Evidence map›Paper›PMID 41735859›Full record

Observational studyThe journal of headache and pain2026

Triggers, prodrome, aura, and headache interactions in migraine with typical aura: a prospective deep-phenotyping study.

Srdjan Mavija, Aleksandra Radojičić, Igor Petrušić

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in The journal of headache and pain, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

3 authors.

Srdjan MavijaNeurology Clinic, University Clinical Centre of the Republic of Srpska, Banja Luka, Republic of Srpska, Bosnia and Herzegovina. mavijasrdjan@gmail.com.
Aleksandra RadojičićHeadache Center, Neurology Clinic, University Clinical Center of Serbia, Belgrade, Serbia.
Igor PetrušićLaboratory for Advanced Analysis of Neuroimages, Faculty of Physical Chemistry, University of Belgrade, Belgrade, Serbia. ip7med@yahoo.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsThis study aimed to prospectively and comprehensively phenotype migraine with typical aura (MwA) attacks, with a particular focus on the interaction between trigger factors and clinical features of the prodrome, aura, and headache phases. A secondary aim was to examine how characteristics of individual phases influence the subsequent course of an attack and to provide data-driven hypotheses relevant for future MwA classification. METHODOLOGY: This was a prospective, multicenter observational study conducted at two tertiary headache clinics. Participants recorded up to three MwA attacks over 12 months using an electronic questionnaire completed within one day after each attack. Data on potential triggers, prodromal symptoms, detailed aura features (visual, somatosensory, and higher cortical dysfunctions), and headache characteristics were collected. Associations between attack phases, including trigger factors, were analyzed.

resultsA total of 90 participants (74% female) reported 144 MwA attacks. Triggers were reported in 82% of attacks, with lack of sleep (36%) and the menstrual cycle (24%) being the most frequent. Prodromal symptoms occurred in 75% of attacks, most commonly neck stiffness (29%) and photophobia (28%). The number of triggers positively correlated with the number of prodromal symptoms (r=0.372, p<0.001). Visual aura occurred in 98% of attacks, with 43% showing sudden onset and 31% presenting as monocular visual disturbances. Somatosensory symptoms were reported in 50% of attacks, and dysphasic symptoms in 40%. The aura preceded headache in 81% of attacks. Severe headache intensity was reported in 62% of cases, while exhaustion occurred in 81%. The presence of tingling, numbness, and dyspraxia during the aura phase was significantly associated with the development of cutaneous allodynia.

conclusionsThese findings suggest that MwA attacks represent a continuous and complex neurobiological process rather than a sequence of isolated phases, in which triggers and prodromal symptoms shape aura complexity, headache severity, and central sensitization. The frequent occurrence of atypical aura durations, sudden onset, and monocular-like visual disturbances in a prospective setting indicates that current MwA diagnostic frameworks may be overly restrictive. A more inclusive classification approach may be required to better capture the clinical heterogeneity of MwA and reduce underdiagnosis or misclassification.

Indexed as

Migraine with AuraProdromal SymptomsAdultFemaleHumansMaleMiddle AgedPhenotypeProspective StudiesAura phenomenologyHeadacheMigraine triggersProdromal symptomsVisual symptoms

Identifiers

PMID41735859
PMCPMC12934116

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.