Item request has been placed! ×
Item request cannot be made. ×
loading  Processing Request

Quantitative analyses of diameter and running pattern of choroidal vessels in central serous chorioretinopathy by en face images.

Item request has been placed! ×
Item request cannot be made. ×
loading   Processing Request
  • Additional Information
    • Source:
      Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN: 2045-2322 (Electronic) Linking ISSN: 20452322 NLM ISO Abbreviation: Sci Rep Subsets: MEDLINE
    • Publication Information:
      Original Publication: London : Nature Publishing Group, copyright 2011-
    • Subject Terms:
    • Abstract:
      This study was to investigate the choroidal vessels in eyes with central serous chorioretinopathy (CSC) quantitatively. We studied 41 CSC eyes and their fellow eyes, and 41 normal eyes of 41 age-adjusted individuals. En-face optical coherence tomography image of the top 25% slab of Haller's layer was analyze. The mean vessel area, vessel length, and vessel diameter were calculated. The running pattern of the vessels was quantified and used to determine the degree of symmetry, the "symmetry index". The vessel area of CSC eyes was not significantly different from that of fellow eyes but significantly larger than that of normal eyes. The vessel length of CSC eyes was not significantly different from fellow eyes but significantly shorter than that of normal eyes. The mean vessel diameter was larger in CSC eyes than in the fellow eyes and the normal eye. The symmetry index was not significantly different in CSC eyes from that of their fellow eyes but was smaller than that of normal eyes. The quantitative analysis showed that eyes with CSC had larger choroidal vessels and asymmetrical vessels running in Haller's layer.
    • References:
      Donald, J. & Gass, M. Pathogenesis of disciform detachment of the neuroepithelium: III. Senile disciform macular degeneration. Am J Ophthalmol 63, 617–645 (1967). (PMID: 10.1016/0002-9394(67)90028-1)
      Liu, B., Deng, T. & Zhang, J. Risk factors for central serous chorioretinopathy: a systematic review and meta-analysis. Retina 36, 9–19 (2016). (PMID: 10.1097/IAE.0000000000000837)
      Kitzmann, A. S., Pulido, J. S., Diehl, N. N., Hodge, D. O. & Burke, J. P. The incidence of central serous chorioretinopathy in Olmsted County, Minnesota, 1980–2002. Ophthalmology 115, 169–173 (2008). (PMID: 10.1016/j.ophtha.2007.02.032)
      Miki, A. et al. Common variants in the complement factor H gene confer genetic susceptibility to central serous chorioretinopathy. Ophthalmology 121, 1067–1072 (2014). (PMID: 10.1016/j.ophtha.2013.11.020)
      Miki, A. et al. Genome-Wide Association Study to Identify a New Susceptibility Locus for Central Serous Chorioretinopathy in the Japanese Population. Invest Ophthalmol Vis Sci 59, 5542–5547 (2018). (PMID: 10.1167/iovs.18-25497)
      de Jong, E. K. et al. Chronic central serous chorioretinopathy is associated with genetic variants implicated in age-related macular degeneration. Ophthalmology 122, 562–570 (2015). (PMID: 10.1016/j.ophtha.2014.09.026)
      Hosoda, Y. et al. CFH and VIPR2 as susceptibility loci in choroidal thickness and pachychoroid disease central serous chorioretinopathy. Proc Natl Acad Sci USA 115, 6261–6266 (2018). (PMID: 10.1073/pnas.1802212115)
      Imamura, Y., Fujiwara, T., Margolis, R. & Spaide, R. F. Enhanced depth imaging optical coherence tomography of the choroid in central serous chorioretinopathy. Retina 29, 1469–1473 (2009). (PMID: 10.1097/IAE.0b013e3181be0a83)
      Maruko, I., Iida, T., Sugano, Y., Ojima, A. & Sekiryu, T. Subfoveal choroidal thickness in fellow eyes of patients with central serous chorioretinopathy. Retina 31, 1603–1608 (2011). (PMID: 10.1097/IAE.0b013e31820f4b39)
      Jirarattanasopa, P. et al. Assessment of macular choroidal thickness by optical coherence tomography and angiographic changes in central serous chorioretinopathy. Ophthalmology 119, 1666–1678 (2012). (PMID: 10.1016/j.ophtha.2012.02.021)
      Kuroda, Y. et al. Increased choroidal vascularity in central serous chorioretinopathy quantified using swept-source optical coherence tomography. Am J Ophthalmol. 169, 199–207 (2016). (PMID: 10.1016/j.ajo.2016.06.043)
