Expression of Selected microRNAs in Migraine: A New Class of Possible Biomarkers of Disease?

: Preliminary but convergent ﬁndings suggest a role for microRNAs (miRNAs) in the generation and maintenance of chronic pain and migraine. Initial observations showed that serum levels of miR-382-5p and miR-34a-5p expression were increased in serum during the migraine attack, with miR-382-5p increasing in the interictal phase as well. By contrast, miR-30a-5p levels were lower in migraine patients compared to healthy controls. Of note, antimigraine treatments proved to be capable of inﬂuencing the expression of these miRNAs. Altogether, these observations suggest that miRNAs may represent migraine biomarkers, but several points are yet to be elucidated. A major concern is that these miRNAs are altered in a broad spectrum of painful and non-painful conditions, and thus it is not possible to consider them as truly “migraine-speciﬁc” biomarkers. We feel that these miRNAs may represent useful tools to uncover and deﬁne different phenotypes across the migraine spectrum with different treatment susceptibilities and clinical features, although further studies are needed to conﬁrm our hypothesis. In this narrative review we provide an update and a critical analysis of available data on miRNAs and migraines in order to propose possible interpretations. to providing reliable biomarkers for theoretical and practical scientiﬁc advances.


Introduction
Migraine is a primary headache disorder defined by the recurrence of attacks of throbbing pain typically located on one side of the head, with medium-high intensity, worsening with routine physical activities. The attacks last from 4 to 72 h. The pain is often accompanied by photo-and/or phonophobia and nausea and/or vomiting [1]. In around 30% of patients, a headache is preceded by visual, sensitive or aphasic symptoms, defining a subtype of the disease spectrum called "migraine with aura" [1].
According to the Global Burden of Disease Study 2019, migraine is the second most disabling disease in terms of years lived with disability [2]. In addition to the burden on personal life, migraine has a negative impact on multiple areas of the lives of those affected (school, social activities, work), resulting in a huge socio-economic impact on society [3,4].
Depending on the median frequency of headache, migraine is defined as episodic migraine (EM) for those who have less than 15 headache days per month, or chronic migraine (CM) in those who have at least 15 headache days per month, 8 of which with migraine features, for at least three months [1]. Chronification of migraine is often associated with a progressive increase in the intake of acute medications, a condition known Table 1. Summary of neurophysiological, neuroimaging and biochemical parameters that have been proposed as biomarkers of episodic migraine, chronic migraine and medication overuse headache.
Andersen et al. first detected the aberrant serum expression of 32 miRNAs in migraine patients in 2016 and identified a nine-fold increase in miR-34a-5p expression with a fourfold increase in miR-382-5p expression during the migraine attack when compared to the interictal phase [46]. Intriguingly, they also detected a significant higher miR-382-5p expression in migraine patients during the interictal period when compared to healthy subjects, and thus proposed this miRNA as a possible actor in migraine pathophysiology and a specific biomarker of the disease [46]. A main limitation of the study was that the migraine population was not well characterized, thus it was not possible to correlate the results obtained with the migraine phenotype (episodic or chronic) and with headache features.
A previously suggested hypothesis was that miR-382-5p serum expression was explained by increased blood-brain barrier permeability, which was suggested to occur during the migraine attack in a pre-clinical model [47], but this hypothesis has never been confirmed in humans and needs further confirmation.
Previous studies revealed that both miR-382-5p and miR-34a-5p negatively modulate target genes linked to GABAergic facilitating signaling, a neurotransmitter involved in trigeminal pain analgesia [46]. This may represent a protective compensatory mechanism in migraine self-limitation; indeed, higher GABA levels have been detected in the cerebrospinal fluid and in the saliva during migraine attacks [48,49].
The seminal work of Gallelli et al. paved the way for the identification of miRNAs as potential peripheral biological markers of drug response. They demonstrated lower miR-34a-5p and miR-375-5p expression in serum and saliva of children and adolescents treated with magnesium and acute nonsteroidal anti-inflammatory drugs (NSAIDs) compared to untreated subjects with migraine without aura [50]. It is noteworthy that in the first cohort of patients, the expression of these specific miRNAs was comparable to a group of healthy controls [50].
A recent study specifically analyzed miR-382-5p and miR-34a-5p expression in subjects with EM or CM and MOH (CM-MOH) [51]. The authors described a significantly higher interictal expression of miR-34a-5p and miR-382-5p in the plasma of CM-MOH subjects [51]. This analysis detected for the first time the association between specific miRNAs and the migraine phenotype as well as disease severity [51]. Notably, in this study CGRP plasma levels positively correlated with miR-382-5p and miR-34a-5p expression [51].
