Clinical Study | Open Access
Kiyoko Gocho, Sachiko Kikuchi, Takenori Kabuto, Shuhei Kameya, Kei Shinoda, Atsushi Mizota, Kunihiko Yamaki, Hiroshi Takahashi, "High-Resolution En Face Images of Microcystic Macular Edema in Patients with Autosomal Dominant Optic Atrophy", BioMed Research International, vol. 2013, Article ID 676803, 12 pages, 2013. https://doi.org/10.1155/2013/676803
High-Resolution En Face Images of Microcystic Macular Edema in Patients with Autosomal Dominant Optic Atrophy
The purpose of this study was to investigate the characteristics of microcystic macular edema (MME) determined from the en face images obtained by an adaptive optics (AO) fundus camera in patients with autosomal dominant optic atrophy (ADOA) and to try to determine the mechanisms underlying the degeneration of the inner retinal cells and RNFL by using the advantage of AO. Six patients from 4 families with ADOA underwent detailed ophthalmic examinations including spectral domain optical coherence tomography (SD-OCT). Mutational screening of all coding and flanking intron sequences of the OPA1 gene was performed by DNA sequencing. SD-OCT showed a severe reduction in the retinal nerve fiber layer (RNFL) thickness in all patients. A new splicing defect and two new frameshift mutations with premature termination of the Opa1 protein were identified in three families. A reported nonsense mutation was identified in one family. SD-OCT of one patient showed MME in the inner nuclear layer (INL) of the retina. AO images showed microcysts in the en face images of the INL. Our data indicate that AO is a useful method to identify MME in neurodegenerative diseases and may also help determine the mechanisms underlying the degeneration of the inner retinal cells and RNFL.
Autosomal dominant optic atrophy (ADOA; MIM no. 165500), also known as Kjer’s disease , is the most common hereditary ocular neuropathy with a prevalence of 1/12,000–1/50,000 [2–4]. ADOA is characterized by a decrease in the visual acuity that develops in childhood, temporal palor of the optic discs, centrocecal scotoma, and color vision defects [5, 6]. Histopathological studies of human eyes with ADOA showed diffuse atrophy of the retinal ganglion cell (RGC) layer that predominated in the central retina [7, 8].
ADOA has considerable intra- and interfamilial clinical variability with incomplete penetrance estimated to be about 90% in the familial forms of the disease . Mutations in the optic atrophy 1 gene, OPA1 (MIM no. 605290), located on chromosome 3q28-q29, are responsible for about 60–80% of the cases of ADOA [10–12].
OPA1 encodes a mitochondrial dynamin-related GTPase, which is anchored to the mitochondrial inner membrane [13, 14]. Although the Opa1 protein is ubiquitously expressed in human tissues, a strong expression of the Opa1 protein has been reported in the RGC layer . The Opa1 protein has multiple functions and plays a key role in the fusion of mitochondria and thus in organizing the mitochondrial network [13, 14]. The other functions of the Opa1 protein are related to oxidative phosphorylation, maintenance of the membrane potential [11, 16, 17], maintenance of mtDNA [18, 19], organizing the cristae, and control of mitochondrial apoptosis through the compartmentalization of cytochrome C [17, 20]. Mutations of the OPA1 gene result in a loss of function in most ADOA patients indicating that haploinsufficiency is involved in the pathomechanism of the disease . However, to date, there is no clear evidence to suggest a further role for the OPA1 gene in the degeneration of RGCs in ADOA.
Recently, Barboni et al. detected “microcystic macular edema (MME)” in the inner nuclear layer (INL) of patients with Leber’s hereditary optic neuropathy (LHON) and ADOA . The INL is predominantly made up of the nuclei of the horizontal, bipolar, and amacrine cells. MME was originally identified in patients with multiple sclerosis (MS) by Gelfand et al., and it was characterized by cystic lacunar areas of hyporeflectivity with clear boundaries in the spectral domain optical coherence tomographic (SD-OCT) images . They suggested that MME represented a breakdown of the blood-retina barrier caused by subclinical uveitis or retinitis. Abegg et al. noted similar changes in a case of compressive optic neuropathy due to a glioma, but they suggested retrograde transsynaptic degeneration as the cause of MME . Balk et al. noted similar characteristics in a case of recurrent optic neuritis not due to multiple sclerosis adding inflammation as a possible cause of MME .
