Inherited retinal dystrophies (IRD) are a heterogeneous group of rare chronic disorders caused by genetically determined degeneration of photoreceptors and retinal pigment epithelium cells. Ultra-widefield (UWF) imaging is a useful diagnostic tool for evaluating retinal integrity in IRD, including Stargardt disease, retinitis pigmentosa, cone dystrophies, and Best vitelliform dystrophy. Color or pseudocolor and fundus autofluorescence images obtained with UWF provide previously unavailable information on the retinal periphery, which correlates well with visual field measurement or electroretinogram. Despite unavoidable artifacts of the UWF device, the feasibility of investigations in infants and in patients with poor fixation makes UWF imaging a precious resource in the diagnostic armamentarium for IRD.
Inherited retinal dystrophies (IRD) are a heterogeneous group of rare chronic disorders caused by genetically determined degeneration of photoreceptors or retinal pigment epithelium (RPE) cells.
Color and fundus autofluorescence ultra-widefield (UWF) imaging have added novel insights in the interpretation of both macular and peripheral changes occurring in IRD.
UWF imaging aids in the diagnosis and monitoring of patients with IRD; UWF changes correlate well with functional damage on visual field test and electroretinogram.
Advantages of digital UWF imaging systems include enhanced resolution, easier acquisition with non-compliant patients (i.e., children), and avoidance of pupil dilation.
Future investigations on structure–function and phenotype–genotype correlations using UWF will increase our understanding of the complex spectrum of IRD.
Inherited retinal dystrophies (IRD) are a heterogeneous group of rare chronic disorders caused by genetically determined degeneration of photoreceptors or retinal pigment epithelium (RPE) cells. IRD are heterogeneous in terms of onset of symptoms and severity of clinical manifestations. IRD can be clinically categorized into four groups: rod-dominant diseases, cone-dominant diseases, generalized retinal degenerations, and vitreoretinal disorders [1, 2]. An additional group of IRD includes pure macular diseases, namely Stargardt disease (STGD1), pattern dystrophy, Best vitelliform dystrophy (BVD), Sorsby disease, North Carolina dystrophy, and Doyne honeycomb dystrophy .
Specific complaints, age of onset, inheritance pattern, and electro-functional tests (such as full-field electroretinogram (ERG) and multifocal ERG) may suggest the site of retinal dysfunction and, in specific cases, the gene defect.
There is currently no specific treatment for any form of retinal dystrophy; antioxidant drugs, such as lutein, photoprotection, and low-vision aids are the only therapeutic alternatives offered nowadays. Nevertheless, early diagnosis and better characterization are important for accurate information on prognosis, genetic counseling, and gene-targeted therapeutic options available in the future. The aim of the present narrative review is to elucidate the role of non-invasive imaging in IRD, focusing on widefield (WF) and ultra-widefield (UWF) imaging devices. This article is based on previously conducted studies and does not contain any studies with human participants or animals performed by any of the authors.
Non-invasive Imaging and Widefield Application in IRD
Fundus autofluorescence (FAF) is one of the most informative techniques in patients with IRD. Two types of FAF are mostly used in clinical practice: short wavelength autofluorescence (SW-FAF), with an emitting light of 488 nm, is specific for lipofuscin, and near-infrared autofluorescence (NIR-FAF), with an emitting light of 787 nm, is specific for melanin. The changes on SW- and NIR-FAF provide useful information about the pathophysiology of IRD. SW-FAF shows hyper-autofluorescence in the case of lipofuscin buildup  or outer retinal disruption ; on the other hand, hypo-autofluorescence corresponds to areas of RPE loss (as RPE atrophy) or masquerading of normal RPE autofluorescence (such as pigment clumping) [6,7,8]. SW-FAF signal may also transiently increase after blue light exposure; this phenomenon has been called photobleaching. The optical pigments of photoreceptors normally absorb light in the same spectrum of SW-FAF; illumination with blue light induces an isomerization of the optical pigments from the 11-cis to all-trans conformation, resulting in a temporary loss of their absorption properties . Photobleaching might differ between healthy and diseased eyes, including intermediate age-related macular degeneration  and IRD .
Fundus fluorescein angiography (FFA) and indocyanine green angiography (ICGA) evaluate the retinal and choroidal perfusion  and the presence of rare complications of IRD, such as cystoid macular edema (CME) or choroidal neovascularization (CNV) . While they are useful at the first diagnosis, they are poorly applicable in monitoring patients with IRD.
