ATP2B2 encodes the PMCA2 Ca2+ pump that plays an important role in maintaining ion homeostasis in hair cells among others by extrusion of Ca2+ from the stereocilia to the endolymph. Several mouse models have been described for this gene; mice heterozygous for loss-of-function defects display a rapidly progressive high-frequency hearing impairment. Up to now ATP2B2 has only been reported as a modifier, or in a digenic mechanism with CDH23 for hearing impairment in humans. Whole exome sequencing in hearing impaired index cases of Dutch and Polish origins revealed five novel heterozygous (predicted to be) loss-of-function variants of ATP2B2. Two variants, c.1963G>T (p.Glu655*) and c.955delG (p.Ala319fs), occurred de novo. Three variants c.397+1G>A (p.?), c.1998C>A (p.Cys666*), and c.2329C>T (p.Arg777*), were identified in families with an autosomal dominant inheritance pattern of hearing impairment. After normal newborn hearing screening, a rapidly progressive high-frequency hearing impairment was diagnosed at the age of about 3–6 years. Subjects had no balance complaints and vestibular testing did not yield abnormalities. There was no evidence for retrocochlear pathology or structural inner ear abnormalities. Although a digenic inheritance pattern of hearing impairment has been reported for heterozygous missense variants of ATP2B2 and CDH23, our findings indicate a monogenic cause of hearing impairment in cases with loss-of-function variants of ATP2B2.
Hearing impairment (HI) is an important cause of social burden worldwide (WHO 2008). The reported incidence in early childhood varies from 1 to 3/1000 (Wroblewska-Seniuk et al. 2017). It is estimated that early onset sensorineural HI (SNHI) is hereditary in about 50% of the cases and in 20% of the cases nonsyndromic SNHI is inherited in an autosomal dominant pattern (Smith et al. 2005). Until now, more than 60 loci and 37 genes have been identified for autosomal dominant nonsyndromic SNHI (Hereditary Hearing loss Homepage). Still, for many subjects with congenital or childhood-onset HI, a genetic diagnosis cannot be provided (Zazo Seco et al. 2017). For several of the genes (recently) described to be associated with early onset HI, defects have so far been found in only a few or one single family. To confirm the association of such genes with HI, additional supportive data are required. Mouse models have contributed such evidence for several genes and have been of great significance by providing candidate genes for HI in humans (Brown et al. 2008; Friedman et al. 2007; Wesdorp et al. 2018).
The plasma membrane Ca2+ ATPase 2 (PMCA2), encoded by Atp2b2, has already been known for 2 decades to be essential for hearing and balance in mouse (e.g. the deafwaddler mouse) (Street et al. 1998). It is one of the two PMCAs with a tissue-specific expression; PMCA2 is mainly expressed in the inner ear, the cerebellum and the mammary gland. Alternative splicing of Atp2b2 transcripts results in several PMCA2 isoforms, e.g. PMCA2 w/a, or z/a [for review (Strehler and Zacharias 2001)]. Isoform PMCA2 w/a is the major PMCA2 isoform in the organ of Corti and is encoded by a transcript with three alternatively spliced exons at the first alternative splice site, site A (Grati et al. 2006; Hill et al. 2006). Given the structural and functional homology of the inner ear in mice, rat and human, PMCA2 was anticipated to be critical for hearing in humans as well, and indications for that have already been reported. A hypofunctional variant of PMCA2 (p.Val586Met) was found to aggravate HI in a family with a homozygous CDH23 variant (Schultz et al. 2005). Moreover, digenic inheritance of SNHI was suggested in an isolated case with heterozygous missense variants in both ATP2B2 and CDH23 (Ficarella et al. 2007). Furthermore, SNHI in cases with the 3p deletion syndrome (MIM 613792) was suggested to be correlated with haploinsufficiency of ATP2B2 (McCullough et al. 2007). A heterozygous missense variant in ATP2B2 has recently been associated with ataxia but without HI; the identified variant functionally affected a PMCA2 isoform that is expressed in the cerebellum but not prominently in the inner ear (Vicario et al. 2018). Finally, two de novo truncating variants in ATP2B2 have been reported in a study on autism (Takata et al. 2018). These studies, however, do not provide evidence for a causative association of ATP2B2 with monogenic SNHI.
