Cytokines as new biomarkers of skin wound vitality.


Journal

International journal of legal medicine
ISSN: 1437-1596
Titre abrégé: Int J Legal Med
Pays: Germany
ID NLM: 9101456

Informations de publication

Date de publication:
Nov 2021
Historique:
received: 13 11 2020
accepted: 25 06 2021
pubmed: 28 7 2021
medline: 9 11 2021
entrez: 27 7 2021
Statut: ppublish

Résumé

The diagnosis of skin wound vitality is currently based on standard histology, but histological findings lack sensitivity in case of a short survival time. New reliable biomarkers of vitality are therefore strongly needed. We assessed the ability of 10 candidate cytokines (IFN-γ, IL-1β, IL-2, IL-4, IL-6, IL-8, IL-10, IL-12p70, IL-13, TNF-α) to discriminate between vital and early post-mortem wounds. Twenty-four cadavers with a recent open skin wound (< 3 h) were included (20 men, 4 women, mean age = 51.0 ± 24.3 years). An early post-mortem wound was performed in an uninjured skin area, and both wounds were sampled at the autopsy (post-mortem interval (PMI) = 66.3 ± 28.3 h). Needle-puncture sites related to resuscitation cares were included as very early post-mortem wounds (n = 6). In addition to standard histology, cytokines levels were simultaneously measured in each sample using a multiplex sandwich immunoassay, then normalized on healthy skin levels. A quantitative evaluation of IL-8-positive cells in ante- and post-mortem wound samples was also performed. In the training set of samples (n = 72), cytokine levels were significantly higher in vital wounds (mean age = 47 ± 53 min) than in post-mortem wounds (mean PMI = 6.9 ± 9.0 h) (p < 0.2), except for two cytokines (IFN-γ and IL-2). IL-8 was the best discriminatory cytokine (Se = 54%, Sp = 100%, AUC = 0.79), while a multivariate model combining IL-4 and IL12p70 was a bit more discriminant (Se = 55%, Sp = 100%, AUC = 0.84). In the validation set (n = 72), the discriminatory power of the cytokines and the predictive model was slightly lower, with IL-8 remaining the best cytokine (Se = 46%, Sp = 96%, AUC = 0.75). The predictive model remained highly specific (Sp = 100%). Both the cytokines and the predictive model allowed the iatrogenic injuries to be correctly classified as post-mortem wounds. Standard histology and immunohistochemistry showed 21% sensitivity and a specificity of 79% and 100%, respectively. Only two iatrogenic wounds could be properly categorized histologically. This study suggests that cytokines could be useful biomarkers of skin wound vitality and that the immunoassay method could be more sensitive than immunohistochemistry to identify wounds with a short survival time. Further research is underway to confirm these preliminary data.

Sections du résumé

BACKGROUND BACKGROUND
The diagnosis of skin wound vitality is currently based on standard histology, but histological findings lack sensitivity in case of a short survival time. New reliable biomarkers of vitality are therefore strongly needed. We assessed the ability of 10 candidate cytokines (IFN-γ, IL-1β, IL-2, IL-4, IL-6, IL-8, IL-10, IL-12p70, IL-13, TNF-α) to discriminate between vital and early post-mortem wounds.
METHODS METHODS
Twenty-four cadavers with a recent open skin wound (< 3 h) were included (20 men, 4 women, mean age = 51.0 ± 24.3 years). An early post-mortem wound was performed in an uninjured skin area, and both wounds were sampled at the autopsy (post-mortem interval (PMI) = 66.3 ± 28.3 h). Needle-puncture sites related to resuscitation cares were included as very early post-mortem wounds (n = 6). In addition to standard histology, cytokines levels were simultaneously measured in each sample using a multiplex sandwich immunoassay, then normalized on healthy skin levels. A quantitative evaluation of IL-8-positive cells in ante- and post-mortem wound samples was also performed.
RESULTS RESULTS
In the training set of samples (n = 72), cytokine levels were significantly higher in vital wounds (mean age = 47 ± 53 min) than in post-mortem wounds (mean PMI = 6.9 ± 9.0 h) (p < 0.2), except for two cytokines (IFN-γ and IL-2). IL-8 was the best discriminatory cytokine (Se = 54%, Sp = 100%, AUC = 0.79), while a multivariate model combining IL-4 and IL12p70 was a bit more discriminant (Se = 55%, Sp = 100%, AUC = 0.84). In the validation set (n = 72), the discriminatory power of the cytokines and the predictive model was slightly lower, with IL-8 remaining the best cytokine (Se = 46%, Sp = 96%, AUC = 0.75). The predictive model remained highly specific (Sp = 100%). Both the cytokines and the predictive model allowed the iatrogenic injuries to be correctly classified as post-mortem wounds. Standard histology and immunohistochemistry showed 21% sensitivity and a specificity of 79% and 100%, respectively. Only two iatrogenic wounds could be properly categorized histologically.
CONCLUSION CONCLUSIONS
This study suggests that cytokines could be useful biomarkers of skin wound vitality and that the immunoassay method could be more sensitive than immunohistochemistry to identify wounds with a short survival time. Further research is underway to confirm these preliminary data.

Identifiants

pubmed: 34313846
doi: 10.1007/s00414-021-02659-z
pii: 10.1007/s00414-021-02659-z
doi:

Substances chimiques

Biomarkers 0
Cytokines 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2537-2545

Informations de copyright

© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Références

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Auteurs

Pierre-Antoine Peyron (PA)

Department of Forensic Medicine, CHU Montpellier, University of Montpellier, Montpellier, France. pa-peyron@chu-montpellier.fr.

Sophie Colomb (S)

Department of Forensic Medicine, CHU Montpellier, University of Montpellier, Montpellier, France.

Dorian Becas (D)

Department of Forensic Medicine, CHU Montpellier, University of Montpellier, Montpellier, France.

Aurélie Adriansen (A)

Department of Forensic Medicine, CHU Montpellier, University of Montpellier, Montpellier, France.

Guillaume Gauchotte (G)

Department of Biopathology, Forensic Pathology, CHRU Nancy, INSERM U1256, Université de Lorraine, Vandoeuvre-lès-Nancy, France.

Laurent Tiers (L)

IRMB, INM, INSERM, CHU Montpellier, (LBPC-PPC), University of Montpellier, Montpellier, France.

Grégory Marin (G)

Department of Biostatistics and Medical Information, CHU Montpellier, University of Montpellier, Montpellier, France.

Sylvain Lehmann (S)

IRMB, INM, INSERM, CHU Montpellier, (LBPC-PPC), University of Montpellier, Montpellier, France.

Eric Baccino (E)

Department of Forensic Medicine, CHU Montpellier, University of Montpellier, Montpellier, France.

Constance Delaby (C)

IRMB, INM, INSERM, CHU Montpellier, (LBPC-PPC), University of Montpellier, Montpellier, France.
Sant Pau Memory Unit, Department of Neurology, Institut D'Investigacions Biomèdiques Sant Pau, Hospital de Sant Pau, Universitat Autònoma de Barcelona, Barcelona, Spain.

Christophe Hirtz (C)

IRMB, INM, INSERM, CHU Montpellier, (LBPC-PPC), University of Montpellier, Montpellier, France.

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