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Clinical patterns and risk factors in scleritis: a multicentric study in Colombia

  • Inflammatory Disorders
  • Published:
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Abstract

Purpose

This study aims to describe the clinical characteristics of scleritis in a large cohort of Colombian patients and identify factors associated with the clinical presentation.

Methods

Retrospective case series of patients with scleritis from 2015 to 2020. Clinical records were obtained from seven uveitis referral centers in Colombia. Patients with a diagnosis of episcleritis were excluded.

Results

We evaluated 389 patients with scleritis (509 eyes). There was a female predominance (75.6%) with a mean age of 51 ± 15 years. Most cases were noninfectious (94.8%) and unilateral (69.2%). The most frequent type of inflammation was diffuse anterior scleritis (41.7%), followed by nodular scleritis (31.9%) and necrotizing scleritis (12.3%). Systemic autoimmune diseases were found in 41.3% of patients, the most common being rheumatoid arthritis (18.5%) and granulomatosis with polyangiitis (5.9%). Polyautoimmunity was found in 10.4% of those with a systemic autoimmune disease. The most frequent treatment was systemic steroids (50.9%), followed by systemic NSAIDs (32.4%). Steroid-sparing immunosuppression was required in 49.1% of patients. Systemic autoimmune diseases were more common in patients with necrotizing scleritis and those older than 40 years of age. Best-corrected visual acuity of 20/80 or worse at presentation was more common in necrotizing scleritis and subjects with associated uveitis, ocular hypertension, or who were over 40 years of age.

Conclusions

This is the first study in Colombia and the largest in Latin America describing the clinical characteristics and presentation patterns of scleritis. The most common presentation was in females, with unilateral, anterior diffuse noninfectious scleritis. Systemic autoimmune diseases and polyautoimmunity were frequent, as was the need for steroid-sparing immunosuppression. Age over 40 and necrotizing scleritis were associated with higher odds of having a systemic autoimmune disease and worse visual acuity at presentation.

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Data availability

The information in the databases used in this article is freely accessible and is available for research purposes.

Abbreviations

ANA:

Antinuclear antibodies

ANCA:

Anti-neutrophil cytoplasmic antibodies

BCVA:

Best-corrected visual acuity

GPA:

Granulomatosis with polyangiitis

HLA-B27:

Human leukocyte antigen B27

IQRs:

Interquartile range (IQRs)

NS:

Necrotizing scleritis

NSAIDs:

Systemic non-steroidal anti-inflammatory drugs

OR:

Odds ratio

PolyA:

Polyautoimmunity

PUK:

Peripheral ulcerative keratitis

RA:

Rheumatoid arthritis

RF:

Rheumatoid factor

SD:

Standard deviation

SSI:

Steroid-sparing immunosuppression

References

  1. Okhravi N, Odufuwa B, McCluskey P et al (2005) Scleritis. Surv Ophthalmol 50(4):351–363. https://doi.org/10.1016/j.survophthal.2005.04.001

    Article  PubMed  Google Scholar 

  2. Turk MA, Rosenbaum JT (2021) A good detective never misses a clue: why the epidemiology of scleritis deserves our attention. Arthritis Rheumatol 73(7):1127–1128. https://doi.org/10.1002/art.41724

    Article  PubMed  Google Scholar 

  3. Homayounfar G, Nardone N, Borkar DS et al (2013) Incidence of scleritis and episcleritis: Results from the pacific ocular inflammation study. Am J Ophthalmol 156(4):752-758.e3. https://doi.org/10.1016/j.ajo.2013.05.026

    Article  PubMed  Google Scholar 

  4. Honik G, Wong IG, Gritz DC (2013) Incidence and prevalence of episcleritis and scleritis in Northern California. Cornea 32(12):1562–1566. https://doi.org/10.1097/ICO.0b013e3182a407c3

    Article  PubMed  Google Scholar 

  5. Braithwaite T, Adderley NJ, Subramanian A et al (2021) Epidemiology of scleritis in the United Kingdom from 1997 to 2018: population-based analysis of 11 million patients and association between scleritis and infectious and immune-mediated inflammatory disease. Arthritis Rheumatol 73(7):1267–1276. https://doi.org/10.1002/art.41709

    Article  PubMed  Google Scholar 

  6. Wakefield D, Di Girolamo N, Thurau S et al (2005) Scleritis: immunopathogenesis and molecular basis for therapy. Prog Retin Eye Res 35:44–62. https://doi.org/10.1016/j.preteyeres.2013.02.004

    Article  CAS  Google Scholar 

  7. Cunningham ET, McCluskey P, Pavesio C et al (2016) Scleritis. Ocul Immunol Inflamm 24(1):2–5. https://doi.org/10.1016/j.preteyeres.2013.02.004

