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Multicenter Study
. 2024 Nov;44(11):3331024241299453.
doi: 10.1177/03331024241299453.

Exploring the multifaceted characteristics of aura in migraine: A multicenter, cross-sectional study

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Free article
Multicenter Study

Exploring the multifaceted characteristics of aura in migraine: A multicenter, cross-sectional study

Giorgio Dalla Volta et al. Cephalalgia. 2024 Nov.
Free article

Abstract

Background: Migraine with aura (MwA) is a debilitating disorder characterized by paroxysmal attacks of pain preceded or accompanied by reversible neurological symptoms. While the pathophysiology remains unclear, trigeminovascular system activation and cortical spreading depression have been implicated. This study aims to comprehensively investigate and characterize the diverse clinical features and manifestations of aura, as well as the types of acute medications self-administered for aura management.

Methods: A multicenter, cross-sectional study was conducted using data from the Italian Headache Registry (RICe). Aura characteristics, frequency, duration and associated migraine premonitory symptoms were collected. Acute medication use and timing (headache or aura phase) were assessed.

Results: The study included 272 patients with a diagnosis of MwA. Most patients (99.3%) experienced typical aura symptoms, with visual aura (96.3%) being the most prevalent, followed by sensory (33.0%) and speech and/or language aura (25.6%). Brainstem aura (8.5%) and motor aura (1.8%) were less common. Notably, 13.0% of patients reported aura relapses within 24 hours. Triptans (39.7%), non-steroidal anti-inflammatory drugs (47.8%) and nutraceuticals (59.9%) were commonly used for acute aura management.

Conclusions: This study reports several different aura manifestations, highlighting atypical features, aura relapse rates and treatment approaches for aura. These findings could contribute to a deeper understanding of aura and its management in clinical settings.

Keywords: brainstem aura; cortical spreading depression; headache; visual aura.

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Conflict of interest statement

Declaration of conflicting interestsThe authors declared the following potential conflicts of interest with respect to the research, authorship and/or publication of this article: PG received personal fees from Allergan, Eli Lilly, Novartis, Amgen and TEVA; grants from Amgen, TEVA, Eli-Lilly, Allergan and Chiesi; is on the Scientific Advisory Board for Endosome Therapeutics; and is a founding scientist of FloNext srl, Spinoff of the University of Florence. FDC received personal fees from TEVA, Eli Lilly and Novartis. LFI received personal fees from Eli-Lilly and TEVA, and a travel grant from Lundbeck. SS reports personal fees as a speaker or advisor from Abbott, Allergan-AbbVie, AstraZeneca, Eli Lilly, Lundbeck, Novartis, NovoNordisk, Pfizer and Teva, and research grants from Novartis. RO reports personal fees from Novartis, Eli Lilly and Teva, and non-financial support from Novartis, Allergan, Eli Lilly and Teva. SG received personal fees from Allergan/AbbVie, Eli Lilly, Novartis, Teva and Lundbeck. Grazia Sances received personal fees as a speaker or was on the Advisory Board for Eli-Lilly, Novartis, TEVA, Lundbeck and Pfizer. RDI received speaker honoraria and advisory board participation: Eli-Lilly, TEVA, Lundbeck, Pfizer, AbbVie; MPP received speaker honoraria and advisory board participation from Abbvie, Idorsia, Eli-Lilly, Novartis, Pfizer, TEVA. The other authors have no conflicting interests.

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