Adaptive optics (AO) technology has enabled clinicians to view the retina with high microscopic lateral resolution [26, 27]. This technique has been used to analyze the cone photoreceptor mosaic in eyes with inherited retinal degenerations [28, 29]. It has also been used to analyze the inner retinal layers, for example, the retinal nerve fiber layer . However, this new technology has not been used to analyze the inner layers of the retina in patients with MME. AO has a transverse resolution of approximately 1.6 μm compared to commercial OCT systems with a resolution of approximately 15 μm. This higher resolution should help in detecting and evaluating en face images of MME.
Thus, the purpose of this study was to investigate the characteristics of MME determined from the en face images obtained by an AO fundus camera in patients with ADOA and also to try to determine the mechanisms underlying the degeneration of the inner retinal cells and RNFL by AO. To accomplish this, 6 patients from 4 families with the OPA1 gene were studied.
The protocol of this study conformed to the tenets of the Declaration of Helsinki and was approved by the Institutional Review Board of the Nippon Medical School. Six consecutive cases of ADOA patients from 4 families who visited Nippon Medical School Chiba Hokusoh Hospital from December 2010 through April 2013 were studied. A written informed consent was obtained from the six patients after an explanation of the nature and possible complications of the experimental protocol.
2.1. Clinical Examinations
The ophthalmological examinations included measurements of the best-corrected visual acuity (BCVA), determination of the refractive error (spherical equivalent), slit-lamp biomicroscopy, ophthalmoscopy, fundus photography, fluorescein angiography (FA), perimetry, SD-OCT, infrared imaging, and full-field electroretinography (ERG). The visual fields were obtained by Goldman perimetry and Humphrey Visual Field Analyzer (Model 745i; Carl Zeiss Meditec, Inc., Dublin, California). The Swedish interactive threshold algorithm standard strategy was used with program 30-2 of the Humphrey Visual Field Analyzer. Color vision was evaluated with the Farnsworth Panel D-15. SD-OCT (Carl Zeiss Meditec) images were obtained from all of the patients. The B-scan retinal images were composed of 27,000/s consecutive A-scans acquired through the center of the macula horizontally for Figures 5(b) and 8(a). In all patients, the fixation was centered on the macula. For Figure 8(b), we moved a horizontal scan line manually to the area containing the MME detected by AO with centered patient fixation. For RNFL thickness analysis, we performed a vertical SD-OCT scan at about 1 mm from the edge of optic disc with centered fixation. The total scan depth was 2 mm, the axial resolution was 5 μm, and transverse resolution was 15 μm. The images presented are 6-mm-long scans except for Figure 5(b) which has been cut to fit AO images. The 512 × 128 Macular Cube scan protocol was used to obtain the en face OCT images. With this protocol, 128 cross-sectional B-scan images were obtained, each composed of 512 A-scans. In all patients, fixation was centered on the macula. Full-field scotopic and photopic ERGs were recorded using an extended testing protocol incorporating the International Society for Clinical Electrophysiology of Vision standards .
2.2. Genetic Testing
Blood samples were collected from the patients, and genomic DNA was isolated from peripheral white blood cells with a blood DNA isolation kit (NucleoSpin Blood XL; Macherey Nagel, Germany). The DNA was used as a template to amplify the OPA1 gene. Coding regions and flanking introns of the OPA1 gene were amplified by polymerase chain reaction (PCR) with published primers . The PCR products were purified (ExoSAP-IT; USB Corp., USA), and both strands of the gene were sequenced with an automated sequencer (Bio Matrix Research; Chiba, Japan).
RT-PCR was used to amplify the cDNAs of OPA1. The mRNAs were obtained from peripheral white blood cells with the TRIzol reagent (Invitrogen, CA, USA), and template cDNAs were generated with random hexamer primers. We designed exon-spanning primer pairs and used them to amplify exon 18 to exon 20 of the OPA1 cDNA. They are forward primer (5′-GTTGAACAACAGGCTGATAG-3′) and reverse primer (5′-GCTTGATATCCACTGTGGTG-3′). The recovered DNAs were subcloned into the StrataClone PCR cloning vector (Stratagene; CA, USA). Plasmid DNAs from 20 positive clones were purified with the Qiagen Plasmid Purification Kit (Qiagen, CA, USA) and sequenced with an automated sequencer (Bio Matrix Research; Chiba, Japan).