Optical coherence tomography (OCT) assesses the state of the vitreoretinal interface, the inner retinal layers, the photoreceptors, and the RPE; OCT also confirms the presence of specific features, including vitelliform accumulation in Best disease, flecks in STGD1, and foveal cavitation in certain cone-rod dystrophies [14, 15]. OCT angiography (OCTA) has added novel insights in the interpretation of vascular changes occurring in the macula in patients with IRDs. OCTA combines information from morphology and perfusion at the level of the superficial capillary plexus and the deep capillary plexus of the inner retina, at the choriocapillaris, and the choroidal layer. OCTA has shown interesting changes in a wide variety of IRD, including STGD1 , retinitis pigmentosa (RP) , and BVD . Whereas the scanning range of most commercially available OCTA devices is still limited to the posterior pole, technical advances now allow scanning of larger areas of the retina (up to 80°) by montage of multiple scans [19, 20]. A swept-source OCTA device (PlexElite, Carl Zeiss Meditec, Dublin, CA, USA) has been applied to investigate the grade of peripheral perfusion impairment in patients with RP ; further studies are needed to clarify the peripheral vascular involvement in other IRDs.
Traditional fundus retinography and fluorangiographic photograms include only the central 30° or 55° of the retina; this field of view is optimal for detecting pathologic changes of the optic nerve head, the papillary region, and the macula, but is inadequate for the imaging of the medium-far and of the very-far retinal periphery. In recent years, dedicated non-mydriatic wide-angle digital cameras have been developed to obtain UWF imaging of the retina, including the Optos Optomap® (Dumfermline, Scotland, UK), the ZEISS Clarus 500 (Dublin, USA) , and the Centervue Eidon device (Padova, Italy) . UWF imaging allows simultaneous evaluation of the peripheral and central retina without the requirement of eye steering; UWF imaging has revealed interesting details about peripheral retinal lesions in IRDs [24, 25].
Advantages of digital UWF imaging systems include enhanced resolution, short image acquisition and processing time, the possibility of image manipulation and transmission, good-quality capturing in eyes with cataract or media opacities, easier procedure with non-compliant pediatric patients, and avoidance of pupil dilation [26, 27]. UWF systems combine standard fundus photography (either true color or pseudocolor) with other retinal investigations, namely FFA, ICGA, red-free filter, and FAF. While confocal scanning laser ophthalmoscopy (cSLO) such as the Heidelberg Spectralis operates with SW-FAF and NIR-FAF filters only, UWF devices are coupled with novel technologies for FAF signal generation. Optos Optomap is embedded with a green-light autofluorescence (excitation 518 nm); as green-light autofluorescence has a smaller rate of absorption by macular pigments, it better discriminates FAF anomalies in the perifoveal retina . Eidon contains a “true color” confocal scanner which captures images with three different sources: LED (440–650 nm), infrared (825–870 nm), and blue light (440–475 nm). The Eidon system separates short and long FAF emission wavelengths, obtaining a spectrally resolved FAF or color-FAF [29,30,31]. This imaging technique has revealed interesting new details in patients with IRD .
STGD1 is a recessive inherited disease with an incidence of 8–10 per 100,000 persons, caused by autosomal mutations in the ABCA4, ELOVL4, or PROM1 genes [33, 34]. The pathognomonic features of STGD1 include yellow or white fish-shaped flecks and photoreceptors, RPE, and choriocapillaris atrophy at the posterior pole. STGD1 is a progressive disease; however, the rate of disease progression changes varies considerably between subjects . The number of flecks tends to increase with time with a radial, centrifugal pattern; indeed, UWF imaging is able to show lesions extending beyond the vascular arcades, in contrast to conventional imaging (Fig. 1). Both SW-FAF and NIR-FAF are reliable techniques for monitoring the progression of the disease [36, 37]. Moreover, spectrally resolved FAF allowed the distinction of two types of flecks: the first type is located centrally and shows green emission fluorescent component (500–560 nm) and disruption of outer retinal bands on OCT; the other type is located mainly peripherally and shows red emission fluorescent component (560–700 nm) and only minor alterations of outer retinal layers on OCT . RPE atrophy can also spread outside the vascular arcades in later stages of STGD1 disease, sparing the peripapillary region (Fig. 2) [38, 39].
A novel classification of UWF FAF patterns in STGD1 has been published and is based on the distribution of flecks and RPE atrophy extension (Table 1) . UWF imaging is particularly useful in characterizing the type III pattern, in which RPE atrophy extends towards the equator. The type III pattern has the worst prognosis: it is associated with severe alterations on OCT and vascular capillary damage in the central retina on OCTA, compared with other patterns . Moreover, patients with widespread disease on UWF imaging present with a greater constriction of peripheral isopters, more dysfunction on ERG, and worse best corrected visual acuity (BCVA) compared to patients with disease confined to the macula .
