Risk factors for secondary Glaucoma in patients with Vogt-Koyanagi-Harada disease

Carlos Alvarez-Guzman1,2, Curt Hartleben-Matkin2, Raul E. Ruiz-Lozano1, Alejandro Rodriguez-Garcia1,3, Manuel E. Quiroga-Garza1, Jorge E. Valdez-Garcia1
1Tecnologico de Monterrey, Escuela de Medicina y Ciencias de la Salud, Instituto de Oftalmologia y Ciencias Visuales, Monterrey, Mexico
2Fundación de Asistencia Privada Conde de Valenciana, IAP, Ciudad de México, Ciudad de México, Mexico
3Instituto de Oftalmologia y Ciencias Visuales (1er Piso Ote.) Hospital Zambrano Hellion Tec Salud, Mexico, Mexico

Tóm tắt

Identify the prevalence and risk factors for secondary glaucoma among Mexican-mestizo patients with Vogt-Koyanagi-Harada Disease (VKH). Retrospective cohort study analyzing the demographic, clinical, and epidemiological variables. Risk estimates were calculated using a Cox proportional hazards regression model. One hundred eyes of 50 patients, 44 (88%) women and 6 men (12%) with a median age of 35.5 years (IQR 29–46) and a median follow-up time of 72 months (IQR 13.7–126.7) were analyzed. The prevalence of glaucoma was 20%, with angle-closure accounting for 70% of all cases. Significant clinical risk factors for glaucoma development were a chronic recurrent stage at presentation (RR 2.88, 95% CI 1.11–12.63, p = 0.037), ≥ 2 episodes of recurrent anterior uveitis (RR 8.52, 95% CI 2.02–35.92, p < 0.001), angle-closure disease (ACD, RR 7.08, 95% CI 2.44–20.48, p < 0.001), iris bombé (RR 5.0, 95% CI 2.10–11.90, p < 0.001), and peripapillary atrophy (RR 3.56, 95% CI 1.43–8.85, p < 0.001). Exposure to > 24 months of oral (RR 9.33, 95% CI 2.21–39.28, p < 0.001) or > 12 months of topical corticosteroids (RR 3.88, 95% CI 1.31–11.46, p = 0.007) were associated with an increased likelihood for secondary glaucoma development. Glaucoma is a frequent complication of VKH, often attributed to mixed pathogenic mechanisms. Chronic disease at presentation, recurrent inflammation, angle-closure mechanisms, iris bombé, and peripapillary atrophy represent clinically significant risk factors for developing secondary glaucoma. Prompt and aggressive steroid-spearing immunosuppressive therapy for adequate inflammation control may lower the risk of glaucoma in VKH.

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Tài liệu tham khảo

Aggarwal K, Agarwal A, Deokar A et al (2017) Distinguishing features of acute Vogt-Koyanagi-Harada disease and acute central serous chorioretinopathy on optical coherence tomography angiography and en face optical coherence tomography imaging. J Ophthalmic Inflamm Infect 7:3

Chow A, Burkemper B, Varma R, Rodger DC, Rao N, Richter GM (2018) Comparison of surgical outcomes of trabeculectomy, Ahmed shunt, and Baerveldt shunt in uveitic glaucoma. J Ophthalmic Inflamm Infect 8:9

Herbort CP Jr, Abu El Asrar AM, Takeuchi M et al (2019) Catching the therapeutic window of opportunity in early initial-onset Vogt-Koyanagi-Harada uveitis can cure the disease. Int Ophthalmol 39:1419–1425

Concha del Rio LE, Arellanes-Garcia L (2010) Vogt-Koyanagi-Harada disease in the developing world. Int Ophthalmol Clin 50:189–199

O'Keefe GA, Rao NA (2017) Vogt-Koyanagi-Harada disease. Surv Ophthalmol 62:1–25

Read RW, Rechodouni A, Butani N et al (2001) Complications and prognostic factors in Vogt-Koyanagi-Harada disease. Am J Ophthalmol 131:599–606

