Clinical Overview of Leber Hereditary Optic Neuropathy

Almina Stramkauskaitė
Department of Ophthalmology, Lithuanian University of Health Sciences, Medical Academy, Kaunas, Lithuania

Ieva Povilaitytė
Department of Ophthalmology, Lithuanian University of Health Sciences, Medical Academy, Kaunas, Lithuania

Brigita Glebauskienė
Department of Ophthalmology, Lithuanian University of Health Sciences, Medical Academy, Kaunas, Lithuania

Rasa Liutkevičienė*
Department of Ophthalmology, Lithuanian University of Health Sciences, Medical Academy, Kaunas, Lithuania
Neuroscience Institute, Lithuanian University of Health Sciences, Medical Academy, Kaunas, Lithuania

Abstract. Leber hereditary ptic neuropathy (LHON) is a disease of young adults with bilateral, painless, subacute visual loss. The peak age of onset of LHON is in the second and third decades of life. Men are 4 times more likely to be affected than women. In about 25-50% of cases, both eyes are affected simultaneously. In unilateral cases, the other eye is usually affected 2 to 3 months later. Visual acuity deteriorates to counting fingers or worse with a dense central or centrocecal scotoma. In the subacute phase, the optic disc may appear hyperemic with swelling of the peripapillary retinal nerve fibre layer, peripapillary telangiectasias, and increased vascular tortuosity. Ocular coherence tomography of the macula shows marked thinning of the ganglion cell complex even at this stage. The diagnosis of LHON is made in a subject with a consistent clinical history and/or one of three common pathogenic mitochondrial DNA (mtDNA) variants identified by molecular genetic testing. Idebenone was approved by the European Medicines Agency under exceptional circumstances for the treatment of LHON. Current evidence suggests some benefit to vision in a subset of affected individuals treated with idebenone, particularly when treated within the first year of onset of vision loss. In this article, we discuss aetiology, clinical features, diagnosis, differential dignosis, prognosis and treatment.
Keywords: Leber hereditary optic neuropathy, aetiology, clinical features, diagnosis, treatment.

Paveldimos Lėberio optinės neuropatijos klinikinė apžvalga

Santrauka. Paveldima Lėberio optinė neuropatija (PLON) jaunų suaugusiųjų liga, pasireiškianti abipusiu, beskausmiu, poūmiu regos praradimu. PLON dažniausiai prasideda antrame ir trečiame gyvenimo dešimtmetyje. Vyrai šia liga serga 4 kartus dažniau nei moterys. Apie 25–50% atvejų, abi akys pažeidžiamos tuo pačiu metu. Vienpusio regos nervo pažeidimo atvejais, kitoje akyje panašūs simptomai pasireiškia po 2–3 mėnesių. Regos aštrumas mažėja iki pirštų skaičiavimo ar dar blogiau, taip pat nustatoma centrinė ar centrocekalinė skotoma. Poūmėje fazėje stebimas hiperemiškas regos nervo diskas kartu su peripapiliniu tinklainės nervinių skaidulų pluošto (TNSP) paburkimu, peripapilinėmis telangiektazijomis, ir padidėjusiu kraujagyslių vingiuotumu. Optinėje koherentinėje tomografijoje (OKT) stebimas žymus ganglinių ląstelių suplonėjimas geltonojoje dėmėje. PLON diagnozė nustatoma remiantis nuoseklia klinikine istorija ir/ar molekuliniais genetiniais tyrimais, nustačius vieną iš trijų patogenetinių mitochondrinės DNR (mtDNR) mutacijų. Idebenonas buvo patvirtintas Europos vaistų agentūros, PLON gydymui. Įrodyta, kad regėjimas pagerėjo daliai pacientų, kai gydymas idebenonu buvo pradėtas per pirmuosus metus nuo regos aštrumo blogėjimo. Šiame straipsnyje aptariame PLON etiologiją, klinikinius požymius, diagnozę ir gydymą.
Raktiniai žodžiai: Paveldima Lėberio optinė neuropatija, etiologija, klinikiniai požymiai, diagnozė, gydymas.

