Objectives: We and others showed that migraineurs are at increased risk of subclinical and clinical ischemic brain lesions. Migraineurs also have a higher prevalence of frequent syncope and orthostatic intolerance, symptoms that are associated with transient reductions in cerebral blood flow. In this study, we assessed whether these autonomic symptoms may contribute to the increased risk of brain lesions in migraine.Methods: Migraineurs (n 5 291) and controls (n 5 140) from the population-based, cross-sectional CAMERA (Cerebral Abnormalities in Migraine, an Epidemiologic Risk Analysis) cohort (aged 30-60 years, and free of other neurologic symptoms) underwent 1) brain MRI scan, and 2) structured telephone interview including questions on frequent syncope ($5/lifetime) and orthostatic intolerance.Results: Frequent syncope (odds ratio [OR] 5 2.7; 95% confidence interval: 1.3-5.5) and orthostatic intolerance (OR 5 2.0 [1.1-3.6]) were independent risk factors for high load of deep white matter lesions. Effects were strongest in women and similar in migraineurs and controls. Migraine diagnosis did not mediate or moderate these associations. Individuals with orthostatic intolerance had higher prevalence of high periventricular white matter lesion load (OR 5 1.9 [1.1-3.5]). Syncope and orthostatic intolerance were not related to subclinical infarcts or infratentorial lesions. Migraine is a common neurovascular brain disorder characterized by attacks of disabling headache, autonomic dysfunction, and sometimes aura symptoms.
Conclusions:1 Although suffering a migraine attack is ranked among the most painful and disabling disorders, 2 the disease migraine is commonly not believed to have long-term brain consequences.However, we found in the population-based CAMERA (Cerebral Abnormalities in Migraine, an Epidemiologic Risk Analysis) study that female migraineurs are at increased risk of deep white matter hyperintense lesions (WMLs), and that both male and female migraineurs have a higher prevalence of infratentorial brain lesions, including hyperintense brainstem lesions and cerebellar infarcts.3,4 This association was not modified by cardiovascular risk factors or use of vasoconstricting antimigraine medication. These MRI lesions appear to have developed subclinically, but they might still be relevant in view of the findings of a meta-analysis showing that migraine is a risk factor for ischemic stroke.5 Furthermore, WMLs have in general a predictive value for future stroke and cognitive and functional decline. 6 The mechanisms leading to increased risk of brain lesions in migraineurs remain unknown.