2.3. Adaptive Optics (AO) Flood Illumination Image Acquisition
Fundus images were obtained with an infrared AO retinal camera (rtx1, Imagine Eyes, Orsay, France) . This system was used in earlier investigations to image individual cone photoreceptors [27, 29, 34, 35] and other retinal structures [27, 36]. In our study, the AO instrument illuminated a 4-degree square field of the retina with 850 nm infrared flashes to acquire en face images of the retina with a transverse optical resolution of 250 line pairs/mm. Successive AO images were taken at adjacent retinal locations with an angular spacing of 2 degrees in the horizontal and vertical directions. This procedure allowed for a horizontal and vertical overlap of at least 2 degree between successive images. Prior to each acquisition, the focusing depth was adjusted to the inner nuclear layer. The resulting images were stitched together by superimposing retinal vessel landmarks with an image editing software (GIMP, The GIMP Development Team; Image J, National Institute of Health, Bethesda, MD). The size of each pixel was typically 0.8 μm when calculated at the retinal plane, and the values were adjusted for variations in the axial length of the eye . We also analyzed normal controls and patients with advanced glaucoma to determine whether MME was present. They were 50 normal controls and 5 advanced glaucomatous retinas. There were 27 men and 23 women whose age ranged from 18 to 57 years (mean, years) in this normal control group. There were 3 men and 2 women whose age ranged from 37 to 57 years (mean, years) in the glaucoma group. The focusing depth was adjusted to the INL.
3.1. Clinical Findings
We studied 6 patients from 4 families with ADOA, (Figure 1) and the clinical characteristics of these 6 patients are summarized in Table 1. The decimal BCVA of all patients was reduced with a range from 0.7 to 0.07. The Goldmann kinetic visual fields showed a centrocecal scotoma in three patients and a blind spot enlargement in the other three patients. Temporal optic disc palor was seen in all patients. Ito et al. reported that the retinal nerve fiber layer (RNFL) in the macular area of patients with ADOA was significantly thinner than that in control subjects by SD-OCT . They also showed that the RNFL in the temporal areas of circular scans around the optic disc was almost lost while the nasal areas were relatively well preserved.
|Best corrected visual acuity (decimal).|
bRetinal nerve fiber layer.
We performed a vertical SD-OCT scan at about 1 mm from the edge of optic disc. The results in the ADOA patients showed that the temporal RNFL was very thin in all of the patients (Figure 2). FA did not show any leakage in Patients 1-II-1 and 2-II-1 (data not shown). We did not perform FA on the other 4 patients.
The clinical findings of a representative case are shown in Figure 3 (Patient 1-II-1). Fundus examinations showed temporal palor of the optic discs (Figure 3(a)). A centrocecal scotoma was observed in the Goldmann kinetic visual fields test (Figure 3(b)). Panel D-15 showed that the confusion pattern was consistent with a tritan axis, blue-yellow defect in each eye (Figure 3(c)). The a- and b-waves of the scotopic and photopic full-field ERGs were of normal amplitudes. The amplitudes of the photopic negative response (PhNR) of the cone ERGs which is believed to originate from inner retinal layers have been reported to be reduced in ADOA patients . In this case, the PhNR of the cone ERG was decreased, and the peak of the PhNR was a positive potential relative to the baseline (Figure 3(d)).
3.2. Molecular Genetic Findings
We identified one already reported pathogenic mutation and three new mutations in the four families (Table 2). Patient 1-II-1 was found to have a new heterozygous G to A mutation at position −1 of intron 18 that is likely to abolish the 3′ splice acceptor site (c.1771-1G>A; Figures 4(a) and 4(b)). The family history revealed no other members including her parents with any eye disease. We could not test the genetics in other family members because she was not willing to have them tested. Although this mutation has never been reported, a mutation at position −2 of intron 18 (c.1771-2A>G) has been reported to be pathogenic with a splicing defect .
|Reference sequence NM_015560.2.|
To investigate the impact of the splice acceptor site mutation, we analyzed OPA1 transcripts expressed in the white blood cells from this patient. Two distinct RT-PCR products were obtained from the patient (data not shown). To separate the mutant transcripts from wild-type transcripts, the RT-PCR products were cloned into a cloning vector. Twenty clones from the patient were sequenced to verify the inserts, and 5 of them showed truncated inserts with a skipping of exon 19 (Figures 4(c)–4(e)). This skipping would yield a truncated protein with a premature termination codon due to a frameshift (p.N591GfsX18).