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* Corresponding author: Rasa Liutkevičienė, Department of Ophthalmology, Lithuanian University of Health Sciences, Medical Academy, Eiveniu 2 str., Kaunas LT-50161, Lithuania. Tel.: +370-326740. E-mail: rasa.liutkeviciene@lsmuni.lt

Received: 16/03/2022. Revised: 15/05/2022. Accepted: 17/05/2022
Copyright © 2022 Almina Stramkauskaitė, Ieva Povilaitytė, Brigita Glebauskienė, Rasa Liutkevičienė. Published by Vilnius University Press.This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Introduction

Leber hereditary optic neuropathy (LHON) is the most common primary mitochondrial DNA disease, with the majority of patients having one of three primary mtDNA point mutations, namely m.3460G > A (MTND1), m.11778G > A (MTND4), and m.14484T > C (MTND6) [1]. In addition to the three primary mutations, approximately 30 different point mutations have been associated with LHON, which are divided into two groups: the “top-14”, which include the three primary mutations, and a group of cases that occur only in a family or in single cases [2]. LHON is characterized by bilateral, subacute loss of vision due to preferential loss of retinal ganglion cells (RGCs) in the inner retina, resulting in optic nerve degeneration. The dead RGCs are then unable to send visual signals to the brain, resulting in output that is not processed properly, leading to blindness and extreme visual impairment. RGCs loss occurs in about 50% of males and about 10-15% of females. Recovery of lost vision is possible depending on the mutation [3]. LHON is not age-dependent as it affects people in all age groups, but it is reported that males between the ages of 20 and 30 are most commonly affected [4]. The mutation in the mitochondrial genome (mtDNA) occurs in the subunit encoding complex-I (CI) of the electron transport chain, NADH:ubiquinone oxidoreductase, and the mutation usually involves the replacement of a single amino acid. This in turn leads to a lack of energy in neurons, causing neuronal death [5]. Apart from CI dysfunction, impairment of the glutamate transport system and increased oxidative stress also lead to RGCs dysfunction and death [6]. Currently available treatments reduce optic nerve stress to some extent, but do not completely eliminate the condition [7]. Therefore, in this article, we discuss aetiology, clinical features, diagnosis, and treatment.

Aetiology

LHON is a maternally inherited mitochondrial disorder that results in central scotoma due to thinning of the retinal nerve fiber layer and death of RGCs [8–10]. Because this inherited disease usually involves a mutation in the mtDNA that is passed through maternal inheritance, there is a history of vision loss in maternal relatives in more than half of families. Surprisingly, there is no family history in up to 40% of cases, but this is mainly because tracing is difficult, as de novo mutations are particularly rare [11–13]. The severity of LHON depends on whether the factors are homoplasmic or heteroplasmic [14]. While milder LHON mutations are homoplasmic, more severe CI mutations are both homoplasmic, leading to optic atrophy, and heteroplasmic, leading to basal ganglia degeneration, dystonia, as well as Leigh syndrome [8].

Many pathogenetic mechanisms of LHON are known, including CI dysfunction with decreased adenosine triphosphate (ATP) synthesis. Oxidative phosphorylation (OXPHOS) is responsible for the majority of ATP synthesis, and a chain of five respiratory complexes located at the inner mitochondrial membrane plays a central role in this process. All three missense mutations (ND1, ND4, ND6) of LHON are subunits of complex I. Therefore, damage to the respiratory chain can lead to a lack of ATP synthesis, resulting in RGCs degeneration or death [8,10,15]. Due to apoptotic RGCs, visual signals do not reach the brain, thus the output is not processed properly, resulting in blindness and severe visual damage. Although the visual loss is painless, inflammation of the optic nerves may cause discomfort in rare cases [3,16]. In some studies, the respiratory chain was impaired in patients with the m. 11778G > A mutation, but not in those with the m. 3460G > A mutation. The outcome of respiratory impairment in LHON is controversial and further studies are needed [10].

Apart from the impairment of CI, caused by energetic failure, an impaired respiratory chain can lead to increased production of ROS, so that increased levels of oxidative stress also accounts for the degeneration of the RGCs [6,17]. Mitochondria are responsible for the majority of ROS production, while ROS can damage any cell [17]. Although the primary LHON mutation is a prerequisite, secondary factors are responsible for the risk of vision loss [6]. Cigarette smoking is associated with either the onset or progression of LHON, and heavy smokers are more susceptible to the disease. Heavy drinkers tend to develop an increased risk of vision loss, although the progression of the disease is not as severe as with smoking [18]. Interestingly, some studies report that vitamin B12 deficiency contributes to the development of LHON due to a lack of relevant metabolic cofactors [19].