Although analyzed as a secondary endpoint, miR-382-5p and miR-34a-5p expression was reduced two months after detoxification from acute medications (in-hospital detoxification program), regardless of the clinical outcome [51]. This observation suggests the possibility of a direct role for acute medications in the expression of both miRNAs. miR-382-5p and miR-34a-5p were also negatively modulated by erenumab, a monoclonal antibody directed against the CGRP receptor, in a population of difficult-to-treat CM patients with and without MOH [52]. The expression of each miRNA was reduced after three monthly s.c. administrations of erenumab, irrespective of the clinical outcome, which suggests a direct role for CGRP in miRNA regulation [52]. By contrast, central sensitization improved only in migraine patients who responded to erenumab treatment with an at least 30% reduction in monthly migraine days [52].
2.2. miR-382-5p and miR-34a-5p in Pain and Putative Mechanisms miR-34a expression was reported to be altered in several human diseases besides migraine, including osteoarthritis [53,54], Alzheimer's disease [55], cancer [56,57] and leukemia [58]. The connection between miR-34a and these pathologies resides in its strong contribution to the regulation of cell cycles and apoptosis, with miR-34a being a major transcriptional target of p53 [59,60]. The involvement of miR-34a in several painful and non-painful conditions clearly suggests that, when considered alone, it cannot represent a migraine-specific biomarker. Nonetheless, it may still play a role as part of a multibiomarker panel signature of migraine [7].
Regarding pain-related disorders, miR-34a plays a role in the modulation of the inflammatory response [61,62]. Upregulation of mir-34a has been reported in osteoarthritic tissues specimens and in patients with low back pain related to intervertebral disc degeneration [63][64][65]. miR-34a expression was enhanced by IL-1β release [53], although miR-34a itself can up-regulate the IL-1β/cyclooxygenase 2 (COX-2)/Prostaglandin E2 (PEG2) inflammation pathway [66] by targeting the deacetylase silencing information regulator 1 (SIRT1) [66][67][68]. miR-34a also inhibits SIRT1 by increasing the acetylation of the nuclear factor kappa B (NF-κB) P65 subunit, ultimately enhancing the transcription of inflammatory mediators, including IL-1β, IL-6 and tumor necrosis factor-α [67,69]. In an animal model of inflammatory pain, Chen et al. reported an increase in miR-34a expression in the spinal cord and showed that its inhibition by a miR-34a antagonist exerted analgesic effects by increasing spinal SIRT1 expression [68]. The inhibition of SIRT1 was reported to enhance the release of CGRP in rat trigeminal ganglia in vitro, probably as a consequence of IL-1β/COX-2/PGE2 pathway activation [66]. Other genes coding for proteins that are involved in chronic pain pathways have been validated as targets of miR-34a, such as sodium voltage-gated channel beta subunit 2 (Scn2b) and vesicle-associated membrane protein 2 (VAMP2) [70]. This latter belongs to the SNARE (soluble N-ethyl-maleimide-sensitive factor attachment protein receptor) protein complex that regulates presynaptic neurotransmitter release as well as neurotransmitter receptor trafficking and synaptic plasticity [71], whose variants have been reported to be linked with migraine susceptibility [72]. It must be noted that miR-34a was found to be down-regulated in rats' dorsal root ganglions 12 days after the experimental induction of neuropathic pain, with the concomitant up-regulation of VAMP2 [70]. Since the increase of synaptic proteins is related to higher glutamate release [73], this may ultimately lead to an enhancement of nociception. Nonetheless, miR-34a was predicted to target the genes coding for specific GABA receptors subunits (GABBR2, Gamma-aminobutyric acid type B receptor subunit 2; GABRA3, Gamma-aminobutyric acid receptor subunit alpha-3) [46]. In this context, an up-regulation of this microRNA, as reported in serum of migraine patients, could contribute to the reduction of the GABA inhibitory signal [46]. Although some controversies exist, it is reasonable to assert that the role of miR-34a may vary across different pain disorders according to the time of evaluation and, more importantly, depending on specimen collection. However, together these observations strongly point towards the contribution of miR-34a to the regulation of pain-related neurotransmission.
