Molecular Vision 2017; 23:548-560
<http://www.molvis.org/molvis/v23/548>
Received 01 April 2017 | Accepted 08 August 2017 | Published 10 August 2017
Molecular Vision 2017; 23:548-560
<http://www.molvis.org/molvis/v23/548>
Received 01 April 2017 |
Accepted 08 August 2017 |
Published 10 August 2017
Eric D. Gaier,1 Katherine Boudreault,1 Isao Nakata,1 Maria Janessian,1 Philip Skidd,2 Elizabeth DelBono,1 Keri F. Allen,1 Louis R. Pasquale,1,3 Emily Place,1 Dean M. Cestari,1 Rebecca C. Stacy,1 Joseph F. Rizzo III,1 Janey L. Wiggs1
1Department of Ophthalmology, Harvard Medical School, Massachusetts Eye and Ear Infirmary Boston, MA; 2Departments of Ophthalmology and Neurology, University of Vermont College of Medicine, Burlington, MA; 3Channing Division of Network Medicine, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA
Correspondence to: Janey L. Wiggs, Massachusetts Eye and Ear Infirmary, 243 Charles St., Boston, MA, 02114; Phone: (617) 573-3670; FAX: (617) 573-6439; email: janey_wiggs@meei.harvard.edu
Purpose: Inherited optic neuropathy is genetically heterogeneous, and genetic testing has an important role in risk assessment and counseling. The purpose of this study is to determine the prevalence and spectrum of mutations in a group of patients referred for genetic testing to a tertiary center in the United States. In addition, we compared the clinical features of patients with and without mutations in OPA1, the gene most commonly involved in dominantly inherited optic atrophy.
Methods: Clinical data and genetic testing results were reviewed for 74 unrelated, consecutive patients referred with a history of insidious, relatively symmetric, bilateral visual loss secondary to an optic neuropathy. Patients were evaluated for disease-causing variants in OPA1, OPA3, WFS1, and the entire mitochondrial genome with DNA sequencing and copy number variation (CNV) testing.
Results: Pathogenic DNA variants were found in 25 cases, with the majority (24 patients) located in OPA1. Demographics, clinical history, and clinical features for the group of patients with mutations in OPA1 were compared to those without disease-causing variants. Compared to the patients without mutations, cases with mutations in OPA1 were more likely to have a family history of optic nerve disease (p = 0.027); however, 30.4% of patients without a family history of disease also had mutations in OPA1. OPA1 mutation carriers had less severe mean deviation and pattern standard deviation on automated visual field testing than patients with optic atrophy without mutations in OPA1 (p<0.005). Other demographic and ocular features were not statistically significantly different between the two groups, including the fraction of patients with central scotomas (42.9% of OPA1 mutation positive and 66.0% of OPA1 mutation negative).
Conclusions: Genetic testing identified disease-causing mutations in 34% of referred cases, with the majority of these in OPA1. Patients with mutations in OPA1 were more likely to have a family history of disease; however, 30.4% of patients without a family history were also found to have an OPA1 mutation. This observation, as well as similar frequencies of central scotomas in the groups with and without mutations in OPA1, underscores the need for genetic testing to establish an OPA1 genetic diagnosis.
Inherited optic neuropathy is an important cause of blindness worldwide [1]. Genetic optic neuropathies can be inherited as an autosomal dominant (AD), autosomal recessive (AR), X-linked recessive (XR), or mitochondrial (maternal) trait. Dominantly inherited optic atrophy is the most common form with prevalence ranging from 1/10,000 in Denmark to 1/30,000 elsewhere [2-4]. Between 40% and 90% of dominantly inherited optic neuropathy cases are reportedly caused by mutations involving OPA1 (Gene ID 165500, OMIM 605290) [3,5-9], depending on the population. OPA1-related optic neuropathy is typically characterized by insidious symmetric visual loss and dyschromatopsia beginning within the first two decades of life [2,7]. Optic nerve head pallor and excavation are frequently present, especially in the temporal sector. Syndromic optic neuropathy, which includes neurologic signs and symptoms (such as sensorineural hearing loss and progressive external ophthalmoplegia), has been estimated to occur in 10–30% of patients with disease-causing OPA1 variants [10,11].