Clinical features

Based on the clinical features of LHON, it is generally divided into an acute and a chronic phase, while some studies also describe a presymptomatic phase [20–23]. The latter stage shows ophthalmoscopic changes, such as edema of the retinal nerve fiber layer, tortuosity of the small vessels, and peripapillary microangiopathy [24]. More comprehensive testing may reveal more subtle manifestations of optic nerve dysfunction. According to the literature, asymptomatic carriers of LHON mutation 1178 may have dyschromatopsia with predominantly red/green color discrimination and decreased spatial contrast sensitivity [25]. Not all individuals who are carriers of the mutation, suffer from visual impairment. However, the majority of carriers present with LHON symptoms between the ages of 15 and 35 years, and the disease predominantly affects males, with an estimated male-to-female ratio of 5:1 [26]. The onset of the disease is characterised by acute, painless loss of central vision, with both eyes affected simultaneously in approximately 25% of cases [26]. Although this disease usually occurs bilaterally, it occurs asynchronously. Initially, only one eye is affected, while the other eye becomes damaged within a year. Considering that vision loss is painless, discomfort may rarely occur due to inflammation of the optic nerves [3,4]. A sudden onset of blurred and cloudy vision are the most common initial symptoms of the acute phase of LHON [22,27,28]. Presymptomatic ophthalmoscopic manifestations may persist throughout life in many patients, but once central vision disappears, some new ophthalmoscopic features may appear, such as edema of superior and inferior fibre arcades and axonal loss within the papillomacular bundle (PMB) [24,29]. These fundus changes are visible either before or later after vision loss [30]. Vision deterioration becomes more severe after four to six weeks, with visual acuity typically being 6/60. Loss of colour discrimination and either central or centrocaecal scotoma is also observed [31,32]. Although this phase usually lasts several weeks, approximately 20% to 30% of patients do not show any ophthalmoscopic abnormalities during the acute phase [33]. Later, the edema of the nerve fibres decreases, and the chronic phase is usually reached more than a year after the onset of the disease [34]. Due to the early failure of the PMB, most of the remaining nerve fibers degenerate, resulting in complete optic atrophy, which is more pronounced on the temporal side [23,27,35]. Although affected individuals with the 14484 mutation or aged < 20 years may recover spontaneously, recovery of vision is usually minimal and the prognosis of visual recovery is poor [10,27,33,36]. In the chronic phase, vision loss is usually not progressive, and the majority of patients are considered legally blind [37,38]. Vision loss stabilizes and reaches its nadir within 6-12 months after the onset of the disease [33,36]. When a patient is diagnosed in the late stages and has no maternal history, a brief differential diagnosis is required. It takes at least one month to obtain the results of molecular testing. For this reason, comprehensive testing, including neuroimaging of the retina, optic nerves, chiasm, and optic tracts, should not be delayed in order to make the correct diagnosis and treatment. However, neither gender nor mutation status is responsible for the timing or severity of vision loss [23].
According to the consensus, LHON has the following stages (Table 1):

Table 1. Leber hereditary optic neuropathy stages

Asymptomatic (the carriers of the mutation).	Subacute (from the manifestation of LHON to 6 months).	Dynamic (from months 6 to 12).	Chronic >(more than 12 months).
Using OCT, thickening of the temporal retinal nerve fibre layer was confirmed in asymptomatic individuals with an LHON-causing mtDNA pathogenic variant, providing evidence that the PMB is particularly vulnerable in LHON [39].	Patients are usually asymptomatic until they develop visual disturbance in the central visual field in the first eye (acute phase). Similar symptoms appear in the other eye on average two to three months later, so that in the majority of cases both eyes are affected within six months. Unilateral optic nerve damage is very rare in patients with LHON, and in such cases another underlying pathologic process should be actively excluded. The most common feature is an enlarging central or centrocecal scotoma. As the size and density of the visual field defect increases, visual acuity deteriorates to the level of finger counting or worse. At this stage, specific changes of the ocular fundus can be observed even in asymptomatic patients: retinal telangiectasias of the peripapillary vessels, edema of the peripapillary retinal nerve fibre layer, which progress and eventually lead to atrophy of the optic nerve [40].	The fundus changes that occur in the subacute stage slowly regress: the edema of the peripapillary retinal nerve fibre layer recedes [40].	At this stage, optic nerve atrophy progresses at different rates: it can be observed from 6 weeks to more than 1 year after the loss of vision. The central or centrocyclic scotoma enlarges. Most patients remain severely visually impaired and meet the legal requirements for blind registration. OCT shows thinning of the retinal fibre layer, especially in the temporal zones [37].

