A novel pathogenic CACNA1A variant causing episodic ataxia type 2 (EA2) spectrum phenotype in four family members and a novel combined therapy

Episodic ataxias (EAs) are rare neurological disorders characterized by recurrent episodes of cerebellar ataxia with an imbalance of stance and gait, limb ataxia, dysarthria, and nystagmus, often triggered by physical or emotional stress, or alcohol and accompanied by nausea and vomiting (for review see [1, 2]). Currently, there are at least seven known subtypes of EA. Among them, EA1 and EA2 are clinically most relevant [2]. EA2 has its onset typically in adolescence, but some cases with a late onset have been reported [3]. EA2 episodes generally last between minutes and hours, and are accompanied by migraine-like cephalgia in around 50% of patients [4]. EA 2 patients frequently develop slowly progressive interictal ataxia and distinct central ocular motor dysfunctions, e.g., mainly gaze-evoked or downbeat nystagmus [4, 5]. EA2 is an inherited autosomal-dominant channelopathy, caused by pathogenic variants affecting the CACNA1A gene on chromosome 19p13, which encodes the alpha-1A subunit of the P/Q-type voltage-gated calcium channel (Cav2.1) [1, 6]. The latter is found ubiquitously in the nervous system with high expression levels in cerebellar Purkinje cells [7, 8]. EA2 shares molecular pathologic similarities with spinocerebellar ataxia type 6 (SCA6), familial hemiplegic migraine (FHM) and epileptic encephalopathy, also carrying mutations in the CACNA1A gene. Typically, cases of FHM present with missense mutations, SCA6 with a C-terminal polyglutamine expansion and EA2 harbors point mutations resulting in premature stop codons as well as small or large deletions, insertions and missense mutations [2]. During the last decades, an increasing number of CACNA1A variants have been described. Here, we report on a female patient with a novel pathogenic CACNA1A variant and give insights into the heterogeneous phenotypes within her family. A 47-year-old white Caucasian female presented to our tertiary outpatient center with recurrent attacks of postural imbalance (no vertigo sensu stricto, no nausea or vomiting) with the feeling of falling forward, and an associated holocephalic headache that began around the age of 15 years. The attacks occurred daily, most often in stressful situations and usually lasted for several hours. No other triggers were evident. By the time the patient presented to us, she felt permanently dizzy and posturally unstable in between the attacks, rendering her dependent on regular help in her daily routine. There was no catamnestic report of seizures or syncopes. Her clinical and neuro-ophthalmological examination revealed a cerebellar ocular motor dysfunction with bilateral horizontal gaze-evoked and rebound-nystagmus, saccadic pursuit in all directions, hypermetric horizontal and vertical saccades, reduced optokinetic nystagmus in all directions, and an most probably centrally impaired horizontal vestibulo-ocular reflex bilaterally (video head-impulse test: gain of 0.44 on the right and 0.35 on the left). Bithermal caloric testing showed a central preponderance of left-beating nystagmus without spontaneous nystagmus (warm right – 3.8°/s, warm left + 22.9°/s, cold right 6.4°/s, cold left – 2.0°/s). Finger-to-finger following showed slightly hypermetric movements. Romberg’s test revealed an imbalance in tandem stance. Quantitative gait analysis with the GAITRite system * Josef Penkava josef.penkava@med.uni-muenchen.de


Dear Sirs,