Less frequent findings have been described on UWF FAF, including a hyper-autofluorescent ring at the transition between diseased and healthy retina, an oval-shaped hyper-autofluorescence outside the arcades, and mottled peripheral FAF changes (Fig. 3) . Recently, peripheral pigmented retinal lesions resembling congenital hypertrophy of the RPE (CHRPE) have also been reported in patients with STGD1 [44, 45]. Patients with peripheral pigmented hypertrophy featured decreased visual acuity, large central scotomas, abnormal ERG, and more widespread involvement of the peripheral retina compared with patients without CHRPE-like lesions.
In conclusion, UWF imaging has allowed a shifting paradigm in STGD1 and other ABCA4-related diseases from a pure macular dystrophy to a more generalized affection. Although STGD1 predominantly involves the macula in the first stages, significant retinal changes extend to the periphery with the progression of the disease. According to some authors, type III STGD1 with peripheral involvement represents a different phenotype of STGD1 rather than a progression of center-involving disease.
Retinitis Pigmentosa and Pigmentary Dystrophies
The term retinitis pigmentosa (RP) embraces a heterogeneous group of inherited dystrophies characterized by progressive degeneration of rods and secondary involvement of cones. RP can be inherited as autosomal dominant, autosomal recessive, or X-linked disease; rarely, it can originate from spontaneous mutations .
Night blindness and peripheral visual field defect are the most common symptoms at the onset of RP; gradual central visual acuity loss may take place in advanced stages. The pathogenesis of RP is complex: loss of photoreceptors is accompanied by changes in the RPE and retinal glia; ultimately, the inner retinal neurons, blood vessels, and the optic nerve head are affected. Pigment clumping in the mid and extreme periphery, vessel attenuation, and CME are the typical fundus findings.
UWF imaging is revealed a precious tool to diagnose and monitor patients suffering from RP; a complex grading of RP changes has been recently proposed that is based on UWF FAF (Table 2) . Different phenotypes of decreased autofluorescence (DAF) have been described in RP; patients with widespread DAF (grade 4) (especially if featuring nummular DAF) are significantly older than other groups (Fig. 4) .
Patients with RP exhibit a ring of perifoveal hyper-autofluorescence; this line is thought to be the landmark between preserved central fovea and diseased retina [47,48,49]. The area external to this ring correlates with the extent of visual field damage [50,51,52]. UWF FAF has a greater predictive value for estimating residual retinal sensitivity than OCT ; in fact, hypo-autofluorescence on UWF FAF correlates with functional scotomas on Goldmann perimetry with an agreement of 91%, whereas normal autofluorescence corresponds to normal visual fields with an agreement of 85% .
In selected cases, UWF imaging also allows genotypic/phenotypic correlation in patients with RP. Patients with RHO, USH2A, CEP290, RPGRIP1, and RPGR mutations usually show a prominent hyper-autofluorescent ring at the macula; patients with PRPF31 mutations show a similar ring of autofluorescence in the macula and a circular pattern of coarse DAF in the mid-periphery . A second ring of macular hyper-autofluorescence has been found in patients with USH2A mutations. A peripheral patchy pattern of hyper/hypo-autofluorescence has been described in patients with RHO or RPGR mutations, while diffuse hypo-autofluorescence is distinctive for USH2A or RDS/PRPH2 mutations . Patients with X-linked RP present radial hyper-autofluorescence starting from the mid-periphery and pointing towards the posterior pole [55, 56]. Finally, one patient with CRB1 mutation demonstrated para-arterial preservation of the RPE .
Pigmented paravenous retinochoroidal atrophy (PPRCA) is a rare retinal dystrophy characterized by bilateral retinal and RPE atrophy and pigment clumping along the large retinal veins; PPRCA is part of the spectrum of RP [57, 58]. The diagnosis is clinical and its exact pathogenesis is not clear. On UWF pseudocolor photographs, pigment appears as bone spicule, coarse clumps, or fine granular accumulations starting from the optic disc and expanding into the mid-periphery . UWF FAF shows well-demarcated perivenular hypo-autofluorescence corresponding to RPE atrophy and pigmentation (Fig. 5) . A crescent-like hyper-autofluorescent demarcation can be noticed at the border between the normal and affected retina or along the retinal veins, with or without central hypo-autofluorescence (Fig. 5) . Widefield OCTA revealed a relative sparing of the retinal capillary plexuses (superficial and deep), with diffuse defects in the choriocapillaris corresponding to RPE atrophy .
