Chromatic pupilloperimetry for objective diagnosis of Best vitelliform macular dystrophy

被引:8
|
作者
Ben Ner, Daniel [1 ,2 ]
Sher, Ifat [1 ]
Hamburg, Amit [1 ,2 ]
Mhajna, Mohamad O. [1 ,2 ]
Chibel, Ron [1 ,2 ]
Derazne, Estela [2 ]
Sharvit-Ginon, Inbal [3 ,4 ]
Pras, Eran [2 ,5 ]
Newman, Hadas [2 ,6 ]
Levy, Jaime [7 ]
Khateb, Samer [7 ]
Sharon, Dror [7 ]
Rotenstreich, Ygal [1 ,2 ]
机构
[1] Sheba Med Ctr, Goldschleger Eye Inst, Room 220, IL-5262100 Tel Hashomer, Israel
[2] Tel Aviv Univ, Sackler Fac Med, Tel Aviv, Israel
[3] Bar Ilan Univ, Dept Psychol, Ramat Gan, Israel
[4] Joseph Sagol Neurosci Ctr, Sheba Med Ctr, Ramat Gan, Israel
[5] Assaf Harofeh Med Ctr, Dept Ophthalmol, Matlows Ophthalmo Genet Lab, Zerifin, Israel
[6] Tel Aviv Sourasky Med Ctr, Ophthalmol Dept, Tel Aviv, Israel
[7] Hadassah Hebrew Univ, Dept Ophthalmol, Med Ctr, Jerusalem, Israel
来源
CLINICAL OPHTHALMOLOGY | 2019年 / 13卷
关键词
Best vitelliform macular dystrophy; pupillary light reflex; perimetry; pupilloperimetry; visual field; FUNDUS AUTOFLUORESCENCE; ELECTROOCULOGRAPHY; PUPILLOMETER; PERIMETRY;
D O I
10.2147/OPTH.S191486
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose: To determine the pupil response of Best vitelliform macular dystrophy (BVMD) patients for focal blue and red light stimuli presented at 76 test points in a 16.2 degrees visual field (VF) using a chromatic pupilloperimeter. Methods: An observational study was conducted in 16 participants: 7 BVMD patients with a heterozygous BEST1 mutation and 9 similar-aged controls. All participants were tested for best-corrected visual acuity, chromatic pupilloperimetry and Humphrey perimetry. Percentage of pupil contraction (PPC), maximal pupil contraction velocity (MCV) and latency of MCV (LMCV) were determined. Results: The mean PPC and MCV recorded in BVMD patients in response to red stimuli were lower by >2 standard errors (SEs) from the mean of controls in 47% and 43% of VF test points, respectively. The mean PPC and MCV recorded in the patients in response to blue stimuli were lower by >2 SEs from the mean of controls in 36% and 24% of VF test points, respectively. The patients' mean and median MCV recorded in response to red light correlated with their Humphrey mean deviation score (r=-0.714, P=0.071 and r=-0.821, P=0.023, respectively) and visual acuity (r=0.709, P=0.074 and r=0.655, P=0.111, respectively). A substantially shorter mean LMCV was recorded in BVMD patients compared to controls in 54% and 93% of VF test points in response to red and blue light, respectively. Receiver operating characteristic analysis for LMCV in response to red light identified a test point at the center of the VF with high diagnostic accuracy (area under the curve of 0.94). Conclusion: Chromatic pupilloperimetry may potentially be used for objective noninvasive assessment of rod and cone cell function in different locations of the retina in BVMD patients.
引用
收藏
页码:465 / 475
页数:11
相关论文
共 50 条
  • [41] PHOTORECEPTOR INNER SEGMENT MORPHOLOGY IN BEST VITELLIFORM MACULAR DYSTROPHY
    Scoles, Drew
    Sulai, Yusufu N.
    Cooper, Robert F.
    Higgins, Brian P.
    Johnson, Ryan D.
    Carroll, Joseph
    Dubra, Alfredo
    Stepien, Kimberly E.
    RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES, 2017, 37 (04): : 741 - 748
  • [42] A Spontaneous Nonhuman Primate Model of Best Vitelliform Macular Dystrophy
    Xu, Mingming
    Xue, Ying
    Cao, Yingxue
    Yang, Ziqi
    Sun, Zehui
    Mai, Xiaomei
    Shi, Le
    Qing, Wenjie
    Li, Yuying
    Yi, Wei
    Liu, Xialin
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2024, 65 (07)
  • [43] OCT features in Vitelliform Macular Dystrophy (Best's disease)
    Leveziel, N
    Souied, E
    Benhamou, N
    Coscas, G
    Soubrane, G
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2003, 44 : U711 - U711
  • [44] Unilateral best vitelliform macular dystrophy- a case series
    Ratra, Dhanashree
    Karra, Abhishek
    DOCUMENTA OPHTHALMOLOGICA, 2025, : 111 - 116
  • [45] Still no evidence for heterogeneity in Best's vitelliform macular dystrophy
    Graff, C
    Wadelius, C
    JOURNAL OF MEDICAL GENETICS, 1996, 33 (07) : 630 - 630
  • [46] Lack of evidence for genetic heterogeneity in Best vitelliform macular dystrophy
    Mansergh, F
    Meitinger, T
    Rodolph, G
    Humphries, P
    Farrar, GJ
    JOURNAL OF MEDICAL GENETICS, 1998, 35 (01) : 85 - 86
  • [47] CLINICAL AND MOLECULAR GENETIC ANALYSIS OF BEST VITELLIFORM MACULAR DYSTROPHY
    Boon, Camiel J. F.
    Theelen, Thomas
    Hoetsloot, Elisabeth H.
    Van Schooneveld, Mary J.
    Keunen, Jan E. E.
    Cremers, Frans P. M.
    Klevering, B. Jeroen
    Hoyng, Carel B.
    RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES, 2009, 29 (06): : 835 - 847
  • [48] BEST1 mutations in Japanese patients with Best vitelliform macular dystrophy
    Katagiri, Satoshi
    Hayashi, Takaaki
    Sekiryu, Tetsuju
    Gekka, Tamaki
    Akahori, Masakazu
    Sasano, Hiroyuki
    Ohkuma, Yasuhiro
    Iwata, Takeshi
    Tsuneoka, Hiroshi
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2014, 55 (13)
  • [49] Deep Learning to distinguish Best vitelliform macular dystrophy (BVMD) from adult vitelliform macular degeneration (AVMD)
    Crincoli, Emanuele
    Zhao, Zhanlin
    Walker, Juliana Estrada
    Mehanna, Carl Joe
    Halouani, Safa
    Miere, Alexandra
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2022, 63 (07)
  • [50] BEST VITELLIFORM DYSTROPHY
    BLODI, CF
    STONE, EM
    OPHTHALMIC PAEDIATRICS AND GENETICS, 1990, 11 (01): : 49 - 59