Evidence map›Paper›PMID 42494172›Full record

ArticleBrain and behavior2026

Atogepant Reduces Psychological Dependence on Acute Treatments Evaluated With the Leeds Dependence Questionnaire: A Prospective Study.

Luigi Francesco Iannone, Marina Romozzi, Alberto Boccalini, Flavia Lo Castro, Claudia Altamura, Fabrizio Vernieri, Simona Guerzoni

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Article in Brain and behavior, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Luigi Francesco IannoneDepartment of Biomedical, Metabolic, and Neural Science, University of Modena and Reggio Emilia, Modena, Italy.
Marina RomozziDipartimento Universitario di Neuroscienze, Università Cattolica del Sacro Cuore, Roma, Italy.
Alberto BoccaliniDepartment of Digital and Predictive Medicine, Pharmacology and Clinical Metabolic Toxicology, Headache Center and Drug Abuse, Laboratory of Clinical Pharmacology and Pharmacogenomics, AOU Policlinico di Modena, Modena, Italy.
Flavia Lo CastroDepartment of Digital and Predictive Medicine, Pharmacology and Clinical Metabolic Toxicology, Headache Center and Drug Abuse, Laboratory of Clinical Pharmacology and Pharmacogenomics, AOU Policlinico di Modena, Modena, Italy.
Claudia AltamuraHeadache Unit, Fondazione Policlinico Universitario Campus Bio-Medico, Roma, Italy.
Fabrizio VernieriHeadache Unit, Fondazione Policlinico Universitario Campus Bio-Medico, Roma, Italy.
Simona GuerzoniDepartment of Digital and Predictive Medicine, Pharmacology and Clinical Metabolic Toxicology, Headache Center and Drug Abuse, Laboratory of Clinical Pharmacology and Pharmacogenomics, AOU Policlinico di Modena, Modena, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe Leeds Dependence Questionnaire (LDQ) is a validated tool for assessing psychological dependence across various substances and has been adapted for use in headache patients. No study has yet explored the effects of preventive anti-CGRP treatments like atogepant on psychological dependence related to acute migraine medications.

methodsWe conducted a prospective, real-world, single-center study on patients with migraine who were treated with atogepant 60 mg daily for 12 weeks. LDQ scores were assessed at baseline and after 12 weeks. Monthly headache days (MHDs), acute medication use, and presence of psychiatric comorbidities were collected. A linear mixed-effects model evaluated the effect of treatment over time, adjusting for medication overuse (MO) status and psychiatric comorbidities.

resultsWe included 43 patients (69.8% with chronic migraine, 67.4% with MO). The LDQ total score significantly decreased from 7.95 ± 5.79 to 6.42 ± 5.08 after treatment (mean difference: -1.53, p = 0.032). Significant improvements were seen in three specific LDQ items reflecting loss of control, compulsive use, and psychological distress. No significant correlation was found between the reduction in LDQ score and the change in acute medication use. Mixed-effects modeling confirmed a significant effect of treatment (p = 0.022), but independent of MO or MOH status or psychiatric comorbidities.

conclusionPreventive treatment with atogepant is associated with a significant reduction in psychological dependence on acute migraine medications, as measured by the LDQ. These findings support the need to assess dependence-like behavior in clinical migraine care and highlight the potential behavioral benefits of effective preventive treatments.

Indexed as

Migraine DisordersAdultFemaleHumansMaleMiddle AgedProspective StudiesSurveys and QuestionnairesTreatment Outcomeacute treatmentsatogepantdependence‐likemigraine

Identifiers

PMID42494172
PMCPMC13396879

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.