Here, we report four different heterozygous truncating variants and one canonical splice site variant in ATP2B2 in families with nonsyndromic progressive SNHI. In two of the families, the variants are de novo. All variants affect exons, or their splice sites, that encode the ortholog of the rat PMCA2 w/a isoform. This isoform is highly abundant in stereocilia of outer hair cells (OHC) and to a lesser extent at the apical surface of inner hair cells (IHC) (Hill et al. 2006).
Materials and methods
This study was approved by the medical ethics committee of the Radboud University Medical Center in Nijmegen, the Netherlands and was carried out according to the Declaration of Helsinki. Written informed consent was obtained from all participants or their legal representatives. Medical history was taken from all participants, with special attention paid to (acquired) HI and vestibular symptoms. Affected individuals underwent general ear, nose and throat (ENT) examinations in the Radboud University Medical Center or findings of ENT examination were taken from their medical history. Pure tone audiometry (PTA) was performed according to current standards in a sound-attenuating booth, where air conduction hearing thresholds for the frequencies from 250 Hz to 8 kHz were measured. Bone conduction thresholds were measured for the frequencies 500 Hz–8 kHz. The age- and gender-specific 95th percentile thresholds for individual hearing levels for each frequency were derived from the International Organisation for Standardization; ISO 7029:2017. Individuals were considered affected when pure tone thresholds for at least three frequencies were below the 95th percentile (P95) for the better hearing ear. The GENDEAF guidelines for the description of audiological data were applied in this study (Mazzoli et al. 2003). GraphPad Prism 6.0 (GraphPad, San Diego, CA, USA) was used to calculate an age-related typical audiogram (ARTA), based on linear regression, for the ages of 10–70 years as described (Huygen et al. 2003). Speech perception was assessed in a sound-attenuating booth with standard monosyllabic consonant–vowel–consonant Dutch word lists (Bosman and Smoorenburg 1995). Otoacoustic emissions and click-evoked brainstem-evoked response audiometric (BERA) measurements were performed according to current standards. In the Netherlands, the first step of newborn hearing screening is carried out by the detection of transient evoked otoacoustic emissions (TEOAE) (van der Ploeg et al. 2012). If applicable, results of newborn hearing screening were assessed by hetero-anamnesis of parents. Vestibular function was assessed by electronystagmography (ENG), caloric irrigation testing, rotary chair stimulation and video head impulse tests (vHIT), as described previously (Oonk et al. 2015). Additionally, cervical and ocular vestibular-evoked myogenic potentials (cVEMP/oVEMP) were measured to assess saccular and utricular function, respectively, as described (Papathanasiou et al. 2014; Vanspauwen et al. 2017). When responses were seen at ≤ 100 dB hearing level in cVEMP testing, saccular function was considered as present, otherwise absent (Papathanasiou et al. 2014). For oVEMPs, this normal value is ≤ 140 dB force level (Vanspauwen et al. 2017).
Subjects V.2 of family W18-0139 and I.1 of family W17-0883 were not able to participate in clinical evaluations, but retrospective data were analyzed. Subjects IV.3, IV.4 and V.1 of family W18-0139 did not consent for the study.
DNA was extracted from peripheral blood samples according to standard procedures. Exomes were enriched with the Agilent SureSelectXT Human AllExon v4 or v5 kit (Santa Clara, CA, USA) and sequencing was performed on an Illumina HiSeq4000 system by BGI Europe (Copenhagen, Denmark). Read alignment to the human reference genome (GrCH37/hg19) and variant calling was performed using BWA (Li and Durbin 2009) and GATK (Broad Institute, Cambridge, MA, USA) software, respectively. Variant annotation was performed using a custom-designed in-house annotation and variant evaluation pipeline. First, whole exome sequence (WES) data were analyzed for variants in a panel of 142 genes known to be associated with nonsyndromic HI and relatively common syndromic forms of HI (gene list version DG 2.5; Hereditary Hearing Loss Exome Panel Genome Diagnostics Nijmegen-Maastricht, see Online Resource Table S1) in a diagnostic setting. Variants in the 142 deafness-associated genes were classified according to guidelines from the Association for Clinical Genetic Science and the Dutch Society of Clinical Genetic Laboratory Specialists (Wallis et al. 2013). To address other recently published deafness genes, WES data of all subjects were reanalyzed with the most recent version of the gene panel, version DG 2.11, which consists of 159 deafness genes, see Online Resource Table S1. Variants of the complete exome were evaluated according to the criteria described in the supplemental methods section (see Online Resource).