Patient 2-II-1 was found to have a new heterozygous single base-pair deletion at position 1899 (c.1899delT). This would yield a truncated protein with a premature termination codon due to a frameshift (p.I633MfsX12). We could not test the genetic changes in other family members because they were not willing to have them tested. Although this mutation is a novel mutation, two small deletion mutations within the same exon (c.1881_1882delAG, c.1892_1893delAT) have been reported as pathogenic mutations for ADOA [40, 41].
Patient 3-III-1 was found to have a reported nonsense mutation. A heterozygous C to T mutation at position 1096 (c.1096C>T) directly changed an arginine at amino acid position 366 to a stop codon (R366X). This mutation was confirmed to be pathogenic by several studies [10, 42, 43].
Patients 4-II-1, 4-III-1, and 4-III-2 from the same family were found to have a new heterozygous single base-pair deletion at amino acid position 1102 (c.1102delT) that would yield a truncated protein with a premature termination codon due to a frameshift (p.R368GfsX4).
All three new mutations identified caused a frameshift with premature termination codon. These mutations would likely be pathogenic by the mechanism of haploinsufficiency as reported .
3.3. High-Resolution Imaging of Microcystic Macular Edema (MME) by SD-OCT and Adaptive Optics
The SD-OCT images of Patient 1-II-1 showed cystic lacunar areas of hyporeflectivity with clear boundaries, or MME, which were compatible with the characteristics suggested by Gelfand et al. (Figure 5(b)) . Wolff et al.  reported that microcysts could also be observed using en face OCT imaging. En face OCT imaging of Patient 1-II-1 revealed that cysts were located in the superior, nasal, and inferior macular quadrants in both eyes (Figures 6(a) and 6(b)). AO imaging obtained from the same area showed high-resolution en face images of the microcysts in the inner layer of the retina (Figures 5(d) and 5(e)). They were of various sizes and appeared as dark reflectance areas outlined by hyperreflective regions. Most were oval shaped (Figures 5(d) and 5(e)). Similar structures were not found in more than 50 normal controls and 5 patients with advanced glaucoma in our department. We have not examined a patient with MS or optic nerve atrophy other than those with ADOA.
Abegg et al. and Wolff et al. have reported that an area with MME is seen with different patterns as hyporeflective regions in the IR images in the perimacular area [24, 44]. The IR images of our ADOA cases also had ring-shaped hyporeflective regions in the perimacular area (Figures 5(a), 7(b), and 7(c)). The hyporeflective region in the IR image coincided well with the area containing the microcystic structures in the AO images (Figures 7(a)–7(d)).
B-scan and en face SD-OCT images of Patient 2-II-1 did not show the MME clearly; however, the IR image had a crescent-shaped perimacular hyporeflective region (Figures 6(c), 6(d), and 8(a)–8(d)). In the crescent-shaped area, the en face AO image showed microcystic structures (Figures 8(e)–8(g)). The number of microcysts was fewer in Patient 2-II-1 than in Patient 1-II-1; however, the clarity of the microcysts was the same in these two patients (Figures 5(e) and 8(g)).
Although we analyzed the other 4 patients extensively, we did not find microcystic structures in their AO images. The refractive error and axial length were not significantly different in all six patients.
Over 200 mutations in the OPA1 gene have been identified in patients with ADOA (HGMD professional, Institute of Medical Genetics in Cardiff). Approximately one-half of the OPA1 mutations lead to premature termination codons from nonsense mutations or frameshifts from small insertions, deletions, or splice site mutations . These truncated mRNAs are unstable and get degraded by specific pathways, that is, nonsense-mediated mRNA decay, which are in-built protective cellular mechanisms against mutant proteins with possible dominant negative effect [42, 46, 47]. The reduced Opa1 protein expression levels observed in these reported cases support the role of haploinsufficiency in ADOA. These results strongly suggest that the three new heterozygous mutations with premature termination codon identified in this study are pathogenic.
Gelfand et al. reported that MME was associated with lower visual acuity and a thinner RNFL in patients with MS . In our cases, Patient 1-II-1 with the poorest BCVA had the clearest MME in her SD-OCT and AO images. Our vertical SD-OCT image between the optic disc and macular region showed that the temporal RNFL was almost completely absent in all of the patients. However, among these patients, Patient 1-II-1 had the thinnest RNFL in the peripheral region of the vertical scan. Our data are consistent with the hypothesis that the degree of MME is related to the disease severity.
