Usher syndrome is an inherited and irreversible disease that manifests as retinitis pigmentosa (RP) and bilateral neurosensory hearing loss. Mutations in Usherin 2A (USH2A) are not only a frequent cause of Usher syndrome, but also nonsyndromic RP. Although gene- and cell-based therapies are on the horizon for RP and Usher syndrome, studies characterizing natural disease are lacking. In this retrospective analysis, retinal function of USH2A patients was quantified with electroretinography. Both groups had markedly reduced rod and cone responses, but nonsyndromic USH2A patients had 30 Hz-flicker electroretinogram amplitudes that were significantly higher than syndromic patients, suggesting superior residual cone function. There was a tendency for Usher syndrome patients to have a higher distribution of severe mutations, and alleles in this group had a higher odds of containing nonsense or frame-shift mutations. These data suggest that the previously reported severe visual phenotype seen in syndromic USH2A patients could relate to a greater extent of cone dysfunction. Additionally, a genetic threshold may exist where mutation burden relates to visual phenotype and the presence of hearing deficits. The auditory phenotype and allelic hierarchy observed among patients should be considered in prospective studies of disease progression and during enrollment for future clinical trials.
Usher syndrome is an inherited autosomal recessive condition affecting both hearing and vision, specifically manifesting as retinitis pigmentosa (RP) and bilateral neurosensory hearing loss1,2,3,4. It is the most common cause of deaf-blindness and currently irreversible. The retinal phenotype is characterized by night-blindness, a constricting visual field, and classic pigmentary degeneration seen on imaging2, 5, 6. Usher syndrome is categorized clinically into three types (Usher syndrome types 1–3) based predominantly on the onset and progression of hearing loss. Usher syndrome type 1 typically exhibits congenital hearing loss, childhood-onset RP, and possible vestibular dysfunction. Usher syndrome type 2 is characterized by mild, non-progressive hearing loss and early adulthood-onset of RP. Usher syndrome type 3 is the rarest, typically manifesting with progressive hearing loss, early-onset RP, and sporadic vestibular dysfunction7, 8. In addition to this traditional classification, the diagnosis can be refined with genetic testing, as mutations in at least 13 genes are known to cause Usher syndrome9. These genes are typically involved in ciliary transport or scaffolding proteins important for cellular structure and morphology5, 10,11,12,13,14,15.
Previously, Usher syndrome was thought to affect approximately 1 in 25,000 individuals, but recent epidemiologic data suggest a higher prevalence16. This could be due in part to cases in which there is a subtle hearing phenotype, resulting in an incomplete diagnosis of isolated RP. Interestingly, mutations in some genes leading to Usher syndrome can also manifest as nonsyndromic RP (NSRP) in other individuals, with mutations in Usherin 2A (USH2A) being a frequent cause of both17,18,19,20,21,22,23. Recently, a multi-center analysis of a large USH2A patient cohort found different visual outcomes in patients with Usher syndrome compared to NSRP24. Syndromic patients tended to exhibit worse visual outcomes as measured by subjective tests of visual function and harbored a higher proportion of truncating mutations. Another study also assessed syndromic and nonsyndromic USH2A patients but found no difference in retinal disease progression when comparing patients with the p.(Cys759Phe) amino acid substitution in USH2A, which is associated with NSRP, to patients with a p.(Glu767Serfs*21) frameshift in USH2A, which is implicated in Usher syndrome6. Differences in statistical modeling of progression, follow-up time, and the genotypes of interest in each study may account for the differing results, highlighting the need for further investigation. Assessing functional outcomes in syndromic and nonsyndromic USH2A patients is essential for patient management and counseling. Furthermore, understanding natural disease is necessary for future clinical trials so physicians can conclude if treatments are efficacious and which patients are most likely to benefit7, 25.
The present study sought to elucidate differences in cone function between Usher syndrome and NSRP due to mutations in the same USH2A gene. Patients were examined in a single electrophysiology clinic using objective visual function data, specifically the 30 Hz-flicker full-field electroretinogram (ffERG). The 30 Hz-flicker ffERG is a commonly used outcome measure of visual function and prognosis in RP patients26,27,28,29,30,31. This particular ffERG measures cone function by exposing the patient to a light stimulus at a rate of 30 flashes per second after the retina is bleached to suppress rod responses, resulting in a predominantly L- and M-cone response. While the rod response aids in diagnosis and is typically severely diminished or completely extinguished in Usher syndrome and RP, the 30 Hz-flicker is useful for assessing retinal function in clinical practice, as cones are affected later in the disease course26, 27, 31, 32. The mutation spectrum was also assessed in this cohort of USH2A patients and compared to the findings of previous studies.