Like miR-34a, miR-382-5p was predicted to target the GABRA5 (Gamma-aminobutyric acid receptor subunit alpha-5) GABA receptor subunit and also IL-10RA [46]. Thus, the observed up-regulation in the serum levels of miR-382-5p in migraine patients may be explained by reduced GABAergic and anti-inflammatory signaling [46,74,75]. The increased miR-382-5p serum levels in migraine patients may be also related to high protein levels of transforming growth factor β (TGF-β). In agreement with this hypothesis, increased TGF-β levels were found in the plasma and cerebrospinal fluid of patients with EM [76,77]. TGF-β is able to increase the expression of miR-382-5p [78][79][80] by inhibiting transcription factors' repressors [81]. TGF-β modulated miR-382-5p in vitro (human CD34+ stem cells), resulting in the increased accumulation of reactive oxygen species (ROS). ROS accumulation was explained by miR-382-5p-induced inhibition of superoxide dismutase 2 (SOD2), a direct target of this mRNA [79,80]. This latter issue appears to be relevant in the context of migraine pain, since oxidative stress and mitochondrial dysfunction was suggested as actors in migraine pathophysiology [82][83][84]. miR-382-5p regulation is also influenced by the long non-coding RNA Ftx (lncRNA Ftx), which exerts its action as a competing endogenous RNA (ceRNA), competing with miR-382-5p at targets level [85]. An increase in miR-382-5p expression together with a down-regulation of lncRNA Ftx and neuregulin-1 (Nrg-1) was reported in an animal model of neuropathic pain [85]. The lack of inhibition exerted by lncRNA Ftx on miR-382, is supposed to increase the inhibition of Nrg-1, thus facilitating pain and inflammation [85]. The involvement of Nrg-1 in pain was also reported in an animal model of inflammatory pain. Its reduction has been found in the dorsal root ganglia and spinal cord of mice, contributing to hypersensitivity [86]. Notably, increasing Nrg-1 expression facilitates analgesia and tissue repair by modulating glial cells proliferation, central nervous system injury repair and the reduction of the release of pro-inflammatory cytokine [85,[87][88][89]. Increased miR-382-5p expression in pain conditions may also be related to nuclear factor kappa B (NF-κB) signaling, implicated in migraine pain [90][91][92]. NF-κB acts as a transcription factor for many miRNAs [93], including miR-382 [94]. Indeed, the inhibition of NF-κB significantly suppressed miR-382 in vitro [94].  These observations suggest that the activation of the inflammatory pathways may lead to an up-regulation of miR-34a and miR-382 which in turn modulate the release of inflammatory and pain mediators (Figure 1).

Role of miR-30a in Migraine and Pain
Like many other miRNAs, miR-30a can target several different genes [97][98][99][100], of which many are connected with pathways related with pain transmission/modulation. Zhai and Zhu reported lower serum miR-30a levels in migraine patients compared to healthy subjects [93] (Tables 2 and 3). Interestingly, the authors also showed that miR-30a overexpression can degrade calcitonin/alpha-CGRP (Calca) gene in vitro, thus reducing CGRP levels [93].

Role of miR-30a in Migraine and Pain
Like many other miRNAs, miR-30a can target several different genes [97][98][99][100], of which many are connected with pathways related with pain transmission/modulation. Zhai and Zhu reported lower serum miR-30a levels in migraine patients compared to healthy subjects [93] (Tables 2 and 3). Interestingly, the authors also showed that miR-30a overexpression can degrade calcitonin/alpha-CGRP (Calca) gene in vitro, thus reducing CGRP levels [93].
TGF-β is known to downregulate miR-30a [101,102]. Given that high protein levels of TGF-β were found in migraine patients [74,75], it is worth speculating that, in contrast to what happens with miR-382, the increased TGF-β levels might negatively regulate miR-30a expression. This would lead to increased Calca expression and, consequently, to augmented CGRP levels. This pathway appears to be relevant for migraine, as it was hypothesized that Calca degradation may represent a protective mechanism in migraine progression [93].
