Current partner codePEPTIDESDE
NCT05812742·Not applicable·INTERVENTIONAL

Chasing Biomarkers in Post-concussion Syndrome

Status

Completed

Phase

Not applicable

Enrollment

86

Locations

0

Results

Not posted

Publications

0

Study summary

What the protocol is testing.

The goal of this study was to investigate the biomarkers, neurofilament light chain, inflammatory markers, calcitonin-gene-related peptide, and metabolites from the kynurenine pathway in patients with severe post-concussive symptoms. The main question it aimed to answer was: * Are the biomarker concentrations significantly changed in patients with severe post-concussive symptoms compared to healthy individuals? * Do the biomarker concentrations change at follow-up? Participants were recruited from a recently published randomized controlled trial (Clinicaltrials.gov no. NCT02337101 / PMID: 31891145 ). The biomarker concentrations were compared to a healthy control group recruited from the Blood Bank at Aarhus University Hospital in 2022.

Full detailed description

In the previously published RCT-study (PMID: 31891145), 86 participants with severe post-concussive symptoms provided blood samples at baseline (4 months after the concussion). Severe post-concussive symptoms were defined as having a Rivermead Post Concussion Questionnaire \>20. Around 7 months later, a follow-up blood sample was obtained from 54 participants. These blood samples were used to investigate blood biomarkers for the condition.

Interventions

Treatment arms and agents.

BEHAVIORAL

Early intervention programme

For more information, please go to the original registration of the RCT-study (NCT02337101) or the published article (PMID: 31891145).

BEHAVIORAL

Enhanced usual care

For more information, please go to the original registration of the RCT-study (NCT02337101) or the published article (PMID: 31891145).

Timeline

From registration to results.

  1. First posted

    Apr 14, 2023

  2. Study start

    Mar 2015

  3. Primary completion

    Jul 2023

  4. Study completion

    Jul 2023

  5. Results posted

    Not reported

  6. Registry updated

    Apr 16, 2024

Outcomes

What the study measures.

Primary outcomes

Neurofilament light chain at baseline (primary outcome)

Time frame · The baseline blood sample was taken up to 7 months after the concussion (4 months median).

The investigators hypothesized: The concentration of neurofilament light chain (ng/L) is significantly increased at baseline in patients compared to the healthy control group.

Neurofilament light chain at follow-up (primary outcome)

Time frame · The follow-up blood sample was taken up to 12 months after baseline (7 months median) after the baseline blood sample.

The investigators hypothesized: 1)The neurofilament light chain concentration (ng/L) normalizes (decreases) at follow-up compared to the baseline concentration in patients.

Self-reported post-concussion symptoms score (primary outcome)

Time frame · The baseline symptom score (RPQ) was obtained from the patients up to 7 months after the concussion (4 months median), and the follow-up score was obtained up to 16 months (10.5 median) after the concussion

The symptom score was measured at both baseline and follow-up using the Rivermead Post-Concussion Symptoms Questionnaire (RPQ) which is a self-reported questionnaire. The Rivermead Post-Concussion Symptoms Questionnaire contains 16 items which is rated from 0 (not experienced) to 4 (a severe problem). The total score thus ranges on a scale between 0-64.

Calcitonin-gene related peptide at baseline (CGRP)

Time frame · The baseline blood sample was taken up to 7 months after the concussion (4 months median).

The investigators hypothesized: The concentration of calcitonin gene-related peptide (pg/mL) is decreased compared to the healthy control group at baseline

Calcitonin-gene related peptide at follow-up (CGRP)

Time frame · The follow-up blood sample was taken up to 12 months after baseline (7 months median) after the baseline blood sample.

The investigators hypothesized: The CGRP concentrations (pg/mL) will normalize (increase) at follow-up compared to baseline.

Secondary outcomes

Quinolinic acid at baseline

Time frame · The baseline blood sample was taken up to 7 months after the concussion (4 months median).

