The electrophysiological footprint of CACNA1A disorders.

Elisabetta Indelicato, Iris Unterberger, Wolfgang Nachbauer, Andreas Eigentler, Matthias Amprosi, Fiona Zeiner, Edda Haberlandt, Manuela Kaml, Elke Gizewski, Sylvia Boesch

Journal: Journal of neurology 2021;268(7):2493-2505

PMID: 33544220

Abstract

OBJECTIVES

CACNA1A variants underlie three neurological disorders: familial hemiplegic migraine type 1 (FHM1), episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6). EEG is applied to study their episodic manifestations, but findings in the intervals did not gain attention up to date.

METHODS

We analyzed repeated EEG recordings performed between 1994 and 2019 in a large cohort of genetically confirmed CACNA1A patients. EEG findings were compared with those of CACNA1A-negative phenocopies. A review of the related literature was performed.

RESULTS

85 EEG recordings from 38 patients (19 EA2, 14 FHM1, 5 SCA6) were analyzed. Baseline EEG was abnormal in 55% of cases (12 EA2, 9 FHM1). The most common finding was a lateralized intermittent slowing, mainly affecting the temporal region. Slowing was more pronounced after a recent attack but was consistently detected in the majority of patients also during the follow-up. Interictal epileptic discharges (IEDs) were detected in eight patients (7 EA2,1 FHM1). EEG abnormalities and especially IEDs were significantly associated with younger age at examination (16 ± 9 vs 43 ± 21 years in those without epileptic changes, p = 0.003) and with earlier onset of disease (1 (1-2) vs 12 (5-45) years, p = 0.0009). EEG findings in CACNA1A-negative phenocopies (n = 15) were largely unremarkable (p = 0.03 in the comparison with CACNA1A patients).

CONCLUSIONS

EEG abnormalities between attacks are highly prevalent in episodic CACNA1A disorders and especially associated with younger age at examination and earlier disease onset. Our findings underpin an age-dependent effect of CACNA1A variants, with a more severe impairment when P/Q channel dysfunction manifests early in life.

Address: Center for Rare Movement Disorders Innsbruck, Department of Neurology, Medical University of Innsbruck, Anichstrasse 35, 6020, Innsbruck, Austria.; Epileptology Division, Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.; Department of Pediatrics I, Medical University of Innsbruck, Innsbruck, Austria.; Department of Pediatrics, City Hospital, Dornbirn, Austria.; Department of Neuroradiology, Medical University of Innsbruck, Innsbruck, Austria.; Center for Rare Movement Disorders Innsbruck, Department of Neurology, Medical University of Innsbruck, Anichstrasse 35, 6020, Innsbruck, Austria. [email protected].
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