In line with the above-mentioned observation, low levels of miR-30a were also found in animal models of neuropathic pain [103,104]. The involvement of miR-30a in pain modulation resides in its ability to regulate different pathways contributing to pain. For instance, miR-30a directly binds phosphatidyl Inositol 3-kinase (PI3K) [105] and Becn1 [106], the gene coding for Beclin 1, a core subunit of the PI3K complex. Up-regulation of miR-30a inhibits the PI3K/Akt/mTOR signaling pathway, thus resulting in a reduced central sensitization and pain relief [107][108][109]. In addition, miR-30a targets ten-eleven translocation methylcytosine dioxygenase 1 (TET1) [110], which is involved in the DNA demethylation of some genes linked to pain hypersensitivity, like brain-derived neurotrophic factor (BDNF) [111,112]. Accordingly, miR-30a levels were also found to be reduced in rats with spinal cord injuries, thus confirming the hypothesis that miR-30a may have a protective role when it comes to neuropathic pain [104].
Taken together, these findings support the role of miR-30a in pain modulation and suggest that a down-regulation of miR-30a in pain conditions may lead to an up-regulation of different pro-nociceptive effectors possibly involved in migraine pain. The overexpression of miR-30a may be a useful pathway to counteract pain in general and possibly also in migraine pain (Figure 1).

Role of Other miRNAs in Migraine and Pain
Recently, the micro-MIG study corroborated the hypothesis that the expression of different miRNA expression is altered in EM and CM when compared to a control group, although no specific miRNAs were identified [113].
Furthermore, differential expressions of miRNAs were reported in the serum and in circulating blood monocytes of people with migraine without aura compared to healthy controls. These alterations were predominantly represented by the downregulation of miR-181a, let-7b and miR-22, with only miR-27b found to be upregulated. Interestingly, the altered expression of these aforementioned miRNAs has been linked to a higher cardiovascular risk, potentially correlating with the well-known relationship between migraine and vascular dysfunction [94]. Along with miR-382-5p and miR-34a-5p, Andersen and co-workers also found increased levels of miR-29c-5p and miR-26b-3p in EM patients, suggesting a further dysregulation of GABAergic and interleukin (IL4 and IL1RA) signaling [46].
A subsequent in-depth analysis supported the link between migraine and endothelial dysfunction, demonstrating an altered expression of miRNAs related with endothelial function (miR-155, miR-126 and let-7) in EM patients without vascular risk factors when compared to healthy subjects [95]. Burstein et al. described alteration of up to 27 miRNAs in the periosteum of CM patients when compared to healthy controls [114]. These alterations led to an upregulated expression of 25 genes involved in inflammatory response and a downregulation in 11 genes involved in the opposite task [114].
A recent review suggested that migraine and major depression may share a similar mRNAs profile [115]. Indeed, among 12 miRNAs previously studied in migraine, 11 were also altered in depressive disorders. This observation further suggests caution in interpreting these miRNAs as single migraine-specific biomarkers [115].
Several miRNAs were studied during celecoxib administration [116]. miR-590-5p, in particular, appears a to be a target as it is specifically dysregulated in humans during migraine attack, in subjects with Complex Regional Pain syndrome and in mice with experimentally-induced chronic pain conditions [116].
More recently, a significant reduction in miR-375 expression, a specific miRNA related to cancer, metabolic and inflammatory diseases [117], was identified in the serum and saliva of migraine children taking symptomatic (NSAIDs) and preventive (long-term magnesium) drugs [50].
Finally, there is evidence of miRNA variation related to non-drug interventions, as suggested by the alteration in has-miR-590-5p and has-miR-660-3p expression induced by a 6-week ketogenic diet [96]. The precise biochemical mechanisms underlying this phenomenon are elusive, but the Authors invoked the antioxidant and antiinflammatory effects of the diet, together with the restoration of a physiological cortical excitability [118,119].
It is worth reporting that negative results failing to confirm changes in miRNA expression in migraine patients have also been published, with the main limitation generally represented by low sample sizes and limited statistical power [120].
A deep analysis of the role of miRNAs in non-migraine pain conditions is beyond the scope of the present review, but some of the clinical and preclinical findings derived from studies on pain may indirectly and effectively delineate the relationship between miRNA expression and migraine. In recent years, various pain models, such as inflammatory, neuropathic or diabetic pain models have included the evaluation of miRNAs [121]. Depending on the study conducted, both overexpression and suppression were reported in association with pain exacerbation [122]. miRNA expression varied across studies depending on the tissue specimen, the site of the nociceptive pathway evaluated and the time of collection after the experimental injury, thus showing a time and space-dependent expression [123][124][125][126]. In mice models of peripheral nerve injury, miR-21 was found consistently increased across various studies [127][128][129][130]. Bai et al. injected the complete Freund's adjuvant (CFA) in the masseter muscle of rats and subsequently analyzed the ipsilateral trigeminal ganglion specimen. They found that several miRNAs (miR-29a, miR-99, miR-124a and miR-134) were downregulated in the following hours, with a subsequent upregulation rebound days after the injection [123].
