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Incidence of uveitis and macular edema among patients taking fingolimod 0.5 mg for multiple sclerosis
Journal of Ophthalmic Inflammation and Infection volume 10, Article number: 24 (2020)
Patients with multiple sclerosis (MS) have a higher incidence of uveitis compared with the general population. Fingolimod, a first line disease modifying drug used in multiple sclerosis, may cause macular edema and thus requires ophthalmic examination. However, murine models and anecdotal reports suggest fingolimod may reduce the incidence of uveitis.
To report the incidence of uveitis and macular edema among those on fingolimod 0.5 mg (Gilenya®) therapy for multiple sclerosis (MS).
Retrospective review of patients on fingolimod who developed uveitis and/or macular edema.
No patients had an occurrence or history of uveitis. Four of the 188 (2.13%) patients developed macular edema without ocular inflammation. One of the 188 (0.53%) patients developed Acute Macular Neuroretinopathy.
Patients taking fingolimod have a lower incidence of uveitis than expected in a population of MS patients.
Multiple sclerosis (MS) is an inflammatory demyelinating disease which targets the central nervous system in a delayed-type hypersensitivity reaction. Fingolimod (Gilenya®, Novartis) reduces both the number of relapses and progression of disease in the relapsing remitting variant of MS by preventing the migration of lymphocytes [1, 2]. Fingolimod-associated macular edema (FAME) is a known complication requiring ophthalmic examination [3,4,5]. Uveitis can cause vision loss and may be 20 times more likely in MS when compared to the general population [6,7,8,9,10,11]. The recommendation of pretreatment ophthalmic exams and monitoring while on fingolimod presents a unique opportunity to evaluate MS patients who may have undiagnosed uveitis and to follow for its development.
Herein we report an incidence of uveitis and macular edema among patients on the FDA-approved dose of fingolimod 0.5 mg for MS.
The electronic health record at The Retina Institute (St. Louis) was reviewed for patients referred for screening exams due to fingolimod use. Each case was examined for a past history, recurrence, or new occurrence of uveitis. Snellen visual acuity was reviewed as well as time of exposure to fingolimod. Optical coherence tomography (OCT) and biomicroscopy results were available for all patients. The incidence of optic neuritis, FAME, and other visually significant ocular comorbidities were also recorded.
A total of 188 patients met the study criteria over a period of 104 months. None had or developed uveitis [6,7,8,9,10,11]. One of the 188 (0.53%) developed acute macular neuroretinopathy (AMN). Twenty six of 188 (13.83%) had a history of optic neuritis and 7 (3.7%) had a new occurrence during the course of the study. The mean follow up on fingolimod was 60.9 months with a range of 1–104 months. Three patients discontinued treatment after 57, 43, and 13 months due to nonophthalmic reasons. Visual acuity (VA) was 20/40 or better in 93% of eyes, 5% had visual acuity 20/50 to 20/200, and 2% had worse VA than 20/200. The visual acuity of two eyes was worse than 20/400 as a result of optic neuritis. Additional causes of vision loss in the patients with vision worse than 20/100 were optic neuritis, ischemic optic neuropathy, ruptured globe, keratoconus, macular hole, and amblyopia.
Fingolimod-associated macular edema (FAME)
Three of the 188 patients (1.6%) developed FAME (Fig. 1). Fingolimod was continued and each was successfully treated with either topical steroids, NSAIDs, or a combination of the two. None of these patients had any other identifiable cause of macular edema. Another 65-year-old female with a 57 month exposure to fingolimod developed macular edema 2 weeks after cataract extraction. She was successfully treated with topical and subtenons steroids while continuing the fingolimod.
No patient had a history of or developed uveitis during the follow up period.
One 27-year-old female presented with unilateral photopsia and a paracentral scotoma 5 months after beginning fingolimod. Her migraines were treated with sumatriptan and she took lisdexamfetamine for weight control. Otherwise, she denied recent viral prodrome, vaccinations, pregnancy, oral contraceptive pills (OCPs), and international travel. VA was 20/20 and dilated fundus examination revealed a subtle reddish lesion just superior to the fovea of the right eye consistent with acute macular neuroretinopathy (Fig. 2). The patient’s visual defect faded and the flashes of light resolved by 5 months after presentation. She remained stable throughout her 13 months of follow up.