Episodic ataxias (EAs) are rare neurological disorders characterized by recurrent episodes of cerebellar ataxia with an imbalance of stance and gait, limb ataxia, dysarthria, and nystagmus, often triggered by physical or emotional stress, or alcohol and accompanied by nausea and vomiting (for review see [1,2]). Currently, there are at least seven known subtypes of EA. Among them, EA1 and EA2 are clinically most relevant [2]. EA2 has its onset typically in adolescence, but some cases with a late onset have been reported [3]. EA2 episodes generally last between minutes and hours, and are accompanied by migraine-like cephalgia in around 50% of patients [4]. EA 2 patients frequently develop slowly progressive interictal ataxia and distinct central ocular motor dysfunctions, e.g., mainly gaze-evoked or downbeat nystagmus [4,5]. EA2 is an inherited autosomal-dominant channelopathy, caused by pathogenic variants affecting the CACNA1A gene on chromosome 19p13, which encodes the alpha-1A subunit of the P/Q-type voltage-gated calcium channel (Cav2.1) [1,6]. The latter is found ubiquitously in the nervous system with high expression levels in cerebellar Purkinje cells [7,8]. EA2 shares molecular pathologic similarities with spinocerebellar ataxia type 6 (SCA6), familial hemiplegic migraine (FHM) and epileptic encephalopathy, also carrying mutations in the CACNA1A gene. Typically, cases of FHM present with missense mutations, SCA6 with a C-terminal polyglutamine expansion and EA2 harbors point mutations resulting in premature stop codons as well as small or large deletions, insertions and missense mutations [2]. During the last decades, an increasing number of CACNA1A variants have been described. Here, we report on a female patient with a novel pathogenic CACNA1A variant and give insights into the heterogeneous phenotypes within her family.
A 47-year-old white Caucasian female presented to our tertiary outpatient center with recurrent attacks of postural imbalance (no vertigo sensu stricto, no nausea or vomiting) with the feeling of falling forward, and an associated holocephalic headache that began around the age of 15 years. The attacks occurred daily, most often in stressful situations and usually lasted for several hours. No other triggers were evident. By the time the patient presented to us, she felt permanently dizzy and posturally unstable in between the attacks, rendering her dependent on regular help in her daily routine. There was no catamnestic report of seizures or syncopes.
Her clinical and neuro-ophthalmological examination revealed a cerebellar ocular motor dysfunction with bilateral horizontal gaze-evoked and rebound-nystagmus, saccadic pursuit in all directions, hypermetric horizontal and vertical saccades, reduced optokinetic nystagmus in all directions, and an most probably centrally impaired horizontal vestibulo-ocular reflex bilaterally (video head-impulse test: gain of 0.44 on the right and 0.35 on the left). Bithermal caloric testing showed a central preponderance of left-beating nystagmus without spontaneous nystagmus (warm right -3.8°/s, warm left + 22.9°/s, cold right 6.4°/s, cold left -2.0°/s). Finger-to-finger following showed slightly hypermetric movements. Romberg's test revealed an imbalance in tandem stance. Quantitative gait analysis with the GAITRite system 1 3 objectified a dynamic instability due to incipient impaired cerebellar postural adjustment. Cranial MRI showed several small supratentorial white matter lesions, but no distinct vermian atrophy as is sometimes reported in EA 2 [1].
Genetic testing using next-generation sequencing and Sanger sequencing methods (i.e. enrichment of the genes CACNA1A, CACNB4, KCNA1, SCN2A, and SLC1A3, followed by next-generation sequencing of coding exons as well as conserved parts of splice sites, and bioinformatic data analysis; hereby, in a first step an analysis of variants of the CACNA1A gene was performed prior to confirmation of the variant by amplification with polymerase chain reaction and analysis by Sanger sequencing after a second, independent DNA extraction from the original blood sample) revealed a novel, heterozygous, pathogenic [9,10]  (Exome Aggregation Consortium) or GnomAD (Genome Aggregation database). Other translational stop variants in the CACNA1A gene have been described in EA2 patients before [11,12].