Regarding space-dependent expression, Kusuda et al. found a downregulation of miR-1, miR-16 and miR-206 in the dorsal roots of rats injected with CFA in the left hind paw. By contrast, concomitant analysis of the spinal dorsal horn showed a tardive upregulation of the same set of miRNAs [125].
These findings are consistent with the tissue-specific action of miRNAs involved in pain modulations, suggesting that the same miRNA may differently influence gene expression depending on the tissue specimen.
Human studies have focused primarily on detecting circulating miRNAs in cohorts of patients affected by chronic pain conditions, such as fibromyalgia, complex regional pain syndromes, inflammatory and irritable bowel syndromes, osteoarthritis and others. Given the large number of heterogeneous studies, only a fraction of findings has been consistently confirmed [131]. In fibromyalgia, the severity of pain inversely correlated with miR-320 and miR-145 levels [132,133]. A reduced expression of miR-320 was associated with chronic pain development in a cohort of patients who experienced motor vehicle collisions [134]. A consistent finding in studies investigating osteoarthritic pain is the general upregulation of miR-146, an alteration that was normalized by successfully treatment with balneotherapy [135].
miRNA expression was also explored as a possible diagnostic biomarker of pain disorders [129]. For instance, Dayer et al. proposed miR-320 and miR-98-5p as possible biomarkers for distinguishing neuropathic from non-neuropathic pain conditions [136].
Finally, there is increasing evidence from animal models of the potential role of miRNAs as a therapeutic target.
As previously mentioned, treatment with a miR-34a antagonist was effective in inducing analgesia in a rodent model of inflammatory pain induced by CFA [68,70]. Similarly, many other mimics or inhibitors of different miRNAs have been tested in several animal models of pain, proving their effectiveness [137,138].
There are currently several therapeutic strategies (polymeric vectors, lipid-based delivery systems, viral vectors) under consideration for both increasing and decreasing specific miRNA expression in selected tissues [139,140]. Some crucial aspects are yet to be addressed, namely the necessity to find vectors able to safely cross the blood-brain barrier, the evaluation of the drug-related toxicity and the ability to selectively target specific miRNAs to reduce the interaction with other genes not related to the target disease.

Discussion
Migraine represents a leading cause of disability, affecting young and adult people during the most productive years of their life. It also imposes an enormous economic burden on the society, mainly attributed to indirect related costs, such as work presenteeism and absenteeism.
Novel drug therapies modulating the CGRP pathways are now available, but their high cost and the presence of resistant patients imposes the need to continue research on novel therapeutic targets as well as on specific predictive biomarkers. Several biological and instrumental evaluations were suggested as potential migraine biomarkers, including genetic profiles, plasma and CSF neurotransmitters (CGRP, PACAP, VIP, glutamate), cytokines and neuroimaging alterations [7]. Although promising, none of these may truly be considered a solid biomarker, and further confirmation studies are needed. miRNAs have attracted the attention of the scientific community, initially to better understand the epigenetic impact of several physiological processes and, more recently, as possible diagnostic, monitoring and predictive biomarkers in a broad spectrum of pain and non-pain conditions. The data from the literature summarized here suggest that miRNAs may well have a place in the network of pathophysiological alterations that reflect the complexity of migraine.
Validated biological biomarkers may allow several steps forward in the management of migraine and primary headaches: (i) the refinement of the diagnosis according to biological features; (ii) the prediction of the response to advanced therapies; (iii) the improved selection of patients for clinical trials or in everyday practice; (iv) the identification of novel molecular targets for drugs development. Recent but increasing evidence suggests a role for miR-382-5p, miR-34a-5p and miR-30a in migraine.
These miRNAs are associated with migraine phenotypes and disease severity as suggested by their expression in peripheral blood mononuclear cells of EM or CM-MOH patients [51]. Notably, the association between miRNAs levels and the migraine phenotypes survived a multivariate correction for age, sex, disease duration and CGRP levels. Furthermore, miR-382-5p and miR-34a-5p expression in peripheral blood mononuclear cells of subjects of these two clinical populations positively correlated with CGRP plasma levels. In this context, it is worth mentioning that an increased expression of both miRNAs was also reported in a population of difficult-to-treat CM patients with and without medication overuse [52]. Collectively, these findings support a role for miR-382-5p and miR-34a-5p in migraine, which is partly, but probably not entirely, related to the interaction with the CGRP pathway.
