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Suboptimal therapy controls clinically apparent disease but not subclinical progression of Vogt-Koyanagi-Harada disease

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Abstract

Purpose To evaluate clinical and angiographic differences in patients with Vogt-Koyanagi-Harada (VKH) disease during the early 4-month treatment phase with high- or medium-dose systemic corticosteroid therapy. Methods VKH patients treated at the Centre for Ophthalmic Specialized Care, Lausanne, Switzerland (n = 4), or the Department of Ophthalmology, Tokyo Medical and Dental University, Tokyo, Japan (n = 5), underwent a pre-treatment indocyanine green angiography (ICGA) and a follow-up ICGA four months after treatment began. Lausanne patients received high-dose, systemic corticosteroid therapy, with or without immunosuppressive therapy. Tokyo patients received medium-dose systemic corticosteroid therapy that included 3 days of intravenous pulse methylprednisolone. ICGA signs including choroidal stromal vessel hyperfluorescence and leakage, hypofluorescent dark dots (HDD), fuzzy vascular pattern of large stromal vessels and disc hyperfluorescence were retrospectively compared. Results The pre-treatment ICGA demonstrated that each of the nine patients had choroidal inflammatory foci, as indicated by HDD. At 4-month follow-up, clinical and fluorescein findings had improved almost equally in both groups. HDD had resolved in the Lausanne group but persisted in the Tokyo group. Sunset glow fundus occurred in three of the Tokyo patients and none of the Lausanne patients. Conclusions Submaximal doses of inflammation suppressive therapy are sufficient to suppress clinically apparent disease but not the underlying lesion process. This explains the propensity for sunset glow fundus in seemingly controlled disease.

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References

  1. Sugita S, Takase H, Taguchi C et al (2006) Ocular infiltrating CD4+T cells from patients with Vogt-Koyanagi-Harada disease recognize human melanocyte antigens. Invest Ophthalmol Vis Sci 47:2547–2554. doi:10.1167/iovs.05-1547

    Article  PubMed  Google Scholar 

  2. Bouchenaki N, Herbort CP (2004) Stromal choroiditis. In: Pleyer U, Mondino B (eds) Essentials in ophthalmology: uveitis and immunological disorders. Springer, Berlin, pp 234–253

    Google Scholar 

  3. Sonoda S, Nakao K, Ohba N (1999) Extensive chorioretinal atrophy in Vogt-Koyanagi-Harada disease. Jpn J Ophthalmol 43:113–119. doi:10.1016/S0021-5155(98)00066-5

    Article  CAS  PubMed  Google Scholar 

  4. Rao NA (2006) Treatment of Vogt-Koyanagi-Harada disease by corticosteroids and immunosuppressive agents. Ocul Immunol Inflamm 14:71–72. doi:10.1080/09273940600674368

    Article  PubMed  Google Scholar 

  5. Bouchenaki N, Morisod L, Herbort CP (2006) Vogt-Koyanagi-Harada syndrome: importance of rapid diagnosis and therapeutic intervention. Klin Monatsbl Augenheilkd 216:1–5

    Google Scholar 

  6. Keino H, Goto H, Ususi M (2002) Sunset glow fundus in Vogt-Koyanagi-Harada disease with or without chronic inflammation. Graefes Arch Clin Exp Ophthalmol 240:878–882. doi:10.1007/s00417-002-0538-z

    Article  PubMed  Google Scholar 

  7. Yang P, Wang H, Zhou H et al (2002) Clinical manifestations and diagnosis of Vogt-Koyanagi-Harada syndrome. Zhonghua Yan Ke Za Zhi 38:736–739

    PubMed  Google Scholar 

  8. Foster DJ, Cano MR, Green RL, Rao NA (1990) Echographic features of the Vogt-Koyanagi-Harada Syndrome. Arch Ophthalmol 108:1421–1426

    Google Scholar 

  9. Bouchenaki N, Cimino L, Auer C, Tran VT, Herbort CP (2002) Assessement and classification of choroidal vasculitis in posterior uveitis using indocyanine green angiography. Klin Monatsbl Augenheilkd 219:243–249. doi:10.1055/s-2002-30661

    Article  PubMed  Google Scholar 

  10. Khairallah M, Ben Yahia S, Attia S et al (2006) Indocyanine green angiographic features in multifocal chorioretinitis associated with West Nile virus infection. Retina 26:358–359. doi:10.1097/00006982-200603000-00019

    Article  PubMed  Google Scholar 

  11. Machida S, Tanaka M, Murai K, Takahashi T, Tazawa Y (2004) Choroidal circulatory disturbance in ocular sarcoidosis without the appearance of retinal lesions or loss of visual function. Jpn J Ophthalmol 48:392–396. doi:10.1007/s10384-004-0087-6

    Article  PubMed  Google Scholar 

  12. Howe L, Stanford M, Graham E, Marshall J (1998) Indocyanine green angiography in inflammatory eye diseases. Eye 12:761–767

    PubMed  Google Scholar 

  13. Harada T, Kanbara Y, Takeuchi T, Niwa T, Majima T (1997) Exploration of Vogt-Koyanangi Harada syndrome by infrared choroidal angiography with indocyanine green. Eur J Ophthalmol 7:163–170

    CAS  PubMed  Google Scholar 

  14. Oshima Y, Harino S, Hara Y, Tano Y (1996) Indocyanine green angiographic findings in Vogt-Koyanagi-Harada disease. Am J Ophthalmol 122:58–66

