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Substance P mediates reduced pneumonia rates after traumatic brain injury.

Publication ,  Journal Article
Yang, S; Stepien, D; Hanseman, D; Robinson, B; Goodman, MD; Pritts, TA; Caldwell, CC; Remick, DG; Lentsch, AB
Published in: Crit Care Med
September 2014

OBJECTIVES: Traumatic brain injury results in significant morbidity and mortality and is associated with infectious complications, particularly pneumonia. However, whether traumatic brain injury directly impacts the host response to pneumonia is unknown. The objective of this study was to determine the nature of the relationship between traumatic brain injury and the prevalence of pneumonia in trauma patients and investigate the mechanism of this relationship using a murine model of traumatic brain injury with pneumonia. DESIGN: Data from the National Trauma Data Bank and a murine model of traumatic brain injury with postinjury pneumonia. SETTING: Academic medical centers in Cincinnati, OH, and Boston, MA. PATIENTS/SUBJECTS: Trauma patients in the National Trauma Data Bank with a hospital length of stay greater than 2 days, age of at least 18 years at admission, and a blunt mechanism of injury. Subjects were female ICR mice 8-10 weeks old. INTERVENTIONS: Administration of a substance P receptor antagonist in mice. MEASUREMENTS AND MAIN RESULTS: Pneumonia rates were measured in trauma patients before and after risk adjustment using propensity scoring. In addition, survival and pulmonary inflammation were measured in mice undergoing traumatic brain injury with or without pneumonia. After risk adjustment, we found that traumatic brain injury patients had significantly lower rates of pneumonia compared to blunt trauma patients without traumatic brain injury. A murine model of traumatic brain injury reproduced these clinical findings with mice subjected to traumatic brain injury demonstrating increased bacterial clearance and survival after induction of pneumonia. To determine the mechanisms responsible for this improvement, the substance P receptor was blocked in mice after traumatic brain injury. This treatment abrogated the traumatic brain injury-associated increases in bacterial clearance and survival. CONCLUSIONS: The data demonstrate that patients with traumatic brain injury have lower rates of pneumonia compared to non-head-injured trauma patients and suggest that the mechanism of this effect occurs through traumatic brain injury-induced release of substance P, which improves innate immunity to decrease pneumonia.

Duke Scholars

Published In

Crit Care Med

DOI

EISSN

1530-0293

Publication Date

September 2014

Volume

42

Issue

9

Start / End Page

2092 / 2100

Location

United States

Related Subject Headings

  • Wounds, Nonpenetrating
  • Trauma Centers
  • Substance P
  • Sex Factors
  • Respiration, Artificial
  • Pneumonia
  • Neurokinin-1 Receptor Antagonists
  • Middle Aged
  • Mice, Inbred ICR
  • Mice
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Yang, S., Stepien, D., Hanseman, D., Robinson, B., Goodman, M. D., Pritts, T. A., … Lentsch, A. B. (2014). Substance P mediates reduced pneumonia rates after traumatic brain injury. Crit Care Med, 42(9), 2092–2100. https://doi.org/10.1097/CCM.0000000000000486
Yang, Sung, David Stepien, Dennis Hanseman, Bryce Robinson, Michael D. Goodman, Timothy A. Pritts, Charles C. Caldwell, Daniel G. Remick, and Alex B. Lentsch. “Substance P mediates reduced pneumonia rates after traumatic brain injury.Crit Care Med 42, no. 9 (September 2014): 2092–2100. https://doi.org/10.1097/CCM.0000000000000486.
Yang S, Stepien D, Hanseman D, Robinson B, Goodman MD, Pritts TA, et al. Substance P mediates reduced pneumonia rates after traumatic brain injury. Crit Care Med. 2014 Sep;42(9):2092–100.
Yang, Sung, et al. “Substance P mediates reduced pneumonia rates after traumatic brain injury.Crit Care Med, vol. 42, no. 9, Sept. 2014, pp. 2092–100. Pubmed, doi:10.1097/CCM.0000000000000486.
Yang S, Stepien D, Hanseman D, Robinson B, Goodman MD, Pritts TA, Caldwell CC, Remick DG, Lentsch AB. Substance P mediates reduced pneumonia rates after traumatic brain injury. Crit Care Med. 2014 Sep;42(9):2092–2100.

Published In

Crit Care Med

DOI

EISSN

1530-0293

Publication Date

September 2014

Volume

42

Issue

9

Start / End Page

2092 / 2100

Location

United States

Related Subject Headings

  • Wounds, Nonpenetrating
  • Trauma Centers
  • Substance P
  • Sex Factors
  • Respiration, Artificial
  • Pneumonia
  • Neurokinin-1 Receptor Antagonists
  • Middle Aged
  • Mice, Inbred ICR
  • Mice