Prognostic value of pretreatment indocyanine green angiography in the acute uveitic phase of Vogt-Koyanagi-Harada disease.

Item request has been placed! ×
Item request cannot be made. ×
loading   Processing Request
  • Additional Information
    • Source:
      Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 101468102 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1755-3768 (Electronic) Linking ISSN: 1755375X NLM ISO Abbreviation: Acta Ophthalmol Subsets: MEDLINE
    • Publication Information:
      Publication: Oxford, UK : Wiley-Blackwell
      Original Publication: Oxford, UK ; Malden, MA : Blackwell Munksgaard
    • Subject Terms:
    • Abstract:
      Purpose: To investigate the prognostic value of pretreatment indocyanine green angiographic (ICGA) features in initial-onset acute uveitis associated with Vogt-Koyanagi-Harada (VKH) disease.
      Methods: Retrospective analysis of 84 patients (168 eyes). Main outcome measures were final visual acuity, development of 'sunset glow fundus' (SGF) and progression to chronic recurrent evolution.
      Results: Thirty-eight patients (76 eyes) presented in the phase preceding anterior segment (AS) inflammation (early presentation) and 46 patients (92 eyes) had AS inflammation at presentation (late presentation). The mean number of hypofluorescent dark dots (HDDs) and frequency of disc hyperfluorescence were more in the late presentation group (p < 0.001 for both comparisons), whereas the early presentation group showed higher frequencies of peripapillary punctate choroidal hyperfluorescence (p < 0.001) and hypofluorescent patches involving macula corresponding to the areas of exudative retinal detachment (p = 0.012). The mean number of HDDs and the frequency of disc hyperfluorescence were higher among eyes that developed SGF (p < 0.001 for both comparisons) and eyes that progressed to chronic recurrent evolution (p < 0.001; p = 0.001, respectively). The frequencies of peripapillary punctate choroidal hyperfluorescence and hypofluorescent patches corresponding to the areas of exudative retinal detachment were less in the eyes that developed SGF (p = 0.019; p = 0.003, respectively). Punctate choroidal hyperfluorescence elsewhere was less frequent in the eyes that developed SGF (p < 0.001) and eyes that progressed to chronic recurrent evolution (p = 0.002).
      Conclusions: Pretreatment ICGA has a prognostic value in initial-onset acute uveitis associated with VKH disease.
      (© 2023 Acta Ophthalmologica Scandinavica Foundation. Published by John Wiley & Sons Ltd.)
    • References:
      Abouammoh, M.A., Gupta, V., Hemachandran, S., Herbort, C.P. & Abu El‐Asrar, A.M. (2016) Indocyanine green angiographic findings in initial‐onset acute Vogt‐Koyanagi‐Harada disease. Acta Ophthalmologica, 94, 573–578.
      Abu El‐Asrar, A.M., Al Mudhaiyan, T., Al Najashi, A.A., Hemachandran, S., Hariz, R., Mousa, A. et al. (2017) Chronic recurrent Vogt‐Koyanagi‐Harada disease and development of ‘sunset glow fundus’ predict worse retinal sensitivity. Ocular Immunology and Inflammation, 25, 475–485.
      Abu El‐Asrar, A.M., Al Rashed, F.A., AlBloushi, A.F., Tobaigy, M.F., Gikandi, P.W., Herbort, C.P., Jr. et al. (2023) Therapeutic window of opportunity in the acute uveitic phase of Vogt‐Koyanagi‐Harada disease: prevention of late autoimmune complications by early intervention. Acta Ophthalmologica, 101, e236–e245.
      Abu El‐Asrar, A.M., Al Tamimi, M., Hemachandran, S., Al‐Mezaine, H.S., Al‐Muammar, A. & Kangave, D. (2013) Prognostic factors for clinical outcomes in patients with Vogt‐Koyanagi‐Harada disease treated with high‐dose corticosteroids. Acta Ophthalmologica, 91, e486–e493.
      Abu El‐Asrar, A.M., Dosari, M., Hemachandran, S., Gikandi, P.W. & 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 Ophthalmologica, 95, 85–90.
      Abu El‐Asrar, A.M., Hemachandran, S., Al‐Mezaine, H.S., Kangave, D. & Al‐Muammar, A.M. (2012) The outcomes of mycophenolate mofetil therapy combined with systemic corticosteroids in acute uveitis associated with Vogt‐Koyanagi‐Harada disease. Acta Ophthalmologica, 90, e603–e608.