A total of 10 patients were diagnosed with Usher syndrome type IIA and 10 patients were diagnosed with recessive NSRP based on clinical history, family history, dilated fundus exam, presence or absence of subjective hearing loss, and genetic confirmation of two or more USH2A mutations. The diagnosis was supported by multimodal retinal imaging (Fig. 1) and/or ffERG scotopic b-wave responses that were decreased to a greater extent than photopic responses, indicative of a rod-cone dystrophy. Clinical and genetic findings of the cohort are provided in Tables 1 and 2. The average age of the Usher syndrome group was 33 (n = 10) compared to 44 (n = 10) in the NSRP group (p = 0.16). Four eyes had best-corrected visual acuity (BCVA) of 20/100 or worse in Usher syndrome patients. In NSRP patients, one eye was less than 20/100, which was in the context of cystoid macular edema (CME). Three of ten Usher syndrome patients had a bulls-eye pattern of macular atrophy or significant maculopathy in both eyes. One NSRP patient had a bulls-eye pattern of atrophy bilaterally. On fundoscopy, nine Usher syndrome patients had evident intraretinal pigment migration. In the youngest patient (P10), no intraretinal pigment migration was observed. In the NSRP group, seven patients had intraretinal pigment migration. No patient showed evidence of CME on SD-OCT in either eye of Usher syndrome patients, compared to three NSRP patients. Two patients (P8 and P14) underwent previous audiometry for which P8 (Usher syndrome) was found to have bilateral neurosensory hearing loss. P14 (NSRP) underwent audiometry to screen for hearing loss after receiving results of genetic testing, which was in the normal range.
Results of ffERG testing are presented in Table 3. Eight patients in each group underwent electroretinography. NSRP patients had mean 30 Hz-flicker amplitudes of 17.04 ± 16.7 μV (mean ± SD), compared to Usher syndrome patients, 2.13 ± 1.64 μV (Fig. 2). 30 Hz-flicker amplitudes were compared between groups using the Wilcoxon rank-sum test (p = 0.0023). Seven of eight patients in the Usher syndrome group required Burien-Allen (BA) contact lens electrodes compared to three of eight NSRP patients. All others used Dawson, Trick, and Litzkow (DTL) recording electrodes. Of the 10 total patients whose recordings were performed with BA contact lens electrodes, four (P3, P4, P6, P8) also had prior DTL recordings performed during the same visit; all four DTL recordings were nondetectable. Five of eight Usher syndrome patients had an implicit time delay in 30 Hz-flicker recordings compared to all NSRP patients (p = 0.20). Scotopic b-wave amplitudes were recorded in a total of 12 patients (24 eyes). Scotopic b-waves were extinguished in all 10 eyes of Usher syndrome patients and 10 of 14 eyes of NSRP patients.
The genetic profile of all patients are provided in Table 2, and each USH2A mutation identified in the cohort is tabulated in Supplemental Table 1. All patients had family histories consistent with an autosomal recessive inheritance pattern. No patients in this cohort were related to each other. P19 reported a family history of parental consanguinity. The distribution of severe mutations was assessed between groups. A severe mutation was defined as a nonsense mutation or an indel (insertion or deletion) resulting in an out-of-frameshift. The percentage of Usher syndrome patients having at least one severe mutation was 70% compared to 30% of NSRP patients (p = 0.089). In the Usher syndrome group, 45% (9/20) of alleles had a nonsense mutation or an indel resulting in an out-of-frameshift compared to 15% (3/20) of NSRP patients. The odds ratio for an allele containing a frameshift or nonsense mutation in the Usher syndrome group compared to the NSRP group was 4.6 (confidence interval: 1.1 to 20, p = 0.039). Two patients in the Usher syndrome group harbored two truncating alleles compared to no patients in the NSRP group. Mutations were known to be in trans or homozygous in 5 of 10 Usher syndrome patients and 6 of 10 NSRP patients. The phase of the two USH2A mutations was unknown in the remaining patients. A 27 base-pair deletion was identified in P10 (Usher syndrome), which included the loss of a splice-site acceptor. As it is not clear if this allele is affected more by aberrant splicing or a frameshift, it was not counted as severe to maintain a conservative analysis. A homozygous, in-frame duplication was identified in P19 (NSRP) and thus not considered severe based on our criteria, as the amino acid reading frame is unaffected. One of 10 patients in the Usher syndrome group and three of 10 patients in the NSRP group harbored at least one variant affecting splicing. One patient (P12) was identified to have three variants in USH2A, in which the variant affecting splicing was found to be in trans to the two missense variants.
