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Background <p>Objective biochemical markers for stratifying brachial plexus injury (BPI) severity remain lacking. Platelet-activating factor (PAF), an inflammatory mediator implicated in neurological damage, has not been evaluated in traumatic BPI. We investigated whether serum PAF levels predict complete injury and correlate with nerve conduction impairment.</p> Methods <p>This retrospective case-control study analyzed 102 traumatic BPI patients (43 complete, 59 incomplete) and 51 matched controls enrolled between January 2020 and December 2023. Serum PAF and nerve conduction velocities (NCV) of median, radial, and ulnar nerves were measured. Multivariable logistic regression, restricted cubic spline (RCS) modeling, and ROC analysis were performed.</p> Results <p>BPI patients exhibited elevated PAF versus controls (171.8±26.1 vs. 147.7±12.1 pg/mL, <i>P</i>&lt;0.001) and reduced mean NCV (19.8±2.6 vs. 64.0±6.1 m/s, <i>P</i>&lt;0.001).PAF correlated inversely with NCV (ρ=-0.50, <i>P</i>&lt;0.001). Complete injuries showed higher PAF (189.3±23.5 vs. 158.9±19.8 pg/mL, P&lt;0.001) and lower NCV (all P&lt;0.001). PAF (OR=1.151 per pg/mL, 95% CI: 1.033–1.284, P=0.011) and mean NCV (OR=0.012, P=0.014) independently predicted complete injury. RCS analysis revealed a nonlinear threshold at 165 pg/mL (OR=5.247, 95% CI: 2.808-9.803). PAF achieved good discrimination (AUC=0.840, sensitivity 84%, specificity 68%), though inferior to NCV (AUC=0.982). A multivariable model combining PAF, NCV, and injury-to-detection interval reached near-perfect discrimination (AUC=0.997). </p> Conclusions <p>Serum PAF independently predicts complete BPI with a nonlinear threshold at 165 pg/mL. While electrophysiological assessment remains the gold standard, PAF demonstrates potential as a rapid, minimally invasive screening tool in acute settings where immediate nerve conduction studies are unavailable, particularly for triaging patients requiring urgent intervention. </p>

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Elevated platelet-activating factor levels predict complete brachial plexus injury: a retrospective case-control study

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年3月9日

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  • Ziyang Zhang,
  • Guoxu Ma,
  • Tingting Dang,
  • Yonglu Huang,
  • Fan Gong,
  • Jianke Wu,
  • Xiaoliang Li,
  • Jian Gao,
  • Hanlin Zhang,
  • Yi Ding,
  • Tianyu Zhou,
  • Bowen Zhang

摘要

Background

Objective biochemical markers for stratifying brachial plexus injury (BPI) severity remain lacking. Platelet-activating factor (PAF), an inflammatory mediator implicated in neurological damage, has not been evaluated in traumatic BPI. We investigated whether serum PAF levels predict complete injury and correlate with nerve conduction impairment.

Methods

This retrospective case-control study analyzed 102 traumatic BPI patients (43 complete, 59 incomplete) and 51 matched controls enrolled between January 2020 and December 2023. Serum PAF and nerve conduction velocities (NCV) of median, radial, and ulnar nerves were measured. Multivariable logistic regression, restricted cubic spline (RCS) modeling, and ROC analysis were performed.

Results

BPI patients exhibited elevated PAF versus controls (171.8±26.1 vs. 147.7±12.1 pg/mL, P<0.001) and reduced mean NCV (19.8±2.6 vs. 64.0±6.1 m/s, P<0.001).PAF correlated inversely with NCV (ρ=-0.50, P<0.001). Complete injuries showed higher PAF (189.3±23.5 vs. 158.9±19.8 pg/mL, P<0.001) and lower NCV (all P<0.001). PAF (OR=1.151 per pg/mL, 95% CI: 1.033–1.284, P=0.011) and mean NCV (OR=0.012, P=0.014) independently predicted complete injury. RCS analysis revealed a nonlinear threshold at 165 pg/mL (OR=5.247, 95% CI: 2.808-9.803). PAF achieved good discrimination (AUC=0.840, sensitivity 84%, specificity 68%), though inferior to NCV (AUC=0.982). A multivariable model combining PAF, NCV, and injury-to-detection interval reached near-perfect discrimination (AUC=0.997).

Conclusions

Serum PAF independently predicts complete BPI with a nonlinear threshold at 165 pg/mL. While electrophysiological assessment remains the gold standard, PAF demonstrates potential as a rapid, minimally invasive screening tool in acute settings where immediate nerve conduction studies are unavailable, particularly for triaging patients requiring urgent intervention.