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MicroRNA Profile and Erenumab Treatment

Not Applicable
Completed
Conditions
Migraine
Interventions
Genetic: Blood sampling for microRNA testing
Registration Number
NCT04659226
Lead Sponsor
University of L'Aquila
Brief Summary

Erenumab, a monoclonal antibody acting on the calcitonin gene-related peptide (CGRP) receptor, is an effective and safe migraine-specific preventive drug. The use of migraine-specific preventive drugs paves the way for a novel method to study migraine pathogenesis. Migraine is a complex disorder with several genetic and epigenetic influence, including that of microRNA. Several microRNAs, including those of inflammation and of endothelial function, have high expression levels in subjects with migraine; however, the findings of the available studies are insufficient to provide epigenetic biomarkers for migraine. Besides, little evidence is available on the role of migraine preventive treatments in the expression of microRNA. The study aims at evaluating the expression profiles of microRNAs before and after erenumab treatment prescribed according to clinical indication. The study will include women with episodic or chronic migraine treated with erenumab 140 mg monthly according to the Summary of Product Characteristics and local reimbursement criteria. The study will compare the expression profile of microRNAs in women with episodic and chronic migraine; besides, it will investigate differences in migraine-associated microRNA expression according to age, migraine characteristics, pain intensity, response to erenumab, migraine-related impact and disability.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
40
Inclusion Criteria
  • Women aged 25 to 50 years
  • Chronic or episodic migraine with or without aura diagnosed according to the International Classification of Headache Disorders - 3rd edition
  • Receiving a first prescription of erenumab for migraine prevention according to the Summary of Product Characteristics and local reimbursement criteria
  • At least 1 year from migraine onset
  • Provided informed consent
Exclusion Criteria
  • Headache other than migraine
  • Prior exposure to erenumab or other monoclonal antibodies targeting CGRP or its receptor
  • Use of any migraine preventive treatment in the last 60 days or 5 half-lives or 4 months if ever treated with botulinum toxin A
  • Pregnant or nursing
  • Body Mass Index <18 or >30 Kg/m2
  • Heavy smoking (more than 20 cigarettes per day)
  • Myocardial infarction, stroke, transient ischemic attack, unstable angina, or coronary artery bypass surgery or other revascularization procedures within 12 months prior to first visit
  • Illicit drug abuse
  • Major psychiatric disorders
  • Infective or inflammatory diseases
  • Any chronic medication prescribed for indications different from migraine within 60 days before study initiation

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Episodic or chronic migraineBlood sampling for microRNA testingWomen starting treatment with erenumab according to clinical indication
Primary Outcome Measures
NameTimeMethod
Fold changes in microRNA serum concentration - Episodic migraine3 months per each patient

Relative quantification of circulating microRNAs expression changes in women with episodic migraine after a 3-month treatment with erenumab with respect to pre-treatment. Data will be obtained by real-time polymerase chain reaction on microfluidic cards. Details on tested microRNAs are provided at the following link: https://assets.thermofisher.com/TFS-Assets/GSD/Reference-Materials/tac-advanced-miRNA-assay-list.xlsx

Fold changes in microRNA serum concentration - Chronic migraine3 months per each patient

Relative quantification of circulating microRNAs expression changes in women with chronic migraine after a 3-month treatment with erenumab with respect to pre-treatment. Data will be obtained by real-time polymerase chain reaction on microfluidic cards. Details on tested microRNAs are provided at the following link: https://assets.thermofisher.com/TFS-Assets/GSD/Reference-Materials/tac-advanced-miRNA-assay-list.xlsx

Secondary Outcome Measures
NameTimeMethod
Subgroup analyses3 months per each patient

Subgroup analyses of patients stratified according to age, migraine characteristics, response to erenumab, and migraine-related impact and disability. Data will be obtained by real-time polymerase chain reaction on microfluidic cards. Details on tested microRNAs are provided at the following link: https://assets.thermofisher.com/TFS-Assets/GSD/Reference-Materials/tac-advanced-miRNA-assay-list.xlsx

Baseline comparison between episodic and chronic migraineBaseline

Relative quantification of microRNA expression levels at baseline in women with chronic compared with episodic migraine. Data will be obtained by real-time polymerase chain reaction on microfluidic cards. Details on tested microRNAs are provided at the following link: https://assets.thermofisher.com/TFS-Assets/GSD/Reference-Materials/tac-advanced-miRNA-assay-list.xlsx

Trial Locations

Locations (1)

University of L'Aquila

🇮🇹

L'Aquila, Italy

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