Short wavelength autofluorescent (SW-AF) and spectral-domain optical coherence tomography (SD-OCT) imaging were obtained for all patients. Four patients (P7, P9, P13, P20) had bilateral advanced disease, rendering the ellipsoid zone (EZ) line length and AF ring diameters unmeasurable; the left eye of one patient (P4) had a macular hole that prevented accurate EZ-line and ring visualization. One patient (P17) had a granular AF ring that was not quantifiable. CME was observed on SD-OCT for three patients (P15, P18, P20) but did obscure the EZ-line. No patients warranted exclusion due to poor imaging quality. For all eyes with an AF ring, it was visible within the central 30 degrees of the retina. AF ring diameters were generally symmetrical between eyes, and 15 of 16 patients had horizontal diameters that were larger than vertical diameters. Mean EZ-line length between both eyes were 2425 µm for Usher syndrome patients and 3145 µm for NSRP patients (p = 0.38); Usher syndrome patients had mean horizontal and vertical ring diameters of 3633 μm and 3044 μm, respectively, compared to a horizontal diameter of 3915 μm (p = 0.71) and vertical diameter of 3101 μm (p = 0.94) in NSRP patients (Fig. 3).
A 41-year-old female with RP and two confirmed pathogenic USH2A mutations, c.10073G > A and c.920_923dupGCCA, did not have an auditory phenotype documented on previous intake forms or clinic notes. As subjective hearing loss could not be confirmed, this patient was excluded from analyses (see methods). Of interest, she did undergo previous audiometry for the work-up of tinnitus, which was found to be within the normal range for all tested frequencies. FfERG scotopic b-waves and 30 Hz-flicker amplitudes for this patient were higher than all patients in the cohort (Supplemental Table 2). Multimodal retinal imaging was performed in this patient, which was consistent with RP (Supplemental Fig. 2).
Usher syndrome presents with considerable genetic and phenotypic variability between individuals. Mutations in at least 13 genes are known to cause Usher syndrome but may manifest as a different clinical entity in other patients. In addition to USH2A, mutations in CLRN1 are also known to cause both Usher syndrome and NSRP33. Furthermore, a longer list of genes are associated with both Usher syndrome and nonsyndromic recessive deafness (CDH23, CIB2, DFNB31, MYO7A, PCDH15, and USH1C)5. In these cases, differences in the mutational spectrum may relate to disease manifestation. For MYO7A and CDH23, truncating mutations are reported to be more commonly associated with Usher syndrome, while ‘leaky’ splice site and missense mutations manifest as nonsyndromic deafness34, 35. RP with hearing deficits have also been reported in the context of X-linked RPGR mutations, albeit less frequently36. The present study focused specifically on Usher syndrome and recessive NSRP due to mutations in USH2A, and is first to elucidate differences in cone function between these groups.
Overall, our data suggest that patients with Usher syndrome due to USH2A mutations have a more attenuated 30 Hz-flicker response compared to their NSRP counterparts (Fig. 2). NSRP patients in this retrospective analysis had a mean 30 Hz-flicker amplitude of 17 µV at an average age of 44 years old (n = 8). Usher syndrome patients in our cohort had inferior cone function with a mean 30 Hz-flicker amplitude of 2.1 μV at a younger average age of 33 years old (n = 8). 30 Hz-flicker ffERGs are a useful outcome measure to assess, as scotopic responses are affected earlier and often already extinguished in both RP and Usher syndrome at presentation. Photopic 30 Hz-flicker response is an outcome in previous landmark clinical trials assessing the efficacy of dietary supplements for RP27,28,29 and published actuarial tables provide conversions for 30 Hz-flicker amplitudes into prognoses for patient counseling26. Together, these data suggest that the presence of subjective hearing loss in USH2A patients may be predictive of worse cone function and thus visual phenotype. Interestingly, these large differences in retinal function did not corroborate structural measurements obtained from multimodal imaging in both groups, which would have been predicted based on the stark difference in 30 Hz-flicker amplitudes (Fig. 3). Future comparisons may require more subjects to detect a potential statistical difference. Alternatively, the difference in ERG amplitudes may reflect the number of healthy cone photoreceptors in the peripheral retina, as an ERG represents an average of the entire fundus. In contrast, structural measurements in this study were within the macula, which is affected later in the disease course. Lastly, functional loss precedes structural changes, hence an ERG is a more sensitive test to detect changes in the retina. As a result, structural measurements for both groups may be assessed more effectively as a progression rate over a longitudinal follow-up, as opposed to in cross-section.
The Usher syndrome group was more likely to be enriched with disease alleles containing either an indel or nonsense mutation, which generally has a more deleterious effect on protein structure (Table 1). Allelic hierarchy has been reported previously and was confirmed in this study19. It is possible that a genetic threshold exists in which the combined burden of the two alleles is severe enough to cause hearing loss in addition to the retinal phenotype. Alternatively, differential disruption of USH2A isoforms or their expression patterns in photoreceptor and inner ear cells may account for variable hearing deficits. The genetic heterogeneity and frequent occurrence of compound heterozygous mutations in USH2A patients, however, make it difficult to confirm this hypothesis.