Mean 20x coverage of the enriched regions in WES ranged between 93.5 and 98.0%. Copy number variation (CNV) was addressed by depth of coverage analysis with CoNIFER as described (Krumm et al. 2012; Pfundt et al. 2017). Segregation analysis of selected variants was carried out by Sanger Sequencing, as described (Wesdorp et al. 2018). Primer sequences are available upon request. Confirmation of parental identities in the cases with de novo variants was performed with the AmpFLSTR™ Identifiler™ kit, according to the manufacturer’s protocol (Applied Biosystems, Thermo Fisher Scientific MA, USA).
Sequencing of CDH23 for individuals I.1 and II.1 of family W17-0883 and III.3 of family W18-0139 was performed by massive parallel ion semiconductor sequencing as described (Diekstra et al. 2015).
Loss-of-function variants in ATP2B2 are associated with hearing impairment
An otherwise healthy subject of Dutch origin with childhood-onset, rapidly progressive nonsyndromic SNHI (family W18-0138, III.1, Fig. 1) was referred to our out-patient clinic for etiologic consultation. First, GJB2 was screened in routine diagnostics, which revealed a heterozygous variant of uncertain significance c.647G>T (NM_004004; p.Arg216Ile) [DFNA3A, (MIM 601544); DFNB1, (MIM 220290)]. This variant was not associated with autosomal dominant HI as it was inherited from the unaffected mother. In addition, no variant was identified in the second GJB2 allele by Sanger sequencing. Therefore, defects in GJB2 were not considered to underlie the HI in the presented case. Subsequently, WES was performed, which revealed neither other (likely) pathogenic variants in genes of the deafness gene panel (version DG 2.5), nor CNVs of these genes. Finally, analysis of the complete WES data (beyond the gene panel for deafness) was carried out. Truncating variants and variants of canonical splice sites were considered potentially deleterious. Furthermore, other potentially pathogenic variants that met the criteria as provided in the supplemental methods section were considered (See Online Resource). This analysis revealed a truncating variant in ATP2B2: c.955delG (NM_001001331.2, p.Ala319fs), which was neither present in our in-house database (~ 20,000 exomes) nor in gnomAD (version r2.02) (Lek et al. 2016). Importantly, the ATP2B2 variant was not found in the parents and as both parental identities were confirmed, the variant was considered to be de novo (Fig. 1). Several heterozygous missense and truncating defects of the mouse ortholog of ATP2B2 were associated with early onset, progressive high-frequency HI (Bortolozzi et al. 2010; Carpinelli et al. 2013; Kozel et al. 1998; McCullough and Tempel 2004; Spiden et al. 2008; Street et al. 1998; Takahashi and Kitamura 1999; Tsai et al. 2006; Watson and Tempel 2013; Xu et al. 2011). Therefore, we regarded the ATP2B2 variant to be an excellent candidate cause of the HI in this subject.
To confirm the association of ATP2B2 defects with SNHI in humans, WES data of about 700 index cases were analyzed for truncating variants and variants in canonical splice sites in this gene. In 110 of these cases, a dominant inheritance pattern of HI was indicated by the referring clinician. Defects of known genes associated with HI were previously excluded for these cases in routine diagnostics, as indicated in the methods section. Three cases were found to have nonsense variants in ATP2B2, and one case a variant in a canonical splice site (Table 1). All four cases had a reported onset of HI in the first decade (Table 2). Segregation analysis of the ATP2B2 variants in the respective families demonstrated that the c.1963G>T variant in subject III.2 of family W17-4352 was de novo, as it was not detected in the parents (Fig. 1) while both parental identities were confirmed. In families W17-0883 and W18-0111, the identified ATP2B2 variants co-segregated with the HI in three and one affected family members, respectively. In family W18-0139, the ATP2B2 variant was present in two participating family members with early onset HI (IV.2 and V2) but also in individual III.3 who reported a late onset of HI, at the age of 55 years.
