Elevated Tau in Military Personnel Relates to Chronic Symptoms Following Traumatic Brain Injury.


Journal

The Journal of head trauma rehabilitation
ISSN: 1550-509X
Titre abrégé: J Head Trauma Rehabil
Pays: United States
ID NLM: 8702552

Informations de publication

Date de publication:
Historique:
pubmed: 30 4 2019
medline: 6 7 2021
entrez: 30 4 2019
Statut: ppublish

Résumé

To understand the relationships between traumatic brain injury (TBI), blood biomarkers, and symptoms of posttraumatic stress disorder (PTSD), depression, and postconcussive syndrome symptoms. Cross-sectional cohort study using multivariate analyses. One hundred nine military personnel and veterans, both with and without a history of TBI. PTSD Checklist-Civilian Version (PCL-C); Neurobehavioral Symptom Inventory (NSI); Ohio State University TBI Identification Method; Patient Health Questionnaire-9 (PHQ-9); Simoa-measured concentrations of tau, amyloid-beta (Aβ) 40, Aβ42, and neurofilament light (NFL). Controlling for age, sex, time since last injury (TSLI), and antianxiety/depression medication use, NFL was trending toward being significantly elevated in participants who had sustained 3 or more TBIs compared with those who had sustained 1 or 2 TBIs. Within the TBI group, partial correlations that controlled for age, sex, TSLI, and antianxiety/depression medication use showed that tau concentrations were significantly correlated with greater symptom severity, as measured with the NSI, PCL, and PHQ-9. Elevations in tau are associated with symptom severity after TBI, while NFL levels are elevated in those with a history of repetitive TBIs and in military personnel and veterans. This study shows the utility of measuring biomarkers chronically postinjury. Furthermore, there is a critical need for studies of biomarkers longitudinally following TBI.

Identifiants

pubmed: 31033745
doi: 10.1097/HTR.0000000000000485
pmc: PMC6814502
mid: NIHMS1517748
pii: 00001199-202001000-00007
doi:

Substances chimiques

Amyloid beta-Peptides 0
Biomarkers 0
Neurofilament Proteins 0
neurofilament protein L 0
tau Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

66-73

Subventions

Organisme : Intramural NIH HHS
ID : Z99 NR999999
Pays : United States

Commentaires et corrections

Type : CommentIn

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Auteurs

Cassandra L Pattinson (CL)

National Institute of Nursing Research, National Institutes of Health, Bethesda, Maryland (Drs Pattinson, Guedes, Lai, and Gill, Ms Motamedi, and Messrs Devoto and Peyer); Center for Neuroscience and Regenerative Medicine, Rockville, Maryland (Dr Shahim and Mss Taylor and Dunbar); National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland (Dr Shahim); Henry M. Jackson Foundation, Bethesda, Maryland (Mss Taylor and Dunbar and Dr Roy); and Uniformed Services University of the Health Sciences, Department of Medicine, Bethesda, Maryland (Dr Roy).

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Classifications MeSH