The incidence of uveitis in this cohort (n = 188) using fingolimod for MS was zero. The incidence of uveitis in MS patients is variable yet none in our cohort had a typical uveitis occurrence despite a mean observation period greater than 5 years [6,7,8,9, 12,13,14,15,16]. Lim et al. previously pooled data on the incidence of uveitis from the MS fingolimod studies . The mean observation period was 627 days and included a range of fingolimod doses compared with placebo and interferon beta-1a. The authors reported a first time uveitis occurrence in 0.09% of patients on fingolimod (dose range 0.5 mg to 5 mg), 0.2% in the placebo group, and 0.09% in the interferon group. Of the 139 with a uveitis history, 5 (3.6%) had recurrence while on fingolimod. One in 8 (12.5%) patients on placebo had recurrence while 4 of 15 (26.67%) taking interferon had recurrent uveitis. Though the MS fingolimod studies were not designed to evaluate the effect of fingolimod on the prevention of uveitis or a reduction in uveitis recurrence, the data suggest those on placebo had double the rate of uveitis occurrence compared with those on fingolimod. Those taking intramuscular interferon had a similar rate of first time uveitis. The rate of recurrent uveitis in those taking a placebo was over 3 times those on fingolimod, while recurrence in those taking interferon was just over 7 times those on fingolimod. In the last 8 years since we began screening patients on fingolimod we noted an unusually low incidence of concomitant uveitis despite the diagnosis of MS. We cannot comment on the rate of recurrence since none of our cohort had a prior history of uveitis. However, this retrospective review confirms a low initial occurrence of uveitis in patients taking fingolimod for MS. Varying doses of fingolimod and interferon beta-1a were included in the data compiled by Lim et al. . Our current study is unique in that it includes only the FDA-approved 0.5 mg dose of fingolimod. In addition, the cohort is a relatively homogenous group without a history of uveitis who were observed for a significantly longer period (mean > 5 years).
Fingolimod limits lymphocytic migration by targeting sphingosine-1-phosphate (S1P) receptors found in lymphocytic tissue, endothelium, and leukocytes [1, 2, 17]. It is therefore not unreasonable to hypothesize that there is a limitation of lymphocytic migration through the blood-retinal barrier as well when patients are exposed to fingolimod. There is precedence for fingolimod’s ophthalmic anti-inflammatory effect in experimental autoimmune uveitis. Murine studies have confirmed active disease suppression, maintenance of disease remission, and increased vascular barrier integrity when subjects are exposed to fingolimod [18, 19]. We hypothesize fingolimod’s anti-inflammatory effect could partly explain the lack of uveitis in our cohort that would typically be associated with MS.
One patient developed AMN. There is no consensus on a unifying mechanism of AMN though it is most strongly associated with flu-like illnesses, influenza vaccination, and OCP’s [20,21,22,23,24,25]. The patient in our cohort had other risk factors for AMN including lisdexamfetamine and migraine headaches. Lisdexamfetamine acts by facilitating the release of norepinephrine and dopamine, known vasoconstrictors. Therefore, her AMN was likely due to relative ischemia from vasoconstriction rather than a manifestation of inflammation within the retinal vasculature. The latter seems unlikely since she nor any other patient in our cohort developed typical clinical findings consistent with uveitis. There is no known direct link between AMN and MS alone, although it has been associated with acute demyelinating optic neuritis [26, 27]. In a prospective study of 114 patients with acute optic neuritis, Deschamps et al. found 6 developed AMN . Therefore it remains that the development of AMN in our patient is likely coincidental since she had no history of optic neuritis.
The average time to the development of uveitis after an MS diagnosis ranges from 3.6 to 9 years [6,7,8,9]. We did not include time since the onset of MS diagnosis since this information was not available on every patient. Yet the mean follow up on fingolimod was 60.9 months and was likely adequate considering the average onset of uveitis after MS. Further, the length of time of MS was at least the same or greater than the fingolimod exposure (mean = 60.9 months) since MS was the indication for fingolimod use in all patients.