    CAS  PubMed  Google Scholar 

  15. Okada AA, Mizusawa T, Sakai J, Usui M (1998) Videofunduscopy and videoangiography using the scanning laser ophthalmoscope in Vogt-Koyanagi-Harada disease. Br J Ophthalmol 82:1175–1181

    Article  CAS  PubMed  Google Scholar 

  16. Bouchenaki N, Herbort CP (2001) The contribution of indocyanine green angiography to the appraisal and management of Vogt Koyanagi-Harada. Ophthalmology 108:54–64. doi:10.1016/S0161-6420(00)00428-0

    Article  CAS  PubMed  Google Scholar 

  17. Bouchenaki N, Herbort CP (2000) Indocyanine green angiography (ICGA) in the assessement and follow-up of choroidal inflammation in active chronically evolving Vogt-Koyanagi-Harada disease. In: Dodds EM, Couto CA (eds) Uveitis in the third millenium. Elsevier, Amsterdam, pp 35–38

    Google Scholar 

  18. Herbort CP, LeHoang P, Guex-Crosier Y (1998) Schematic interpretation of indocyanine green angiography in posterior uveitis using a standard protocol. Ophthalmology 105:432–440. doi:10.1016/S0161-6420(98)93024-X

    Article  CAS  PubMed  Google Scholar 

  19. Altan-Yaycioglu R, Akova YA, Akca S, Yilmaz G (2006) Inflammation of the posterior uvea: findings on fundus fluorescein and indocyanine green angiography. Ocul Immunol Inflamm 14:171–179. doi:10.1080/09273940600660524

    Article  PubMed  Google Scholar 

  20. Kohno T, Miki T, Shiraki K et al (1999) Subtraction ICG angiography in Harada’s disease. Br J Ophthalmol 83:822–833

    Article  CAS  PubMed  Google Scholar 

  21. Herbort CP, Mantovani A, Bouchenaki N (2007) Indocyanine green angiography in Vogt-Koyanagi-Harada disease: angiographic signs and utility in patient follow-up. Int Ophthalmol 27:173–182. doi:10.1007/s10792-007-9060-y

    Article  PubMed  Google Scholar 

  22. Herbort CP, Probst K, Cimino L, Tran VT (2004) Differential inflammatory involvement in retina and choroid in birdshot chorioretinopathy. Klin Monatsbl Augenheilkd 221:351–356. doi:10.1055/s-2004-812827

    Article  CAS  PubMed  Google Scholar 

  23. 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. doi:10.1016/S0002-9394(01)00925-4

    Article  CAS  PubMed  Google Scholar 

  24. Damico FM, Kiss S, Young LH (2005) Vogt-Koyanagi-Harada disease. Semin Ophthalmol 20:183–190. doi:10.1080/08820530500232126

    Article  PubMed  Google Scholar 

  25. Sasamoto Y, Ohno S, Matsuda H (1990) Studies on corticosteroid therapy in Vogt-Koyanagi-Harada disease. Ohthalmologica 201:162–167

    CAS  Google Scholar 

  26. Yamanaka E, Ohguro N, Yamamoto S et al (2002) Evaluation of pulse corticosteroid therapy for Vogt-Koyanagi-Harada disease assessed by optical coherence tomography. Am J Ophthalmol 134:454–456. doi:10.1016/S0002-9394(02)01575-1

    Article  CAS  PubMed  Google Scholar 

  27. Read RW, Yu F, Accorinti M et al (2006) Evaluation of the effect on outcomes of the route of administration of corticosteroids in acute Vogt-Koyanagi-Harada disease. Am J Ophthalmol 142:119–124. doi:10.1016/j.ajo.2006.02.049

    Article  CAS  PubMed  Google Scholar 

  28. Keino H, Goto H, Mori H, Iwasaki T, Ususi M (2006) Association between severity of inflammation in CNS and development of sunset glow fundus in Vogt-Koyanagi-Harada disease. Am J Ophthalmol 141:1140–1142. doi:10.1016/j.ajo.2006.01.017

    Article  PubMed  Google Scholar 

  29. Suzuki S (1999) Quantitative evaluation of “sunset glow” fundus in Vogt-Koyanagi-Harada disease. Jpn J Ophthalmol 43:327–333. doi:10.1016/S0021-5155(99)00016-7

    Article  CAS  PubMed  Google Scholar 

  30. Al-Kharashi AS, Aldibhi H, Al Fraykh H, Kangave D, El-Asrar Abu (2007) Prognostic factors in Vogt-Koyanagi-Harada disease. Int Ophthalmol 27:201–210. doi:10.1007/s10792-007-9062-9

    Article  PubMed  Google Scholar 

  31. Bykhovskaya I, Thorne JE, Kempen JH, Dunn JP, Jabs DA (2005) Vogt-Koyanagi-Harada disease: clinical outcomes. Am J Ophthalmol 140:674–678

    PubMed  Google Scholar 

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Correspondence to Carl P. Herbort.

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Kawaguchi, T., Horie, S., Bouchenaki, N. et al. Suboptimal therapy controls clinically apparent disease but not subclinical progression of Vogt-Koyanagi-Harada disease. Int Ophthalmol 30, 41–50 (2010). https://doi.org/10.1007/s10792-008-9288-1

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  • DOI: https://doi.org/10.1007/s10792-008-9288-1

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