OPA1 is a nuclear gene encoding a dynamin-related GTPase that is ubiquitously expressed and localizes to the inner mitochondrial membrane [12-14]. There are eight alternatively spliced isoforms [15], and disease-causing variants are found throughout the OPA1 coding sequence. The OPA1 protein is highly expressed in neuronal tissues, including retinal ganglion cells, and participates in multiple processes, including mitochondrial fission/fusion, oxidative phosphorylation, and apoptosis [16-18]. The molecular and cellular mechanisms responsible for OPA1-mediated optic neuropathy are only partially understood, and clinical studies of patients with mutations in OPA1 have been limited with respect to the clinical features examined [3,5-9,19,20]. More than 300 independent disease-causing OPA1 variants have been characterized (Mitodyn) [21,22]. Although the majority of mutations in OPA1 are missense or nonsense alleles, approximately 10–13% of patients with inherited optic atrophy have been reported to have large-scale chromosomal deletions or insertions (copy number variants, or CNVs) affecting OPA1 [23].
Inherited forms of optic neuropathy are also caused by mutations involving mitochondrial DNA-encoded genes ND4 (OMIM 516006) and ND6 (OMIM 516006) in patients with Leber hereditary optic neuropathy (LHON; OMIM 535000), mutations in OPA3 (OMIM 606580) in AD optic atrophy associated with cataract (OMIM 1653000), and mutations in WFS1 (OMIM 606201) in AR optic atrophy associated with sensorineural hearing loss, diabetes mellitus, and diabetes insipidus (OMIM 222300) [24,25]. Nine other genes are rare causes of optic atrophy inherited primarily as AR traits [4,26-29].
Genetic counseling can be challenging for many optic atrophy families that are too small to confidently differentiate AD, AR, and mitochondrial inheritance from inspection of the pedigree. Genetic testing can help inform genetic counseling for these patients and their families by revealing the disease-causing variant and associated inheritance pattern. Additionally, genetic testing can identify specific mutations that in some cases may be relevant to disease outcomes. Although genetic testing for optic atrophy is offered by several Clinical Laboratory Improvement Amendments (CLIA)–certified laboratories, the mutation detection rates, classifications of disease-causing variants, and clinical features of mutation carriers have not been comprehensively reported [30].
We selected a cohort of consecutively identified patients referred to our genetic testing laboratory who were predominately referred from a single clinical service with a history of insidious, relatively symmetric, bilateral visual loss secondary to an optic neuropathy. We report on the mutation prevalence and variant spectrum for this group of unrelated patients and compare the clinical features of patients with disease-causing OPA1 variants with cases without an identified genetic cause of disease.
The Institutional Review Board at the Massachusetts Eye and Ear Infirmary (MEEI) approved this Health Insurance Portability and Accountability Act (HIPAA)–compliant study that adhered to the Declaration of Helsinki and to the ARVO statement on human subjects. Seventy-four unrelated patients with presumed inherited optic atrophy referred for genetic testing between 2006 and 2014 were included in the study. Most patients were referred from the MEEI Neuro-Ophthalmology service (61 patients) with the remaining patients referred from the National Ophthalmic Disease Genotyping Network (eyeGENE; seven patients), MEEI glaucoma service (one patient), and other physicians not at MEEI (five patients). We obtained written informed consent from each patient.
Patients referred for genetic testing had a clinical presentation of insidious, generally symmetric bilateral visual loss in the context of optic nerve pallor and increased cupping that, in the absence of an alternative etiology such as metabolic condition, toxic disorder, neoplastic or paraneoplastic disorder, inflammatory disease (including demyelination), or infection, was suggestive of optic atrophy on a genetic basis. Genomic DNA was extracted from blood, buccal swab, or mouth wash samples according to approved protocols [31]. Blood was obtained by venous puncture (usually from the antecubital vein) into two 10 ml heparinized tubes. Lymphocytes pellets were prepared from each tube and DNA was extracted from each lymphocyte pellet using established protocols [31]. DNA samples were stored at -80 °C until used for sequencing.
