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碧萝芷®缓解糖尿病患者的慢性静脉功能不全:一项补充剂注册研究。

Pycnogenol® relieves chronic venous insufficiency (CVI) in diabetics: a supplement registry study.

作者信息

Belcaro Gianni, Cesarone Maria R, Scipione Claudia, Scipione Valeria, Cornelli Umberto, Cotellese Roberto, Ippolito Edmondo, Dugall Mark, Hosoi Morio, Corsi Marcello, Feragalli Beatrice, Bavera Pietro

机构信息

Irvine3 and Nicolaides Labs, Circulation Sciences, Pescara, Italy -

San Valentino, Vascular Screening Center, Pescara, Italy -

出版信息

Minerva Surg. 2025 Feb;80(1):36-43. doi: 10.23736/S2724-5691.24.10444-3. Epub 2024 Sep 11.

Abstract

BACKGROUND

The aim of this supplement registry study was to evaluate the efficacy of Pycnogenol in controlling signs and symptoms of chronic venous insufficiency (CVI), diabetic microangiopathy and microcirculatory parameters - in diabetic patients with CVI and microangiopathy. These CVI patients are eligible for medical procedures as their incompetent superficial veins can be treated with repeated sclerotherapy and or local surgery according to needs.

METHODS

During this registry study, only non-interventional managements were used. The effects of the use of elastic compression with standard management (SM) was compared to Pycnogenol intake (150 mg/day) and SM, without using elastic compression for 8 weeks.

RESULTS

Fifty-eight diabetic patients with CVI completed the study with 28 subjects supplemented with Pycnogenol and 30 in the control group. The two groups completing 8 weeks were comparable at baseline. After 8 weeks, no side effects were observed; the compliance was optimal with >98.5% of the supplement capsules correctly used. The tolerability to stockings was lower (73% of stockings were not fully used for the whole day). There were no dropouts. Venous pressures were comparable in the two groups at baseline. Microcirculatory and clinical measurements of the patients were comparable at inclusion. After 8 weeks, the differences between Pycnogenol and elastic compression were statistically significant for skin resting flux (RF), rate of ankle swelling (RAS), transcutaneous PO2 and PCO2 indicating a significant improvement in microcirculatory perfusion with Pycnogenol in comparison with elastic compression. In parallel, clinical symptoms assessed by the Composite Symptom Score (CSS), the venous Clinical severity Score (VCSS) and the Venous Disability Score (VDS), were significantly lower in the Pycnogenol group than in the compression group, indicating a significant clinical effect of Pycnogenol compared to elastic compression (P<0.05). Pycnogenol showed important antioxidant properties and lowered oxidative stress as seen also in previous studies.

CONCLUSIONS

This registry study confirms the clinical and microcirculatory efficacy of Pycnogenol in CVI in diabetics. The study indicates the significant supplementary, clinical role of Pycnogenol in the management of this common clinical condition over a short period of time, possibly preventing ulcerations.

摘要

背景

本补充剂注册研究的目的是评估碧萝芷在控制慢性静脉功能不全(CVI)、糖尿病微血管病变的体征和症状以及微循环参数方面的疗效——针对患有CVI和微血管病变的糖尿病患者。这些CVI患者有资格接受医疗程序,因为他们功能不全的浅表静脉可根据需要通过重复硬化疗法和/或局部手术进行治疗。

方法

在本注册研究期间,仅采用非介入性管理。将使用弹性压迫联合标准管理(SM)的效果与摄入碧萝芷(150毫克/天)联合SM的效果进行比较,8周内不使用弹性压迫。

结果

58例患有CVI的糖尿病患者完成了研究,其中28例受试者补充了碧萝芷,30例在对照组。完成8周的两组在基线时具有可比性。8周后,未观察到副作用;依从性最佳,超过98.5%的补充剂胶囊正确使用。对弹力袜的耐受性较低(73%的弹力袜未全天充分使用)。没有受试者退出。两组在基线时静脉压力具有可比性。患者的微循环和临床测量在纳入时具有可比性。8周后,碧萝芷组和弹性压迫组在皮肤静息通量(RF)、踝部肿胀率(RAS)、经皮氧分压(PO₂)和二氧化碳分压(PCO₂)方面的差异具有统计学意义,表明与弹性压迫相比,碧萝芷可显著改善微循环灌注。同时,碧萝芷组通过综合症状评分(CSS)、静脉临床严重程度评分(VCSS)和静脉残疾评分(VDS)评估的临床症状明显低于压迫组,表明与弹性压迫相比,碧萝芷具有显著的临床效果(P<0.05)。如先前研究所示,碧萝芷具有重要的抗氧化特性并降低了氧化应激。

结论

本注册研究证实了碧萝芷在糖尿病患者CVI中的临床和微循环疗效。该研究表明,碧萝芷在短期内对这种常见临床病症的管理中具有显著的补充临床作用,可能预防溃疡形成。

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