    Article  PubMed  CAS  Google Scholar 

  8. Dutta Majumder P, Agrawal R, McCluskey P et al (2020) Current approach for the diagnosis and management of noninfective scleritis. Asia-Pacific J Ophthalmol 10(2):212–223. https://doi.org/10.1097/APO.0000000000000341

    Article  Google Scholar 

  9. Akpek EK, Thorne JE, Qazi FA et al (2004) Evaluation of patients with scleritis for systemic disease. Ophthalmology 111(3):501–506. https://doi.org/10.1016/j.ophtha.2003.06.006

    Article  PubMed  Google Scholar 

  10. Jain V, Garg P, Sharma S (2009) Microbial scleritis - experience from a developing country. Eye 23(2):255–261. https://doi.org/10.1038/sj.eye.6703099

    Article  PubMed  CAS  Google Scholar 

  11. Lavric A, Gonzalez-Lopez JJ, Majumder PD et al (2016) Posterior scleritis: analysis of epidemiology, clinical factors, and risk of recurrence in a cohort of 114 patients. Ocul Immunol Inflamm 24(1):6–15. https://doi.org/10.3109/09273948.2015.1005240

    Article  PubMed  Google Scholar 

  12. Sainz De La Maza M, Molina N, Gonzalez-Gonzalez LA et al (2012) Clinical characteristics of a large cohort of patients with scleritis and episcleritis. Ophthalmology 119(1):43–50. https://doi.org/10.1016/j.ophtha.2011.07.013

    Article  PubMed  Google Scholar 

  13. Tanaka R, Kaburaki T, Ohtomo K et al (2018) Clinical characteristics and ocular complications of patients with scleritis in Japanese. Jpn J Ophthalmol 62(4):517–524. https://doi.org/10.1007/s10384-018-0600-y

    Article  PubMed  CAS  Google Scholar 

  14. Sainz De La Maza M, Molina N, Gonzalez-Gonzalez LA et al (2012) Scleritis therapy. Ophthalmology. 119(1):51–8. https://doi.org/10.1016/j.ophtha.2011.07.043

    Article  PubMed  Google Scholar 

  15. Cuchacovich TM, Pacheco BP, Merino BG et al (2000) Clinical features and response to systemic treatment in episcleritis and scleritis resistant to local treatment. Rev Med Chil 128(11):1205–1214. https://doi.org/10.4067/S0034-98872000001100004

    Article  CAS  Google Scholar 

  16. de Oliveira MD, Curi ALL, Fernandes RS et al (2009) Scleritis: clinical characteristics, systemic associations, treatment and outcome in 100 patients. Arq Bras Oftalmol 72(2):231–235. https://doi.org/10.1590/s0004-27492009000200019

    Article  Google Scholar 

  17. Parra AGM, Miyazaki FH, Ribeiro RM et al (2010) Análise de 29 casos de esclerite. Experiência de um serviço de Reumato-Oftalmologia. Arq Bras Oftalmol 73(3):250–3. https://doi.org/10.1590/s0004-27492010000300008

    Article  PubMed  Google Scholar 

  18. Sen HN, Sangave AA, Goldstein DA et al (2011) A standardized grading system for scleritis. Ophthalmology 118(4):768–771. https://doi.org/10.1016/j.ophtha.2010.08.027

    Article  PubMed  Google Scholar 

  19. Watson PG, Hayreh SS (1976) Scleritis and episcleritis. Br J Ophthalmol 60(3):163–191. https://doi.org/10.1136/bjo.52.4.348

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  20. Moussa G, Bassilious K, Mathews N (2021) A novel excel sheet conversion tool from Snellen fraction to LogMAR including ‘counting fingers’, ‘hand movement’, ‘light perception’ and ‘no light perception’ and focused review of literature of low visual acuity reference values. Acta Ophthalmol 99(6):e963–e965. https://doi.org/10.1111/aos.14659

    Article  PubMed  Google Scholar 

  21. Day AC, Donachie PHJ, Sparrow JM et al (2015) The Royal College of Ophthalmologists’ National Ophthalmology Database study of cataract surgery: report 1, visual outcomes and complications. Eye 29(4):552–560. https://doi.org/10.1038/eye.2015.3

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  22. Abd El Latif E, Seleet MM, El Hennawi H et al (2019) Pattern of scleritis in an Egyptian cohort. Ocul Immunol Inflamm 27(6):890–896. https://doi.org/10.1080/09273948.2018.1544372

    Article  PubMed  CAS  Google Scholar 

  23. de-la-Torre A, López-Castillo CA, Rueda JC, Mantilla RD, Gómez-Marín JE, Anaya JM (2009) Clinical patterns of uveitis in two ophthalmology centres in Bogota. Colombia. Clin Exp Ophthalmol 37(5):458–66. https://doi.org/10.1111/j.1442-9071.2009.02082.x

