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Biomarkers for recurrent pressure injury risk in persons with spinal cord injury
Authors:Katie Schwartz  M. Kristi Henzel  Mary Ann Richmond  Jennifer K. Zindle  Jacinta M. Seton  David P. Lemmer
Affiliation:1. Louis Stokes Cleveland Veterans Affairs Medical Center (LSCVAMC), Cleveland, Ohio, USA;2. Louis Stokes Cleveland Veterans Affairs Medical Center (LSCVAMC), Cleveland, Ohio, USA;3. Department of Physical Medicine and Rehabilitation, Case Western Reserve University, Cleveland, Ohio, USA "ORCIDhttps://orcid.org/0000-0002-8382-574X;4. Department of Physical Medicine and Rehabilitation, Case Western Reserve University, Cleveland, Ohio, USA;5. Louis Stokes Cleveland Veterans Affairs Medical Center (LSCVAMC), Cleveland, Ohio, USA "ORCIDhttps://orcid.org/0000-0003-1731-2062;6. Louis Stokes Cleveland Veterans Affairs Medical Center (LSCVAMC), Cleveland, Ohio, USA "ORCIDhttps://orcid.org/0000-0001-5771-6294
Abstract:Objective: To investigate potential linkages between pressure injury (PrI) recurrence following spinal cord injury (SCI) and muscle-based and circulatory biomarkers, specifically fatty metabolites and inflammatory cytokines.

Design: Observational study.

Setting: Tertiary Care Center.

Participants: 30 individuals with complete or incomplete SCI. Study participants either had never developed a PrI (Group I) or had a history of recurrent PrI (Group II).

Interventions: Not applicable.

Outcome Measures: Gluteal muscle histology, immunohistochemistry, muscle-based and circulatory fatty metabolites and inflammatory cytokines.

Results: Gluteal intramuscular adipose tissue (IMAT) was greater than 15% in most Group II (83%) individuals. Muscle tissue histology confirmed intramuscular structural differences. Fatty acid binding protein 4 (FABP4) and fatty acid binding protein 3 (FABP3) were reliably detected in muscle and blood and significantly correlated with IMAT (P? Conclusion: Identifying individuals with SCI at highest risk for recurrent PrI may impact patient management. IMAT content evaluation illustrates that muscle quality is a key biomarker. Low circulatory inflammatory biomarker expression potentially limits clinical significance for between group differences. Circulatory levels of FABP4 hold great potential as a recurrent PrI risk biomarker.
Keywords:Biomarkers  Fatty metabolites  Inflammatory cytokines  Pressure ulcer  Spinal cord injuries
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