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      Acellular Dermal Matrix Used in Diabetic Foot Ulcers: Clinical Outcomes Supported by Biochemical and Histological Analyses

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          Abstract

          Diabetic foot ulcer (DFU) is a diabetes complication which greatly impacts the patient’s quality of life, often leading to amputation of the affected limb unless there is a timely and adequate management of the patient. DFUs have a high economic impact for the national health system. Data have indeed shown that DFUs are a major cause of hospitalization for patients with diabetes. Based on that, DFUs represent a very important challenge for the national health system. Especially in developed countries diabetic patients are increasing at a very high rate and as expected, also the incidence of DFUs is increasing due to longevity of diabetic patients in the western population. Herein, the surgical approach focused on the targeted use of the acellular dermal matrix has been integrated with biochemical and morphological/histological analyses to obtain evidence-based information on the mechanisms underlying tissue regeneration. In this research report, the clinical results indicated decreased postoperative wound infection levels and a short healing time, with a sound regeneration of tissues. Here we demonstrate that the key biomarkers of wound healing process are activated at gene expression level and also synthesis of collagen I, collagen III and elastin is prompted and modulated within the 28-day period of observation. These analyses were run on five patients treated with Integra ® sheet and five treated with the injectable matrix Integra ® Flowable, for cavitary lesions. In fact, clinical evaluation of improved healing was, for the first time, supported by biochemical and histological analyses. For these reasons, the present work opens a new scenario in DFUs treatment and follow-up, laying the foundation for a tailored protocol towards complete healing in severe pathological conditions.

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          Most cited references43

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          Diabetic Foot Ulcers and Their Recurrence.

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            Inter-Society Consensus for the Management of Peripheral Arterial Disease (TASC II).

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              Growth factors and cytokines in wound healing.

              Wound healing is an evolutionarily conserved, complex, multicellular process that, in skin, aims at barrier restoration. This process involves the coordinated efforts of several cell types including keratinocytes, fibroblasts, endothelial cells, macrophages, and platelets. The migration, infiltration, proliferation, and differentiation of these cells will culminate in an inflammatory response, the formation of new tissue and ultimately wound closure. This complex process is executed and regulated by an equally complex signaling network involving numerous growth factors, cytokines and chemokines. Of particular importance is the epidermal growth factor (EGF) family, transforming growth factor beta (TGF-beta) family, fibroblast growth factor (FGF) family, vascular endothelial growth factor (VEGF), granulocyte macrophage colony stimulating factor (GM-CSF), platelet-derived growth factor (PDGF), connective tissue growth factor (CTGF), interleukin (IL) family, and tumor necrosis factor-alpha family. Currently, patients are treated by three growth factors: PDGF-BB, bFGF, and GM-CSF. Only PDGF-BB has successfully completed randomized clinical trials in the Unites States. With gene therapy now in clinical trial and the discovery of biodegradable polymers, fibrin mesh, and human collagen serving as potential delivery systems other growth factors may soon be available to patients. This review will focus on the specific roles of these growth factors and cytokines during the wound healing process.
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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                Int J Mol Sci
                Int J Mol Sci
                ijms
                International Journal of Molecular Sciences
                MDPI
                1422-0067
                30 June 2021
                July 2021
                : 22
                : 13
                : 7085
                Affiliations
                [1 ]Department of Advanced Medical and Surgical Sciences, University of Campania Luigi Vanvitelli, Piazza Miraglia 2, 80138 Naples, Italy; ferdinando.campitiello@ 123456unicampania.it (F.C.); angeladellacorte@ 123456live.it (A.D.C.); Dr.scialla@ 123456gmail.com (G.S.); silvestro.canonico@ 123456unicampania.it (S.C.)
                [2 ]Department of Experimental Medicine, Section of Biotechnology, Medical Histology and Molecular Biology, University of Campania Luigi Vanvitelli, Via L. De Crecchio 7, 80138 Naples, Italy; marcella.cammarota@ 123456unicampania.it (M.C.); antonella.dagostino@ 123456unicampania.it (A.D.); giulia.ricci@ 123456unicampania.it (G.R.); antonietta.stellavato@ 123456unicampania.it (A.S.); adripirozzi@ 123456gmail.com (A.V.A.P.); chiara.schiraldi@ 123456unicampania.it (C.S.)
                Author notes
                [†]

                Co-last authors.

                Author information
                https://orcid.org/0000-0002-6443-5092
                https://orcid.org/0000-0002-2199-170X
                https://orcid.org/0000-0002-1066-843X
                Article
                ijms-22-07085
                10.3390/ijms22137085
                8267704
                34209306
                bae183b9-a5dc-4f46-8bc6-a4d597d1384c
                © 2021 by the authors.

                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/).

                History
                : 10 May 2021
                : 23 June 2021
                Categories
                Article

                Molecular biology
                diabetic foot ulcer,biomaterials,biochemical and histological analyses
                Molecular biology
                diabetic foot ulcer, biomaterials, biochemical and histological analyses

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