Other variants that could potentially be causative for HI in the families were addressed (Online Resource Tables S2 and S3). For families W18-0138 and W17-4352, both a dominant and recessive inheritance patterns were addressed. 11 variants met the described criteria and their segregation in the respective families was determined (Online Resources Fig. S1 and Table S2). In families W18-0138 and W17-4352, identified variants with a potentially dominant effect were not de novo but derived from a normal hearing parent and, therefore, considered unlikely to be pathogenic. Variants with a potentially recessive effect were only found in DNM1 (family W17-4352), a gene that is associated with deafness in mouse (Boumil et al. 2010). However, the variant of one of the alleles was predicted to be synonymous and to have no effect on splicing. In the families with dominantly inherited HI, only one candidate variant, c.3226G>C (p.Asp1076His) in MYO6, co-segregated with the HI in family W18-0111.
Since digenic and modifier mechanisms have been described for the combination of CDH23 and ATP2B2 variants (Ficarella et al. 2007; Schultz et al. 2005), we evaluated all rare variants in CDH23 in the index cases. CDH23 was completely covered in WES by at least ten reads for all coding exons. Six rare variants, named VC1–VC6, were identified and segregation analysis was performed (Online Resource Table S3 and Fig. S1). Four variants (VC1–VC4) are missense variants predicted to have a deleterious effect by at least two of the employed pathogenicity prediction tools. VC2 and VC3 are located in cis on the paternal allele and are co-inherited with the ATP2B2 variant in family W18-0111. VC1 and VC4 co-occurred with the de novo variants in families W18-0138 and W17-4352, respectively. Therefore, no segregation analysis was carried out. For an intronic (VC5) and a synonymous (VC6) variant, no effects on splicing or protein function were predicted. Also, VC5 does not co-segregate with the ATP2B2 variant (and HI) in family W17-0883. Sequencing of CDH23 was performed in individuals I.1 and II.1 (W17-0883) to identify other variants in this gene that might contribute the HI. This revealed only common variants. VC6 co-occurred with the ATP2B2 variant in subjects IV.2 and V2 of family W18-0139, but not in individual III.3. The latter reported to have developed HI around the age of 55 years. Sequencing of CDH23 in this individual revealed that he carries the VC1 variant heterozygously.
Characteristics of ATP2B2-associated HI
None of the affected subjects or their parents reported exposure to excessive noise, long-term usage of antibiotics, history of head trauma or meningitis. Subjects III.3 and IV.2 of family W18-0139 reported complaints of tinnitus. All four subjects who underwent newborn hearing screening passed the first screening (Table 2). HI in all except two participating affected subjects was bilateral, sensorineural, symmetric, and mild to profound. For individual IV.2 of family W18-139, who repeatedly underwent ear surgery of the left ear, and I.1 of family W17-0883 who had a conductive HI on his left ear due to previous cholesteatoma surgery, only data of the right ears are depicted and included in further evaluations. For the other subjects, mean air conduction threshold values are depicted in Fig. 2 and employed in further analyses. Audiogram configurations were (steeply) downsloping (Fig. 2) and the age of onset was in the first decade with one exception (Table 2). Subject III.3 of family W18-0139 reported an onset age of 55 years, but no audiometry was performed before the age of 64 years. His hearing is clearly below the P95 for presbyacusis for the higher frequencies. Other affected subjects (IV.3, IV.4 and V.1) in this family did not participate in the clinical and genetic evaluations, but on hetero-anamnesis they had an early childhood onset of HI. Subject III.3 reported that his father, paternal aunts and grandmother had HI early in life and that they were wearing hearing aids.
Speech reception thresholds in general were lower than or comparable to pure tone average thresholds (0.5–2 kHz), indicating the absence of retrocochlear pathology. This was confirmed by BERA measurements in four subjects (Online Resource Table S4, data not shown).
