Case Series: Vestibular Migraines in Fragile X Premutation Carriers

Author:

Tak YeEun12,Tassone Flora13ORCID,Hagerman Randi J.14ORCID

Affiliation:

1. University of California Davis School of Medicine, Sacramento Campus, Sacramento, CA 95817, USA

2. Medical Investigation of Neurodevelopmental Disorders (MIND) Institute, University of California Davis Health, Sacramento, CA 95616, USA

3. Department of Biochemistry and Molecular Medicine, University of California Davis, Sacramento, CA 95817, USA

4. Department of Pediatrics, University of California Davis Health, Sacramento, CA 95817, USA

Abstract

Background: Vestibular migraine (VM) is one of the most common causes of recurrent vertigo and presents with a history of spontaneous or positional vertigo with a history of migraine headaches. While research has identified a high prevalence of migraine headaches and vestibular deficits among fragile X premutation carriers, there has been no discussion about VM within this population. Objective: This case series and review seeks to describe the clinical characteristics and pathophysiology of VM among individuals with the fragile X premutation. We also seek to discuss treatment and future steps in addressing VM in this population. Methods: A review of the literature regarding vestibular migraine and presentation of migraine headaches and vestibular deficits among premutation carriers was performed. A detailed clinical history of migraine headaches and vertigo was obtained from three patients with the fragile X premutation seen by the senior author (RJH). Results: All three cases first developed symptoms of migraine headaches earlier in life, with the development of VM near menopause. Two of the three cases developed progressive balance issues following the development of VM. All three cases found that their VM episodes were improved or resolved with pharmacological and/or lifestyle interventions. Conclusions: It is important to recognize VM among premutation carriers because beneficial treatments are available. Future studies are needed regarding the prevalence of VM and the relationship to subsequent FXTAS. The pathophysiology of VM remains uncertain but possibilities include mitochondrial abnormalities, cranial nerve VIII toxicity secondary to neurotoxic protein accumulation, and calcitonin gene-related peptide (CGRP) signaling dysfunction due to altered levels of fragile X messenger ribonucleoprotein (FMRP).

Funder

NICHD

MIND Institute IDDRC

Victor La Fave III fund

Tides fund

Publisher

MDPI AG

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