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The Impact of N-Acetylcysteine on Autologous Fat Graft: First-in-Human Pilot Study

BACKGROUND: Our goal was to determine whether N-acetylcysteine (NAC) administered to the tumescent solution can reduce oxidative stress and increase autologous fat graft (AFG) viability. METHODS: The study included 15 women with a mean age of 31.8 years (range 23–39 years) who underwent breast asymm...

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Autores principales: Pietruski, Piotr, Paskal, Wiktor, Paluch, Łukasz, Paskal, Adriana M., Nitek, Żaneta, Włodarski, Paweł, Walecki, Jerzy, Noszczyk, Bartłomiej
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8481185/
https://www.ncbi.nlm.nih.gov/pubmed/32221675
http://dx.doi.org/10.1007/s00266-020-01633-1
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author Pietruski, Piotr
Paskal, Wiktor
Paluch, Łukasz
Paskal, Adriana M.
Nitek, Żaneta
Włodarski, Paweł
Walecki, Jerzy
Noszczyk, Bartłomiej
author_facet Pietruski, Piotr
Paskal, Wiktor
Paluch, Łukasz
Paskal, Adriana M.
Nitek, Żaneta
Włodarski, Paweł
Walecki, Jerzy
Noszczyk, Bartłomiej
author_sort Pietruski, Piotr
collection PubMed
description BACKGROUND: Our goal was to determine whether N-acetylcysteine (NAC) administered to the tumescent solution can reduce oxidative stress and increase autologous fat graft (AFG) viability. METHODS: The study included 15 women with a mean age of 31.8 years (range 23–39 years) who underwent breast asymmetry correction with AFG harvested from both thighs. One thigh was infiltrated with a standard tumescent fluid (control graft) and other with a NAC-enriched tumescent fluid (NAC-treated graft). Each participant had breast MRI imaging before and 6 months after the procedure. Also, adipose tissue samples from each graft were subjected to biochemical analysis, flow cytometric assay and qRT-PCR to determine the markers of oxidative stress, angiogenesis and adipogenesis. RESULTS: Concentration and activity of superoxide dismutase in the NAC-treated grafts turned out to be significantly higher than in the control grafts, in both fresh (p = 0.041 and p = 0.023, respectively) and frozen samples (p = 0.004 and p = 0.003, respectively). The level of nitric oxide in frozen samples from the control grafts was significantly higher than in the NAC-treated grafts (p = 0.009). iNOS was the only qRT-PCR target showing significant intergroup differences, with higher transcription levels observed in the control grafts (p = 0.027). Breast volumetric analysis demonstrated that the NAC-treated group had a 12.19% lower resorption rate than the control group, although it was found to be statistically insignificant (p = 0.149). No postoperative complications were observed during a 6-month follow-up. CONCLUSIONS: Some results of this study are promising. Further studies on larger groups are needed to determine NAC impact on AFG. LEVEL OF EVIDENCE IV: This journal requires that authors assign a level of evidence to each article. For a full description of these Evidence-Based Medicine ratings, please refer to the Table of Contents or the online Instructions to Authors www.springer.com/00266. TRIAL REGISTRY NAME: The Impact of N-Acetylcysteine on Volumetric Retention of Autologous Fat Graft for Breast Asymmetry Correction. REGISTRATION IDENTIFICATION NUMBER: NCT03197103. URL FOR THE REGISTRY: https://clinicaltrials.gov/ct2/show/NCT03197103?term=acetylcysteine&rank=6 ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00266-020-01633-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-84811852021-10-08 The Impact of N-Acetylcysteine on Autologous Fat Graft: First-in-Human Pilot Study Pietruski, Piotr Paskal, Wiktor Paluch, Łukasz Paskal, Adriana M. Nitek, Żaneta Włodarski, Paweł Walecki, Jerzy Noszczyk, Bartłomiej Aesthetic Plast Surg Original Article BACKGROUND: Our goal was to determine whether N-acetylcysteine (NAC) administered to the tumescent solution can reduce oxidative stress and increase autologous fat graft (AFG) viability. METHODS: The study included 15 women with a mean age of 31.8 years (range 23–39 years) who underwent breast asymmetry correction with AFG harvested from both thighs. One thigh was infiltrated with a standard tumescent fluid (control graft) and other with a NAC-enriched tumescent fluid (NAC-treated graft). Each participant had breast MRI imaging before and 6 months after the procedure. Also, adipose tissue samples from each graft were subjected to biochemical analysis, flow cytometric assay and qRT-PCR to determine the markers of oxidative stress, angiogenesis and adipogenesis. RESULTS: Concentration and activity of superoxide dismutase in the NAC-treated grafts turned out to be significantly higher than in the control grafts, in both fresh (p = 0.041 and p = 0.023, respectively) and frozen samples (p = 0.004 and p = 0.003, respectively). The level of nitric oxide in frozen samples from the control grafts was significantly higher than in the NAC-treated grafts (p = 0.009). iNOS was the only qRT-PCR target showing significant intergroup differences, with higher transcription levels observed in the control grafts (p = 0.027). Breast volumetric analysis demonstrated that the NAC-treated group had a 12.19% lower resorption rate than the control group, although it was found to be statistically insignificant (p = 0.149). No postoperative complications were observed during a 6-month follow-up. CONCLUSIONS: Some results of this study are promising. Further studies on larger groups are needed to determine NAC impact on AFG. LEVEL OF EVIDENCE IV: This journal requires that authors assign a level of evidence to each article. For a full description of these Evidence-Based Medicine ratings, please refer to the Table of Contents or the online Instructions to Authors www.springer.com/00266. TRIAL REGISTRY NAME: The Impact of N-Acetylcysteine on Volumetric Retention of Autologous Fat Graft for Breast Asymmetry Correction. REGISTRATION IDENTIFICATION NUMBER: NCT03197103. URL FOR THE REGISTRY: https://clinicaltrials.gov/ct2/show/NCT03197103?term=acetylcysteine&rank=6 ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00266-020-01633-1) contains supplementary material, which is available to authorized users. Springer US 2020-03-27 2021 /pmc/articles/PMC8481185/ /pubmed/32221675 http://dx.doi.org/10.1007/s00266-020-01633-1 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Pietruski, Piotr
Paskal, Wiktor
Paluch, Łukasz
Paskal, Adriana M.
Nitek, Żaneta
Włodarski, Paweł
Walecki, Jerzy
Noszczyk, Bartłomiej
The Impact of N-Acetylcysteine on Autologous Fat Graft: First-in-Human Pilot Study
title The Impact of N-Acetylcysteine on Autologous Fat Graft: First-in-Human Pilot Study
title_full The Impact of N-Acetylcysteine on Autologous Fat Graft: First-in-Human Pilot Study
title_fullStr The Impact of N-Acetylcysteine on Autologous Fat Graft: First-in-Human Pilot Study
title_full_unstemmed The Impact of N-Acetylcysteine on Autologous Fat Graft: First-in-Human Pilot Study
title_short The Impact of N-Acetylcysteine on Autologous Fat Graft: First-in-Human Pilot Study
title_sort impact of n-acetylcysteine on autologous fat graft: first-in-human pilot study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8481185/
https://www.ncbi.nlm.nih.gov/pubmed/32221675
http://dx.doi.org/10.1007/s00266-020-01633-1
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