Genetic testing was done at the MEEI CLIA–certified genetic diagnostic laboratory (CLIA number 22D1037777). Initially, the genetic testing procedures for optic atrophy were limited to PCR amplification of the OPA1 coding sequence (NM_130837.2) followed by Sanger sequencing. In 2012, we developed a next-generation sequencing (NGS) test using selective exon capture for OPA1, OPA3, WFS1, and the entire mitochondrial genome (Genetic Eye Disease test, GEDi test; 31). In total (Sanger sequencing and GEDi NGS testing), 74 unrelated patients underwent genetic analysis. Initially, 62 patients were tested for OPA1 variants using Sanger sequencing and OPA1 multiplex ligation-dependent probe amplification (MLPA), and point variants or CNVs were found in 21 patients (Appendix 1). Sufficient DNA was not available for further analysis in three additional cases. The remaining 38 patients (62 – minus 21 cases where mutations were found and minus the three cases without sufficient DNA) were further studied using the NGS GEDi test, along with an additional 12 patients who were newly referred for testing. The additional 12 cases who were taken directly to GEDi testing also had an evaluation for CNVs using OPA1 MLPA. The GEDi testing identified three additional OPA1 point mutations and a single case with a mitochondrial DNA mutation known to cause LHON (m.11778G>A) in the combined group of 38 patients from Sanger and the newly referred 12 patients. If a disease-causing variant was identified, then testing of family members was offered. For patients with OPA1 variants, five affected family members with variants were identified, and these cases were included in the comparison of clinical features.
For the Sanger sequencing test, all OPA1 exons (NM_130837.2, isoform 8; ENST00000361510) and 100 base pairs of the flanking intron sequence were amplified using a standard nested PCR approach. Oligonucleotides for amplification and sequencing were selected using Primer3 software (provided by Massachusetts Institute of Technology, Cambridge, MA) and were located at least 40 bp from each exon’s splice site. Primer sequences are available on request. PCR was performed in a thermal cycler in a total volume of 25 μl containing 50 ng genomic DNA; 1.5 mM MgCl2; 200 μM each of dATP, dCTP, dGTP, and dTTP; 100 ng forward PCR primer, 100 ng reverse PCR primer; 20 mM Tris-HCl (pH 8.4); 50 mM KCl; and 0.5 U Taq DNA polymerase (Platinum Taq; Invitrogen-Life Technologies, Rockville, MD). Cycling conditions were as follows: an initial denaturing step of 5 min at 94 °C; 35 cycles of denaturation (94 °C for 45 s), annealing (primer-specific annealing temperature for 60 s), elongation (72 °C for 45 s), and a final elongation step of 5 min at 72 °C. Amplified genomic DNA was directly sequenced using sequencing chemistries (BIGDYE Terminators; Applied Biosystems Inc., Foster City, CA) and an automated sequencer (model ABI PRISM 3730xl DNA Analyzer; Applied Biosystems Inc.). Next-generation sequencing was performed using the GEDi diagnostic panel that covers the coding and intronic regions of three optic atrophy-related genes (OPA1, OPA3, and WFS1), as well as the mitochondrial genome as previously described [31].
To assess the likelihood of pathogenicity for missense variants, we used the following criteria: rare (<1%) or novel based on the publically available sequence database from the National Heart, Lung, and Blood Institute Exome Sequencing Project (NHLBI ESP) and the Exome Consortium (ExAC), evolutionarily conserved, and expected to be pathogenic based on the results of two online pathogenicity programs: PolyPhen-2 and SIFT [32,33]. Frameshift and nonsense mutations were assessed for pathogenicity using MutationTaster [34]. MLPA was used to identify CNVs using a kit from MRC Holland (P229 OPA1 probemix, Amsterdam, the Netherlands). At least three separate MLPA reactions were conducted for each patient. PCR products were separated on Applied Biosystem’s ABI 3130XL capillary sequencers. Analysis was performed using the Coffalyser software (MRC Holland, Amsterdam, The Netherlands). Mitochondrial DNA variants were assessed according to the algorithm outlined by Wang et al. [35], which accounts for allele frequency (<0.2%), degree of heteroplasmy, and matrilinear inheritance. Heteroplasmy was assessed with analysis of the sequence data.
