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Japanese Journal of Ophthalmology

, Volume 58, Issue 1, pp 47–55 | Cite as

Width of abnormal ganglion cell complex area determined using optical coherence tomography to predict glaucoma

  • Ulfah RimayantiEmail author
  • Miftahul Akhyar Latief
  • Paramastri Arintawati
  • Tomoyuki Akita
  • Junko Tanaka
  • Yoshiaki Kiuchi
Clinical Investigation

Abstract

Purposes

We examined the relationships of ganglion cell complex (GCC) parameters determined on spectral-domain optical coherence tomography (SD-OCT), especially the width of abnormal areas, and its ability to detect various stages of glaucoma.

Methods

OCT parameters of glaucomatous and normal eyes were determined with the RTVue SD-OCT. Widths of abnormal GCC areas marked by either red or yellow on the OCT significance map were quantified with image J software. The relationships between the abnormal GCC area and other GCC parameters [thickness, focal loss volume (FLV), and global loss volume (GLV)] and the peripapillary retinal nerve fiber layer (RNFL) thickness were determined using regression analyses. The potential of using the GCC and RNFL parameters to discriminate between glaucomatous and normal eyes was examined using the area under the curve (AUC) of receiver operating characteristics (ROC).

Results

One hundred and eighteen glaucomatous eyes and 45 normal control eyes were studied. Nonlinear models best described the relationships between abnormal GCC area and other GCC parameters. Scatter plots showed changes in the average thickness of the GCC and RNFL, and the average sizes of the GLV preceded changes of abnormal areas of the GCC. The width of the abnormal areas on the GCC thickness map was comparable with other parameters for diagnosing glaucoma.

Conclusions

OCT thickness parameters appeared to decrease faster than the area parameter at the initial stage of glaucoma. The sizes of abnormal areas of the GCC were the most pertinent parameters for detecting glaucoma.

Keywords

Ganglion cell complex (GCC) abnormal GCC area Glaucoma Optical coherence tomography 

Notes

Acknowledgments

Professional medical English editing: This manuscript was edited by Dr. Duco Hamasaki in Florida and Dr. Brian Quinn, editor-in-chief, Japan Medical Communication.

Conflicts of interest

U. Rimayanti, None; M. Akhyar Latief, None; P. Arintawati, None; T. Akita, None; J. Tanaka, None; Y. Kiuchi, None.

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Copyright information

© Japanese Ophthalmological Society 2013

Authors and Affiliations

  • Ulfah Rimayanti
    • 1
    Email author
  • Miftahul Akhyar Latief
    • 1
  • Paramastri Arintawati
    • 2
  • Tomoyuki Akita
    • 3
  • Junko Tanaka
    • 3
  • Yoshiaki Kiuchi
    • 1
  1. 1.Department of Ophthalmology and Visual Science, Graduate School of Biomedical SciencesHiroshima UniversityHiroshimaJapan
  2. 2.Department of OphthalmologyMedical Faculty of Diponegoro UniversitySemarangIndonesia
  3. 3.Department of Epidemiology, Infectious Disease Control and Prevention, Graduate School of Biomedical SciencesHiroshima UniversityHiroshimaJapan

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