# Decoding migraine disorders: parathyroid hormone-related peptide receptors as key genetic drivers

**Authors:** Andreia Dias, Marta Ferreira, Mariana Santos, Alda Sousa, Carla Oliveira, Miguel Alves-Ferreira, Carolina Lemos

PMC · DOI: 10.1093/braincomms/fcaf142 · Brain Communications · 2025-04-28

## TL;DR

This study identifies parathyroid hormone-related genes as potential biomarkers for female migraine patients, offering new insights for targeted therapies.

## Contribution

The first-time identification of PTH1R and PTH2 as key genetic drivers in female migraine patients.

## Key findings

- PTH1R and PTH2 were upregulated in female migraine patients compared to controls.
- Metabolic and G-protein coupled receptor pathways were upregulated in female migraine patients.
- Immune-related pathways were downregulated in migraine patients compared to controls.

## Abstract

Migraine is a complex neurological disorder, and the most common migraine categories are migraine with aura and without aura. The higher prevalence of migraine in related individuals compared to the general population indicates a potential genetic predisposition; however, gene expression, which is influenced by both genetic and environmental factors, can also be a major factor in the migraine susceptibility. Given the high number of Portuguese migraine patients whose diagnosis and treatment have not yet been well established, we decided to carry out a whole transcriptome analysis within a migraine Portuguese cohort. This study aims to identify potential biomarkers that could contribute to improved migraine therapy. We performed total RNA sequencing on whole blood samples from 15 migraine patients and 12 age-matched controls. Differential expression analysis and gene set enrichment analysis were performed in different migraine subgroups. Finally, we performed the protein-protein interaction networks of differentially expressed genes. Gene set enrichment analysis comparing migraine patients with controls highlighted upregulated pathways linked to metabolism, and downregulated immuno-inflammatory pathways. Moreover, the groups of female migraine patients and female migraine without aura patients emphasized significant upregulated pathways, including G protein-coupled receptors signalling pathways, when compared with female controls. Interestingly, we found two important differentially expressed genes related to parathyroid hormone: PTH1R and PTH2. PTH1R was upregulated in female migraine without aura versus female controls, while PTH2 was both upregulated between female migraine patients and female controls, as well as between female migraine without aura and controls. Here, we show, for the first time, the involvement of parathyroid hormone receptors and their associated gene expression patterns in female migraine patients. These molecules stand out as sturdy and promising biomarkers for innovative therapeutic in female migraine patients.

Dias et al. analysed gene expression in Portuguese migraine patients, revealing upregulated metabolic and G-protein coupled receptor pathways and downregulated immune pathways. Notably, PTH1R and PTH2 were upregulated in female migraine groups, highlighting parathyroid hormone receptors as potential biomarkers for female migraine patients.

Graphical Abstract

## Linked entities

- **Genes:** PTH1R (parathyroid hormone 1 receptor) [NCBI Gene 5745], PTH2 (parathyroid hormone 2) [NCBI Gene 113091]
- **Diseases:** migraine (MONDO:0005277)

## Full-text entities

- **Genes:** PTH2 (parathyroid hormone 2) [NCBI Gene 113091] {aka TIP39}, PTH (parathyroid hormone) [NCBI Gene 5741] {aka FIH1, PTH1}, PTH1R (parathyroid hormone 1 receptor) [NCBI Gene 5745] {aka EKNS, PFE, PTHR, PTHR1}
- **Diseases:** Migraine (MESH:D008881), inflammatory (MESH:D007249), migraine with aura and without aura (MESH:D020326), neurological disorder (MESH:D009461)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12034459/full.md

## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC12034459/full.md

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Source: https://tomesphere.com/paper/PMC12034459