    Article  PubMed  Google Scholar 

  24. Lane J, Nyugen E, Morrison J et al (2018) Clinical features of scleritis across the Asia-Pacific Region. Ocul Immunol Inflamm 27(6):920–926. https://doi.org/10.1080/09273948.2018.1484496

    Article  PubMed  Google Scholar 

  25. Bin Ismail MA, Lim RHF, Fang HM, Wong EPY, Ling HS, Lim WK, Teoh SC, Agrawal R (2017) Ocular autoimmune systemic inflammatory infectious study (OASIS)-report 4: analysis and outcome of scleritis in an East Asian population. J Ophthalmic Inflamm Infect 7(1):6. https://doi.org/10.1186/s12348-017-0124-5

    Article  PubMed  PubMed Central  Google Scholar 

  26. Erkanli L, Akova YA, Guney-Tefekli E, Tugal-Tutkun I (2010) Clinical features, prognosis, and treatment results of patients with scleritis from 2 tertiary eye care centers in Turkey. Cornea. 29(1):26–33. https://doi.org/10.1097/ICO.0b013e3181ac9fad

    Article  PubMed  Google Scholar 

  27. Anaya JM, Ramirez-Santana C, Alzate MA et al (2016) Autoimmune Ecol Front Immunol 26(7):139. https://doi.org/10.3389/fimmu.2016.00139

    Article  CAS  Google Scholar 

  28. Rojas-Villarraga A, Amaya-Amaya J, Rodriguez-Rodriguez A et al (2012) Introducing polyautoimmunity: secondary autoimmune diseases no longer exist. Autoimmune Dis 1(1):1–9. https://doi.org/10.1155/2012/254319

    Article  Google Scholar 

  29. Arellano-Martinez A, Gonzalez-Diaz V, Cerpa-Cruz S et al (2017) Prevalence of poliautoimmunity and family autoimmunity in Mexico. Ann Rheum Dis 76:1446. https://doi.org/10.1136/annrheumdis-2017-eular.6952

    Article  Google Scholar 

  30. Malagón C, del Gomez M, P, Mosquera C, et al (2019) Juvenile polyautoimmunity in a rheumatology setting. Autoimmun Rev 18(4):369–381. https://doi.org/10.1016/j.autrev.2018.11.006

    Article  PubMed  Google Scholar 

  31. Lachmann SM, Hazleman BL, Watson PG (1978) Scleritis and associated disease. Br Med J 14 1(6105):88–90. https://doi.org/10.1136/bmj.1.6105.88

    Article  CAS  Google Scholar 

  32. Lin P, Bhullar SS, Tessler HH et al (2008) Immunologic markers as potential predictors of systemic autoimmune disease in patients with idiopathic scleritis. Am J Ophthalmol 145(3):463–472. https://doi.org/10.1016/j.ajo.2007.09.024

    Article  PubMed  CAS  Google Scholar 

  33. Gonzalez-Gonzalez LA, Molina-Prat N, Doctor P (2014) Clinical features and presentation of posterior scleritis: a report of 31 cases. Ocul Immunol Inflamm 22(3):203–207. https://doi.org/10.3109/09273948.2013.840385

    Article  PubMed  Google Scholar 

  34. Villota C, Roa OZ, Díaz M, Gutiérrez JM, Fernández-Ávila DG (2015) AB1114 prevalence of HLA-B27 in a cohort of transplant of a university hospital in Colombia. Ann Rheum Dis 74:1273–1273

    Article  Google Scholar 

  35. Romero-Sanchez C, Chila-Moreno L, Gómez A, Casas GMC, Bautista-Molano W, Briceño I, Rueda JC, De Avila J, Londono J, Valle-Onate R (2018) The frequency of HLA-B27 in a Colombian population with signs of spondyloarthritis. Curr Rheumatol Rev 14(3):246–250. https://doi.org/10.2174/1573397113666170329121552

    Article  PubMed  Google Scholar 

  36. Satoh M, Chan EK, Ho LA, Rose KM, Parks CG, Cohn RD, Jusko TA, Walker NJ, Germolec DR, Whitt IZ, Crockett PW, Pauley BA, Chan JY, Ross SJ, Birnbaum LS, Zeldin DC, Miller FW (2012) Prevalence and sociodemographic correlates of antinuclear antibodies in the United States. Arthritis Rheum. 64(7):2319–27. https://doi.org/10.1002/art.34380

    Article  PubMed  PubMed Central  Google Scholar 

  37. Marin GG, Cardiel MH, Cornejo H, Viveros ME (2009) Prevalence of antinuclear antibodies in 3 groups of healthy individuals: blood donors, hospital personnel, and relatives of patients with autoimmune diseases. J Clin Rheumatol. 15(7):325–9. https://doi.org/10.1097/RHU.0b013e3181bb971b