In our cohort of 20 patients, exactly 31 unique disease-causing variants were identified in USH2A. Of these, the most common variants were c.2299delG, c.10073G > A, and c.10712C > T. The c.2299delG variant is the most frequent disease-causing variant of Usher syndrome in multiple studies37,38,39, and was not found in the NSRP group. c.10712C > T mutations were only identified in Usher syndrome patients in this cohort, and previous studies have also associated this particular variant with RP and an auditory phenotype19. This missense mutation causes the reading frame to be interrupted by a premature STOP codon; mRNA produced might be targeted for nonsense-mediated decay. Interestingly, Lenassi et al. found the c.10073G > A, c.2276G > T, and c.12575G > A mutations to be ‘retinal disease specific’ and hypothesized the presence of one of these mutations leads to a nonsyndromic manifestation, largely independent of the second mutation19. Our mutational analysis found this to be possible. P13 and P16, both NSRP, harbored homozygous c.10073G > A and c.2276G > T variants, respectively. Similarly, the presented case study featured a patient with the ‘retina-specific’ c.10073G > A mutation17, 19, 21. This patient had a normal audiogram across all frequencies in addition to scotopic B-wave and 30 Hz-flicker amplitudes that were higher than all patients in the cohort.
There are previous studies with contrasting findings. Sandberg et al. compared patients with the p.(Cys759Phe) amino acid substitution in USH2A, which is known to cause NSRP, with patients that had a p.(Glu767fs*21) truncating mutation, known to cause Usher syndrome. No differences in disease progression were detected6. Our cohort observed only one patient (P13, NSRP) with the p.(Cys759Phe) substitution in USH2A and three patients (P1, P5, P9) with the p.(Glu767fs*21) truncating mutation, preventing a meaningful comparison within this study. However, conclusions from the present study are in accordance with the previously mentioned multi-center cohort study performed in Europe that found Usher syndrome patients to be diagnosed earlier, became visually impaired sooner by subjective functional testing, and have a higher frequency of truncating mutations compared to NSRP patients24. Visual prognoses were determined in their cohort with visual acuity and field measurements, which were superior in NSRP. Our retrospective analysis confirms a severe visual phenotype in Usher syndrome, elucidates differences in visual function with an objective test, and is the first to document differences in ffERG cone responses between these populations, an important index in RP research and clinical practice.
There are limitations to our study. Patients underwent ffERG testing with BA contact lens or DTL recording electrodes. Four Usher syndrome patients in this cohort underwent recordings with both DTL-recording electrodes and BA contact lenses in the same visit, with undetectable waveforms in the former. The increased use of BA contact lens electrodes in the Usher syndrome group likely decreased the potential difference between groups, which was still statistically significant. Prospective investigations and clinical trials would benefit from the use of a single type of recording electrode to compare cone function over time. Another limitation is the aforementioned genetic heterogeneity of Usher syndrome and RP, which lends smaller cohorts difficult to interpret. Of the 20 patients in this cohort, 4 were homozygous for USH2A mutations. In compound heterozygotes it is difficult to parse the contribution of a specific mutation to disease phenotype without a larger cohort. Lastly, using subjective hearing loss to diagnosis either Usher syndrome or NSRP likely leads to misclassification of patients with a subtle hearing phenotype that is undetectable to the patient. However, using subjective hearing loss as a criterion was useful in stratifying differences in auditory phenotype and can guide genetic screening and counseling. Still, a more sophisticated and quantifiable measure of hearing loss may reveal other correlations between particular mutations and auditory or visual manifestations. Future investigations should consider comparing visual outcomes to a quantifiable measure of auditory function, such as a standardized audiometry.
There is currently no cure for Usher syndrome. Standard management typically involves monitoring complications of RP and providing assistive hearing devices such as hearing aids or cochlear implants40. However, after previous demonstration of safety and efficacy in macaques, clinical trials for Usher syndrome type IB are underway that involve subretinal administration of UshStat® (EIAV-CMV-MYO7A) (NCT01505062)41. Recently, a preclinical anti-sense oligonucleotide has also shown promise in an Usher syndrome type 1C mouse model after being identified in an in vitro screen. By blocking an aberrant splice site, vestibular and auditory rescue is achieved in this model42. Specific to USH2A, investigators corrected the effects of a deep intronic mutation in patient-derived fibroblasts43. With gene- and cell-based therapies becoming a reality, studies characterizing natural disease become essential for assessing treatment efficacy. This study not only provides objective functional data comparing retinal function between Usher syndrome and NSRP caused by mutations in the same gene, but may also prove useful for retina specialists counseling USH2A patients.