      Abu El‐Asrar, A.M., Struyf, S., Van den Broeck, C., Van Damme, J., Opdenakker, G., Geboes, K. et al. (2007) Expression of chemokines and gelatinase B in sympathetic ophthalmia. Eye (London, England), 21, 649–657.
      AlBloushi, A.F., Alfawaz, A.M., AlZaid, A., Alsalamah, A.K., Gikandi, P.W. & Abu El‐Asrar, A.M. (2021) Incidence, risk factors and surgical outcomes of cataract among patients with Vogt‐Koyanagi‐Harada disease. Ocular Immunology and Inflammation, 29, 128–136.
      Bacsal, K., Wen, D.S. & Chee, S.P. (2008) Concomitant choroidal inflammation during anterior segment recurrence in Vogt‐Koyanagi‐Harada disease. American Journal of Ophthalmology, 145, 480–486.
      Bouchenaki, N. & Herbort, C.P. (2001) The contribution of indocyanine green angiography to the appraisal and management of Vogt‐Koyanagi‐Harada disease. Ophthalmology, 108, 54–64.
      Chee, S.P. & Jap, A. (2013) The outcomes of indocyanine green angiography monitored immunotherapy in Vogt‐Koyanagi‐Harada disease. The British Journal of Ophthalmology, 97, 130–133.
      Chee, S.P., Jap, A. & Cheung, C.M. (2010) The prognostic value of angiography in Vogt‐Koyanagi‐Harada disease. American Journal of Ophthalmology, 150, 888–893.
      Fang, W. & Yang, P. (2008) Vogt‐Koyanagi‐Harada syndrome. Current Eye Research, 33, 517–523.
      Fardeau, C., Tran, T.H., Gharbi, B., Cassoux, N., Bodaghi, B. & LeHoang, P. (2007) Retinal fluorescein and indocyanine green angiography and optical coherence tomography in successive stages of Vogt‐Koyanagi‐Harada disease. International Ophthalmology, 27, 163–172.
      Gocho, K., Kondo, I. & Yamaki, K. (2001) Identification of autoreactive T cells in Vogt‐Koyanagi‐Harada disease. Investigative Ophthalmology & Visual Science, 42, 2004–2009.
      Herbort, C.P., Mantovani, A. & Bouchenaki, N. (2007) Indocyanine green angiography in Vogt‐Koyanagi‐Harada disease: angiographic signs and utility in patient follow‐up. International Ophthalmology, 27, 173–182.
      Kawaguchi, T., Horie, S., Bouchenaki, N., Ohno‐Matsui, K., Mochizuki, M. & Herbort, C.P. (2010) Suboptimal therapy controls clinically apparent disease but not subclinical progression of Vogt‐Koyanagi‐Harada disease. International Ophthalmology, 30, 41–50.
      Miyanaga, M., Kawaguchi, T., Miyata, K., Horie, S., Mochizuki, M. & Herbort, C.P. (2010) Indocyanine green angiography findings in initial acute pretreatment Vogt‐Koyanagi‐Harada disease in Japanese patients. Japanese Journal of Ophthalmology, 54, 377–382.
      Rao, N.A. (2007) Pathology of Vogt‐Koyanagi‐Harada disease. International Ophthalmology, 27, 81–85.
      Yamaki, K., Gocho, K., Hayakawa, K., Kondo, I. & Sakuragi, S. (2000) Tyrosinase family proteins are antigens specific to Vogt‐Koyanagi‐Harada disease. Journal of Immunology, 165, 7323–7329.
      Yamaki, K., Kondo, I., Nakamura, H., Miyano, M., Konno, S. & Sakuragi, S. (2000) Ocular and extraocular inflammation induced by immunization of tyrosinase related protein 1 and 2 in Lewis rats. Experimental Eye Research, 71, 361–369.
      Yang, P., Ren, Y., Li, B., Fang, W., Meng, Q. & Kijlstra, A. (2007) Clinical characteristics of Vogt‐Koyanagi‐Harada syndrome in Chinese patients. Ophthalmology, 114, 606–614.
    • Grant Information:
      IFKSURC-1-2103 Deputyship for Research & Innovation, Ministry of Education in Saudi Arabia
    • Contributed Indexing:
      Keywords: Vogt‐Koyanagi‐Harada disease; chronic recurrent evolution; indocyanine green angiography; prognosis; uveitis; ‘sunset glow fundus’
    • Accession Number:
      IX6J1063HV (Indocyanine Green)
      0 (Coloring Agents)
    • Publication Date:
      Date Created: 20231222 Date Completed: 20240708 Latest Revision: 20240708
    • Publication Date:
      20240708
    • Accession Number:
      10.1111/aos.16613
    • Accession Number:
      38131519