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纤维蛋白凝块和富含白细胞的富血小板纤维蛋白显示出相似的释放动力学和生长因子含量:一项初步研究。

Fibrin clot and Leukocyte-rich platelet-rich fibrin show similar release kinetics and amount of growth factors: a pilot study.

机构信息

Department of Orthopaedic Surgery, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-Cho, Chuo-Ku, Kobe, 650-0017, Japan.

出版信息

J Orthop Surg Res. 2023 Mar 25;18(1):238. doi: 10.1186/s13018-023-03709-5.

DOI:10.1186/s13018-023-03709-5
PMID:36964579
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10039559/
Abstract

BACKGROUND

In knee arthroscopic surgery, fibrin clot (FC) and leukocyte-rich platelet-rich fibrin (L-PRF) may be used in augmentation for meniscal repair. Studies have investigated growth factors released from FC and L-PRF; however, it is difficult to compare FC and L-PRF between different studies. Direct comparison of growth factors that may support meniscal healing released from FC and L-PRF may be beneficial in deciding whether to use FC or L-PRF. If no significant difference is seen, the surgeon may decide to use FC which is easier to prepare compared to L-PRF. The purpose of this pilot study is to investigate the release amount and pattern of basic fibroblast growth factor (bFGF), platelet-derived growth factor AB (PDGF-AB), transforming growth factor β1 (TGF-β1), vascular endothelial growth factor (VEGF), and stromal cell-derived factor 1 (SDF-1) from FC and L-PRF.

METHOD

Twenty milliliters (ml) of whole blood was collected from each of the four volunteers. Ten milliliters of whole blood was allocated for preparation of FC and 10 ml for L-PRF. FC and L-PRF were separately placed in 5 ml of culture media. Five milliliters of the culture media was sampled and refilled at 15 min, 1 day, 3 days, 1 week and 2 weeks. The collected culture was used to quantify bFGF, PDGF-AB, TGF-β1, VEGF, and SDF-1 release by Enzyme-linked immune-sorbent assay (ELISA). Mann-Whitney U test was performed to assess significance of differences in amount of each growth factor released between FC and L-PRF. Significance was accepted at P value less than 0.05.

RESULTS

At two weeks, the cumulative release of TGF-β1 was the highest among all the growth factors in both FC and L-PRF (FC:19,738.21 pg/ml, L-PRF: 16,229.79 pg/ml). PDGF-AB (FC: 2328 pg/ml, L-PRF 1513.57 pg/ml) had the second largest amount, followed by VEGF (FC: 702.06 pg/ml, L-PRF 595.99 pg/ml) and bFGF (FC: 23.48 pg/ml, L-PRF 18.2 pg/ml), which order was also common in both FC and L-PRF. No significant difference in final release amount and pattern was seen between FC and L-PRF.

CONCLUSION

The current pilot study showed that cumulative release amount and release pattern of PDGF-AB, VEGF, TGF-β1, and bFGF did not significantly differ between FC and L-PRF during the two weeks of observation.

摘要

背景

在膝关节镜手术中,纤维蛋白凝块(FC)和富含白细胞的富血小板纤维蛋白(L-PRF)可用于半月板修复的增强。已有研究调查了从 FC 和 L-PRF 释放的生长因子;然而,很难在不同的研究中比较 FC 和 L-PRF。直接比较从 FC 和 L-PRF 释放的可能支持半月板愈合的生长因子可能有助于决定是否使用 FC 或 L-PRF。如果没有看到显著差异,外科医生可能会决定使用 FC,因为与 L-PRF 相比,FC 更容易准备。本初步研究的目的是调查纤维蛋白凝块(FC)和富含白细胞的富血小板纤维蛋白(L-PRF)中碱性成纤维细胞生长因子(bFGF)、血小板衍生生长因子 AB(PDGF-AB)、转化生长因子 β1(TGF-β1)、血管内皮生长因子(VEGF)和基质细胞衍生因子 1(SDF-1)的释放量和释放模式。

方法

从四名志愿者每人采集 20 毫升(ml)全血。将 10 毫升全血分配用于制备 FC 和 10 毫升用于 L-PRF。FC 和 L-PRF 分别放置在 5 毫升的培养基中。在 15 分钟、1 天、3 天、1 周和 2 周时取样并补充 5 毫升培养物。收集的培养物用于通过酶联免疫吸附测定(ELISA)定量 bFGF、PDGF-AB、TGF-β1、VEGF 和 SDF-1 的释放。采用曼-惠特尼 U 检验评估 FC 和 L-PRF 之间释放的每种生长因子量的差异的显著性。接受 P 值小于 0.05 的显著性。

结果

在两周时,TGF-β1 的累积释放量在 FC 和 L-PRF 中所有生长因子中最高(FC:19738.21pg/ml,L-PRF:16229.79pg/ml)。PDGF-AB(FC:2328pg/ml,L-PRF 1513.57pg/ml)含量第二大,其次是 VEGF(FC:702.06pg/ml,L-PRF 595.99pg/ml)和 bFGF(FC:23.48pg/ml,L-PRF 18.2pg/ml),这一顺序在 FC 和 L-PRF 中也很常见。FC 和 L-PRF 之间在最终释放量和释放模式上没有显著差异。

结论

本初步研究表明,在两周的观察期内,FC 和 L-PRF 之间 PDGF-AB、VEGF、TGF-β1 和 bFGF 的累积释放量和释放模式没有显著差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/901a/10039559/043490f08fcd/13018_2023_3709_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/901a/10039559/e14a8bcce254/13018_2023_3709_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/901a/10039559/67fbe92f6d31/13018_2023_3709_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/901a/10039559/0560a611cde0/13018_2023_3709_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/901a/10039559/043490f08fcd/13018_2023_3709_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/901a/10039559/e14a8bcce254/13018_2023_3709_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/901a/10039559/67fbe92f6d31/13018_2023_3709_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/901a/10039559/0560a611cde0/13018_2023_3709_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/901a/10039559/043490f08fcd/13018_2023_3709_Fig4_HTML.jpg

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