This retrospective analysis was approved by the Edward S. Harkness Eye Institute and Columbia University Internal Review Boards and adhered to the tenets of the Declaration of Helsinki. The data presented in this study, including images and genetic testing results, are not identifiable to individual patients. Informed consent for participation was obtained as outlined in the Columbia University Medical Center IRB-approved protocol, AAAR0284. Patients diagnosed with Usher syndrome or NSRP at the Harkness Eye Institute electrodiagnostics clinic were considered for inclusion in electroretinogram or mutational analyses based upon: (1) if they harbored at least two pathogenic or likely pathogenic USH2A variants and (2) had prior documentation of the presence or absence of subjective hearing loss on clinic notes or patient intake forms. It is important to note that all patients in the NSRP group reported no hearing loss on an intake form or during the clinic visit as per the physician note, meaning the auditory phenotype was not assumed to be normal if it was not stated explicitly. Twenty-seven patients presenting to clinic between 2010 and 2016 were found to have at least two USH2A mutations. Out of the 27 patients, seven were excluded from analyses for the following reasons: USH2A variants occurred in cis (one patient); two USH2A variants were reported as benign (one patient); other identified gene variants could reasonably account for disease phenotype with no accompanying co-segregation analysis (three patients); there was a confounding history of subjective hearing loss, which is the independent variable in each analysis performed (one patient); or there was no documentation of the presence or absence of hearing loss (one patient). The 20 included USH2A patients were analyzed in two groups, Usher syndrome (n = 10) and NSRP (n = 10). Multimodal imaging was acquired in all patients and a total of 16 patients underwent ffERG testing.
For all patients, DNA was isolated from whole blood lymphocytes for sequencing. Most patients (15 of 20) had genetic testing for a panel of genes known to cause Usher syndrome or RP by next generation sequencing and subsequent confirmation with Sanger sequencing at the Casey Eye Institute Diagnostic Laboratory (Portland, Oregon), Molecular Vision Laboratory (Hillsboro, Oregon), or Columbia University Medical Center Pathology Department (New York, NY). Whole exome sequencing was performed on three patients by the Columbia University Medical Center Pathology Department (New York, NY). The remaining two patients had genetic testing performed at the National Institute on Deafness and Other Communication Disorders (Bethesda, Maryland) and the John and Marcia Carver Nonprofit Genetic Testing Laboratory (Iowa City, IA). USH2A variants were analyzed by Alamut software version 2.2 (Interactive Biosoftware, Rouen, France).
FfERGs were acquired with the Diagnosys Espion Electrophysiology System (Diagnosys LLC, Lowell, MA, USA) from both eyes using DTL recording electrodes in accordance to the International Society for Clinical Electrophysiology of Vision (ISCEV) standards in scotopic and photopic states44, 45. When the 30 Hz-flicker amplitudes were lower than five microvolts or predicted to be lower than five microvolts based on exam, Burian-Allen contact lens electrodes were used to record the 30 Hz-flicker responses that are subsequently processed through narrow band-passed filtering with computed averaging26, 44, 46, 47. The amplitudes obtained from both eyes were measured by a single user with Espion V6.0.56 software (Diagnosys LLC, Lowell, MA, USA), which calculates the amplitude from trough to peak of the first visible waveform, as performed previously46, 48,49,50. Amplitudes of both eyes were averaged and compared between the two groups.
Fundus SW-AF and SD-OCT images were obtained in all patients after dilation using Spectralis HRA + OCT device (Heidelberg Engineering, Heidelberg, Germany). SW-AF images were acquired using a 30-degree field of view with 1536 × 1536 pixel resolution. SW-AF imaging utilized a 521nm barrier filter and 486nm wavelength stimulus. The external horizontal and vertical ring diameter of SW-AF imaging was measured manually using Spectralis software (Heidelberg Eye explorer, software version 1.9.10, Heidelberg Engineering, Heidelberg, Germany). SD-OCT was obtained with an 870nm light source and automatic real-time registration of the fundus infrared reflectance image. Horizontal scans (high resolution mode, 9mm, ART, average of a minimum of 50 images) through the fovea provided a view of the EZ-line and was measured manually using Spectralis software. All measurements were obtained by a single observer (T.C), who was masked to whether the patient was in the Usher syndrome or NSRP group.
All statistical analyses were performed using Stata/IC software version 13.0 (StataCorp LLC, College Station, Texas). 30 Hz-flicker ffERG amplitudes were compared between Usher syndrome and NSRP patients using a Wilcoxon-rank sum test. Right and left eyes were averaged prior to statistical analysis. To compare the distribution of patients harboring at least one frameshift (indel) or nonsense mutation, a Fisher’s exact test was used (Table 4, row 4). To account for a possible correlation of observations from the same subject, the odds of having either an indel or nonsense mutation in one allele was compared between both groups by fitting logistic regression models using generalized estimating equations. In this case, the outcome variable was whether an allele had either a nonsense mutation or an indel resulting in an out-of-frame shift (Table 4, row 5). Structural measurements acquired from SD-OCT (EZ-line length) and SW-AF imaging (horizontal and vertical ring diameters) were compared using a two-tailed Student’s t test with unequal variance. Measurements for the right and left eye were averaged prior to comparing groups for all indices. A p value less than 0.05 was considered statistically significant in all results reported. All values are expressed as mean ± standard deviation (SD) unless otherwise indicated.