Demographic, medical, and ophthalmic data were extracted from the medical record masked to OPA1 mutation status. Onset of symptoms was extracted from the history of present illness. Family history was considered positive if an immediate family member or multiple extended family members were reported to have unexplained vision loss or optic atrophy.
The clinical evaluation of each patient was performed by the MEEI Neuro-Ophthalmology service and included best-corrected Snellen visual acuity; pupillary exam; color discrimination using Ishihara pseudoisochromatic plates; applanation tonometry of intraocular pressure (IOP); dilated stereoscopic funduscopy, including subjective assessment of the cup-to-disc ratio (CDR); assessment of visual fields with static perimetry (Humphrey) using the 24–2 threshold program, kinetic (Goldmann) perimetry, or both. Visual acuity recorded in Snellen equivalents was converted to the LogMAR scale. Absolute asymmetry was calculated by taking the absolute LogMAR difference. Normalized asymmetry was calculated by dividing the absolute asymmetry by the averaged acuity between the two eyes. Patients were considered to have dyschromatopsia if they could read the control plate but could not read all Ishihara plates.
Reliable visual fields were available for 47 patients (37 on the Humphrey visual field [HVF] analyzer and ten on the Goldmann perimeter) and were systematically analyzed for each patient by an ophthalmologist masked to OPA1 mutation status. The visual field analysis was modified from a previously described method [36]. Only visual fields with reliability indices of ≤33% fixation losses, ≤20% false positive responses, and ≤20% false negative responses were used for analysis. From the extracted visual field global indices (pattern standard deviation [PSD] and mean deviation [MD]), absolute and normalized asymmetries were calculated. The pattern of visual loss was characterized as whether it involved the central field (including the cecocentral and paracentral regions), peripheral visual field (including nasal step, Bjerrum, and temporal wedge zones), or both (Appendix 2). These regions were presumed to be abnormal if there was a cluster of three or more contiguous points with retinal sensitivity depression of 0.5 log unit (−5 dB) relative to age-matched controls on the pattern deviation plot. Goldmann fields were interpreted using the same topographical descriptors by two investigators (EDG, KB) independently with complete agreement.
Statistical analyses were conducted using IBM SPSS Statistics (Version 22) software. Discrete variables were tested using the chi-square (χ2) test. Continuous variables were tested using the Student t test (unpaired; unequal variance assumed). Bonferroni corrections for multiple comparisons were applied for each measure within each of the three analyses, including demographic/historical data, details of the clinical examination, and results of perimetry where indicated. In all cases, a p value of less than 0.05 was considered statistically significant. Post-hoc power calculations were completed using G*Power 3 (Appendix 3). As post-hoc power calculations suggested that the study was best powered to detect differences between OPA1 mutation positive (M+) and OPA1 mutation negative (M-) cases in visual field parameters (>90% power), and family history of disease (>69% power), we focused on those features.
Seventy-four unrelated patients with optic atrophy were tested for clinically relevant variants in up to three genes and the entire mitochondrial genome using Sanger and next-generation sequencing. We used the following criteria to classify nuclear DNA variants as clinically relevant: 1) rare [<1%] in the general population (Exome Aggregate Consortium); 2) predicted to be pathogenic by PolyPhen2, SIFT, and MutationTaster; 3) evolutionarily conserved [genomic evolutionary rate profile, GERP]); and 4) segregation with disease status (if family members were available). Mitochondrial variants were classified according to the algorithm outlined by Wang et al. [35] that includes frequency of the potentially pathogenic allele (<0.2%), measure of heteroplasmy, and matrilineal inheritance (if possible from the pedigree information). Using these criteria, clinically relevant variants (mutations) were identified in 25 of 74 cases overall. Mutations in OPA1 were found in 24 cases, and a homoplasmic mitochondrial DNA variant (m.11778G>A) known to cause LHON was found in one case (Figure 1, Table 1, Table 2 and Table 3). Mutations in OPA3 or WFS1 were not observed in this cohort. The mutations in OPA1 included five missense alleles, two nonsense, and three insertions or deletions causing a shift of the reading frame (Table 1). The known recurrent deletion at Val958 (chr3:193,384,959–62,delTTAG [15];) was observed in six unrelated cases.
