Plasma calcitonin gene–related peptide and nerve growth factor as headache and pain biomarkers in recently deployed soldiers with and without a recent concussion

Author:

Scher Ann I.1,McGinley James S.2,VanDam Lyndsey R.3,Campbell Amanda M.3,Chai Xiyun4,Collins Billy5,Klimp Scott A.6,Finkel Alan G.7ORCID,Schwab Karen1,Lipton Richard B.8,Johnson Kirk W.3

Affiliation:

1. Uniformed Services University of the Health Sciences Bethesda Maryland USA

2. Vector Psychometric Group Chapel Hill North Carolina USA

3. Pain Research, Eli Lilly and Company Indianapolis Indiana USA

4. Precision Medicine Neuroscience, AbbVie Chicago Illinois USA

5. US Public Health Service Commissioned Corps Fayetteville North Carolina USA

6. Womack Army Medical Center Fort Bragg North Carolina USA

7. Carolina Headache Institute Durham North Carolina USA

8. Albert Einstein College of Medicine Bronx New York USA

Abstract

AbstractObjectiveThe objective of this study was to characterize the utility of calcitonin gene–related peptide (CGRP) and nerve growth factor (NGF) as potential biomarkers for headache and pain disorders in the post–military deployment setting.BackgroundThe need to improve recognition, assessment, and prognoses of individuals with posttraumatic headache or other pain has increased interest in the potential of CGRP and NGF as biomarkers.MethodsThe Warrior Strong Study (NCT01847040) is an observational longitudinal study of United States–based soldiers who had recently returned from deployment to Afghanistan or Iraq from 2009 to 2014. The present nested cross‐sectional analysis uses baseline data collected from soldiers returning to Fort Bragg, North Carolina.ResultsIn total, 264 soldiers (mean (standard deviation [SD] age 28.1 [6.4] years, 230/264 [87.1%] men, 171/263 [65.0%] White) were analyzed. Mean (SD) plasma levels of CGRP were 1.3 (1.1) pg/mL and mean levels of NGF were 1.4 (0.4) pg/mL. Age was negatively correlated with NGF (−0.01 pg/mL per year, p = 0.007) but was not associated with CGRP. Men had higher mean (SD) CGRP plasma levels than women (1.4 95% confidence interval [CI; 1.2] vs. 0.9 95% CI [0.5] pg/mL, p < 0.002, Kruskal–Wallis test). CGRP levels were lower in participants who had a headache at the time of the blood draw (1.0 [0.6] pg/mL vs. 1.4 [1.2] pg/mL, p = 0.024). NGF was lower in participants with continuous pain (all types; 1.2 [0.4] vs. 1.4 [0.4] pg/mL, p = 0.027) and was lower in participants with traumatic brain injury (TBI) + posttraumatic headache (PTH) versus TBI without PTH (1.3 [0.3] vs. 1.4 [0.4] pg/mL, p = 0.021). Otherwise, CGRP and NGF were not associated with migraine‐like headache, TBI status, or headache burden as measured by the number of medical encounters in crude or adjusted models.ConclusionIn this exploratory study, plasma levels of NGF and CGRP showed promise as biomarkers for headache and other types of pain. These findings need to be replicated in other cohorts.

Funder

Center for Neuroscience and Regenerative Medicine

Congressionally Directed Medical Research Programs

Eli Lilly and Company

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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