Figure 1. (a, b) Bilateral optic nerve atrophy.

Figure 2. OCT shows thinning of retinal nerve fiber layer.

Diagnosis

LHON is a poorly diagnosed disease. Correct identification of LHON is critical because of its similarity to several diseases such as isolated optic neuritis or neuromyelitis optica. Attention in the clinical setting is important to correctly identify the disease and exclude other pathologies [41,42]. Molecular genetic testing for pathogenic variants of mtDNA, a multi-gene panel, or complete sequencing of mtDNA are performed to identify LHON. Although the identification of specific mutations in mtDNA plays a central role, other data, such as medical history, fundus, OCT, and magnetic resonance imaging (MRI), are also relevant to the diagnosis of the disease [13]. Some studies recommend that an electrocardiogram be obtained in all patients with LHON because of possible cardiac abnormalities [43–45].

Differential diagnosis

There is a wide spectrum of acute and chronic optic neuropathies with varying aetiology and variable visual prognosis. The results of ophthalmologic examination, neurologic examination, and imaging studies can aid in diagnosis and treatment. The two main diseases that should be differentiated are: optic neuritis and dominant optic atrophy.

Optic neuritis (ON). The main symptoms of ON are very similar to LHON. Symptoms at a young age, mostly in females (ratio of females to males 3:1, in the case of LHON mostly in males), low visual acuity, central scotoma, colour vision loss, pain with eye movements, visual evoked potentials (VEPs) may show a delayed response and reduced P100 amplitude. Rapid recovery and a good therapeutic response to metilprednisolone within a few weeks confirm the diagnosis of optic neuritis. Because of the strong association between optic neuritis and multiple sclerosis, an MRI of the brain should be ordered [46,47].

Dominant optic atrophy (DOA). DOA has an insidious onset with mild visual loss beginning in the first two decades of life. Unlike LHON, patients are asymptomatic in the early stages. Patients are often identified only by testing based on a family history or a diagnosis of bilateral optic atrophy. Patients often present with visual acuity of 0.6 or better. Although visual prognosis varies widely at DOA, visual performance is better compared with LHON, with an average visual acuity of 0.3 to 0.1 [23]. Approximately 50-60% of people with DOA have a mutation in OPA -1(3q28-q29) [48,49].

Ischemic optic neuropathy (ION) and increased intracranial pressure (IIcP). ION shows optic nerve edema in the acute stage and diffuse optic atrophy in the chronic stage. In patients older than 55 years, arterial ischemic optic neuropathy should be ruled out by determining C-reactive protein and erythrocyte sedimentation rate and consulting a reumatologist who will decide whether to biopsy the temporal artery. If bilateral optic nerve edema is present, the possibility of elevated intracerebral pressure (ICP) should be considered. Symptoms of elevated ICP may include headache, dizziness, nausea, and vomiting. An imaging study should be performed in consultation with a neurologist [46].

Normal tension glaucoma (NTG) may have similar clinical features, such as visual acuity loss, paracentral defects, and thinning of the neuroretinal rim on OCT. However, NTG manifests in the older population with an average age of approximately 64 years and older [50]. Arcuate visual field defects, excavation of the inferior rim, and thinning of the inferior optic nerve also distinguish NTG from other mitondrial neuropathies, however genetic testing confirms the LHON diagnosis [51].