Four point mutations in OPA1 were novel: two missense variants (Ser358Asn; Glu499Gly) and two insertion/deletions resulting in premature stop codons and truncated proteins (c.2333_2334insT, Asn700Lysfs*27; c.2881delG, Val883*). None of these mutations were identified in the EXAC database of 60,706 individuals. SIFT and PolyPhen2 predicted that the novel missense alleles are pathogenic, and the GERP scores (5.6 and 5.8, respectively) indicated that the affected amino acids are evolutionarily conserved (Table 2). The patient with the Ser358Asn mutation had an affected mother and grandmother. A family history was not available for the patient with the Glu499Gly allele. The patient with the c.2333_2334insT mutation reported no family history of neurologic disease. The patient with c.2881delG had a maternal grandfather with a similar history of optic atrophy. Insertion and deletion variants cause premature stop codons and were predicted to be disease causing by MutationTaster (Table 2 [34];).
Copy number variation (large insertions or deletions) was evaluated using MLPA. CNVs involving OPA1 were identified in six cases that included five deletions and one insertion (Table 3, Figure 1C,D). The deletions ranged in size from three exons to deletion of the entire gene; three of these deletions have not been previously reported. A novel duplication involving exon 18 was identified in one patient.
The clinical features of 24 patients with mutations in OPA1, as well as five family members with confirmed mutations, were compared to 49 patients in whom we did not identify a mutation. The patient with the LHON-related mitochondrial DNA variant was not included in the comparison analysis.
In the combined OPA1 mutation positive (M+) and OPA1 mutation negative (M-) group, 85% of the cases were self-identified as Caucasian, and 54% were male. Using available information from clinical records, data were collected for visual acuity, family history of disease, age of diagnosis, reason for referral, alcohol and smoking exposure, extraocular neurologic symptoms, dyschromatopsia, relative afferent pupillary defect (RAPD), IOP, CDR, retinal pathology, and visual field defects (Figure 2, Appendix 4). Power calculations (Appendix 3) indicated approximately 70% power to detect significant comparisons between M+ and M- cases for family history, and greater than 90% power to detect differences in visual field parameters: MD and PSD from Humphrey automated visual fields and the location of visual field defects (peripheral). Below, we focus on these clinical features with adequate power for comparison in the M+ and M- cases.
M+ patients reported earlier age of onset of visual symptoms compared to M- cases (M+: 1.7±1.3 decade; M-: 3.0±2.0 decade, p = 0.045; Appendix 4), and 69.6% of M+ patients had a family history of optic atrophy compared to 30.8% of the M- patients (p = 0.027). However, of the patients with optic atrophy without a known family history, 30.4% carried an OPA1 mutation, and 42.9% of patients with a family history of optic atrophy did not have an identified OPA1 mutation (Appendix 4), arguing that OPA1 mutation status cannot be inferred based on family history alone.
Visual field data were available for 93 eyes among 47 patients. The number of unreliable automated HVFs (fixation losses >33%, false positives >20%, or false negatives >20%) was not different between the M+ (13/36 eyes [64%]) and M- groups (16/57 eyes [72%], p = 0.41). Mean deviations (a measure of the overall depression of the visual field) ranged from −0.86 dB to −32.95 dB (Figure 3A). M+ patients had less severe mean deviation compared to the M- patients (M+: −3.88±5.83 dB; M-: −11.49±10.04 dB, p<0.005; Table 4). There was little asymmetry in the mean deviation between the eyes of the M+ and M- patients (Appendix 4; Figure 3B). Pattern standard deviation, a measure of the depth of a localized visual field defect, ranged widely among patients, from 1.48 dB to 12.19 dB (Figure 3C). Average PSDs were statistically significantly lower in the M+ patients compared to the M- patients (M+: 2.29±1.03 dB; M-: 5.49±3.53 dB, p<0.005; Table 4). There was little asymmetry in PSD between the eyes of the M+ and M- patients (Appendix 4; Figure 3D).