FAME occurred in 3 of the 188 (1.6%) patients in the present study. This rate is much higher than the previously documented 0.2% incidence [3, 4, 28]. The mechanism of FAME is not fully understood although it develops within 3 months from initiation of fingolimod therapy in 68% of cases [3, 4]. It has been shown to decrease vascular permeability yet it also increases tight junction permeability resulting in edema formation [1, 29]. The incidence of FAME in those with a history of uveitis was 19% compared with 1% in the FREEDOMS and TRANSFORMS trials in patients taking the 1.25 mg dose of fingolimod . This data suggests a link between uveitis and FAME although there may be a variable effect on vascular permeability that is dependent on the individual’s immune system status [2, 4]. It is possible that those with a history of uveitis may have weakened tight junctions, resulting in a predilection for FAME with S1P receptor activation rather than vascular barrier stabilization . The decreased dose (0.5 mg) of fingolimod now FDA-approved for the treatment of MS may not have such a high association of uveitis and FAME. Our patients with FAME had no history of uveitis or indications of intraocular inflammation, though subclinical uveitis cannot be ruled out in the absence of fluorescein angiography. There was an increased incidence of FAME in this cohort and all cases responded to anti-inflammatory therapy despite continuation of fingolimod.
The strengths of this study include a uniquely long follow up period with a mean of over 5 years, the generalizability of the findings due to exposure to the only FDA-approved dose of fingolimod for adults, and the consistency of examination by ophthalmologists with experience in the evaluation and treatment of anterior, intermediate, and posterior uveitis. No patients were excluded from taking fingolimod. However, as a retrospective review it is possible the referring pattern of the treating neurologists may have introduced some selection bias. This did not occur to our knowledge since the determination of ocular contraindication to fingolimod treatment was the responsibility of the examining ophthalmologist.
Fingolimod is a well tolerated drug. Despite the high incidence of FAME in our cohort it was easily managed with topical therapy. We report a zero incidence of first time uveitis typically associated with MS in patients taking fingolimod and call for further evaluation of its potential use in the management of uveitis.
Availability of data and materials
Data was collected using the electronic health record of The Retina Institute in St. Louis. The datasets generated contain health protected information and are therefore not available to the public.
Fingolimod-associated macular edema
Optical coherence tomography
Acute macular neuroretinopathy
Oral contraceptive pills
McVerry BJ, Garcia JG (2004) Endothelial cell barrier regulation by sphingosine 1-phosphate. J Cell Biochem 92:1075–1085
Mandal P, Gupta A, Fusi-Rubiano W et al (2017) Fingolimod: therapeutic mechanisms and ocular adverse effects. Eye (Lond) 31:232–240
Kappos L, Radue EW, O’Connor P et al (2010) A placebo controlled trial of oral fingolimod in relapsing multiple sclerosis. N Engl J Med 362:387–401
Zarbin MA, Jampol LM, Jager RD et al (2013) Ophthalmic evaluations in clinical studies of fingolimod (FTY720) in multiple sclerosis. Ophthalmology 120:1432–1439
Budde K, Schütz M, Glander P et al (2006) FTY720 (fingolimod) in renal transplantation. Clin Transpl 20:17–24
Kaya D, Kaya M, Özakbaş S, Idiman E (2014) Uveitis associated with multiple sclerosis: complications and visual prognosis. Int J Ophthalmol 7:1010–1013
Le Scanff J, Seve P, Renoux C et al (2008) Uveitis associated with multiple sclerosis. Mult Scler 14:415–417
Thouvenot E, Mura F, De Verdal M et al (2012) Ipsilateral uveitis and optic neuritis in multiple sclerosis. Mult Scler Int 2012:37236
