A High Methylation Level of a Novel -284 bp CpG Island in the RAMP1 Gene Promoter Is Potentially Associated with Migraine in Women

• Published in: Brain sciences Vol. 12; no. 5; p. 526
• Main Authors: Carvalho, Estefânia, Dias, Andreia, Sousa, Alda, Lopes, Alexandra M, Martins, Sandra, Pinto, Nádia, Lemos, Carolina, Alves-Ferreira, Miguel
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 21.04.2022; MDPI
• Subjects: Biomarkers; Bisulfite; Calcitonin; Calcitonin gene-related peptide; CpG islands; Disease; DNA methylation; Epigenetics; Gene expression; Headache; Hypotheses; Migraine; Proteins; RAMP1; Receptor activity modifying proteins; Womens health; United States > US; DNA methylation; migraine; RAMP1; epigenetics
• ISSN: 2076-3425; 2076-3425
• DOI: 10.3390/brainsci12050526

Migraine is a complex neurovascular disorder affecting one billion people worldwide, mainly females. It is characterized by attacks of moderate to severe headache pain, with associated symptoms. Receptor activity modifying protein (RAMP1) is part of the Calcitonin Gene-Related Peptide (CGRP) receptor, a pharmacological target for migraine. Epigenetic processes, such as DNA methylation, play a role in clinical presentation of various diseases. DNA methylation occurs mostly in the gene promoter and can control gene expression. We investigated the methylation state of the promoter in 104 female blood DNA samples: 54 migraineurs and 50 controls. We treated DNA with sodium bisulfite and performed PCR, Sanger Sequencing, and Epigenetic Sequencing Methylation (ESME) software analysis. We identified 51 CpG dinucleotides, and 5 showed methylation variability. Migraineurs had a higher number of individuals with all five CpG methylated when compared to controls (26% vs. 16%), although non-significant ( = 0.216). We also found that CpG -284 bp, related to the transcription start site (TSS), showed higher methylation levels in cases ( = 0.011). This CpG may potentially play a role in migraine, affecting transcription or receptor malfunctioning and/or altered CGRP binding. We hope to confirm this finding in a larger cohort and establish an epigenetic biomarker to predict female migraine risk.