Data from our group suggest that the expression of miR-382-5p and miR-34a-5p may be influenced by migraine treatments. Indeed, detoxification from overused acute drugs and migraine preventive treatment with erenumab negatively modulated the expression of both miRNAs [51,52]. Interestingly this biological effect was independent of the clinical outcome and of the reduction in central sensitization observed in erenumab responders. Accordingly, the baseline expression of miR-382-5p and miR-34a-5p was not capable of predicting the clinical response to erenumab. Although these observations seem to limit the clinical utility of these miRNAs for the prediction and monitoring of drug response, if confirmed, they will definitely provide a new perspective on the pathophysiological investigations of migraine mechanisms based on a more sophisticated subtyping of the large migraine population. Notably, Christensen et al. suggested that migraine responders to erenumab were characterized by a specific CGRP-phenotype, including: (i) an increased migraine-like induction rate to CGRP administration; (ii) a more severe headache during the induction test; and (iii) a long-lasting headache produced by CGRP administration [141].
Interestingly, another link between CGRP and miRNAs was recently reported by Zhai and Zhu [93]. They found reduced levels of miR-30a in migraine patients, a miRNA postulated to negatively modulate the gene coding for CGRP. Thus, miR-30a agonism may also represent an interesting novel therapeutic target for migraine.
The identification of single disease-specific biomarkers represents a priority of researchers operating in the migraine field.
Thus far, the available evidence on the possible role of migraine biomarkers for miR-382-5p, miR-34a-5p and miR-30a is compelling, although not entirely convincing. These molecules are involved in different ways in several processes and diseases related with pain, with a certain degree of complementary and synergic effects. Thus, it seems reasonable to hypothesize that in the future these miRNAs may qualify as part of a multibiomarkers panel signature of migraine, rather than as individual biomarkers. Such a panel will hopefully contribute to the possibility of identifying distinct phenotypes across the migraine spectrum, and ideally it will also help to predict responses to different treatments.
Finally, miRNAs modulation with pharmacological agonists ("agomir") and antagonists ("antagomir") has already been tested in non-migraine pre-clinical and clinical conditions. For instance, antagomirs targeting miR-27b, miR-107 and miR-155 as well as agomirs targeting miR-126 and miR-195 were tested in pre-clinical models of ischemic stroke, with promising pre-clinical results [142]. A miR-34a antagomir also produced analgesic effects in a pre-clinical pain model of the spinal cord [68]. In a phase 1 study, a miR-34a agonist was tested for safety and tolerability in patients with solid neoplasms. A dose-dependent modulation of target genes was demonstrated in white blood cells, but the trial was terminated early due to serious, immune-mediated, adverse events [143]. Constant drug development will hopefully lead to novel second generation miRNAs agomirs and antagomirs with improved safety profiles.
Several unanswered questions call for further research aimed at disentangling the characteristics and direction of the relationship between miRNAs and migraine.
Moreover, it is reasonable to state that miRNAs are involved in other primary and secondary headaches, such as tension-type headache, trigeminal autonomic cephalalgias, and post-traumatic headache. Finally, further investigations are needed to confirm the association between different migraine phenotypes and miRNAs expression.

Conclusions
The initial evidence prompts a possible role for miRNA profiling in migraine research. Clinical data on miR-382-5p, miR-34a-5p and miR-30a seem promising, but their scientific strength is limited by the lack of consistency across studies due to: (i) inhomogeneity or poor definition of migraine cohorts (EM, CM with and without MOH) and related comorbidities, (ii) small sample sizes and (iii) different types of specimens (e.g., blood, saliva, CSF) collected for miRNAs analysis. Further studies are therefore needed to confirm and expand on the role of miRNAs in migraine pathophysiology and management.
In the future, it will be important to tackle the different components of migraine in their dynamic manifestations. Indeed, migraine is a complex disorder characterized by recurring attacks, each defined by a sequence of phases: a prodromal phase, a pain phase either preceded or not by aura symptoms and a postdrome phase. The prodromal and postdrome phases have attracted the attention of the scientific community as they may represent the true timeframe for the study of the mechanisms involved in the origin and cessation of the migraine attack.
The availability of reliable and validated human migraine models will facilitate the study of miRNA expression in the different phases of the migraine cycle, prompting the possibility to set experimentally controlled conditions.