Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2023 Jul 6;12(13):4526.
doi: 10.3390/jcm12134526.

Effects of Fremanezumab on Psychiatric Comorbidities in Difficult-to-Treat Patients with Chronic Migraine: Post Hoc Analysis of a Prospective, Multicenter, Real-World Greek Registry

Affiliations

Effects of Fremanezumab on Psychiatric Comorbidities in Difficult-to-Treat Patients with Chronic Migraine: Post Hoc Analysis of a Prospective, Multicenter, Real-World Greek Registry

Michail Vikelis et al. J Clin Med. .

Abstract

Objective: this post hoc analysis aimed to evaluate the efficacy of fremanezumab in difficult-to-treat chronic migraine (CM) patients with and without psychiatric comorbidities (PCs), mainly anxiety and/or depression.

Methods: We assessed data from CM patients with and without PCs who failed at least 3 preventives and eventually received at least 3 consecutive monthly doses of fremanezumab 225 mg. Outcomes included the crude response (≥50% reduction in monthly headache days (MHDs)) rates to fremanezumab from the baseline to the last clinical follow-up. The changes in MHDs; MHDs of moderate/greater severity; monthly days with intake of abortive medication; and the proportion of patients' changing status from with PCs to decreased/without PCs were also compared. Disability and quality of life (QOL) outcomes were also assessed.

Results: Of 107 patients enrolled, 65 (60.7%) had baseline PCs. The percentage of patients with (n = 38/65; 58.5%) and without (n = 28/42; 66.6%) PCs that achieved a ≥50% reduction in MHDs with fremanezumab was comparable (p = 0.41), whereas MHDs were significantly reduced (difference vs. baseline) in both patients with PCs (mean -8.9 (standard error: 6.8); p < 0.001) and without PCs (-9.8 (7.5); p < 0.001). Both groups experienced significant improvements in all other efficacy, disability, and QOL outcomes at comparable rates, including in MHD reduction. A significant proportion of fremanezumab-treated patients with baseline PCs de-escalated in corresponding severities or even reverted to no PCs (28/65; 43.1%) post-fremanezumab.

Conclusions: fremanezumab appears to be effective as a preventive treatment in difficult-to-treat CM patients with and without PCs while also being beneficial in reducing the severity of comorbid anxiety and/or depression.

Keywords: CGRP; chronic migraine; efficacy; fremanezumab; monoclonal antibodies; psychiatric comorbidities; response.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Changes in mean fremanezumab-related headache efficacy scores from baseline to the last follow-up between treatment groups.
Figure 2
Figure 2
Differences in the number of fremanezumab responders at the last follow-up compared with baseline MHDs between patients with vs. without PCs.

References

    1. Ashina M., Terwindt G.M., Al-Karagholi M.A.-M., de Boer I., Lee M.J., Hay D.L., Schulte L.H., Hadjikhani N., Sinclair A.J., Ashina H., et al. Migraine: Disease characterisation, biomarkers, and precision medicine. Lancet. 2021;397:1496–1504. doi: 10.1016/S0140-6736(20)32162-0. - DOI - PubMed
    1. Breslau N., Lipton R.B., Stewart W.F., Schultz L.R., Welch K.M. Comorbidity of migraine and depression: Investigating potential etiology and prognosis. Neurology. 2003;60:1308–1312. doi: 10.1212/01.WNL.0000058907.41080.54. - DOI - PubMed
    1. Buse D.C., Silberstein S.D., Manack A.N., Papapetropoulos S., Lipton R.B. Psychiatric comorbidities of episodic and chronic migraine. J. Neurol. 2013;260:1960–1969. doi: 10.1007/s00415-012-6725-x. - DOI - PubMed
    1. Ashina S., Serrano D., Lipton R.B., Maizels M., Manack A.N., Turkel C.C., Reed M.L., Buse D.C. Depression and risk of transformation of episodic to chronic migraine. J. Headache Pain. 2012;13:615–624. doi: 10.1007/s10194-012-0479-9. - DOI - PMC - PubMed
    1. Vandervorst F., Van Deun L., Van Dycke A., Paemeleire K., Reuter U., Schoenen J., Versijpt J. CGRP monoclonal antibodies in migraine: An efficacy and tolerability comparison with standard prophylactic drugs. J. Headache Pain. 2021;22:128. doi: 10.1186/s10194-021-01335-2. - DOI - PMC - PubMed