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葡萄种子提取物与微粉化纯化类黄酮组方治疗慢性静脉疾病患者的随机非劣效性试验。

Vitis Vinifera Seed Extract Versus Micronized Purified Flavonoid Fraction for Patients with Chronic Venous Disease: A Randomized Noninferiority Trial.

机构信息

Department of Surgery, Chung-Ang University College of Medicine, Chung-Ang University Hospital, Seoul, Korea.

Department of Surgery, Kyung Hee University Hospital at Gangdong, Kyung Hee University School of Medicine, Seoul, Korea.

出版信息

Ann Vasc Surg. 2024 Dec;109:177-186. doi: 10.1016/j.avsg.2024.06.011. Epub 2024 Jul 14.

Abstract

BACKGROUND

Venoactive drugs (VADs) based on Vitis vinifera extract are widely used in Korea. However, studies on the clinical effects and head-to-head comparisons with other groups of VADs are limited. This trial aimed to evaluate whether Vitis vinifera seed extract was noninferior to the micronized purified flavonoid fraction (MPFF) in relieving venous symptoms and improving quality of life in patients with chronic venous disease.

METHODS

In this double-blind prospective randomized trial, patients from 13 hospitals, who were diagnosed with venous incompetence by duplex ultrasound and classified as clinical class 1, 2, or 3 in the Clinical, Etiological, Anatomical, and Pathophysiological classifications were enrolled. The primary outcome was the change in the Chronic Venous Disease Quality of Life Questionnaire (CIVIQ-20) score at 8 weeks from baseline. Secondary outcomes included changes in the Aberdeen Varicose Vein Questionnaire, visual analog scale, and Venous Clinical Severity Score at 4 and 8 weeks from baseline. Moreover, the change in leg circumferences was measured at 8 weeks and compared to baseline.

RESULTS

In total, 303 patients were enrolled and randomly assigned to receive either Vitis vinifera seed extract (n = 154) or MPFF (n = 149). The CIVIQ-20 scores at 8 weeks were significantly reduced compared to those at baseline in both groups. No significant intergroup difference in the change of CIVIQ-20 at 8 weeks from baseline was observed (-8.31 ± 14.63 vs. -10.35 ± 14.38, P = 0.29, 95% confidence interval -1.65 to 5.72). The lower limit of the 95% confidence interval was within the predefined noninferiority margin of 6.9. Furthermore, the Aberdeen Varicose Vein Questionnaire, visual analog scale, and Venous Clinical Severity Score scores significantly decreased at 4 and 8 weeks after randomization compared with baseline in both groups. No significant differences were observed in the reduction of each score between groups. The calf circumference measured at 8 weeks was significantly reduced compared to that at baseline in patients receiving Vitis vinifera seed extract.

CONCLUSIONS

Vitis vinifera seed extract was noninferior to MPFF in relieving venous symptoms and improving the quality of life in patients with chronic venous disease.

摘要

背景

基于葡萄(Vitis vinifera)提取物的静脉活性药物(VAD)在韩国被广泛应用。然而,关于其临床疗效以及与其他 VAD 组的头对头比较的研究是有限的。本试验旨在评估葡萄种子提取物在缓解静脉症状和改善慢性静脉疾病患者的生活质量方面是否不劣于微粒化纯化黄酮类(FMPFF)。

方法

在这项双盲前瞻性随机试验中,从 13 家医院招募了被超声诊断为静脉功能不全且临床分类为 1、2 或 3 级的静脉疾病患者。主要结局是从基线开始 8 周时慢性静脉疾病生活质量问卷(CIVIQ-20)评分的变化。次要结局包括从基线开始 4 周和 8 周时 Aberdeen 静脉曲张问卷、视觉模拟评分和静脉临床严重程度评分的变化。此外,还在 8 周时测量了小腿围的变化,并与基线进行了比较。

结果

共纳入 303 例患者,并随机分配至接受葡萄种子提取物(n=154)或 FMPFF(n=149)治疗。两组患者在 8 周时的 CIVIQ-20 评分均显著低于基线。两组患者在从基线开始 8 周时 CIVIQ-20 的变化无显著组间差异(-8.31±14.63 与-10.35±14.38,P=0.29,95%置信区间-1.65 至 5.72)。95%置信区间的下限在预设的 6.9 非劣效性边界内。此外,两组患者在随机分组后 4 周和 8 周时的 Aberdeen 静脉曲张问卷、视觉模拟评分和静脉临床严重程度评分均显著低于基线。两组之间各评分的降低无显著差异。与基线相比,接受葡萄种子提取物治疗的患者在 8 周时的小腿围显著缩小。

结论

葡萄种子提取物在缓解静脉症状和改善慢性静脉疾病患者的生活质量方面不劣于 FMPFF。

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