      Kim, Y., Kang, S. & Bai, K. Choroidal thickness in both eyes of patients with unilaterally active central serous chorioretinopathy. Eye 25, 1635 (2011). (PMID: 10.1038/eye.2011.258)
      Sohrab, M., Wu, K. & Fawzi, A. A. A pilot study of morphometric analysis of choroidal vasculature in vivo, using en face optical coherence tomography. PLoS One 7, e48631 (2012). (PMID: 10.1371/journal.pone.0048631)
      Shiihara, H. et al. Automated segmentation of en face choroidal images obtained by optical coherent tomography by machine learning. Jpn J Ophthalmol 62, 643–651 (2018). (PMID: 10.1007/s10384-018-0625-2)
      Hiroe, T. & Kishi, S. Dilatation of Asymmetric Vortex Vein in Central Serous Chorioretinopathy. Ophthalmol Retina 2, 152–161 (2018). (PMID: 10.1016/j.oret.2017.05.013)
      Savastano, M. C., Rispoli, M., Savastano, A. & Lumbroso, B. En face optical coherence tomography for visualization of the choroid. Ophthalmic Surg Lasers Imaging Retina 46, 561–565 (2015). (PMID: 10.3928/23258160-20150521-07)
      Savastano, M. C. et al. Classification of haller vessel arrangements in acute and chronic central serous chorioretinopathy imaged with en face optical coherence tomography. Retina 38, 1211–1215 (2018). (PMID: 10.1097/IAE.0000000000001678)
      Shiihara, H. et al. Running pattern of choroidal vessel in en face OCT images determined by machine learning–based quantitative method. Graefes Arch Clin Exp Ophthal 257, 1879–1887 (2019). (PMID: 10.1007/s00417-019-04399-8)
      Sonoda, S. et al. Structural changes of inner and outer choroid in central serous chorioretinopathy determined by optical coherence tomography. PLoS One 11, e0157190 (2016). (PMID: 10.1371/journal.pone.0157190)
      Henning, R. J. & Sawmiller, D. R. Vasoactive intestinal peptide: cardiovascular effects. Cardiovasc Res 49, 27–37 (2001). (PMID: 10.1016/S0008-6363(00)00229-7)
      Kishi, S. et al. Geographic filling delay of the choriocapillaris in the region of dilated asymmetric vortex veins in central serous chorioretinopathy. PLoS One 13, e0206646 (2018). (PMID: 10.1371/journal.pone.0206646)
      Saito, M., Noda, K., Saito, W. & Ishida, S. Relationship between choroidal blood flow velocity and choroidal thickness in patients with regression of acute central serous chorioretinopathy. Graefes Arch Clin Exp Ophthal 256, 227–229 (2018). (PMID: 10.1007/s00417-017-3791-x)
      Rochepeau, C. et al. Optical coherence tomography angiography quantitative assessment of choriocapillaris blood flow in central serous chorioretinopathy. Am J Ophthalmol 194, 26–34 (2018). (PMID: 10.1016/j.ajo.2018.07.004)
      Al-Sheikh, M. et al. Quantitative features of the choriocapillaris in healthy individuals using swept-source optical coherence tomography angiography. Ophthalmic Surg Lasers Imaging Retina 48, 623–631 (2017). (PMID: 10.3928/23258160-20170802-04)
      Prünte, C. & Flammer, J. Choroidal capillary and venous congestion in central serous chorioretinopathy. Am J Ophthalmol 121, 26–34 (1996). (PMID: 10.1016/S0002-9394(14)70531-8)
      Saito, M. et al. Macular choroidal blood flow velocity decreases with regression of acute central serous chorioretinopathy. Br J Ophthalmol. 97, 775–780 (2013). (PMID: 10.1136/bjophthalmol-2012-302349)
      Mendrinos, E. & Pournaras, C. J. Topographic variation of the choroidal watershed zone and its relationship to neovascularization in patients with age‐related macular degeneration. Acta Ophthalmol. 87, 290–296 (2009). (PMID: 10.1111/j.1755-3768.2008.01247.x)
      Lee, J. E. et al. Topographical relationship between the choroidal watershed zone and submacular idiopathic choroidal neovascularisation. Br J Ophthalmol. 100, 652–659 (2016). (PMID: 10.1136/bjophthalmol-2015-306678)
      Hong, Y. et al. Three-dimensional visualization of choroidal vessels by using standard and ultra-high resolution scattering optical coherence angiography. Opt Express 15, 7538–7550 (2007). (PMID: 10.1364/OE.15.007538)
      Fluss, R., Faraggi, D. & Reiser, B. Estimation of the Youden Index and its associated cutoff point. Bio J 47, 458–472 (2005). (PMID: 10.1002/bimj.200410135)
    • Publication Date:
      Date Created: 20200614 Date Completed: 20201208 Latest Revision: 20210612
    • Publication Date:
      20250114
    • Accession Number:
      PMC7293258
    • Accession Number:
      10.1038/s41598-020-66858-1
    • Accession Number:
      32533066