An ARTA was calculated to provide insight in the progression of the HI per decade (Fig. 2b). The average annual threshold deterioration (ATD) for the ages 10–70 was 0.5 dB/year for the low frequencies (250–500Hz), 1.1 db/y for middle frequencies (1–2 kHz) and 0.7 dB/year for the high frequencies (4–8 kHz). Under the age of 10 years, audiograms tend to be less reliable due to more prevalent otitis media with effusion or less co-operation or cognitive capabilities of the young subjects. To give insight in the HI at this age, we calculated the average thresholds of all subjects with a hearing test at about 5 years of age (Fig. 2b, dashed line).
Five subjects underwent computed tomography (CT) and/or magnetic resonance imaging (MRI) of the bilateral temporal bones/cochlea and cerebellopontine angle, which revealed normal inner and middle ear anatomy, except for the left ear of subject IV.2 of family W18-0139 for reasons already indicated (Table 2).
Results of vestibular testing
Vestibular history was obtained from all subjects and extensive vestibular testing of at least one affected subject per family (except for family W17-4352) revealed only minor vestibular abnormalities (see Online Resource Table S4). Two subjects reported vestibular complaints; one was diagnosed with benign paroxysmal position vertigo (BPPV) and the second had complaints due to a perilymph leakage at cholesteatoma surgery. Saccular function could not be measured in subjects III.1 of family W18-0138 (bilaterally), III.1 (left ear) of W18-0111, and IV.2 of W18-0139 (left ear), whereas utricular function was not measurable in III.1 of family W18-0138. Maximum stimulus levels were reached in all these subjects.
In this study, five families were presented, in which four mono-allelic truncating variants and one canonical splice site variant in ATP2B2 co-segregated with early onset progressive nonsyndromic SNHI and with late-onset SNHI in one subject. All five variants affected the (predicted) ortholog of the w/a isoform of PMCA2, which is the predominant Ca2+ATPase in rodent hair cells and specifically localizes to stereocilia (Grati et al. 2006; Hill et al. 2006). In man, transcripts encoding the w/a isoform of PMCA2 have so far not been identified but the w splicing pattern has been shown (ENSEMBL, UCSC genome browser). See Online Resource Fig. S2 for a schematic representation of the different isoforms and positions of the variants. The truncating variants can be predicted to have a loss-of-function effect. This might also be the case for the splice site variant by inducing skipping of exon 3, retention of intron 3 or the use of an alternative exonic or intronic splice site. Skipping of exon 3 (198 nucleotides) is predicted to result in the depletion of 66 amino acids from the N-terminal part of the protein, including the first transmembrane region (See Online Resource Fig. S3 for splice prediction). Two of the truncating variants occurred de novo, which supports pathogenicity of the variants. A causal association with disease is further strengthened by a pLI score of 1.00 reported for ATP2B2. This score is an indication of extreme loss of function intolerance of ATP2B2 (Lek et al. 2016). The DOMINO variant effect prediction tool, predicts ATP2B2 to be very likely associated with a dominantly inherited disorder (Quinodoz et al. 2017) which is in agreement with the inheritance pattern of HI in the described families.
As digenic inheritance of HI was proposed for mono-allelic missense variants in ATP2B2 and CDH23 (Ficarella et al. 2007), we addressed this type of inheritance in the families in our study. Although rare CDH23 variants co-occurred with ATP2B2 variants in all five index cases, our findings indicate that mono-allelic loss-of-function variants of ATP2B2 are the underlying cause of HI. First, the CDH23 variant VC5 in individuals III.1 and III.2 of family W17-0883 is intronic and predicted not to affect splicing. Furthermore, this variant was not found in the affected family members I.1 and II.1, who also did not carry any other rare CDH23 variants in the coding sequences or flanking intronic regions. Second, the synonymous CDH23 variant VC6 in family W18-0139 is predicted not to affect the existing splice sites nor to introduce such sites. Although this variant did co-segregate with early onset HI in the family, subject III.3 with late-onset HI carried a different CDH23 variant, namely missense variant VC1 that is also seen in the index case of family W18-0138. Third, none of the variants has been classified as (likely) pathogenic in Clinvar (VC1–VC3, (likely) benign; VC4, uncertain significance; VC6, conflicting, UV1/UV2/UV3) and all but one (VC4) occur relatively frequently in gnomAD. Only variants in deep intronic regions or promoter regions were not addressed and can, therefore, not be excluded. CNVs of CDH23 can be excluded for the index cases only. Finally, the affected individual in the family reported by Ficarella et al. was pre-screened only for mutations in GJB6, MYO6, CDH23, and the most common mutations in GJB2 (Ficarella et al. 2007). As many of the known genes associated with recessive HI were not tested, several of which are commonly involved (e.g. MYO15A), defects in other deafness genes cannot be excluded in the reported case. We cannot exclude a modifying effect of the CDH23 variants on HI in the affected subjects in our study, as has been reported for mouse mutants of Atp2b2 (McCullough and Tempel 2004).
