# OnabotulinumToxinA Reduces Pharmacological Burden in Chronic Migraine Patients: A Two-Center Prospective Cohort Study

**Authors:** Danilo Antonio Montisano, Alessandra Parisi, Alberto Raggi, Claudia Altamura, Luigi D’Onofrio, Marilena Marcosano, Luisa Fofi, Alessia Marcassoli, Fabrizio Vernieri, Licia Grazzi

PMC · DOI: 10.3390/toxins18030143 · Toxins · 2026-03-14

## TL;DR

This study found that using OnabotulinumToxinA for chronic migraine reduces the need for other medications and improves symptoms over 12 months.

## Contribution

The study shows that OnabotulinumToxinA leads to discontinuation of previous preventive therapies and conversion from chronic to episodic migraine.

## Key findings

- 28.4% of patients discontinued previous preventive therapies after 12 months of OnabotulinumToxinA treatment.
- 58.9% of patients converted from chronic to episodic migraine within 12 months.
- Improvements in HIT-6 scores, migraine days, and symptomatic medication intake were observed.

## Abstract

Background: Chronic migraine (CM) is a highly disabling and difficult-to-manage condition with a high pharmacological and economic burden. OnabotulinumtoxinA (BTx) was the first treatment specifically approved for CM. The main aim of this study was to assess whether the initiation of BTx is associated with discontinuation of previously prescribed preventive therapies. Methods: This study was a prospective cohort investigation conducted in two headache centers: Carlo Besta (Milan) and Policlinico Campus Bio-Medico (Rome). We included patients with CM and previous oral preventive treatments initiating BTx. We analyzed persistence with preventive therapies over 12 months of follow-up and evaluated the conversion rate from chronic to episodic migraine (EM), along with change in migraine days, symptomatic intake, and HIT-6. Results: A total of 95 patients were included in the main analysis, showing a discontinuation of treatment in 28.4% of patients at 12 months. In the exploratory analysis, a CM to EM conversion rate of 58.9% was achieved at 12 months; meanwhile, HIT-6, migraine days, and symptomatic intake showed a sizeable improvement. Conclusion: Treatment with BTx was associated with a reduction in drug burden at 12 months and a CM to EM conversion rate of almost 60% at 12 months, also contributing to a reduction in the economic burden of the disease.

## Full-text entities

- **Genes:** CALCA (calcitonin related polypeptide alpha) [NCBI Gene 796] {aka CALC1, CGRP, CGRP-I, CGRP-alpha, CGRP1, CT}, SNAR-E (small NF90 (ILF3) associated RNA E) [NCBI Gene 100170220], SNAP25 (synaptosome associated protein 25) [NCBI Gene 6616] {aka CMS18, DEE117, RIC-4, RIC4, SEC9, SNAP}, TAC1 (tachykinin precursor 1) [NCBI Gene 6863] {aka Hs.2563, NK2, NKNA, NPK, TAC2}
- **Diseases:** Headache (MESH:D006261), Neurogenic Pain (MESH:D010146), dysthyroidism (MESH:D049970), sleep disturbances (MESH:D012893), alcohol or drug abuse (MESH:D019966), psychiatric (MESH:D001523), endocrinological diseases (MESH:D004194), depression (MESH:D003866), photophobia (MESH:D020795), injury to (MESH:D014947), nausea (MESH:D009325), anxiety (MESH:D001007), vertigo (MESH:D014717), HIT (MESH:D013921), neurological disorder (MESH:D009461), hypertension (MESH:D006973), insomnia (MESH:D007319), HIT-6 (MESH:D053632), pain disorders (MESH:D013001), MOH (MESH:D051271), Chronic Migraine (MESH:D008881), visual disturbance (MESH:D014786), health (OMIM:603663), allodynia (MESH:D006930), phonophobia (MESH:D012001)
- **Chemicals:** galcanezumab (MESH:C000628360), CM (-), triptans (MESH:D014363), Topiramate (MESH:D000077236), glutamate (MESH:D018698), fremanezumab (MESH:C000604315)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

29 references — full list in the complete paper: https://tomesphere.com/paper/PMC13029949/full.md

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Source: https://tomesphere.com/paper/PMC13029949