Gelfand et al. hypothesized that the presence of MME was associated with a breakdown of the blood-retinal barrier . However, Barboni et al. noted that patients with LHON and DOA do not have any fluorescein leakage as expected for the noninflammatory status of their disease . Our results also showed that genetically identified ADOA patients with MME do not have any signs of leakage from their retinal vessels.
MME has been detected in the INL of the retina with chiasmal glioma . It is highly unlikely that the MME in a patient with brain tumor is due to inflammation of the retina and optic nerve. Thus, Abegg et al. hypothesized that the MME in the INL was due to retrograde transsynaptic degeneration .
It is well established that retrograde transsynaptic degeneration can occur in the human central nervous system [48, 49]. Van Buren observed atrophy of the RGC following a right occipital lobectomy in monkeys . Recently, Jindahra et al. presented evidence of retrograde trans-synaptic degeneration of RGCs identified by SD-OCT following both congenital and acquired lesions of the retrogeniculate visual pathway in humans . In addition, Green et al. reported that the neurodegenerative changes caused by retrograde transsynaptic degeneration in a patient with MS were seen not only in the RNFL and ganglion cell layer but also in the INL of their retina . Their histopathological study showed prominent atrophy of the INL in 40% of the eyes suffering from MS and none of the control eyes. They also recognized that the severity of the INL atrophy appeared to be related to the severity of RGC atrophy. Similar INL vacuoles have been observed histopathologically in rhesus monkeys with idiopathic optic atrophy . Combining these observations with our observations, we suggest the possibility that the dark regions observed in the en face AO images of our ADOA patients are areas of degenerated horizontal, bipolar, and amacrine cells in the INL caused by retrograde transsynaptic degeneration.
The en face MME structures detected by AO were also found in another ADOA patient who did not show MME clearly in the en face and cross-sectional OCT images. These observations indicate that AO might be useful in identifying MME in other neurodegenerative diseases and may also be helpful in determining the mechanisms underlying RGC and INL degeneration.
Our study has a number of limitations. We identified the en face MME in patients with ADOA; however, there are several other diseases that have MME in their SD-OCT images, for example, MS, recurrent optic neuritis, neuromyelitis optica, LHON, and chiasmal glioma. We need to investigate the en face MME structures in patients with such diseases to identify whether they also show the en face MME in their INL and to compare their features to those of en face MME seen in our patient with ADOA. It will probably be helpful in clarifying the pathomechanisms of the degeneration of inner retinal cell degeneration to investigate several diseases with different etiology.
We have found MME in the INL of the ADOA patients, but it is important to note that only in two patients. The cross-sectional nature of our study did not allow us to draw conclusions regarding the evolution of MME in ADOA and the other diseases. To address these issues, systematic longitudinal studies incorporating detailed ophthalmologic assessments in large cohort are needed and may help determine the mechanisms involved in the development of MME. Although the controls in our study including those with advanced glaucoma did not show MME in their en face AO images, we need to determine why patients with advanced glaucoma did not show en face MME despite the RGC loss. We cannot explain why we did not find MME in the other 4 ADOA patients in this study. It may be related to the disease severity; however, patient 2-II-1 showed comparable peripheral RNFL thickness and better BCVA compared to the other ADOA patients without MME. Some other factors may be needed for MME to develop.
In conclusion, our findings showed that genetically identified ADOA patients without any sign of inflammation can have MME in the INL of the retina. Our data indicate that the disease severity may be associated with the presence of MME in the INL as reported, because we found the clearest MME in the patients with poorest BCVA, although some other factors may be needed for MME to develop other than disease severity. Our findings indicate that there is a possibility that retrograde trans synaptic degeneration could cause severe damages in horizontal, bipolar, and amacrine cells in the INL after the optic nerve atrophy. Further studies are needed, and these findings will probably be helpful in clarifying the pathology of the degeneration of inner retinal cells by retrograde transsynaptic degeneration in patients with optic nerve atrophies and in developing new therapies.
Conflict of Interests
The authors declare that they have no conflict of interests associated with this paper.
The authors thank Dr. Duco Hamsaki of the Bascom Palmer Eye Institute, University of Miami School of Medicine, Miami, FL, USA, for discussions and editing their paper.