Nutritional and drug-induced optic neuropathies. Nutrition-induced neuropathies may be caused by deficiencies of vitamins B, B2, B6, B9, B12 [52–54]. Of course, they may also be caused by anorexia nervosa, alcoholism, gastrointestinal problems, or gastrointestinal surgery and must be confirmed by blood tests and by others specialists consultations [55]. Drug-induced optic neuropathies can be caused by ethambutol, linezolid, chloramphenicol, erythromycin and others [23,56–58]. Medical and social history may also be helpful in the differential diagnosis. However, MRI of the brain and orbit must be performed in all cases of optic neuropathy. Compressive and demyelinating lesions may cause edematous or atrophic optic nerves. Symptoms of a compressive lesion may include headache and changes in mood, personality, or memory. An MRI of the brain and orbits will confirm the diagnosis [46].

Treatment

Idebenone (Raxone(®)) is currently the only disease-specific drug approved by the European Medicines Agency in 2015 for the treatment of visual impairment in adolescents and adults with LHON [59,60]. It is a short-chain benzoquinone that is rapidly absorbed and well tolerated [61,62]. Idebenone 300 mg 3 times daily rarely causes adverse symptoms, but the most common side effects include nasopharyngitis, headache, cough, and dizziness [63]. Due to partial structural similarity, idebenone is referred to as a synthetic analogue of coenzyme Q10, but it has different properties and mechanisms of action. Since idebenone has a shorter and less lipophilic tail than coenzyme Q10, its bioactivation occurs mainly in the cytoplasm and does not rely on mitochondrial function. Moreover, idebenone induces respiratory pathways that are independent of mitochondrial CI [61,62,64,65]. Due to its advantageous structure, idebenone can cross membranes and act as a mitochondrial electron transfer agent [61,62,65]. Importantly, idebenone bypasses the disrupted CI and transfers electrons directly to the mitochondrial complex III, resulting in improved energy supply and restoration of inactive but viable retinal ganglion cells, preventing further vision loss and initiating vision restoration [60,65,66]. Many studies have provided convincing evidence that treatment with oral idebenone 900 mg/d for 6 months not only has a beneficial effect on vision, but also improves Tritan colour vision [67,68].

Several studies have been conducted on the treatment of LHON to find the best treatment option for LHON. These include various neuroprotective agents, stem cell therapy, infrared radiation therapy, and even gene therapy [69–71]. The most promising of these methods are gene therapy and stem cell therapy, but more research is needed to evaluate their efficacy. Gene therapy is suitable for LHON because of the easily accessible RGCs layer in the retina. However, inducing genes into the mitochondrial genome is not easy to perform because mitochondria have a double membrane. However, the desired gene can be transferred to the nuclear genome instead. These studies show that the treatment of LHON is promising. Nevertheless, further studies are needed to evaluate adverse effects and determine the longevity of beneficial effects. The use of stem cells to treat LHON is under investigation, but appears promising as well. Mesenchymal stem cells protect RGCs by secreting both neurotrophic factors and anti-inflammatory cytokines. These stem cells were injected into a rat model of glaucoma and a beneficial effect on RGCs axon survival was observed [72].

Bromidine, an α2-agonist used to treat patients with glaucoma, was found to have a stabilizing effect on RGCs. Because the antiapoptotic properties of bromidine act through CI, it would be a perfect treatment for LHON because the major mitochondrial mutations are also found in this complex. However, bromidine is not suitable for prophylaxis of visual disturbances in the second eye, when acute visual disturbance due to LHON is observed in one eye, studies show [73,74].

Some environmental factors such as smoking and alcohol consumption accelerate the risk of vision loss. Therefore, patients should be advised to avoid smoking and minimize alcohol consumption [18,37]. Because vision loss does not usually progress over time, appropriate occupational therapy and low vision aids can improve the quality of life of LHON patients. [37].

Visual prognosis

Visual prognosis is mutation dependent. The highest chances of visual improvement are observed in patients with mutation 14484T > C, while the lowest chances are observed with mutation 11778G > A [10]. Nevertheless, an early age of onset, a subacute course with slow visual deterioration, and a larger optic disc are associated with a better visual prognosis. [75,76]. However, most patients with LHON experience permanent loss of vision, which negatively affects their quality of life [37].

Conclusion

LHON is a rare disease characterized by degeneration of RGCs.

LHON is leading to bilateral visual loss with poor prognosis.

The disease is caused by mitochondrial mutations.

Idebenone, gene and stem cells therapy have provided encouraging results.

At the moment, Idebenone is only an approved treatment for LHON.

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