Photoreceptor changes in Leber hereditary optic neuropathy with m.G11778A mutation

被引:1
|
作者
Miao, Qing-Mei [1 ]
Cheng, Yu -Fang [1 ]
Zheng, Hong-Mei [1 ]
Yuan, Jia-Jia [1 ]
Chen, Chang-Zheng [1 ]
机构
[1] Wuhan Univ, Eye Ctr, Renmin Hosp, Wuhan 430060, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
Leber hereditary optic neuropathy; asymptomatic carriers; photoreceptor; electroretinogram; mitochondrial dysfunction;
D O I
10.18240/ijo.2023.06.15
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
? AIM: To evaluate the functional and structural changes of photoreceptors in patients and asymptomatic carriers with Leber hereditary optic neuropathy (LHON) using full -field electroretinography (FERG) and optical coherence tomography (OCT). ? METHODS: Individuals diagnosed with LHON at the Renmin Hospital of Wuhan University and their family members were included in this cross-sectional observational study. The FERG a-wave amplitude of affected patients and asymptomatic carriers was analyzed. The thickness of the outer nuclear layer (ONL), inner and outer segment (IS/OS) and total photoreceptors in the macular fovea and parafovea were measured. ? RESULTS: This study included 14 LHON patients (mean age: 20.00 & PLUSMN;9.37y), 12 asymptomatic carriers (mean age: 39.83 & PLUSMN;6.48y), and 14 normal subjects (mean age: 24.20 & PLUSMN;1.52y). The FERG results showed that the dark -adapted 3.0 electroretinography and light-adapted 3.0 electroretinography a-wave amplitudes of patients and carriers were significantly decreased (P<0.001). The ONL and photoreceptors layers were slightly thicker in patients than in normal subjects (P<0.05), whereas they were thinner in carriers (P<0.05). There were no differences in IS/OS thickness among the groups (P>0.05). ? CONCLUSION: Photoreceptors function is significantly impaired in LHON-affected patients and asymptomatic carriers. Meanwhile, photoreceptors morphology is slightly altered, mainly manifesting as a change in ONL thickness.
引用
收藏
页码:928 / 932
页数:5
相关论文
共 50 条
  • [1] Photoreceptor changes in Leber hereditary optic neuropathy with m.G11778A mutation
    Qing-Mei Miao
    Yu-Fang Cheng
    Hong-Mei Zheng
    Jia-Jia Yuan
    Chang-Zheng Chen
    International Journal of Ophthalmology, 2023, (06) : 928 - 932
  • [2] PhNR and peripapillary RNFL changes in Leber hereditary optic neuropathy with m.G11778A mutation
    Miao, Qingmei
    Cheng, Yufang
    Zheng, Hongmei
    Yuan, Jiajia
    Chen, Changzheng
    MITOCHONDRION, 2023, 70 : 111 - 117
  • [3] Foveal pit morphological changes in asymptomatic carriers of the G11778A mutation with Leber's hereditary optic neuropathy
    Liu, Xin-Ting
    Shen, Mei-Xiao
    Chen, Chong
    Huang, Sheng-Hai
    Zhuang, Xi-Ran
    Ma, Qing-Kai
    Chen, Qi
    Lu, Fan
    Yuan, Yi-Min
    INTERNATIONAL JOURNAL OF OPHTHALMOLOGY, 2020, 13 (05) : 766 - 772
  • [4] Foveal pit morphological changes in asymptomatic carriers of the G11778A mutation with Leber's hereditary optic neuropathy
    Xin-Ting Liu
    Mei-Xiao Shen
    Chong Chen
    Sheng-Hai Huang
    Xi-Ran Zhuang
    Qing-Kai Ma
    Qi Chen
    Fan Lu
    Yi-Min Yuan
    International Journal of Ophthalmology, 2020, 13 (05) : 766 - 772
  • [5] Hereditary cerebellar ataxia with Leber's hereditary optic neuropathy mitochondrial DNA 11778 mutation
    Murakami, T
    Mita, S
    Tokunaga, M
    Maeda, H
    Ueyama, H
    Kumamoto, T
    Uchino, M
    Ando, M
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 1996, 142 (1-2) : 111 - 113
  • [6] Macular structural changes in Leber's hereditary optic neuropathy with G11778A mutation evaluated by optical coherence tomography
    Liu, Xinting
    Shen, Meixiao
    Yuan, Yimin
    Lu, Fan
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2018, 59 (09)
  • [7] Clinical Characteristics of m.11778G&gt;A Leber Hereditary Optic Neuropathy with Favorable Outcomes
    Kim, Ungsoo Samuel
    Yun, Jeong Seop
    SEMINARS IN OPHTHALMOLOGY, 2024, 39 (04) : 320 - 323
  • [8] MS diagnosis in a male patient with m.11778G > A Leber’s hereditary optic neuropathy
    Pasquale Scoppettuolo
    Cecile Retif
    Stelianos Kampouridis
    Audrey Meunier
    Joachim Schulz
    Neurological Sciences, 2022, 43 : 6117 - 6120
  • [9] Penetrance of leber hereditary optic neuropathy in Chinese individuals with mitochondrial DNA 11778 mutation
    Zhang, Q.
    Guo, X.
    Jia, X.
    Xiao, X.
    Guo, L.
    Li, S.
    Chinese Journal of Medical Genetics, 2001, 18 (06) : 441 - 443
  • [10] Variations in phenotypic expression of the 11778 mutation in a family with Leber's hereditary optic neuropathy
    Challa, P
    Guy, JR
    Dickel, CD
    Hauswirth, WH
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 1997, 38 (04) : 3709 - 3709