Cone dystrophies (CDs) and cone-rod dystrophies (CRDs) are the most common hereditary cone disorders ; CRDs differ from CDs in terms of the impairment of rod function from the early phases of the disease. Two additional forms of localized cone dysfunction syndromes have been described: occult macular dystrophy and peripheral cone dystrophy (PCD) [63, 64].
Fundus examination is normal in the majority of patients; in advanced cases, it may show a macular bullseye aspect with various degrees of retinal and RPE atrophy . Patients with primary cone degeneration and secondary rod disruption may also develop retinal vascular attenuation and peripheral pigment deposits, mimicking RP. FAF, OCT, and OCTA macular abnormalities have been extensively described in patients with CD, CRD, and localized cone dysfunction syndromes [66,67,68,69]. On the other hand, reports on UWF changes in these patients are still scarce.
UWF FAF displays a hyper-autofluorescent macular ring in certain cases of CD and CRD (Fig. 6) ; in the periphery, abnormal FAF inversely correlates with the residual visual function on both Goldmann perimetry and ERG responses . In a large intra-familial study, UWF FAF showed high similarity between siblings but significant diversity between parent–child pairs; this finding suggests that UWF imaging features in CD and CRD—or more generally with IRD—tend to change with age .
In patients with PCD, UWF FAF showed a central bullseye lesion and perimacular hyper-autofluorescence with rounded or scalloped borders and, in the periphery, irregular hyper- and hypo-autofluorescence located mainly in the nasal quadrant and not contiguous with the macular findings . UWF imaging also aided in the differential diagnosis between PCD (which remains a diagnosis of exclusion) and other posterior segment conditions, such as retinal white dot syndromes, autoimmune retinopathies, infectious chorioretinitis, enhanced S-cone syndrome, pericentral retinitis pigmentosa, or STGD1 .
Best vitelliform dystrophy (BVD) is an autosomal dominant macular dystrophy caused by the somatic mutation of the BEST1 gene; the disease belongs to a bigger family of conditions known as bestrophinopathies characterized by the accumulation of lipofuscin and abnormal electro-oculographic (EOG) Arden ratio . Although BVD usually presents with a single lesion (Fig. 7), up to 30% of patients feature multifocal lesions within and outside the foveal region (Fig. 8). In some patients, other less-specific retinal lesions may be found, such as schisis, subretinal fibrosis, or pigment clumping . Extrafoveal lesions are usually smaller than those located into the macula [76, 77]. Despite no study having systematically addressed the changes in the retinal periphery in BVD and other BEST1-related diseases, UWF imaging may significantly help in the assessment and the monitoring of the vitelliform lesions, especially those located in extrafoveal regions.
Ultra-widefield imaging is a useful tool for evaluating retinal integrity in IRD. Color or pseudocolor and FAF images obtained with UWF provide previously unavailable information about the retinal periphery, which correlates well with visual field or ERG measurement in patients with IRD. Physicians should be aware of peripheral image magnification, image distortion, and artifacts of the UWF devices; nevertheless, the feasibility of investigations in infants and in patients with poor fixation makes UWF imaging a precious resource in the diagnostic armamentarium. Future investigations on structure–function and phenotype-genotype correlations using UWF imaging will undoubtedly increase our understanding of the complex spectrum of IRD.
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All named authors meet the International Committee of Medical Journal Editors (ICMJE) criteria for authorship for this article, take responsibility for the integrity of the work as a whole, and have given their approval for this version to be published.
Maria Vittoria Cicinelli, Alessandro Marchese, Maria Pia Manitto, Alessandro Bordato, and Maurizio Battaglia Parodi have no financial disclosures. Francesco Bandello is advisory board member for Allergan, Bayer, Boehringer-Ingelheim, Hoffmann La Roche, Novartis, NTC Pharma, Sifi, Thrombogenics, Zeiss. Francesco Bandello receives personal fees by Sooft. No conflicting relationship exists for any author.
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Cicinelli, M.V., Marchese, A., Bordato, A. et al. Reviewing the Role of Ultra-Widefield Imaging in Inherited Retinal Dystrophies. Ophthalmol Ther 9, 249–263 (2020). https://doi.org/10.1007/s40123-020-00241-1
- Best vitelliform disease
- Fundus autofluorescence
- Inherited retinal dystrophy
- Retinitis pigmentosa
- Stargardt dystrophy
- Ultra-widefield imaging