Manual Goldmann visual field data were available for 20 eyes among ten patients and were included with the visual field loss pattern analysis along with the HVF data. Although most M+ patients had a localized visual field defect (57%, Table 4), only 42.9% had central, paracentral, or centrocecal scotomas. There was no difference in the frequency of central, paracentral, or centrocecal scotomas between the M+ and M- groups (p = 0.248; Table 4). In contrast, the peripheral patterns of field loss (including nasal step, Bjerrum, and temporal wedge patterns) were significantly more common among eyes without mutations in OPA1 (29/47 [62%]) and were infrequently seen in the M+ patients (5/35 [14.3%]; p<0.005; Table 4).
This study reports the clinical profile and genetic testing results for a cohort of patients with insidious, relatively symmetric, bilateral optic neuropathies referred to a tertiary care center in the United States. Genetic testing revealed disease-causing variants in 34% of unrelated cases, with the majority of variants involving OPA1 (24 of 25). The testing also identified eight novel mutations in OPA1, including four point mutations and four CNVs.
Genetic testing in this cohort of patients with optic atrophy provided an opportunity to compare clinical features of patients with mutations in OPA1 to affected patients without mutations in known disease-causing genes. A family history of optic atrophy is more common in OPA1 mutation carriers; however, 30.4% of OPA1 mutation positive cases did not report a family history of disease, and 30.8% of OPA1 mutation negative patients had affected family members. Thus, OPA1 mutation status cannot be presumed from family history alone. A lack of family history in OPA1 mutation carriers could be due to the impact of modifier alleles, de novo mutations, or variable disease expressivity due to stochastic effects. Further study of families without history of disease but with at least one member with a mutation in OPA1 would be interesting and could help differentiate among these possible explanations. Positive family history in OPA1-negative patients supports the hypothesis that other, yet undiscovered, genes are likely to cause this clinical phenotype of inheritable disease.
Differences between OPA1 M+ and M- patients were also observed in visual field data. The overall visual field compromise (i.e., mean deviation score) was greater in patients without mutations in OPA1 compared with those patients with disease-causing variants. Interestingly, although central scotomas are described as a cardinal feature of OPA1-mediated optic atrophy due to the involvement of the retinal ganglion cells in the central maculopapillary bundle [37], only 42.9% of the OPA1 mutation carriers had visual field defects involving the central visual field. Moreover, a significant difference in the frequency of central scotomas between the OPA1 mutation positive and negative groups was not observed. However, patients without mutations in OPA1 were more likely to have peripheral visual field defects, which suggests that this group of patients, which likely includes multiple etiologies, comprises optic neuropathies that preferentially disrupt retinal ganglion cells outside of the maculopapillary bundle. Other clinical features were not significantly different between the M+ and M- groups, underscoring the value of genetic testing to accurately identify carriers of clinically relevant variants.
Overall, fewer mutations in OPA1 (32%) were found among patients in this sample compared to other studies (40–90% [3,5-9];). Many of the previously published studies included only European populations with likely OPA1 founder effects, especially in Denmark [3]. The rate of mutations in OPA1 in the present study is consistent with one other available study from the United States [9]. Some studies with a higher rate of OPA1 variants included only patients with a known family history of optic atrophy which likely explains the higher percentage of patients with dominantly inherited mutations in OPA1. Importantly, the present study includes all patients referred for genetic testing during the designated time period, regardless of family history, which presumably lowers this type of bias. Among the patients with a positive family history of optic neuropathy, mutations in OPA1 were found in 57.1% of cases, comparable to most European studies evaluating frequency of mutations in OPA1 [6,8,9,38]. By comparison, the mutation rate for mitochondrial variants causing LHON was lower than expected [6], although some cases with a history of sequential disease were prescreened for mitochondrial variants by other methods, which could have reduced our opportunity to observe the LHON disease-causing variants in this cohort.