All data generated or analyzed for this study are included in this published article.
Boughman, J. A., Vernon, M. & Shaver, K. A. Usher syndrome: definition and estimate of prevalence from two high-risk populations. J Chronic Dis 36, 595–603 (1983).
Keats, B. J. & Corey, D. P. The usher syndromes. Am J Med Genet 89, 158–166 (1999).
Mehta, D. et al. Outcomes of evaluation and testing of 660 individuals with hearing loss in a pediatric genetics of hearing loss clinic. Am J Med Genet A 170, 2523–2530, doi:https://doi.org/10.1002/ajmg.a.37855 (2016).
Yang, J., Wang, L., Song, H. & Sokolov, M. Current understanding of usher syndrome type II. Front Biosci (Landmark Ed) 17, 1165–1183 (2012).
Mathur, P. & Yang, J. Usher syndrome: Hearing loss, retinal degeneration and associated abnormalities. Biochim Biophys Acta 1852, 406–420, doi:https://doi.org/10.1016/j.bbadis.2014.11.020 (2015).
Sandberg, M. A. et al. Disease course in patients with autosomal recessive retinitis pigmentosa due to the USH2A gene. Invest Ophthalmol Vis Sci 49, 5532–5539, doi:https://doi.org/10.1167/iovs.08-2009 (2008).
Sengillo, J. D., Justus, S., Cabral, T. & Tsang, S. H. Correction of Monogenic and Common Retinal Disorders with Gene Therapy. Genes (Basel) 8, doi:https://doi.org/10.3390/genes8020053 (2017).
Sengillo, J. D., Justus, S., Tsai, Y. T., Cabral, T. & Tsang, S. H. Gene and cell-based therapies for inherited retinal disorders: An update. Am J Med Genet C Semin Med Genet 172, 349–366, doi:https://doi.org/10.1002/ajmg.c.31534 (2016).
Koffler, T., Ushakov, K. & Avraham, K. B. Genetics of Hearing Loss: Syndromic. Otolaryngol Clin North Am 48, 1041–1061, doi:https://doi.org/10.1016/j.otc.2015.07.007 (2015).
Adato, A. et al. Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells. Hum Mol Genet 14, 3921–3932, doi:https://doi.org/10.1093/hmg/ddi416 (2005).
Heissler, S. M. & Manstein, D. J. Functional characterization of the human myosin-7a motor domain. Cell Mol Life Sci 69, 299–311, doi:https://doi.org/10.1007/s00018-011-0749-8 (2012).
Reiners, J., Nagel-Wolfrum, K., Jurgens, K., Marker, T. & Wolfrum, U. Molecular basis of human Usher syndrome: deciphering the meshes of the Usher protein network provides insights into the pathomechanisms of the Usher disease. Exp Eye Res 83, 97–119, doi:https://doi.org/10.1016/j.exer.2005.11.010 (2006).
Reiners, J. et al. Scaffold protein harmonin (USH1C) provides molecular links between Usher syndrome type 1 and type 2. Hum Mol Genet 14, 3933–3943, doi:https://doi.org/10.1093/hmg/ddi417 (2005).
Yang, J. et al. Ablation of whirlin long isoform disrupts the USH2 protein complex and causes vision and hearing loss. PLoS Genet 6, e1000955, doi:https://doi.org/10.1371/journal.pgen.1000955 (2010).
Zou, J. et al. Deletion of PDZD7 disrupts the Usher syndrome type 2 protein complex in cochlear hair cells and causes hearing loss in mice. Hum Mol Genet 23, 2374–2390, doi:https://doi.org/10.1093/hmg/ddt629 (2014).
Kimberling, W. J. et al. Frequency of Usher syndrome in two pediatric populations: Implications for genetic screening of deaf and hard of hearing children. Genet Med 12, 512–516, doi:https://doi.org/10.1097/GIM.0b013e3181e5afb8 (2010).
Bernal, S. et al. Mutations in USH2A in Spanish patients with autosomal recessive retinitis pigmentosa: high prevalence and phenotypic variation. J Med Genet 40, e8 (2003).
Garcia-Garcia, G. et al. Novel deletions involving the USH2A gene in patients with Usher syndrome and retinitis pigmentosa. Mol Vis 20, 1398–1410 (2014).
Lenassi, E. et al. A detailed clinical and molecular survey of subjects with nonsyndromic USH2A retinopathy reveals an allelic hierarchy of disease-causing variants. Eur J Hum Genet 23, 1318–1327, doi:https://doi.org/10.1038/ejhg.2014.283 (2015).
McGee, T. L., Seyedahmadi, B. J., Sweeney, M. O., Dryja, T. P. & Berson, E. L. Novel mutations in the long isoform of the USH2A gene in patients with Usher syndrome type II or non-syndromic retinitis pigmentosa. J Med Genet 47, 499–506, doi:https://doi.org/10.1136/jmg.2009.075143 (2010).