- P. Kjer, “Infantile optic atrophy with dominant mode of inheritance: a clinical and genetic study of 19 Danish families,” Acta Ophthalmologica, vol. 164, pp. 1–147, 1959.
- H. Eiberg, B. Kjer, P. Kjer, and T. Rosenberg, “Dominant optic atrophy (OPA1) mapped to chromosome 3q region. Linkage analysis,” Human Molecular Genetics, vol. 3, no. 6, pp. 977–980, 1994.
- B. Kjer, H. Eiberg, P. Kjer, and T. Rosenberg, “Dominant optic atrophy mapped to chromosome 3q region: II. Clinical and epidemiological aspects,” Acta Ophthalmologica Scandinavica, vol. 74, no. 1, pp. 3–7, 1996.
- W. M. Lyle, Genetic Risks: A Reference for Eye Care Practitioners, University of Waterloo Press, Ontario, Canada, 1990.
- J. B. Caldwell, R. O. Howard, and L. A. Riggs, “Dominant juvenile optic atrophy. A study in two families and review of hereditary disease in childhood,” Archives of Ophthalmology, vol. 85, no. 2, pp. 133–147, 1971.
- C. S. Hoyt, “Autosomal dominant optic atrophy. A spectrum of disability,” Ophthalmology, vol. 87, no. 3, pp. 245–251, 1980.
- P. B. Johnston, R. N. Gaster, V. C. Smith, and R. C. Tripathi, “A clinicopathologic study of autosomal dominant optic atrophy,” American Journal of Ophthalmology, vol. 88, no. 5, pp. 868–875, 1979.
- P. Kjer, O. A. Jensen, and L. Klinken, “Histopathology of eye, optic nerve and brain in a case of dominant optic atrophy,” Acta Ophthalmologica, vol. 61, no. 2, pp. 300–312, 1983.
- A. C. Cohn, C. Toomes, C. Potter et al., “Autosomal dominant optic atrophy: penetrance and expressivity in patients with OPA1 mutations,” American Journal of Ophthalmology, vol. 143, no. 4, pp. 656–662, 2007.
- C. Alexander, M. Votruba, U. E. A. Pesch et al., “OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28,” Nature Genetics, vol. 26, no. 2, pp. 211–215, 2000.
- P. Amati-Bonneau, A. Guichet, A. Olichon et al., “OPA1 R445H mutation in optic atrophy associated with sensorineural deafness,” Annals of Neurology, vol. 58, no. 6, pp. 958–963, 2005.
- C. Delettre, G. Lenaers, J.-M. Griffoin et al., “Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy,” Nature Genetics, vol. 26, no. 2, pp. 207–210, 2000.
- C. Delettre, G. Lenaers, L. Pelloquin, P. Belenguer, and C. P. Hamel, “OPA1 (Kjer type) dominant optic atrophy: a novel mitochondrial disease,” Molecular Genetics and Metabolism, vol. 75, no. 2, pp. 97–107, 2002.
- A. Olichon, E. Guillou, C. Delettre et al., “Mitochondrial dynamics and disease, OPA1,” Biochimica et Biophysica Acta, vol. 1763, no. 5-6, pp. 500–509, 2006.
- U. E. A. Pesch, J. E. Fries, S. Bette et al., “OPA1, the disease gene for autosomal dominant optic atrophy, is specifically expressed in ganglion cells and intrinsic neurons of the retina,” Investigative Ophthalmology and Visual Science, vol. 45, no. 11, pp. 4217–4225, 2004.
- R. Lodi, C. Tonon, M. L. Valentino et al., “Deficit of in vivo mitochondrial ATP production in OPA1-related dominant optic atrophy,” Annals of Neurology, vol. 56, no. 5, pp. 719–723, 2004.
- A. Olichon, L. Baricault, N. Gas et al., “Loss of OPA1 perturbates the mitochondrial inner membrane structure and integrity, leading to cytochrome c release and apoptosis,” Journal of Biological Chemistry, vol. 278, no. 10, pp. 7743–7746, 2003.
- P. Amati-Bonneau, M. L. Valentino, P. Reynier et al., “OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes,” Brain, vol. 131, no. 2, pp. 338–351, 2008.
- G. Hudson, P. Amati-Bonneau, E. L. Blakely et al., “Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance,” Brain, vol. 131, no. 2, pp. 329–337, 2008.