As indicated by the pLI score of 1.00, loss-of-function variants in ATP2B2 are rare. In gnomAD, eight such variants are reported heterozygously, representing 26 alleles. Three of these variants, representing 21 alleles, affect canonical splice sites of the alternatively spliced exons 7–9 at site A and all three are in frame (see Online Resource Fig. S2). One of these three variants, c.1001-1G>A (NM_001001331.2), was identified in 19 non-Finnish Europeans and is predicted to result in the loss of the splice acceptor site of exon 9. This loss potentially results in skipping of this exon and thereby to a shift from splicing pattern w to y at site A (Online Resource Fig. S2). Alternative splicing at site A determines apical targeting of the encoded PMCA2 in hair cells. When alternative splicing at site A resulted in insertion of at least 31 amino acids, the encoded PMCA2 exclusively targeted to the hair bundle (Grati et al. 2006). As exons 7, 8, and 9 encode 11, 20, and 14 amino acids, respectively, skipping of exon 9 results in 31 amino acids encoded at site A (pattern y) and exclusively apical targeting of the protein (Grati et al. 2006). This suggests that the c.1001-1G>A might have no or a milder phenotypic effect compared to ATP2B2 variants identified in the present study.
The other two canonical splice site variants in gnomAD, each representing a single allele, are predicted to result in the loss of the splice donor site of exon 7 and the splice acceptor site of exon 8, respectively. Skipping of exon 7 would lead to a PMCA2 protein with 34 amino acids encoded by exons inserted at site A and thus apical targeting according to Grati et al. (Grati et al. 2006). Skipping of exon 8 would result in a PMCA2 protein with both apical and basolateral distribution in hair cells (Grati et al. 2006). In conclusion, 21 of 26 loss-of-function alleles reported in gnomAD might well lead to no or a mild phenotype.
Two de novo truncating variants in ATP2B2 have been identified in a study on autism spectrum disorders (ASD), which is a complex disorder (Takata et al. 2018). These variants, c.2268C>A (p. Cys756*) and c.3191G>G (p.Trp1064*) according to transcript NM_001001331.2, affect exons 15 and 20 of the transcript, respectively (see Online Resource Fig. S2). Therefore, these variants are predicted to affect all known PMCA2 isoforms and to lead to nonsense-mediated decay. Based on our findings, the de novo ATP2B2 variants identified in the ASD cases are expected to cause HI but this was not reported by the authors. The age of the subjects was not specified but indicated to be more than 2 years. This suggests that these subjects might not yet have developed HI. Alternatively, if they are toddlers, the HI may have mimicked or contributed to symptoms of ASD due to communication problems as has been reported previously (Worley et al. 2011). The subjects in our study did not display signs of ASD and this condition was neither indicated by themselves nor by their parents.
The type of mutations and their distribution in the gene suggest haploinsufficiency as disease mechanism. 4 of 5 presented ATP2B2 variants potentially lead to nonsense-mediated decay (NMD). A haploinsufficiency mechanism is further supported by the findings of McCullough et al. (2007) who demonstrated that SNHI in cases with the 3p-syndrome is associated with loss of ATP2B2 (McCullough et al. 2007). They reported a high-frequency HI with a steeply downsloping audiogram configuration, similar to that in the cases in our study. Malmgren et al. suggested that deletion of ATP2B2 is not sufficient to cause HI (Malmgren et al. 2007). However, the HI in the cases they reported is not sufficiently characterized to support SNHI in all them. For example, HI of one of the included subjects was indicated to be conductive in the original publication (Angeloni et al. 1999; Malmgren et al. 2007; McCullough et al. 2007).