Rivolta, C., Sweklo, E. A., Berson, E. L. & Dryja, T. P. Missense mutation in the USH2A gene: association with recessive retinitis pigmentosa without hearing loss. Am J Hum Genet 66, 1975–1978, doi:https://doi.org/10.1086/302926 (2000).
Seyedahmadi, B. J., Rivolta, C., Keene, J. A., Berson, E. L. & Dryja, T. P. Comprehensive screening of the USH2A gene in Usher syndrome type II and non-syndromic recessive retinitis pigmentosa. Exp Eye Res 79, 167–173, doi:https://doi.org/10.1016/j.exer.2004.03.005 (2004).
Xu, W. et al. Seven novel mutations in the long isoform of the USH2A gene in Chinese families with nonsyndromic retinitis pigmentosa and Usher syndrome Type II. Mol Vis 17, 1537–1552 (2011).
Pierrache, L. H. et al. Visual Prognosis in USH2A-Associated Retinitis Pigmentosa Is Worse for Patients with Usher Syndrome Type IIa Than for Those with Nonsyndromic Retinitis Pigmentosa. Ophthalmology 123, 1151–1160, doi:https://doi.org/10.1016/j.ophtha.2016.01.021 (2016).
Sujirakul, T. et al. Multimodal Imaging of Central Retinal Disease Progression in a 2-Year Mean Follow-up of Retinitis Pigmentosa. Am J Ophthalmol 160, 786–798 e784, doi:https://doi.org/10.1016/j.ajo.2015.06.032 (2015).
Berson, E. L. Long-term visual prognoses in patients with retinitis pigmentosa: the Ludwig von Sallmann lecture. Exp Eye Res 85, 7–14, doi:https://doi.org/10.1016/j.exer.2007.03.001 (2007).
Berson, E. L. et al. A randomized trial of vitamin A and vitamin E supplementation for retinitis pigmentosa. Arch Ophthalmol 111, 761–772 (1993).
Berson, E. L. et al. Clinical trial of lutein in patients with retinitis pigmentosa receiving vitamin A. Arch Ophthalmol 128, 403–411, doi:https://doi.org/10.1001/archophthalmol.2010.32 (2010).
Berson, E. L. et al. Clinical trial of docosahexaenoic acid in patients with retinitis pigmentosa receiving vitamin A treatment. Arch Ophthalmol 122, 1297–1305, doi:https://doi.org/10.1001/archopht.122.9.1297 (2004).
Schatz, A. et al. Transcorneal electrical stimulation for patients with retinitis pigmentosa: a prospective, randomized, sham-controlled exploratory study. Invest Ophthalmol Vis Sci 52, 4485–4496, doi:https://doi.org/10.1167/iovs.10-6932 (2011).
Wu, D. Z., Liang, J., Wu, L., Luo, T. & Yu, M. Quantitative evaluation of flicker ERG waveforms in low vision patients. Yan Ke Xue Bao 8, 122–125 (1992).
Chang, S., Vaccarella, L., Olatunji, S., Cebulla, C. & Christoforidis, J. Diagnostic challenges in retinitis pigmentosa: genotypic multiplicity and phenotypic variability. Curr Genomics 12, 267–275, doi:https://doi.org/10.2174/138920211795860116 (2011).
Khan, M. I. et al. CLRN1 mutations cause nonsyndromic retinitis pigmentosa. Ophthalmology 118, 1444–1448, doi:https://doi.org/10.1016/j.ophtha.2010.10.047 (2011).
Riazuddin, S. et al. Mutation spectrum of MYO7A and evaluation of a novel nonsyndromic deafness DFNB2 allele with residual function. Hum Mutat 29, 502–511, doi:https://doi.org/10.1002/humu.20677 (2008).
Schultz, J. M. et al. Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes. J Med Genet 48, 767–775, doi:https://doi.org/10.1136/jmedgenet-2011-100262 (2011).
Iannaccone, A. et al. Clinical and immunohistochemical evidence for an X linked retinitis pigmentosa syndrome with recurrent infections and hearing loss in association with an RPGR mutation. J Med Genet 40, e118 (2003).
Eudy, J. D. et al. Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa. Science 280, 1753–1757 (1998).
Weston, M. D. et al. Genomic structure and identification of novel mutations in usherin, the gene responsible for Usher syndrome type IIa. Am J Hum Genet 66, 1199–1210 (2000).
Yan, D. et al. Mutation analysis in the long isoform of USH2A in American patients with Usher Syndrome type II. J Hum Genet 54, 732–738, doi:https://doi.org/10.1038/jhg.2009.107 (2009).
Jatana, K. R. et al. Usher syndrome: characteristics and outcomes of pediatric cochlear implant recipients. Otol Neurotol 34, 484–489, doi:https://doi.org/10.1097/MAO.0b013e3182877ef2 (2013).
