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Updated: Aug 23, 2026

Biomarkers in an Animal Model for Revealing Neural, Hematologic, and Behavioral Correlates of PTSD
Published on: October 10, 2012
The inflammatory markers C-reactive protein and serum amyloid A in refugees with and without posttraumatic stress
Hans Peter Söndergaard1, Lars-Olof Hansson, Töres Theorell
1Department of Public Health, Karolinska Institutet, National Swedish Institute for Psychosocial Factors and Health, P.O. Box 230, S-171 77 Stockholm, Sweden. hans.peter.sondergaard@phs.ki.se
Background:
"Stress" is associated with changes in many systems of the body. The aim was to study the markers of the innate immune system, Serum amyloid A (SAA) and C-reactive protein (CRP), in subjects with and without posttraumatic stress disorder (PTSD).
Methods:
Subjects were refugees from Iraq in the age range of 18-48 years who participated in a longitudinal study focusing on life events. Blood samples were taken in the morning and analysed for Serum amyloid A and high sensitivity C-reactive protein (hsCRP).
Results:
Contrary to expectations, serum SAA and hsCRP were lower in PTSD than in non-PTSD subjects. Levels of SAA and CRP were further inversely correlated with serum DHEA-s, but not with cortisol. In cases with PTSD at baseline, there was an inverse relationship between difference in self-rated symptoms of PTSD and difference in log-transformed SAA-thus increasing PTSD intensity was associated with decreasing SAA. No such patterns were obvious with regard to CRP.
Conclusions:
Changes in the innate immune system, as measured by acute phase proteins of hepatic origin, seem to be a feature of PTSD. Further, the inverse correlation between DHEA-s, which has been shown to be changed in PTSD, and the acute phase proteins is of interest.
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