Eight of the variants identified in this study are novel, including novel CNVs. Several other studies have suggested that between 10% and 19% of the mutations in OPA1 are CNVs [3,4,23,38,39]. The present study supports the observation that OPA1 CNVs are relatively common, and collectively, these results indicate that analysis for OPA1 CNVs is a necessary component of OPA1 genetic testing platforms [9].
Determining if a novel DNA variant is the likely cause of disease is a critical aspect of genetic testing. Classification of pathogenic variants depends on allele frequencies in general populations, appropriate control data, evaluating familial segregation data (if available), and functional information. In this study, we used the most rigorous approach possible to classify the newly discovered variants as pathogenic. This approach utilizes the ExAC database of more than 60,000 European Caucasians to assess the allele frequencies of the novel point mutations. All of the novel variants were absent from the ExAC database suggesting that they are exceedingly rare in the general population, as would be expected for a disease-causing variant. Additionally, we relied on evidence of evolutionary conservation and predicted pathogenicity using the well-characterized in silico pathogenicity programs SIFT, PolyPhen2, and MutationTaster. All the novel variants are evolutionarily conserved and predicted to be pathogenic. Familial segregation is helpful for establishing pathogenicity if available, but this was infrequently available in our cohort. Future studies to develop standardized high-throughput assays for OPA1 function would be a valuable tool to assess functional consequences of newly discovered DNA sequence variants.
A strength of this study is the detailed clinical profile for most of cases, making clinical comparisons possible. The present study also has some limitations. First, although the genetic testing approach is comprehensive, it is possible that some existing OPA1 variants were not detected in the OPA1 mutation negative group. Potential false-negatives would likely be rare events that would not significantly impact the overall results. Second, although the sample size was considerable, the study was under-powered to detect differences in many clinical parameters between the two groups. Third, the retrospective design of this study carries its inherent limitations in selection bias and the ability to detect clinical features that might have been relevant in the comparative analysis. Overall, we believe that these limitations do not undermine the general conclusions.
This study reports the prevalence of mutations in currently known genes for a group of patients with insidious, bilateral, relatively symmetric optic neuropathy who were referred for genetic testing because of suspicion of a genetic etiology. The study adds eight novel variants and new detailed clinical information to the current knowledge of OPA1-related inherited optic atrophy. Our study also supports the concept that a clinical examination alone is not sufficient to identify OPA1 variant carriers, and that genetic testing is necessary to establish a genetic diagnosis that informs counseling for these patients and their families. In the future, routine use of genetic testing in patients with this phenotype also might provide a necessary step toward therapeutic opportunities.
Appendix 1. Summary of genetic testing for unrelated optic neuropathy patients.
Appendix 2. Paracentral and peripheral visual field loss definitions for visual fields scoring.
Appendix 3. Post-hoc power analysis results for sociodemographic, clinical and visual field data.
Appendix 4. Demographic, historical, and clinical data collected for optic atrophy cases
We thank the late Simmons Lessell, MD for caring for some of the patients included in the study, and for his monumental contributions to neuro-ophthalmology at the Massachusetts Eye and Ear Infirmary. Financial Support: This work was partially supported by NIH/NEI P30EY014104 and by an Alcon Research Institute Award (JLW). Meeting Presentation: This work was presented at the North American Neuro-Ophthalmology Society Annual Meeting in poster form (2013, Snowbird, UT) and as a platform presentation (2015, San Diego, CA), and in poster form at the Association for Research in Vision and Ophthalmology annual meeting (2013, Seattle, WA). Conflict of Interest: No relevant conflict of interest exists for any author. RCS is an employee of Novartis, a for-profit organization. JFRIII owns equity in Bionic Eye Technologies and Visus Technologies, which are working on implanted and portable devices for the blind, respectively. JFRIII also serves as Medical Director for Neurology and Ophthalmology for Magic Leap, Inc., which is developing a head-mounted “gaming” device. LRP is a consultant for Bausch+Lomb, inc. and is on the Advisory Board for Eyenovia, inc.