Zallocchi, M. et al. EIAV-based retinal gene therapy in the shaker1 mouse model for usher syndrome type 1B: development of UshStat. PLoS One l, e94272, doi:https://doi.org/10.1371/journal.pone.0094272 (2014).
Lentz, J. J. et al. Rescue of hearing and vestibular function by antisense oligonucleotides in a mouse model of human deafness. Nat Med 19, 345–350, doi:https://doi.org/10.1038/nm.3106 (2013).
Slijkerman, R. W. et al. Antisense Oligonucleotide-based Splice Correction for USH2A-associated Retinal Degeneration Caused by a Frequent Deep-intronic Mutation. Mol Ther Nucleic Acids 5, e381, doi:https://doi.org/10.1038/mtna.2016.89 (2016).
Acton, J. H. et al. Evaluation of multimodal imaging in carriers of X-linked retinitis pigmentosa. Exp Eye Res 113, 41–48, doi:https://doi.org/10.1016/j.exer.2013.05.003 (2013).
McCulloch, D. L. et al. ISCEV Standard for full-field clinical electroretinography (2015 update). Doc Ophthalmol 130, 1–12, doi:https://doi.org/10.1007/s10633-014-9473-7 (2015).
Andreasson, S. O., Sandberg, M. A. & Berson, E. L. Narrow-band filtering for monitoring low-amplitude cone electroretinograms in retinitis pigmentosa. Am J Ophthalmol 105, 500–503 (1988).
Sieving, P. A., Arnold, E. B., Jamison, J., Liepa, A. & Coats, C. Submicrovolt flicker electroretinogram: cycle-by-cycle recording of multiple harmonics with statistical estimation of measurement uncertainty. Invest Ophthalmol Vis Sci 39, 1462–1469 (1998).
Burke, T. R. et al. Quantification of peripapillary sparing and macular involvement in Stargardt disease (STGD1). Invest Ophthalmol Vis Sci 52, 8006–8015, doi:https://doi.org/10.1167/iovs.11-7693 (2011).
Lee, W. et al. Genotypic spectrum and phenotype correlations of ABCA4-associated disease in patients of south Asian descent. Eur J Hum Genet, doi:https://doi.org/10.1038/ejhg.2017.13 (2017).
Nong, E., Lee, W., Merriam, J. E., Allikmets, R. & Tsang, S. H. Disease progression in autosomal dominant cone-rod dystrophy caused by a novel mutation (D100G) in the GUCA1A gene. Doc Ophthalmol 128, 59–67, doi:https://doi.org/10.1007/s10633-013-9420-z (2014).
Jonas Children’s Vision Care, and Bernard & Shirlee Brown Glaucoma Laboratory are supported by the National Institute of Health [5P30EY019007, R01EY018213, R01EY024698, R01EY026682, R21AG050437], National Cancer Institute Core [5P30CA013696], the Research to Prevent Blindness (RPB) Physician-Scientist Award, unrestricted funds from RPB, New York, NY, USA. J.D.S. is supported by the RPB Medical Student Eye Research Fellowship. T.C is supported by the International Council of Ophthalmology - Retina Research Foundation Helmerich Fellowship, honoring Mr. W. H. Helmerich III. V.B.M. is supported by NIH grants [R01EY026682, R01EY024665, R01EY025225, R01EY024698 and R21AG050437]. S.H.T. is a member of the RD-CURE Consortium and is supported by the Tistou and Charlotte Kerstan Foundation, the Schneeweiss Stem Cell Fund, New York State [C029572], the Foundation Fighting Blindness New York Regional Research Center Grant [C-NY05-0705-0312], the Crowley Family Fund, and the Gebroe Family Foundation.
The authors declare that they have no competing interests.
Publisher's note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Electronic supplementary material
About this article
Cite this article
Sengillo, J.D., Cabral, T., Schuerch, K. et al. Electroretinography Reveals Difference in Cone Function between Syndromic and Nonsyndromic USH2A Patients. Sci Rep 7, 11170 (2017). https://doi.org/10.1038/s41598-017-11679-y
Structural modeling, mutation analysis, and in vitro expression of usherin, a major protein in inherited retinal degeneration and hearing loss
Computational and Structural Biotechnology Journal (2020)
Severe or Profound Sensorineural Hearing Loss Caused by Novel <i>USH2A</i> Variants in Korea: Potential Genotype-Phenotype Correlation
Clinical and Experimental Otorhinolaryngology (2020)
Baseline Visual Field Findings in the RUSH2A Study: Associated Factors and Correlation With Other Measures of Disease Severity
American Journal of Ophthalmology (2020)
Scientific Reports (2019)
Full-field electroretinography, visual acuity and visual fields in Usher syndrome: a multicentre European study
Documenta Ophthalmologica (2019)