Capillary blood protein markers of posttraumatic headache in children after concussion

Author:

Fan Feiven12,Babl Franz E.1345,Swaney Ella E. K.13,Hearps Stephen J. C.14,Takagi Michael126,Emery-Corbin Samantha J.78,Dagley Laura F.78,Yousef Jumana78,Parkin Georgia M.1,Rausa Vanessa C.13,Anderson Nicholas1,Fabiano Fabian12,Dunne Kevin139,Seal Marc13,Davis Gavin A.110,Attard Chantal13,Anderson Vicki12311,Ignjatovic Vera131213

Affiliation:

1. Murdoch Children’s Research Institute, Melbourne, Victoria;

2. Melbourne School of Psychological Sciences, University of Melbourne, Victoria;

3. Departments of Pediatrics,

4. Critical Care, and

5. Emergency Department, Royal Children’s Hospital, Melbourne, Victoria;

6. Turner Institute for Brain and Mental Health, School of Psychological Sciences, Monash University, Melbourne, Victoria;

7. Advanced Technology and Biology Division, Walter and Eliza Hall Institute, Melbourne, Victoria;

8. Medical Biology, University of Melbourne, Victoria;

9. Department of Rehabilitation Medicine, Royal Children’s Hospital, Melbourne, Victoria;

10. Department of Neurosurgery, Austin and Cabrini Hospitals, Melbourne, Victoria;

11. Psychology Service, Royal Children’s Hospital, Melbourne, Victoria, Australia;

12. Johns Hopkins All Children’s Institute for Clinical & Translational Research, St. Petersburg, Florida; and

13. Department of Pediatrics, School of Medicine, Johns Hopkins University, Baltimore, Maryland

Abstract

OBJECTIVE Posttraumatic headache (PTH) represents the most common acute and persistent symptom in children after concussion, yet there is no blood protein signature to stratify the risk of PTH after concussion to facilitate early intervention. This discovery study aimed to identify capillary blood protein markers, at emergency department (ED) presentation within 48 hours of concussion, to predict children at risk of persisting PTH at 2 weeks postinjury. METHODS Capillary blood was collected using the Mitra Clamshell device from children aged 8–17 years who presented to the ED of the Royal Children’s Hospital, Melbourne, Australia, within 48 hours of sustaining a concussion. Participants were followed up at 2 weeks postinjury to determine PTH status. PTH was defined per clinical guidelines as a new or worsened headache compared with preinjury. An untargeted proteomics analysis using data-independent acquisition (DIA) was performed. Principal component analysis and hierarchical clustering were used to reduce the dimensionality of the protein dataset. RESULTS A total of 907 proteins were reproducibly identified from 82 children within 48 hours of concussion. The mean participant age was 12.78 years (SD 2.54 years, range 8–17 years); 70% of patients were male. Eighty percent met criteria for acute PTH in the ED, while one-third of participants with follow-up experienced PTH at 2 weeks postinjury (range 8–16 days). Hemoglobin subunit zeta (HBZ), cystatin B (CSTB), beta-ala-his dipeptidase (CNDP1), hemoglobin subunit gamma-1 (HBG1), and zyxin (ZYX) were weakly associated with PTH at 2 weeks postinjury based on up to a 7% increase in the PTH group despite nonsignificant Benjamini-Hochberg adjusted p values. CONCLUSIONS This discovery study determined that no capillary blood protein markers, measured at ED presentation within 48 hours of concussion, can predict children at risk of persisting PTH at 2 weeks postinjury. While HBZ, CSTB, CNDP1, HBG1, and ZYX were weakly associated with PTH at 2 weeks postinjury, there was no specific blood protein signature predictor of PTH in children after concussion. There is an urgent need to discover new blood biomarkers associated with PTH to facilitate risk stratification and improve clinical management of pediatric concussion.

Publisher

Journal of Neurosurgery Publishing Group (JNSPG)

Reference43 articles.

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2. Consensus statement on concussion in sport—the 5th international conference on concussion in sport held in Berlin, October 2016.;McCrory P,2017

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