- C. Frezza, S. Cipolat, O. Martins de Brito et al., “OPA1 controls apoptotic cristae remodeling independently from mitochondrial fusion,” Cell, vol. 126, no. 1, pp. 177–189, 2006.
- N. J. Marchbank, J. E. Craig, J. P. Leek et al., “Deletion of the OPA1 gene in a dominant optic atrophy family: evidence that haploinsufficiency is the cause of disease,” Journal of Medical Genetics, vol. 39, no. 8, p. e47, 2002.
- P. Barboni, V. Carelli, G. Savini, M. Carbonelli, C. La Morgia, and A. A. Sadun, “Microcystic macular degeneration from optic neuropathy: not inflammatory, not trans-synaptic degeneration,” Brain, vol. 135, article e239, 2013.
- J. M. Gelfand, R. Nolan, D. M. Schwartz, J. Graves, and A. J. Green, “Microcystic macular oedema in multiple sclerosis is associated with disease severity,” Brain, vol. 135, pp. 1786–1793, 2012.
- M. Abegg, M. Zinkernagel, and S. Wolf, “Microcystic macular degeneration from optic neuropathy,” Brain, vol. 135, article e225, 2012.
- L. J. Balk, J. Killestein, C. H. Polman, B. M. Uitdehaag, and A. Petzold, “Microcystic macular oedema confirmed, but not specific for multiple sclerosis,” Brain, vol. 135, article e226, 2012.
- J. Liang, D. R. Williams, and D. T. Miller, “Supernormal vision and high-resolution retinal imaging through adaptive optics,” Journal of the Optical Society of America A, vol. 14, no. 11, pp. 2884–2892, 1997.
- M. Lombardo, S. Serrao, N. Devaney, M. Parravano, and G. Lombardo, “Adaptive optics technology for High-Resolution retinal imaging,” Sensors, vol. 13, pp. 334–366, 2012.
- J. L. Duncan, Y. Zhang, J. Gandhi et al., “High-resolution imaging with adaptive optics in patients with inherited retinal degeneration,” Investigative Ophthalmology and Visual Science, vol. 48, no. 7, pp. 3283–3291, 2007.
- N. Tojo, T. Nakamura, C. Fuchizawa, T. Oiwake, and A. Hayashi, “Adaptive optics fundus images of cone photoreceptors in the macula of patients with retinitis pigmentosa,” Clinical Ophthalmology, vol. 7, pp. 203–210, 2013.
- K. Takayama, S. Ooto, M. Hangai et al., “High-resolution imaging of the retinal nerve fiber layer in normal eyes using adaptive optics scanning laser ophthalmoscopy,” PLoS ONE, vol. 7, no. 3, Article ID e33158, 2012.
- G. E. Holder, M. G. Brigell, M. Hawlina, T. Meigen, V. Vaegan, and M. Bach, “ISCEV standard for clinical pattern electroretinography—2007 update,” Documenta Ophthalmologica, vol. 114, no. 3, pp. 111–116, 2007.
- Y. Mashima, K. Yamada, M. Wakakura et al., “Spectrum of pathogenic mitochondrial DNA mutations and clinical features in Japanese families with Leber's hereditary optic neuropathy,” Current Eye Research, vol. 17, no. 4, pp. 403–408, 1998.
- C. Viard, K. Nakashima, B. Lamory, M. Pâques, X. Levecq, and N. Château, “Imaging microscopic structures in pathological retinas using a flood-illumination adaptive optics retinal camera,” in Ophthalmic Technologies XXI, vol. 7885 of Proceedings of SPIE, January 2011.
- M. Lombardo, G. Lombardo, P. Ducoli, and S. Serrao, “Adaptive optics photoreceptor imaging,” Ophthalmology, vol. 119, pp. 1498–1498, 2012.
- M. Lombardo, S. Serrao, P. Ducoli, and G. Lombardo, “Variations in image optical quality of the eye and the sampling limit of resolution of the cone mosaic with axial length in young adults,” Journal of Cataract & Refractive Surgery, vol. 38, pp. 1147–1155, 2012.
- I. Audo, M. El Sanharawi, C. Vignal-Clermont et al., “Foveal damage in habitual poppers users,” Archives of Ophthalmology, vol. 129, no. 6, pp. 703–708, 2011.
