Recurrent spontaneous vertigo with interictal headshaking nystagmus
Sun-Uk Lee1, Jeong-Yoon Choi1, Hyo-Jung Kim1
1From the Department of Neurology (S.-U.L., J.-Y.C., J.-S.K.), Seoul National University College of Medicine, Seoul, South Korea; Dizziness Center (S.-U.L., J.-Y.C., J.-S.K.), Clinical Neuroscience Center, and Research Administration Team (H.-J.K.), Seoul National University Bundang Hospital, Seongnam, South Korea.
Recurrent spontaneous vertigo (RSV) with headshaking nystagmus (HSN) may stem from a hyperactive velocity-storage mechanism. This condition often resolves or improves over time, with no patients developing other vestibular disorders.
Area of Science:
- Neuroscience
- Ophthalmology
- Vestibular System Disorders
Background:
- Recurrent spontaneous vertigo (RSV) of unknown etiology is often accompanied by interictal headshaking nystagmus (HSN).
- Understanding the pathophysiology of RSV-HSN is crucial for diagnosis and management.
Purpose of the Study:
- To define a disorder characterized by recurrent spontaneous vertigo (RSV) and interictal headshaking nystagmus (HSN).
- To characterize HSN in patients with RSV-HSN and compare it to other vestibular disorders.
Main Methods:
- Characterized HSN in 35 patients with RSV-HSN.
- Compared HSN characteristics with patients suffering from compensated vestibular neuritis (VN), vestibular migraine (VM), and Ménière disease (MD).
- Assessed time constant (TC) of HSN and horizontal vestibulo-ocular reflex (VOR).
Main Results:
- Patients with RSV-HSN exhibited a significantly larger HSN time constant (12 seconds) compared to VN (5s), VM (5s), and MD (6s).
- Horizontal VOR time constants were also larger in RSV-HSN patients.
- Over half of the patients experienced symptom resolution or improvement within a median follow-up of 12 years.
Conclusions:
- RSV-HSN is linked to a hyperactive and asymmetric velocity-storage mechanism.
- This mechanism likely causes intermittent vertigo attacks when compensation is disrupted.
- The long-term prognosis for RSV-HSN is generally favorable, with no progression to VM, MD, or cerebellar dysfunction observed.
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