘要

近期研究表明,心肌细胞凋亡促使充血性心力衰竭(CHF)病情进展。在本研究中,我们验证了以下假设:美托洛尔联合CHF标准治疗方案(血管紧张素转换酶抑制剂、利尿剂和地高辛)可显著降低CHF患者血浆中凋亡介质可溶性Fas(sFas)和可溶性Fas配体(sFasL)的浓度。采用酶联免疫吸附测定法(ELISA)测定了106例入选时病情稳定的CHF患者血浆中sFas和sFasL的浓度。在基线期以及美托洛尔联合CHF标准治疗方案(即血管紧张素转换酶抑制剂、利尿剂和地高辛)治疗1年后进行超声心动图检查。美托洛尔剂量每两周加倍,直至每日两次、每次50mg,或维持在最大耐受剂量。92例患者有1年后的数据并进行了分析。与基线期相比,美托洛尔联合标准治疗方案治疗1年后,CHF患者血浆中sFas和sFasL浓度显著降低(P<0.01)(sFas分别为5.4±0.2 ng/ml和3.2±0.1 ng/ml,sFasL分别为52.1±2.3 pg/ml和26.7±1.0 pg/ml)。与基线期相比,美托洛尔联合标准治疗方案治疗1年后,左心室(LV)射血分数显著改善(从32.6±0.9%提高到51.5±0.8%;P<0.01),左心室舒张末期内径(从69.8±0.6mm减小到57.7±0.3mm;P<0.01),左心室收缩末期内径(从53.9±0.6mm减小到40.5±0.5mm;P<0.01),左心室舒张末期容积(从254.7±5.0ml减小到164.1±2.2ml;P<0.01),左心室收缩末期容积(从142.0±4.2ml减小到72.2±2.0ml;P<0.01)。此外,6分钟步行试验中的步行距离从基线期的260.3±5.2m显著增加(P<0.01)至治疗1年后的440.9±5.7m。总之,我们证明了CHF患者中美托洛尔联合血管紧张素转换酶抑制剂、利尿剂和地高辛可能通过其抗凋亡作用导致左心室重构逆转。

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