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

IF 4.1 Q1 CLINICAL NEUROLOGY
Brain communications Pub Date : 2025-04-28 eCollection Date: 2025-01-01 DOI:10.1093/braincomms/fcaf142
Andreia Dias, Marta Ferreira, Mariana Santos, Alda Sousa, Carla Oliveira, Miguel Alves-Ferreira, Carolina Lemos
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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.

解码偏头痛:甲状旁腺激素相关肽受体是关键的遗传驱动因素。
偏头痛是一种复杂的神经系统疾病,最常见的偏头痛类型有先兆偏头痛和无先兆偏头痛。与一般人群相比,相关个体偏头痛的患病率较高表明潜在的遗传易感性;然而,受遗传和环境因素影响的基因表达也可能是偏头痛易感性的主要因素。鉴于大量葡萄牙偏头痛患者的诊断和治疗尚未很好地建立,我们决定在葡萄牙偏头痛队列中进行全转录组分析。这项研究旨在确定可能有助于改善偏头痛治疗的潜在生物标志物。我们对15名偏头痛患者和12名年龄匹配的对照组的全血样本进行了总RNA测序。在不同偏头痛亚组中进行差异表达分析和基因集富集分析。最后,我们进行了差异表达基因的蛋白-蛋白相互作用网络。比较偏头痛患者和对照组的基因集富集分析强调了与代谢相关的上调途径和与免疫炎症相关的下调途径。此外,与女性对照组相比,女性偏头痛患者和没有先兆的女性偏头痛患者组强调了显著的上调通路,包括G蛋白偶联受体信号通路。有趣的是,我们发现了两个与甲状旁腺激素相关的重要差异表达基因:PTH1R和PTH2。与女性对照组相比,无先兆的女性偏头痛患者PTH1R上调,而女性偏头痛患者和女性对照组之间以及无先兆的女性偏头痛患者和对照组之间PTH2均上调。在这里,我们首次展示了女性偏头痛患者中甲状旁腺激素受体及其相关基因表达模式的参与。这些分子在女性偏头痛患者的创新治疗中脱颖而出,成为坚固而有前途的生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
7.00
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0.00%
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审稿时长
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