The same heterozygous CACNA1A variant was detected in three family members (Fig. 1) of our index patient, but the clinical phenotypes varied considerably. The 68-year-old mother is suffering from a slowly progressive imbalance of gait for almost 20 years. She negated cephalgia, episodic ataxia or vertigo. Her imbalance of gait is not accompanied by vegetative symptoms such as nausea or emesis. There are no triggers evident. Neurological examination of the oculomotor system revealed a gaze-evoked nystagmus to the right side. Romberg's test showed omnidirectional swaying and finger-to-nose testing showed a slight dysmetria on both sides. Her gait was broad based and atactic. She has been taking acetazolamide (250 mg/days) for about 3 months with no significant amelioration of her symptoms. The 45-yearold brother of our patient reported intermittent cephalgia, which started in his early childhood. He negated any recurrent attacks of postural imbalance, ataxia or vertigo. He does not take any medication regularly apart from NSAR temporarily. Neurological examination was without pathological findings. The 15-year-old nephew of our patient (her brother's son) has suffered from episodic attacks with imbalance of gait, vertigo, and headache, typically lasting for several hours and triggered by stress since the age of 14 years. In between the attacks, he feels asymptomatic.
Pathogenic variants in the CACNA1A gene are known to lead to a broad clinical spectrum including EA2, SCA6, FHM and epileptic encephalopathy. Different variants usually tend to associate with different phenotypes, but sometimes family members harboring the same variant show a wide variability of the neurological manifestations [4,13]. One further reason for the heterogeneous phenotype in our reported family could be incomplete penetrance. There is substantial evidence of intra-familial incomplete penetrance due to a pathogenic CACNA1A variant in the literature [4,14]. Nevertheless, an involvement of other genes and epigenetic mechanisms cannot be excluded.
Therapeutic principles in patients with EA include medical treatment and physiotherapy, occupational therapy to preserve gait function, and speech therapy [15,16]. In a randomized placebo-controlled trial, it was shown that 4-aminopyridine [17] is effective for the symptomatic treatment of EA2 (and downbeat nystagmus) [18]. Our patient did not respond sufficiently to the medical monotherapeutic treatments of choice with 4-aminopyridine (Fampyra™ 20 mg/ days) and acetazolamide (250 mg-500 mg/days, discharged due to intolerable side effects such as paresthesia and kidney dysfunction) [19]. The modified amino acid acetyl-dlleucine has been introduced as a drug for the symptomatic treatment of cerebellar disorders [20,21]. Under reduction of 4-aminopyridine, the patient indicated significant aggravation of her previously described symptoms. Consequently, we reestablished the well tolerated daily dose of 4-aminopyridine (20 mg/days). However, the effect of the medication was not fully satisfactory to the patient. Therefore, we applied ex juvantibus a combined individual therapeutic approach with 4-aminopyridine (Fampyra™ 20 mg/days) and acetyl-dl-leucine (5 g/days) in a second step. Over the ensuing observation period of 12 months, a subjectively relevant improvement of the patient's daily performance, accompanied by a stabilization of objective clinical and functional measures such as videooculography (no deterioration of ocular motor function), gait analysis (increase in velocity and step length) and ataxia scores (SARA score 4) could be observed interictally.
In conclusion, we identified a novel, pathogenic heterozygous CACNA1A variant NM_001127221.1: [c2070_2071delinsGGAG, p.(Phe690Leufs*9)] in a patient with EA2 and three other family members with a long undiagnosed history of the illness and a very heterogeneous phenotype across three generations of the family carrying the identical variant. The analysis of novel CACNA1A variants is an essential step in the in-depth characterization of EA2 patients. Our results might serve for molecular-genetic testing in similar patients, albeit future genetic analyses will most likely use high-throughput sequencing. From a therapeutic perspective after the patient did not respond sufficiently to standard treatment, a novel combination of 4-aminopyridine (Fampyra™ 20 mg/days) to reduce the frequency of attacks, and acetyl-dl-leucine (5 mg/days) to symptomatically alleviate interictal cerebellar ataxia resulted in subjective improvement and no further progression of the disease to date. Such combined therapies might have an over-additive effect because of different modes of action and may open up a new treatment path in EA2 individuals, especially in cases where 4-aminopyridine or acetazolamide medication alone does not alter the course of the disease. However, further randomized placebo-controlled trials in episodic ataxias are needed.