血管性基因疗法 (AGENT) 试验在患有稳定胸痛的患者中进行
Cindy L Grines1, Matthew W Watkins, Greg Helmer
1Division of Cardiology, William Beaumont Hospital, 3601 W 13 Mile Road, Royal Oak, MI 48073-6769, USA. cgrines@beaumont.edu
Circulation
|March 20, 2002
概括
使用腺病毒输送的纤维细胞生长因子4 (Ad5-FGF4) 的血管性基因疗法在治疗心痛方面表现有前途. 在AGENT试验中,Ad5-FGF4在改善缺血性心脏病患者的运动耐受性方面安全有效.
科学领域:
- 心血管医学 心血管医学
- 基因治疗 基因治疗
- 再生医学是一种再生医学.
背景情况:
- 心肌缺血可以通过血管性基因疗法治疗.
- 人类纤维细胞生长因子 (FGF) 的腺病毒介导基因转移在动物模型中显示出有前途.
研究的目的:
- 评估Ad5-FGF4在患有胸痛的患者中的安全性和抗胰岛症作用.
- 为未来的研究选择安全有效的剂量.
主要方法:
- 血管性基因疗法 (AGENT) 试验涉及79名患有稳定性胸痛的患者.
- 患者接受了安慰剂或Ad5-FGF4的五个上升剂量之一通过冠心内给药.
- 安全性和运动跑步机测试 (ETT) 在基线和随访时进行了评估.
主要成果:
- Ad5-FGF4是安全的,耐受性很好,有轻微的副作用,如短暂的发烧或肝酶升高.
- 与安慰剂相比,接受Ad5-FGF4的患者表现出改善运动时间的趋势.
- 一项小组分析显示,在基线ETT≤10分钟的患者中,运动时间显著改善.
结论:
- Ad5-FGF4表现出有利的抗缺血作用,并且在心痛治疗中似乎是安全的.
- 使用Ad5-FGF4的血管性基因转移对治疗胸痛有希望.
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