Serum calcitonin gene-related peptide in patients with persistent post-concussion symptoms, including headache: a cohort study

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  • Peter Preben Eggertsen
  • Johan Palmfeldt
  • Schytz, Henrik Winther
  • Debbie Hay
  • Rikke Katrine Jentoft Olsen
  • Jørgen Feldbæk Nielsen
Background

Calcitonin gene-related peptide (CGRP) plays an important role in migraine pathophysiology, and post-traumatic headache (PTH) frequently presents with migraine-like features. Despite several clinical similarities, few studies have explored CGRP in PTH and concussion. This study investigates serum CGRP levels in patients with persistent post-concussion symptoms (PPCS), including PTH.
Methods

This cohort study was based on serum samples from individuals aged 18–30 years with PPCS who participated in a previously published randomized controlled trial of a non-pharmacological intervention. The primary outcome was serum CGRP concentrations, determined at baseline before randomization and at follow-up 7 months later, using an enzyme-linked immunosorbent assay (ELISA). CGRP levels at baseline were compared with healthy anonymous blood donors in the same age group.
Results

Baseline serum samples were collected from 86 participants with PPCS. The participants were most often female (78%) and migraine-like headache was the most frequent headache phenotype (74%). Serum CGRP levels were higher in participants with PPCS than in 120 healthy individuals (median: 158.5 pg/mL vs. 76.3 pg/mL, p = 0.050). A stratified analysis revealed that females with PPCS had a fivefold higher median than healthy females (166.3 pg/mL vs. 32.1 pg/mL, p = 0.0006), while no differences were observed in males (p = 0.83). At follow-up, CGRP levels decreased with a median change of  – 1.3 pg/mL (95% confidence interval:  – 17.6–0, p = 0.024).
Discussion

Elevated serum levels of CGRP in patients with PPCS and a decrease over time suggest an involvement of CGRP in PTH/PPCS. If confirmed in other studies, it could pave the way for CGRP-targeted therapies, which could have clinical significance.
Original languageEnglish
JournalJournal of Neurology
Volume271
Pages (from-to)2458-2472
ISSN0939-1517
DOIs
Publication statusPublished - 2024

ID: 390407052