Role of Specific microRNAs in Cluster Headache

Background Cluster headache (CH) is a primary headache included in the trigeminal autonomic cephalalgias (TACs) according to the International Calssification of Headache Disorder, Third Edition. CH is characterized by a multifaceted and incompletely understood pathophysiology. The hypothalamus, the trigeminal-vascular complex, and the trigeminal-autonomic reflex are believed to play a significant role. Increasing experimental evidence has highlighted the involvement of specific microRNAs (miRNAs) in the chronic pain and primary headaches, including migraine. miRNAs are small endogenous noncoding RNAs that are around 22 nucleotides in length. miRNAs operate as post-transcriptional regulator of gene expression by promoting messenger RNA (mRNA) degradation or repressing mRNA translation. The regulation process performed by miRNAs is complex and articulated since an individual miRNA might target hundreds of different mRNAs, and conversely, each mRNA may be regulated by multiple miRNAs. It has been estimated that more than 60% of all protein-coding genes are regulated by miRNAs which consequentially determine the pleiotropic modulation of a wide variety of cellular processes involving differentiation, development and signaling. miRNAs are involved in the generation and maintenance of pain and several evidence suggest that specific miRNAs could play a role in migraine. In a recent study, we observed an upregulation of gene expression in two miRNAs, miR-382-5p and miR-34a-5p, in peripheral blood mononuclear cells (PBMCs) in subjects with chronic migraine (CM). These miRNAs are involved in inflammation modulation and the release of γ-aminobutyric acid (GABA) compared to individuals with episodic migraine and healthy subjects (HCs). These findings underscore a correlation between the gene expression of these miRNAs and the migraine phenotype, as well as its severity. Recent studies suggest an active role for certain neuropeptides in CH. The Danish group has indeed demonstrated that the intravenous administration of CGRP, PACAP, or VIP can induce acute CH attacks in at least 50% of participants when studied in the active phase of the disease. As of now, there is no data regarding the potential involvement of miRNAs in CH. This study aims to provide a detailed exploration of the role of miRNAs in cluster headache, contributing to our understanding of the pathophysiology of this primary headache disorder. Furthermore, the results obtained may pave the way for the development of a new generation of molecules that could be used in the field of CH, such as miRNA agonists (Agomir) and antagonists (Antagomir). Aims The primary objective of our current project is to investigate the peripheral expression of miRNAs implicated in pain modulation (miR-382-5p, miR-34a-5p, and miR-155) in subjects with episodic CH in the active phase (eCH-act), episodic CH in the remission phase (eCH-rem), chronic CH (cCH), and healthy control subjects (HC). Methods All subjects will perform a single evaluation over time during which they will undergo: * explanation of study procedures and informed consent signing * screening visit * clinical and demographic data collection (based on revision of a headache diary) * fasting venous blood sampling * administration of questionnaires All subjects will be evaluated in the morning, after night fasting. For subjects affected by cCH or eCH-act, sampling is expected to be carried out in the inter-critical phase, as defined by the absence of CH attacks for at least 3 hours in patients with eCH and for at least 8 hours in patients with cCH. After blood sampling, patients will stay at Center to complete a set of questionnaires. This will allow the investigator to monitor the patients for at least 2 hours, to exclude that a blood sampling is performed immediately before a CH attack. For patients with eCH, the "active" and "remission" phases will be defined as follows: * Active phase: the phase during which CH attacks have been present for at least 7 days. * Remission phase: characterized by an absence of cluster headache attacks for at least 15 consecutive days without pharmacological therapy. miR-382-5p, miR-34a-5p and miRNA-155 gene expression will be evaluated in PBMCs by real-time reverse transcription (RT-PCR). This assessment will be normalized with U6 (a type of small nuclear RNA used as housekeeping gene) and expressed as Relative Quantification (RQ). Plasma levels of CGRP alpha, PACAP and VIP will be measured using validated commercial ELISA kits. A detailed description of the methods planned for the biochemical analyses could be found here: https://doi.org/10.1186/s10194-020-01189-0. The set of clinical questionnaires will include: Migraine Disability Assessment (MIDAS), Headache Impact Test (HIT-6), Cluster headache Impact Questionnarie (CHIQ). Sample size calculation and pre-planned statistical analysis The following parameters were considered for the calculation: Effect Size: 0.5; alpha error: 0.05; beta error: 0.05 (power: 95%); number of groups: 4. Sample size calculation was conducted using the freeware platform G\*Power (ver. 3.1.9.7) for an ANOVA test with Bonferroni correction applied to the 4 groups. The minimum suggested sample size is 76 subjects (19 subjects per group). To account for potential variability, we plan to enroll a total of 100 subjects, with 25 subjects per group. Parametric or non-parametric correlations will be used to measure the relationship between biochemical variables and clinical variables. Multivariate analyses will be performed according to the results of the univariate analysis. Statistical significance will be set at the 5% level (p\<0.05).