Biousse V, Trichet C, Bloch-Michel E, Roullet E (1999) Multiple sclerosis associated with uveitis in two large clinic-based series. Neurology 52:179–181
Jouve L, Benrabah R, Héron E et al (2017) Multiple sclerosis-related uveitis: does MS treatment affect uveitis course? Ocul Immunol Inflamm 25:302–307
Zein G, Berta A, Foster CS (2004) Multiple sclerosis-associated uveitis. Ocul Immunol Inflamm 12:137–142
Lim LL, Silva DG, Lo TC et al (2019) Uveitis in patients with multiple sclerosis in clinical trials of fingolimod: incidence, prevalence, and impact on disease course. Ophthalmology 126:438–444
Porter R (1972) Uveitis in association with multiple sclerosis. Br J Ophthalmol 56:478–481
Graham EM, Francis DA, Sanders MD, Rudge P (1989) Ocular inflammatory changes in established multiple sclerosis. J Neurol Neurosurg Psychiatry 52:1360–1363
Karara AM, Macky TA, Sharawy MH (2013) Pattern of uveitis in an Egyptian population with multiple sclerosis: a hospital-based study. Ophthalmic Res 49:25–29
Vidović T, Cerovski B, Jukić T (2005) The appearance of pars planitis in multiple sclerosis. Coll Antropol 29:203–206
David OJ, Kovarik JM, Schmouder RL (2012) Clinical pharmacokinetics of fingolimod. Clin Pharmacokinet 51:15–28
Raveney BJE, Copland DA, Nicholson LB, Dick AD (2008) Fingolimod (FTY720) as an acute rescue therapy for intraocular inflammatory disease. Arch Ophthalmol 126:1390–1395
Copland DA, Liu J, Schewitz-Bowers LP et al (2012) Therapeutic dosing of fingolimod (FTY720) prevents cell infiltration, rapidly suppresses ocular inflammation, and maintains the blood-ocular barrier. Am J Pathol 180:672–681
Turbeville SD, Cowan LD, Gass JD (2003) Acute macular neuroretinopathy: a review of the literature. Surv Ophthalmol 48:1–11
Bhavsar KV, Lin S, Rahimy E et al (2016) Acute macular neuroretinopathy: a comprehensive review of the literature. Surv Ophthalmol 61:538–565
Rahimy E, Sarra D (2014) Paracentral acute middle maculopathy spectral-domain optical coherence tomography feature of deep capillary ischemia. Curr Opin Ophthalmol 3:207–212
Casalino G, Arrigo A, Romano F (2019) Acute macular neuroretinopathy: pathogenic insights from optical coherence tomography angiography. Br J Ophthalmol 103:410
Munk MR, Jampo LM, Cunha Souza E et al (2016) New associations of classic acute macular neuroretinopathy. Br J Ophthamol 100:389–394
Shah SP, Goren JF, Lazzara MD et al (2013) Aute macular neuroretinopathy associated with the use of norepinephrine reuptake inhibitors: a case series and OCT findings. Retin Cases Brief Rep 7:146–149
Foroozan R, Buono LM, Savino PJ, Sergott RC (2002) Acute demyelinating optic neuritis. Curr Opin Ophthalmol 13:375–380
Deschamps R, Vasseur V, Shor N et al (2019) A new association: acute macular neuroretinopathy in acute optic neuritis. Acta Ophthalmol 97:e753–e756
Cohen JA, Barkhof F, Comi G et al (2010) Oral fingolimod or intramuscular interferon for relapsing multiple sclerosis. N Engl J Med 362:402–415
Cugati S, Chen CS, Lake S, Lee AW (2014) Fingolimod and macular edema:pathophysiology, diagnosis, and management. Neurol Clin Pract 4:402–409
Provided in part by the Retina Research and Development Foundation.
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This study was approved by the Institutional Review Board at St. Luke’s Hospital. Data collection was conducted in a HIPPA compliant fashion and the research adhered to the tenets of the World Medical Association’s Declaration of Helsinki.
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Sonne, S.J., Smith, B.T. Incidence of uveitis and macular edema among patients taking fingolimod 0.5 mg for multiple sclerosis. J Ophthal Inflamm Infect 10, 24 (2020). https://doi.org/10.1186/s12348-020-00215-1
- Cystoid macular edema
- Macular edema
- Multiple sclerosis
- Acute macular neuroretinopathy