Letsel: Analysis of inflammatory cells and mediators in skin wound biopsies to determine wound age in living subjects in forensic medicine, FSI 2015

DOI: 10.1016/j.forsciint.2014.11.014

Authors: Judith Fronczek, Ronald Lulf, H. Ibrahim Korkmaz, Birgit I. Witte, Franklin R.W. van de Goot, Mark P.V. Begieneman, C.G. Schalkwijk, Paul A.J. Krijnen, Lawrence Rozendaal, Hans W.M. Niessen, Udo J.L. Reijnders.

ABSTRACT

Objective

In forensic medicine it is important to determine the age of skin wounds in living subjects. The aim of this study was to assess whether analysis of inflammatory cells and inflammatory mediators in skin biopsies of wounds from living subjects could improve wound age determination.

Methods

Biopsies (n = 101), representing the superficial border area of a skin wound, were taken from skin injuries of known wound age (range: 4.5 hours to 25 days) of living subjects. All biopsies were analyzed for 3 inflammatory cell markers (MPO, CD45 and CD68) and 4 inflammatory mediators (MIP-1, IL-8, CML and vitronectin). For quantification, biopsies were subdivided in 4 different timeframes: 0.2–2 days, 2–4 days, 4–10 days and 10–25 days old wounds. Subsequently, a probability scoring system was developed.

Results

MPO, CD45, MIP-1, IL-8 (inflammatory cell markers) and N(epsilon)-(carboxymethyl)lysine (CML) positivity were maximal in wounds of 0.2–2 days old and then decreased in time. Remarkably, CD45, CD68 and CML showed a minor but non-significant increase again in 10–25 days old wounds. MPO and CD68 positivity was significantly lower in 4–25 days old wounds compared to 0.2–4 days old wounds. MPO positivity was also significantly lower in 10–25 days old wounds compared to 0.2–10 days old wounds. For CD45, MIP-1, IL-8 and CML no significant differences between the age groups were found. In case of vitronectin positivity in the extravasate or when the number of MIP-1 or IL-8-positive cells was more than 10 cells/mm2 the probability that a wound was more than 10 days old was 0%. A probability scoring system of all analyzed markers can be used to calculate individual wound age probabilities in biopsies of skin wounds of living subjects.

Conclusions

We have developed a probability scoring system of inflammatory cells and mediators that can be used to determine wound age in skin biopsies of living subjects.