WES data of index cases were analyzed for other variants in known mouse and/or human deafness genes that could potentially be causative for HI. This revealed only one candidate variant, c.3226G>C (p.Asp1076His) in MYO6, that co-segregated with the HI in family W18-0111. Although a phenotypic effect of this variant cannot be excluded, MYO6 variants with a dominant effect are known to be associated with progressive HI with a different audiogram configuration and in the majority of cases an onset after childhood (Miyagawa et al. 2015; Oonk et al. 2013; Sampaio-Silva et al. 2018; Topsakal et al. 2010). Therefore, the identified variant is unlikely to fully explain the HI in family W18-0111. Also, the HI in family W18-0111 is comparable to that in the other families reported in this study.
13 mouse mutants (deafwaddler) have been described for Atp2b2, 12 of which have been described to display congenital severe-to-profound HI accompanied by a severe vestibular/ataxic phenotype when the mutation is in the homozygous state. The mutations in all 12 affect the w/a isoform of PMCA2. Mice with loss of function Atp2b2 mutations in the heterozogous state display a rapidly progressive early onset HI (before the age of 3–5 weeks) with high-frequency hearing being most severely affected (Carpinelli et al. 2013; McCullough and Tempel 2004; Noben-Trauth et al. 1997; Watson and Tempel 2013). The type of HI in these mice is highly similar to that in the presented affected subjects.
Based on the findings in the presented families, it cannot be determined whether hearing of the affected subjects was abnormal at birth, as all four subjects who underwent newborn hearing screening passed the first test. The TEOAE devices employed in the screening are calibrated to detect thresholds of 35 dB HL or more, for the frequencies between 1 and 4 kHz (van der Ploeg et al. 2012). This means that in case the tested newborns with ATP2B2 defects had elevated thresholds, these were below 35 dB HL for the tested frequencies. Alternatively, only the thresholds for higher frequencies (> 4 kHz) surpassed 35dB, which might have well been the case based on audiogram configuration (Fig. 2b) and the findings in mouse models. Delayed speech development and difficulties at school were the reasons for the parents to have their children’s hearing tested leading to a diagnosis of HI around the age of 2–5 years.
One individual (W18-0139, III.3, Fig. 1) in our study displayed HI with a late onset rather than an early onset. This suggests the existence of modifying (genetic) factors. For mouse, it has been described that small (15%) increases in PMCA2 activity can account for large differences in hearing phenotype (McCullough and Tempel 2004). Therefore, it is tempting to speculate that the late onset of HI in this case might be due to a relatively high inner ear expression of the second ATP2B2 copy. As subject II.3 was indicated to be severely hearing impaired at the age of 30 years, mosaic presence of the ATP2B2 variant in subject III.3 seems unlikely to explain the late onset of his HI. However, as HI is genetically highly heterogeneous the deceased family members I.2, II.1, II.2 and II.3 may have had HI with a different genetic aetiology. Identification of additional families with deletions or truncating variants of ATP2B2 will shed light on the variability of onset age of ATP2B2-associated HI.
In hair cells and endolymph, Ca2+ is important for maintaining the endocochlear potential, contributes to the mechanotransduction (MET) current, affects MET channel activity, tip-link structure, and, although under debate now, it is thought to play a role in the process of fast adaptation [for review see (Bortolozzi and Mammano 2018; Cali et al. 2017; Qiu and Muller 2018)]. PMCA2 is the Ca2+ pump in OHC stereocilia and, therefore, important for Ca2+ homeostasis in these structures. As has been demonstrated for several of the Atp2b2 mutant mice, HI and OHC dysfunctions precede hair cell degeneration and Ca2+ cytotoxicity has been hypothesized to underlie the latter (Bortolozzi et al. 2010; Konrad-Martin et al. 2001; Spiden et al. 2008). Degeneration of both OHCs and IHCs was demonstrated to be most severe at the cochlear base in heterozygous as well as homozygous Atp2b2 mutant mice (Bortolozzi et al. 2010; Spiden et al. 2008). This is in agreement with high-frequency hearing being most severely affected in the presented families. Analogous to what has been described in mice with a heterozygous Atp2b2 mutation, degeneration of OHCs, IHCs and supporting cells is likely to cause the progression of HI to severe-to-profound in humans.