- A. G. Bennett, A. R. Rudnicka, and D. F. Edgar, “Improvements on Littmann's method of determining the size of retinal features by fundus photography,” Graefe's Archive for Clinical and Experimental Ophthalmology, vol. 232, no. 6, pp. 361–367, 1994.
- Y. Ito, M. Nakamura, T. Yamakoshi, J. Lin, H. Yatsuya, and H. Terasaki, “Reduction of inner retinal thickness in patients with autosomal dominant optic atrophy associated with OPA1 mutations,” Investigative Ophthalmology and Visual Science, vol. 48, no. 9, pp. 4079–4086, 2007.
- K. Miyata, M. Nakamura, M. Kondo et al., “Reduction of oscillatory potentials and photopic negative response in patients with autosomal dominant optic atrophy with OPA1 mutations,” Investigative Ophthalmology and Visual Science, vol. 48, no. 2, pp. 820–824, 2007.
- M. Ferré, D. Bonneau, D. Milea et al., “Molecular screening of 980 cases of suspected hereditary optic neuropathy with a report on 77 novel OPA1 mutations,” Human Mutation, vol. 30, no. 7, pp. E692–E705, 2009.
- O. Baris, C. Delettre, P. Amati-Bonneau et al., “Fourteen novel OPA1 mutations in autosomal dominant optic atrophy including two de novo mutations in sporadic optic atrophy,” Human mutation, vol. 21, no. 6, p. 656, 2003.
- U. E. A. Pesch, B. Leo-Kottler, S. Mayer et al., “OPA1 mutations in patients with autosomal dominant optic atrophy and evidence for semi-dominant inheritance,” Human Molecular Genetics, vol. 10, no. 13, pp. 1359–1368, 2001.
- C. Delettre, J.-M. Griffoin, J. Kaplan et al., “Mutation spectrum and splicing variants in the OPA1 gene,” Human Genetics, vol. 109, no. 6, pp. 584–591, 2001.
- B. Wolff, C. Basdekidou, V. Vasseur, M. Mauget-Faÿsse, J. A. Sahel, and C. Vignal, “Retinal inner nuclear layer microcystic changes in optic nerve atrophy: a novel spectral-domain OCT finding,” Retina, vol. 33, no. 10, pp. 2133–2138, 2013.
- M. Ferré, P. Amati-Bonneau, Y. Tourmen, Y. Malthièry, and P. Reynier, “eOPA1: an online database for OPA1 mutations,” Human mutation, vol. 25, no. 5, pp. 423–428, 2005.
- S. Schimpf, S. Schaich, and B. Wissinger, “Activation of cryptic splice sites is a frequent splicing defect mechanism caused by mutations in exon and intron sequences of the OPA1 gene,” Human Genetics, vol. 118, no. 6, pp. 767–771, 2006.
- S. Schimpf, N. Fuhrmann, S. Schaich, and B. Wissinger, “Comprehensive cDNA study and quantitative transcript analysis of mutant OPA1 transcripts containing premature termination codons,” Human Mutation, vol. 29, no. 1, pp. 106–112, 2008.
- G. Holmes and T. G. Stewart, “On the connection of the inferior olives with the cerebellum in man,” Brain, vol. 31, no. 1, pp. 125–137, 1908.
- A. W. Campbell, Histological Studies on the Localisation of Cerebral Function, Cambridge University Press, Cambridge, Mass, USA, 1905.
- J. M. Van Buren, “Trans-synaptic retrograde degeneration in the visual system of primates,” Journal of Neurology, Neurosurgery, and Psychiatry, vol. 26, pp. 402–409, 1963.
- P. Jindahra, A. Petrie, and G. T. Plant, “Retrograde trans-synaptic retinal ganglion cell loss identified by optical coherence tomography,” Brain, vol. 132, no. 3, pp. 628–634, 2009.
- A. J. Green, S. McQuaid, S. L. Hauser, I. V. Allen, and R. Lyness, “Ocular pathology in multiple sclerosis: retinal atrophy and inflammation irrespective of disease duration,” Brain, vol. 133, no. 6, pp. 1591–1601, 2010.
- B. Fortune, L. Wang, B. V. Bui, C. F. Burgoyne, and G. A. Cioffi, “Idiopathic bilateral optic atrophy in the rhesus macaque,” Investigative Ophthalmology and Visual Science, vol. 46, no. 11, pp. 3943–3956, 2005.
Copyright © 2013 Kiyoko Gocho et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.