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The Effect of Platelet-Rich Plasma on the Intra-Articular Microenvironment in Knee Osteoarthritis

Knee osteoarthritis (KOA) represents a clinical challenge due to poor potential for spontaneous healing of cartilage lesions. Several treatment options are available for KOA, including oral nonsteroidal anti-inflammatory drugs, physical therapy, braces, activity modification, and finally operative t...

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Autores principales: Szwedowski, Dawid, Szczepanek, Joanna, Paczesny, Łukasz, Zabrzyński, Jan, Gagat, Maciej, Mobasheri, Ali, Jeka, Sławomir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8197096/
https://www.ncbi.nlm.nih.gov/pubmed/34071037
http://dx.doi.org/10.3390/ijms22115492
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author Szwedowski, Dawid
Szczepanek, Joanna
Paczesny, Łukasz
Zabrzyński, Jan
Gagat, Maciej
Mobasheri, Ali
Jeka, Sławomir
author_facet Szwedowski, Dawid
Szczepanek, Joanna
Paczesny, Łukasz
Zabrzyński, Jan
Gagat, Maciej
Mobasheri, Ali
Jeka, Sławomir
author_sort Szwedowski, Dawid
collection PubMed
description Knee osteoarthritis (KOA) represents a clinical challenge due to poor potential for spontaneous healing of cartilage lesions. Several treatment options are available for KOA, including oral nonsteroidal anti-inflammatory drugs, physical therapy, braces, activity modification, and finally operative treatment. Intra-articular (IA) injections are usually used when the non-operative treatment is not effective, and when the surgery is not yet indicated. More and more studies suggesting that IA injections are as or even more efficient and safe than NSAIDs. Recently, research to improve intra-articular homeostasis has focused on biologic adjuncts, such as platelet-rich plasma (PRP). The catabolic and inflammatory intra-articular processes that exists in knee osteoarthritis (KOA) may be influenced by the administration of PRP and its derivatives. PRP can induce a regenerative response and lead to the improvement of metabolic functions of damaged structures. However, the positive effect on chondrogenesis and proliferation of mesenchymal stem cells (MSC) is still highly controversial. Recommendations from in vitro and animal research often lead to different clinical outcomes because it is difficult to translate non-clinical study outcomes and methodology recommendations to human clinical treatment protocols. In recent years, significant progress has been made in understanding the mechanism of PRP action. In this review, we will discuss mechanisms related to inflammation and chondrogenesis in cartilage repair and regenerative processes after PRP administration in in vitro and animal studies. Furthermore, we review clinical trials of PRP efficiency in changing the OA biomarkers in knee joint.
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spelling pubmed-81970962021-06-13 The Effect of Platelet-Rich Plasma on the Intra-Articular Microenvironment in Knee Osteoarthritis Szwedowski, Dawid Szczepanek, Joanna Paczesny, Łukasz Zabrzyński, Jan Gagat, Maciej Mobasheri, Ali Jeka, Sławomir Int J Mol Sci Review Knee osteoarthritis (KOA) represents a clinical challenge due to poor potential for spontaneous healing of cartilage lesions. Several treatment options are available for KOA, including oral nonsteroidal anti-inflammatory drugs, physical therapy, braces, activity modification, and finally operative treatment. Intra-articular (IA) injections are usually used when the non-operative treatment is not effective, and when the surgery is not yet indicated. More and more studies suggesting that IA injections are as or even more efficient and safe than NSAIDs. Recently, research to improve intra-articular homeostasis has focused on biologic adjuncts, such as platelet-rich plasma (PRP). The catabolic and inflammatory intra-articular processes that exists in knee osteoarthritis (KOA) may be influenced by the administration of PRP and its derivatives. PRP can induce a regenerative response and lead to the improvement of metabolic functions of damaged structures. However, the positive effect on chondrogenesis and proliferation of mesenchymal stem cells (MSC) is still highly controversial. Recommendations from in vitro and animal research often lead to different clinical outcomes because it is difficult to translate non-clinical study outcomes and methodology recommendations to human clinical treatment protocols. In recent years, significant progress has been made in understanding the mechanism of PRP action. In this review, we will discuss mechanisms related to inflammation and chondrogenesis in cartilage repair and regenerative processes after PRP administration in in vitro and animal studies. Furthermore, we review clinical trials of PRP efficiency in changing the OA biomarkers in knee joint. MDPI 2021-05-23 /pmc/articles/PMC8197096/ /pubmed/34071037 http://dx.doi.org/10.3390/ijms22115492 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Szwedowski, Dawid
Szczepanek, Joanna
Paczesny, Łukasz
Zabrzyński, Jan
Gagat, Maciej
Mobasheri, Ali
Jeka, Sławomir
The Effect of Platelet-Rich Plasma on the Intra-Articular Microenvironment in Knee Osteoarthritis
title The Effect of Platelet-Rich Plasma on the Intra-Articular Microenvironment in Knee Osteoarthritis
title_full The Effect of Platelet-Rich Plasma on the Intra-Articular Microenvironment in Knee Osteoarthritis
title_fullStr The Effect of Platelet-Rich Plasma on the Intra-Articular Microenvironment in Knee Osteoarthritis
title_full_unstemmed The Effect of Platelet-Rich Plasma on the Intra-Articular Microenvironment in Knee Osteoarthritis
title_short The Effect of Platelet-Rich Plasma on the Intra-Articular Microenvironment in Knee Osteoarthritis
title_sort effect of platelet-rich plasma on the intra-articular microenvironment in knee osteoarthritis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8197096/
https://www.ncbi.nlm.nih.gov/pubmed/34071037
http://dx.doi.org/10.3390/ijms22115492
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