    Article  PubMed  Google Scholar 

  38. Tervaert JWC (1989) Association between active Wegener’s granulomatosis and anticytoplasmic antibodies. Arch Intern Med 149(11):2461. https://doi.org/10.1001/archinte.149.11.2461

    Article  PubMed  CAS  Google Scholar 

  39. Cohen Tervaert JW, Huitema MG, Sluiter WJ et al (1990) Prevention of relapses in Wegener’s granulomatosis by treatment based on antineutrophil cytoplasmic antibody titre. Lancet 336(8717):709–711. https://doi.org/10.1016/0140-6736(90)92205-v

    Article  Google Scholar 

  40. Fijołek J, Wiatr E et al (2020) Antineutrophil cytoplasmic antibodies (ANCA): their role in pathogenesis, diagnosis, and treatment monitoring of ANCA-associated vasculitis. Cent Eur J Immunol 45(2):218–227. https://doi.org/10.5114/ceji.2019.92494

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  41. Oray M, Meese H, Foster CS (2016) Diagnosis and management of non-infectious immune-mediated scleritis: current status and future prospects. Expert Rev Clin Immunol 12(8):827–837. https://doi.org/10.1586/1744666X.2016.1171713

    Article  PubMed  CAS  Google Scholar 

  42. Gangaputra S, Newcomb CW, Liesegang TL et al (2009) Methotrexate for ocular inflammatory diseases. Ophthalmology 116(11):2188–2198. https://doi.org/10.1016/j.ophtha.2009.04.020

    Article  PubMed  Google Scholar 

  43. Daniel E, Thorne JE, Newcomb CW et al (2010) Mycophenolate mofetil for ocular inflammation. Am J Ophthalmol 149(3):423-432.e2. https://doi.org/10.1016/j.ajo.2009.09.026

    Article  PubMed  CAS  Google Scholar 

  44. Pasadhika S, Kempen JH, Newcomb CW et al (2009) Azathioprine for ocular inflammatory diseases. Am J Ophthalmol 148(4):500-509.e2. https://doi.org/10.1016/j.ajo.2009.05.008

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  45. Ragam A, Kolomeyer AM, Fang C (2014) Treatment of chronic, noninfectious, nonnecrotizing scleritis with tumor necrosis factor alpha inhibitors. Ocul Immunol Inflamm 22(6):469–477. https://doi.org/10.3109/09273948.2013.863944

    Article  PubMed  CAS  Google Scholar 

  46. Villalobos-Pérez A, Reyes-Guanes J, Muñoz-Ortiz J, Estévez-Florez MA, Ramos-Santodomingo M, Balaguera-Orjuela V et al (2021) Referral process in patients with uveitis: a challenge in the health system. Clin Ophthalmol 15:1–10. https://doi.org/10.2147/OPTH.S287766

    Article  PubMed  PubMed Central  Google Scholar 

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Funding

Convocatoria de Investigación Álvaro Rodríguez González Fundación Oftalmológica Nacional.

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Authors and Affiliations

Authors

Contributions

Mariana Cabrera-Pérez, MD, had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis. All authors contributed equally to this work. Concept and design: Mariana Cabrera-Pérez, MD; Alejandra de-la-Torre, MD, PhD; Claudia Duran, MD; Sandra García, MD; Miguel Cuevas, MD; Néstor Carreño, MD; Carlos M Rangel, MD; Diana Pachón, MD. Acquisition, analysis, or interpretation of data: all authors. Drafting of the manuscript: Alejandra de-la-Torre, MD, PhD; Mariana Cabrera-Pérez, MD; Carlos Cifuentes-González, MS; William Rojas-Carabali, MD; María Alejandra Martínez-Ceballos, MD; María Elisa Mejía, MD. Critical revision of the manuscript for important intellectual content: all authors. Statistical analysis: Mariana Cabrera-Pérez, MD. Administrative, technical, or material support: N/A. Supervision: N/A.

Corresponding author

Correspondence to Mariana Cabrera-Pérez.

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Ethics approval

This study adheres to the ethical principles for human research established by the Helsinki Declaration, the Belmont Report, and Colombian Resolution 008430 of 1993. According to the risks contemplated in resolution 8430 from 1993, this investigation is considered without risks. The information in the databases used in this article is freely accessible and is available for research purposes. In the same way, their coding system ensures data confidentiality. The present study was approved by the ethics committee of the Fundación Oftalmológica Nacional.

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The authors declare no competing interests.

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de-la-Torre, A., Cabrera-Pérez, M., Durán, C. et al. Clinical patterns and risk factors in scleritis: a multicentric study in Colombia. Graefes Arch Clin Exp Ophthalmol 260, 3957–3967 (2022). https://doi.org/10.1007/s00417-022-05754-y

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  • DOI: https://doi.org/10.1007/s00417-022-05754-y

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