Herz- und Diabeteszentrum NRW, Ruhr Universität Bochum, Bad Oeynhausen, Germany.
Competence Center for Clinical Studies Bremen, Universität Bremen, Bremen, Germany.
Diabet Med. 2022 Jun;39(6):e14787. doi: 10.1111/dme.14787. Epub 2022 Jan 21.
Cold atmospheric plasma (CAP) has been proven to enhance wound healing in superficial, chronically infected, diabetic foot ulcers. We aimed to investigate the molecular drivers responsible for this macroscopically observed improvement in diabetic wound healing.
Wound exudate was available from each change of dressing within a prospective, randomised, patient-blinded clinical trial. Specific protein level analyses were conducted via multiplex ELISA for wound samples of a representative subcohort (placebo: n = 13; CAP: n = 14). Expression of fibroblast growth factor 2 (FGF-2), vascular endothelial growth factor A (VEGF-A), cytokines and matrix metalloproteinases (MMPs) were evaluated over a treatment period of about 14 days.
Analysis revealed increased levels of the growth factors FGF-2 (placebo: median 46.9 range [32.0-168.6] AU vs. CAP: 113.7[55.8-208.1] AU) and VEGF-A (placebo: 79.7 [52.4-162.7] AU vs. CAP: 120.8 [51.1-198.1] AU) throughout the treatment period and in head-to-head comparison in a daily assessment. CAP-treated wounds showed increased levels of tumour necrosis factor-alpha, interleukins 1α and 8. However, the total protein amounts were not significantly elevated. The total protein amounts of MMPs were not altered by CAP.
Induction of crucial growth factors, like FGF-2 and VEGF-A, and interleukins appears to be an important component of CAP-mediated promotion of granulation, vascularisation and reepithelialisation in the diabetic foot. These findings demonstrate for the first time that CAP-mediated growth factor induction also occurs in persons with diabetes, as previously described only in several in vitro and rodent experiments. Clinical Trial registration KPWTRIAL: NCT04205942, ClinicalTrials.gov.
已证实冷大气压等离子体(CAP)可促进表浅性、慢性感染性、糖尿病足溃疡的愈合。本研究旨在探讨导致糖尿病创面宏观愈合改善的分子驱动因素。
在一项前瞻性、随机、患者盲法临床试验中,可获得每次换药时的创面渗出物。通过多因子 ELISA 对代表性亚组的创面样本(安慰剂:n=13;CAP:n=14)进行特定蛋白水平分析。在大约 14 天的治疗期间,评估成纤维细胞生长因子 2(FGF-2)、血管内皮生长因子 A(VEGF-A)、细胞因子和基质金属蛋白酶(MMPs)的表达情况。
分析显示,在整个治疗期间,生长因子 FGF-2(安慰剂:中位数 46.9[32.0-168.6] AU vs. CAP:113.7[55.8-208.1] AU)和 VEGF-A(安慰剂:79.7[52.4-162.7] AU vs. CAP:120.8[51.1-198.1] AU)的水平升高,并且在每日评估中进行了头对头比较。CAP 治疗的创面显示肿瘤坏死因子-α、白细胞介素 1α 和 8 的水平升高。然而,总蛋白量并没有显著增加。CAP 未改变 MMP 的总蛋白量。
诱导关键生长因子,如 FGF-2 和 VEGF-A 以及白细胞介素,似乎是 CAP 促进糖尿病足肉芽形成、血管生成和再上皮化的重要组成部分。这些发现首次表明,如前所述,CAP 介导的生长因子诱导也发生在糖尿病患者中,而此前仅在几项体外和啮齿动物实验中描述过。临床试验注册号:KPWTRIAL:NCT04205942,ClinicalTrials.gov。