The investigators hypothesized that: The concentration of the neurotoxic metabolite, quinolinic acid (measured in nM), is increased in patients compared to healthy controls

Quinolinic acid at follow-up

Time frame · The follow-up blood sample was taken up to 12 months after baseline (7 months median) after the baseline blood sample.

The investigators hypothesized: The quinolinic acid concentration (nM) normalizes (decreases) at follow-up compared to the baseline concentration.

Neuroprotective index at baseline

Time frame · The baseline blood sample was taken up to 7 months after the concussion (4 months median).

The investigators hypothesized: The ratio between the neuroprotective metabolite kynurenic acid (KYNA) and the neurotoxic metabolite quinolinic acid (KynA/QUIN) is lower than the ratio in healthy individuals at baseline. A higher ratio means a better outcome.

Neuroprotective index at follow-up

Time frame · The follow-up blood sample was taken up to 12 months after baseline (7 months median) after the baseline blood sample.

The investigators hypothesized: The ratio between the neuroprotective metabolite kynurenic acid (KYNA) and the neurotoxic metabolite quinolinic acid (QUIN) normalizes (increases) at follow-up compared to baseline. A higher ratio thus means a better outcome.

Inflammatory markers at baseline

Time frame · The baseline blood sample was taken up to 7 months after the concussion (4 months median).

The investigators hypothesized that: Tumor necrosis factor alpha (TNF-α) and interleukin-6 (IL-6) (both pg/mL) are increased in patients compared to healthy controls.

Inflammatory markers at baseline

Time frame · The baseline blood sample was taken up to 7 months after the concussion (4 months median).

The investigators hypothesized: Basic fibroblast growth factor (Basic FGF), Eotaxin, interferon gamma (IFN-y), interleukin 1 beta (IL-1B), interleukin 8 (IL-8), interleukin 9 (IL-9), interleukin 17 (IL17), Interferon gamma-induced protein 10 (IP-10), monocyte chemoattractant protein 1 (MCP-1), and Macrophage Inflammatory Protein beta (MIP-1b) (all pg/mL) are significantly increased in patients compared to controls (hypothesis is based on a recent study (PMID: 32326805)

Inflammatory markers at follow-up

Time frame · The follow-up blood sample was taken up to 12 months after baseline (7 months median) after the baseline blood sample.

TNF-α and IL-6 (both pg/mL) decreases at follow-up compared to the baseline value in patients.

Eligibility

Who can take part.

Minimum age
18 Years
Maximum age
30 Years
Sex
ALL
Healthy volunteers
Yes

Patients with severe post-concussive symptoms: Inclusion Criteria: 1. Concussion caused by a head trauma based on the diagnostic criteria recommended by the World Health Organization (WHO) Task Force 2. Age between 18 and 30 years 3. Able to understand, speak and read Danish. 4. A score of 20 or more on the Rivermead Post Concussion Symptoms Questionnaire (RPQ). Exclusion Criteria: 1. Objective neurological findings indicating neurological disease or brain damage. 2. Previous concussion leading to persistent post-concussional symptoms within the last two years. 3. Severe misuse of alcohol, prescription drugs and / or illegal drugs. 4. Severe psychiatric, neurological,or other medical disease that would impede participation in the intervention 5. Inability to speak and read Danish Healthy control group (recruited from December 2021 - March 2022): \- Individuals from the Blood Bank at Aarhus University Hospital in Denmark. Inclusion criteria were: 1. Age between 18-30 years 2. Equal distribution between the genders (60 men and 60 women). This number was based on a power analysis using published data from neurofilament light chain.

Study locations

0 registered sites.

No country data reported. Showing up to 24 locations stored in the fast local snapshot.

No study locations reported.

Publications

Results and literature.

No PMID-linked publications were present in this registry snapshot.

Primary links

Continue at the source.

Related trials

More studies on Calcitonin.

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Put the record in context.

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