Abu El-Asrar AM, Dosari M, Hemachandran S, Gikandi PW, Al-Muammar A (2017) Mycophenolate mofetil combined with systemic corticosteroids prevents progression to chronic recurrent inflammation and development of 'sunset glow fundus' in initial-onset acute uveitis associated with Vogt-Koyanagi-Harada disease. Acta Ophthalmol 95:85–90

Rubsamen PE, Gass JD (1991) Vogt-Koyanagi-Harada syndrome. Clinical course, therapy, and long-term visual outcome. Arch Ophthalmol 109:682–687

Arellanes García L, Recillas Gispert C (1998) Síndrome de Vogt Koyanagi Harada. Rev Mex Oftalmol 72:59–74

Pandey A, Balekudaru S, Venkatramani DV, George AE, Lingam V, Biswas J (2016) Incidence and Management of Glaucoma in Vogt Koyanagi Harada disease. J Glaucoma 25:674–680

Yang P, Wang C, Su G et al (2020) Prevalence, risk factors and management of ocular hypertension or glaucoma in patients with Vogt-Koyanagi-Harada disease. Br J Ophthalmol 105:1678–1682

Daniel E, Pistilli M, Kothari S et al (2017) Risk of ocular hypertension in adults with noninfectious uveitis. Ophthalmology 124:1196–1208

Read RW, Holland GN, Rao NA et al (2001) Revised diagnostic criteria for Vogt-Koyanagi-Harada disease: report of an international committee on nomenclature. Am J Ophthalmol 131:647–652

Foster PJ, Buhrmann R, Quigley HA, Johnson GJ (2002) The definition and classification of glaucoma in prevalence surveys. Br J Ophthalmol 86:238–242

Arevalo JF, Lasave AF, Gupta V et al (2016) Clinical outcomes of patients with Vogt-Koyanagi-Harada disease over 12 years at a tertiary center. Ocul Immunol Inflamm 24:521–529

Abu El-Asrar AM, Al Tamimi M, Hemachandran S, Al-Mezaine HS, Al-Muammar A, Kangave D (2013) Prognostic factors for clinical outcomes in patients with Vogt-Koyanagi-Harada disease treated with high-dose corticosteroids. Acta Ophthalmol 91:e486–e493

Al-Kharashi AS, Aldibhi H, Al-Fraykh H, Kangave D, Abu El-Asrar AM (2007) Prognostic factors in Vogt-Koyanagi-Harada disease. Int Ophthalmol 27:201–210

Veerappan M, Fleischman D, Ulrich JN, Stinnett SS, Jaffe GJ, Allingham RR (2017) The relationship of Vogt-Koyanagi-Harada syndrome to ocular hypertension and Glaucoma. Ocul Immunol Inflamm 25:748–752

Forster DJ, Rao NA, Hill RA, Nguyen QH, Baerveldt G (1993) Incidence and management of glaucoma in Vogt-Koyanagi-Harada syndrome. Ophthalmology 100:613–618

Sng CC, Barton K (2015) Mechanism and management of angle closure in uveitis. Curr Opin Ophthalmol 26:121–127

Herbort CP Jr, Tugal-Tutkun I, Khairallah M, Abu El Asrar AM, Pavesio CE, Soheilian M (2020) Vogt-Koyanagi-Harada disease: recurrence rates after initial-onset disease differ according to treatment modality and geographic area. Int Ophthalmol 40:2423–2433

Jap A, Luu CD, Yeo I, Chee SP (2008) Correlation between peripapillary atrophy and corticosteroid therapy in patients with Vogt-Koyanagi-Harada disease. Eye (Lond) 22:240–245

Keino H, Goto H, Usui M (2002) Sunset glow fundus in Vogt-Koyanagi-Harada disease with or without chronic ocular inflammation. Graefes Arch Clin Exp Ophthalmol 240:878–882

Herbort CP Jr, Abu El Asrar AM, Yamamoto JH et al (2017) Reappraisal of the management of Vogt-Koyanagi-Harada disease: sunset glow fundus is no more a fatality. Int Ophthalmol 37:1383–1395

Urzua CA, Herbort C Jr, Valenzuela RA et al (2020) Initial-onset acute and chronic recurrent stages are two distinctive courses of Vogt-Koyanagi-Harada disease. J Ophthalmic Inflamm Infect 10:23