# Clinical predictors of propranolol responsiveness in pediatric migraine: a prospective observational study

**Authors:** Müge Baykan, Elif Didinmez Taşkırdı, Özge Baykan Çopuroğlu, Pınar Gençpınar, Nihal Olgaç Dündar

PMC · DOI: 10.22514/jofph.2026.026 · 2026-03-12

## TL;DR

This study found that propranolol and behavioral therapy both reduce migraine severity in children, with vitamin deficiencies and certain conditions predicting treatment response.

## Contribution

The study identifies clinical and biochemical predictors of propranolol responsiveness in pediatric migraine patients.

## Key findings

- Both propranolol and behavioral therapy significantly reduced migraine frequency and disability in children.
- Vitamin D and B12 deficiencies were linked to poorer treatment outcomes in propranolol-treated patients.
- Benign paroxysmal vertigo and essential tremor predicted better propranolol response in children with migraines.

## Abstract

Background: This study aimed to evaluate the comparative effectiveness 
of propranolol therapy and structured behavioral interventions in reducing 
headache severity in pediatric patients and to identify predictors of treatment 
response. Methods: In this prospective, single-center study, 178 
pediatric patients diagnosed with migraine based on the International 
Classification of Headache Disorders, 3rd edition (ICHD-3) criteria were 
enrolled. Participants were allocated into two groups according to baseline 
Pediatric Migraine Disability Assessment Scale (PedMIDAS) scores: Group 1 
(PedMIDAS <15, n = 88) received standardized behavioral therapy, while Group 2 
(PedMIDAS ≥15, n = 90) received propranolol (1–3 mg/kg/day) for 12 weeks. 
Primary outcomes were predefined as changes in monthly migraine attack frequency, 
PedMIDAS scores, and Visual Analog Scale (VAS)-measured headache intensity. 
Vitamin D deficiency and vitamin B12 deficiency were evaluated as 
biochemical predictors, and adherence was monitored bi-weekly. Results: 
Both groups showed significant improvement at week 12. Monthly migraine attacks 
declined from 3.5 ± 1.6 to 2.1 ± 1.2 in Group 1 and from 6.4 ± 
2.1 to 3.1 ± 1.7 in Group 2. PedMIDAS scores decreased from 8.60 ± 
3.25 to 5.75 ± 2.52 and 24.40 ± 9.65 to 16.11 ± 7.72, 
respectively (p < 0.001 both). VAS scores also improved in both groups 
with no significant between-group difference in percentage reduction. A 
≥50% reduction in attack frequency plus ≥1-grade PedMIDAS 
improvement defined treatment response. In the propranolol group, response was 
independently associated with benign paroxysmal vertigo and essential tremor, 
while vitamin D and vitamin B12 deficiency predicted poorer outcomes. 
Conclusions: Both propranolol and structured behavioral therapy 
effectively reduce migraine-related disability and pain in pediatric patients, 
yielding comparable proportional improvements. The identification of key clinical 
and biochemical predictors supports a personalized treatment approach, 
integrating comorbidity screening and nutritional assessment to optimize 
outcomes. Clinical Trial Registration: ClinicalTrials.gov/NCT07180043, 
retrospectively registered.

## Linked entities

- **Chemicals:** propranolol (PubChem CID 4946), vitamin B12 (PubChem CID 73415824)
- **Diseases:** migraine (MONDO:0005277), essential tremor (MONDO:0003233)

## Full-text entities

- **Diseases:** Vitamin D and B12 deficiencies (MESH:D014806), Headache Disorders (MESH:D020773), epilepsy (MESH:D004827), palpitations (MESH:D006331), cardiac conduction defects (MESH:D000075224), tension-type headache (MESH:D018781), Migraine (MESH:D008881), secondary headaches (MESH:D051271), photophobia (MESH:D020795), depression (MESH:D003866), tumors (MESH:D009369), bipolar disorder (MESH:D001714), major (MESH:D004830), migraine with aura (MESH:D020325), gastrointestinal symptoms (MESH:D012817), phonophobia (MESH:D012001), trauma (MESH:D014947), Essential  tremor (MESH:D020329), paresthesia (MESH:D010292), dizziness (MESH:D004244), infections (MESH:D007239), Vitamin D  deficiency (MESH:D014808), nausea (MESH:D009325), anxiety (MESH:D001007), Headache (MESH:D006261), micronutrient deficiencies (MESH:D007153), social phobia (MESH:D000072861), primary headaches (MESH:D051270), endothelial  dysfunction (MESH:D014652), Paroxysmal Vertigo (MESH:D014717), attention-deficit/hyperactivity disorder (MESH:D001289), inflammation (MESH:D007249), insufficiency (MESH:D000309), psychosis (MESH:D011618), pain (MESH:D010146), neurological disorders (MESH:D009461), bradycardia (MESH:D001919), asthma (MESH:D001249), BPV (MESH:D065635), fatigue (MESH:D005221), vascular malformations (MESH:D054079), functional  impairment (MESH:D003072), anxiety symptoms (MESH:D001008), obsessive-compulsive disorder (MESH:D009771), neuroinflammation (MESH:D000090862), Psychiatric disorders (MESH:D001523)
- **Chemicals:** caffeine (MESH:D002110), calcium (MESH:D002118), vitamin D/B12 (-), homocysteine (MESH:D006710), vitamin  B12 (MESH:D014805), Propranolol (MESH:D011433), vitamin D (MESH:D014807)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC13036611/full.md

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Source: https://tomesphere.com/paper/PMC13036611