PMCA2 is also expressed in the stereocilia of vestibular hair cells (Grati et al. 2006; Street et al. 1998). A vestibular phenotype was only seen in homozygous or compound heterozygous and not in heterozygous Atp2b2 mutant mouse models (Bortolozzi et al. 2010; Carpinelli et al. 2013; Kozel et al. 1998; McCullough and Tempel 2004; Spiden et al. 2008; Street et al. 1998; Sun et al. 2008; Watson and Tempel 2013). This is histologically supported by studies of Takahashi and Kitamura on the “wri” mouse model; in wri/wri homozygotes, severe degeneration is seen in both the cochlea and saccule within 3 months. In heterozygotes, degeneration was only seen in the cochlea (Takahashi and Kitamura 1999). Vestibular complaints were found in only two patients in this study, but can be attributed to other factors than defects in ATP2B2 (Online Resource Table S4). Oculomotor, vHIT, caloric and rotational chair testing yielded no abnormalities, as expected from previous studies in mouse models. In four subjects, we could not determine whether saccular or utricular function was present. First, we measured until 100dB HL (cVEMP) and 140 dB FL (oVEMP), according to protocol. Higher stimulus levels are too uncomfortable for subjects. The contralateral measurements were close to maximum stimulus levels in subjects III.1 of family W18-0111 and IV.2 of W18-0139. It is, therefore, possible that ipsilateral levels could have been measured with stimuli just above the maximum stimulus levels. Second, in about half of all patients who underwent vestibular examination in our clinic prior to cochlear implantation, it was impossible to measure c- and oVEMPs (Beynon, unpublished data). This relates to subject III.1 of W18-0138, who was the only subject with a cochlear implant. Based on the present findings, we concluded that heterozygous loss-of function variants in ATP2B2 are unlikely to be associated with vestibular dysfunction.
In conclusion, we presented heterozygous ATP2B2 defects to be associated with dominantly inherited nonsyndromic SNHI. All but one subject displayed a rapidly progressive high-frequency HI with a congenital or early childhood onset. Four and possibly all five identified variants have a truncating effect. As amino acid substitutions in mouse PMCA2 can lead to loss of function (e.g. Bortolozzi et al. 2010; Spiden et al. 2008), missense variants in ATP2B2 are to be expected as a cause of HI in humans as well. Variants resulting in reduced PMCA2 function might lead to recessive HI, analogous to the deafwaddler (dfw) allele (McCullough and Tempel 2004).
The DOOFNL Consortium consists of M.F. van Dooren, H.H.W. de Gier, E.H. Hoefsloot, M.P. van der Schroeff (ErasmusMC, Rotterdam, The Netherlands), S.G. Kant, L.J.C. Rotteveel (LUMC, Leiden, the Netherlands), J.C.C. Widdershoven, J.R. Hof, E.K. Vanhoutte (MUMC+, Maastricht, The Netherlands), R.J.C. Admiraal, I. Feenstra, H. Kremer, R.J.E. Pennings, H.G. Yntema (Radboudumc, Nijmegen, The Netherlands) R.H. Free and J.S. Klein Wassink-Ruiter (UMCG, Groningen, The Netherlands), R.J. Stokroos, A.L. Smit, M.J. van den Boogaard (UMC, Utrecht, The Netherlands) and F.A. Ebbens, S.M. Maas, A. Plomp, T.P.M. Goderie, P. Merkus and J. van de Kamp (Amsterdam UMC, Amsterdam, The Netherlands).
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This work was financially supported by a grant from the Heinsius Houbolt foundation [to H.K. and R.J.E.P.]. We thank Ilse de Wijs, Genome Diagnostics Radboudumc, for her contribution to DNA analysis.
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Smits, J.J., Oostrik, J., Beynon, A.J. et al. De novo and inherited loss-of-function variants of ATP2B2 are associated with rapidly progressive hearing impairment. Hum Genet 138, 61–72 (2019). https://doi.org/10.1007/s00439-018-1965-1