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肝细胞生长因子对周围动脉疾病患者步行能力的影响

Hepatocyte growth factor for walking performance in peripheral artery disease.

作者信息

McDermott Mary M, Sufit Robert, Domanchuk Kathryn J, Volpe Nicholas J, Kosmac Kate, Peterson Charlotte A, Zhao Lihui, Tian Lu, Zhang Dongxue, Xu Shujun, Ismaeel Ahmed, Ferrucci Luigi, Parekh Nishant D, Lloyd-Jones Donald, Kramer Christopher M, Leeuwenburgh Christiaan, Ho Karen, Criqui Michael H, Polonsky Tamar, Guralnik Jack M, Kibbe Melina R

机构信息

Department of Internal Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL; Department of Preventive Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL.

Northwestern University Feinberg School of Medicine, Department of Neurology, Chicago, IL.

出版信息

J Vasc Surg. 2025 Jun;81(6):1467-1478.e1. doi: 10.1016/j.jvs.2024.12.124. Epub 2025 Jan 6.

Abstract

BACKGROUND

VM202 is a plasmid encoding two isoforms of hepatocyte growth factor. In preclinical studies, hepatocyte growth factor stimulated angiogenesis and muscle regeneration. This preliminary clinical trial tested the hypothesis that VM202 injections in gastrocnemius muscle would improve walking performance in people with mild to moderate and symptomatic lower extremity peripheral artery disease (PAD).

METHODS

In a double-blind clinical trial, patients with PAD were randomized to gastrocnemius muscle injections of either 4 mg of VM202 or placebo every 14 days for four treatments. The primary outcome was 6-month change in 6-minute walk distance. Secondary outcomes included 3-month change in treadmill walking time and gastrocnemius muscle biopsy measures. In this preliminary trial, statistical significance was prespecified as a one-sided P value of less than .10.

RESULTS

Thirty-nine participants with PAD (64.1% Black, 28.2% female) were randomized. Adjusting for age, race, smoking, and baseline performance, VM202 did not improve 6-minute walk at 6-month follow-up, compared with placebo (-13.5 m; 90% confidence interval [CI], -38.5 to +∞). At the 3-month follow-up, VM202 improved the maximum treadmill walking time (+2.38 minutes; 90% CI, +1.08 to +∞; P = .014) and increased central nuclei abundance in gastrocnemius muscle (+5.86; 90% CI, +0.37 to +∞; P = .088), compared with placebo. VM202 did not significantly improve pain-free walking distance (difference, +0.30 minutes; 90% CI, -1.10 to +∞; P = .39), calf muscle perfusion (difference, +1.80 mL/min per 100 g tissue; 90% CI, -3.80 to +∞; P = .33), or the Walking Impairment Questionnaire distance score (difference, +2.02; 90% CI, -8.11 to +∞; P = .40). In post hoc analyses, VM202 significantly improved 6-minute walk in PAD participants with diabetes mellitus at 6-month follow-up (+34.19; 90% CI, 4.04 to +∞; P = .075), but had no effect in people without diabetes (interaction P = .079).

CONCLUSIONS

These data do not support gastrocnemius injections of VM202 to improve 6-minute walk in PAD. Secondary outcomes suggested potential benefit of VM202 on skeletal muscle measures and treadmill walking, whereas post hoc analyses suggested benefit in PAD participants with diabetes.

摘要

背景

VM202是一种编码肝细胞生长因子两种异构体的质粒。在临床前研究中,肝细胞生长因子可刺激血管生成和肌肉再生。这项初步临床试验检验了以下假设:向腓肠肌注射VM202可改善轻至中度有症状的下肢外周动脉疾病(PAD)患者的行走能力。

方法

在一项双盲临床试验中,PAD患者被随机分为两组,每14天向腓肠肌注射4mg VM202或安慰剂,共进行4次治疗。主要结局是6分钟步行距离在6个月时的变化。次要结局包括跑步机行走时间在3个月时的变化以及腓肠肌活检指标。在这项初步试验中,统计学显著性预先设定为单侧P值小于0.10。

结果

39名PAD参与者(64.1%为黑人,28.2%为女性)被随机分组。在对年龄、种族、吸烟情况和基线表现进行调整后,与安慰剂相比,VM202在6个月随访时并未改善6分钟步行距离(-13.5米;90%置信区间[CI],-38.5至正无穷)。在3个月随访时,与安慰剂相比,VM202改善了跑步机最大行走时间(增加2.38分钟;90%CI,+1.08至正无穷;P = 0.014),并增加了腓肠肌中央核丰度(增加5.86;90%CI,+0.37至正无穷;P = 0.088)。VM202并未显著改善无痛步行距离(差异为+0.30分钟;90%CI,-1.10至正无穷;P = 0.39)、小腿肌肉灌注(差异为每100克组织+1.80毫升/分钟;90%CI,-3.80至正无穷;P = 0.33)或步行障碍问卷距离评分(差异为+2.02;90%CI,-8.11至正无穷;P = 0.40)。在事后分析中,VM202在6个月随访时显著改善了糖尿病PAD参与者的6分钟步行距离(增加34.19;90%CI,4.04至正无穷;P = 0.075),但对无糖尿病者无影响(交互作用P = 0.079)。

结论

这些数据不支持通过向腓肠肌注射VM202来改善PAD患者 的6分钟步行距离。次要结局表明VM202对骨骼肌指标和跑步机行走可能有益,而事后分析表明对糖尿病PAD参与者有益。

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