Ganglion Cell Layer Analysis in Nonarteritic Anterior Ischemic Optic Neuropathy in Diabetic Patients: From the Acute to Resolving Phases

被引:0
作者
Hassan, Moutei [1 ]
Ahmed, Bennis [1 ]
Fouad, Chraibi [1 ]
Meriem, Abdellaoui [1 ]
Benatiya, Idriss Andaloussi [1 ]
Faouzi, Belahsen Mohammed [2 ]
机构
[1] Hassan II Univ Hosp Fez, Dept Ophthalmol, Fes, Morocco
[2] Hassan II Univ Hosp Fez, Dept Neurol, Fes, Morocco
来源
JOURNAL OF RESEARCH IN MEDICAL AND DENTAL SCIENCE | 2021年 / 9卷 / 11期
关键词
Nonarteritic anterior ischemic optic neuropathy; Diabetes; Optical coherence tomography; COHERENCE TOMOGRAPHY;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Purpose: The aim of the present study was to assess tomographic changes in CGC in diabetic patients with non-arteritic anterior ischemic optic neuropathy (NOIA-NA) over a 6-month period and to investigate possible correlations with visual acuity and DM. Materials and methods: This is a prospective observational study, conducted at a diabetes referral centre between January 2017 and January 2020. All patients received a complete ophthalmological examination including measurement of best corrected visual acuity (BCVA), a standard automated visual field, and optical coherence tomography of the papilla (the peripapillary retinal nerve fibre layer RNFLp) and macula (the ganglion cell layer). Patients were monitored at 3 and 6 months. At each follow-up visit, visual acuity measurement, OCT, and CV were performed. CGC measurements in the affected eyes were compared with those of a control group. Correlations between the thinning of the CGC and functional parameters such as MAVC and mean deviation (MD) in the acute and chronic phases were analyzed. Results: We included 80 eyes of 80 diabetic patients with NOIA-NA corresponding to our inclusion criteria. The average age was 60.78 +/- 6.88 years with extremes ranging from 40 to 75 years, sex ratio F/H=1.28. The mean CGC thickness was 76.93 +/- 2.96 mu m and 80.03 +/- 1.03 mu m in affected and control eyes, respectively (P=0.001). Compared to the normative OCT baseline, 62.5% of affected eyes showed thinning of the CGC thickness. In contrast, 100% of the eyes showed RNFLp thickening. The rate of CGC thinning increased over time, such that by the third month, 100% of the eyes with NOIA-NA in our study were classified as abnormal. The CGC was significantly thinner between the initial visit and 3 months (76.93 +/- 2.96 mu m vs. 67.12 +/- -3.33 mu m P<0.001) and significantly thinner between the third month follow-up and 6 months (67.12 +/- -3.33 mu m vs. 66.56+/-3.4 mu m P<0.03). The mean percentage of CGC loss after the acute episode was 12.75% (9.81 mu m) at 3 months and 13.47% (10.37 mu m) at 6 months. CGC at the initial visit was found to be significantly associated with VA (r=-0.682; p<0.001) and DM (r=0.946; p<0.001). Similarly, mean CGC thickness at 3 months and 6 months follow-up was significantly associated with VA (r=-0.633, p<0.001 at 3 months and r=-0.654, p<0.001 at 6 months) and DM (r=0.877, p<0.001 at 3 months and r=0.811; p<0.001 at 6 months). Conclusion: This study indicates that early lesions of the CGC occur in diabetic patients with NOIA-NA in the acute phase, that these lesions can be accurately measured with OCT, and that the significant correlation between CGC changes and visual field deficits and VA represents an important structure-function relationship and underscores the importance of OCT in the evaluation of the functional and structural course of eyes with NOIA-NA.
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页码:75 / 79
页数:5
相关论文
共 13 条
[1]   Retinal Ganglion Cell Loss Precedes Retinal Nerve Fiber Thinning in Nonarteritic Anterior Ischemic Optic Neuropathy [J].
Akbari, Mohammadreza ;
Abdi, Parisa ;
Fard, Masoud Aghsaei ;
Afzali, Marjan ;
Ameri, Ahmad ;
Yazdani-Abyaneh, Alireza ;
Mohammadi, Massod ;
Moghimi, Sasan .
JOURNAL OF NEURO-OPHTHALMOLOGY, 2016, 36 (02) :141-146
[2]   Early axonal damage detection by ganglion cell complex analysis with optical coherence tomography in nonarteritic anterior ischaemic optic neuropathy [J].
Arana Larrea, Begoa ;
Galdos Iztueta, Marta ;
Martinez Indart, Lorea ;
Martinez Alday, Nerea .
GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, 2014, 252 (11) :1839-1846
[3]   Pathogenesis of nonarteritic anterior ischemic optic neuropathy [J].
Arnold, AC .
JOURNAL OF NEURO-OPHTHALMOLOGY, 2003, 23 (02) :157-163
[4]   Nonarteritic anterior ischemic optic neuropathy (NAION) and its experimental models [J].
Bernstein, Steven L. ;
Johnson, Mary A. ;
Miller, Neil R. .
PROGRESS IN RETINAL AND EYE RESEARCH, 2011, 30 (03) :167-187
[5]   TOPOGRAPHY OF GANGLION-CELLS IN HUMAN RETINA [J].
CURCIO, CA ;
ALLEN, KA .
JOURNAL OF COMPARATIVE NEUROLOGY, 1990, 300 (01) :5-25
[6]   Ganglion cell analysis at acute episode of nonarteritic anterior ischemic optic neuropathy to predict irreversible damage. A prospective study [J].
De Dompablo, Elisabet ;
Garcia-Montesinos, J. ;
Munoz-Negrete, F. J. ;
Rebolleda, G. .
GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, 2016, 254 (09) :1793-1800
[7]   Dynamics of Retinal Injury after Acute Optic Neuritis [J].
Gabilondo, Inigo ;
Martinez-Lapiscina, Elena H. ;
Fraga-Pumar, Elena ;
Ortiz-Perez, Santiago ;
Torres-Torres, Ruben ;
Andorra, Magi ;
Llufriu, Sara ;
Zubizarreta, Irati ;
Saiz, Albert ;
Sanchez-Dalmau, Bernardo ;
Villoslada, Pablo .
ANNALS OF NEUROLOGY, 2015, 77 (03) :517-528
[8]   Change of Retinal Nerve Layer Thickness in Non-Arteritic Anterior Ischemic Optic Neuropathy Revealed by Fourier Domain Optical Coherence Tomography [J].
Han, Mei ;
Zhao, Chen ;
Han, Quan-Hong ;
Xie, Shiyong ;
Li, Yan .
CURRENT EYE RESEARCH, 2016, 41 (08) :1076-1081
[9]   Optical Coherence Tomography Study of Experimental Anterior Ischemic Optic Neuropathy and Histologic Confirmation [J].
Ho, Joyce K. ;
Stanford, Madison P. ;
Shariati, Mohammad A. ;
Dalal, Roopa ;
Liao, Yaping Joyce .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2013, 54 (09) :5981-5988
[10]  
JOHNSON LN, 1994, J NEURO-OPHTHALMOL, V14, P38