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
  • [31] Functional and clinical data of Best vitelliform macular dystrophy patients with mutations in the BEST1 gene
    Querques, Giuseppe
    Zerbib, Jennyfer
    Santacroce, Rossana
    Margaglione, Maurizio
    Delphin, Nathalie
    Rozet, Jean-Michel
    Kaplan, Josseline
    Martinelli, Domenico
    Delle Noci, Nicola
    Soubrane, Gisele
    Souied, Eric H.
    [J]. MOLECULAR VISION, 2009, 15 (312-14): : 2960 - 2972
  • [32] Natural course of the vitelliform stage in best vitelliform macular dystrophy: a five-year follow-up study
    Battaglia Parodi, Maurizio
    Romano, Francesco
    Arrigo, Alessandro
    Di Nunzio, Carlo
    Buzzotta, Alessio
    Alto, Giorgio
    Bandello, Francesco
    [J]. GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, 2020, 258 (02) : 297 - 301
  • [33] Association of Optic Nerve Head Drusen with Best Vitelliform Macular Dystrophy: A Case Series
    White, Robert J.
    Watson, Daniel J.
    Koozekanani, Dara D.
    Montezuma, Sandra R.
    [J]. CASE REPORTS IN OPHTHALMOLOGY, 2018, 9 (01): : 82 - 92
  • [34] Novel Presenting Phenotype in a Child With Autosomal Dominant Best's Vitelliform Macular Dystrophy
    Abdalla, Yasmine F.
    De Salvo, Gabriella
    Elsahn, Ahmad
    Self, James E.
    [J]. OPHTHALMIC SURGERY LASERS & IMAGING RETINA, 2017, 48 (07) : 580 - 585
  • [35] Optical Coherence Tomography Examination of the Retinal Pigment Epithelium in Best Vitelliform Macular Dystrophy
    Qian, Cynthia X.
    Charran, Dionisio
    Strong, Cameron R.
    Steffens, Timothy J.
    Jayasundera, Thiran
    Heckenlively, John R.
    [J]. OPHTHALMOLOGY, 2017, 124 (04) : 456 - 463
  • [36] Natural course of the vitelliform stage in best vitelliform macular dystrophy: a five-year follow-up study
    Maurizio Battaglia Parodi
    Francesco Romano
    Alessandro Arrigo
    Carlo Di Nunzio
    Alessio Buzzotta
    Giorgio Alto
    Francesco Bandello
    [J]. Graefe's Archive for Clinical and Experimental Ophthalmology, 2020, 258 : 297 - 301
  • [37] Multimodal Imaging Characteristics of Quiescent Type 1 Neovascularization in Best Vitelliform Macular Dystrophy
    Mentes, Jale
    Baris, Mine Esen
    [J]. TURK OFTALMOLOJI DERGISI-TURKISH JOURNAL OF OPHTHALMOLOGY, 2021, 51 (03): : 188 - 191
  • [38] Screening of BEST1 Gene in a Chinese Cohort With Best Vitelliform Macular Dystrophy or Autosomal Recessive Bestrophinopathy
    Tian, Lu
    Sun, Tengyang
    Xu, Ke
    Zhang, Xiaohui
    Peng, Xiaoyan
    Li, Yang
    [J]. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2017, 58 (09) : 3366 - 3375
  • [39] Novel Mutation in BEST1 Associated with Atypical Best Vitelliform Dystrophy
    Matson, Michelle E.
    Ly, Son V.
    Monarrez, Jennifer L.
    [J]. OPTOMETRY AND VISION SCIENCE, 2015, 92 (08) : E180 - E189
  • [40] Genotype-phenotype correlation and longitudinal course in ten families with Best vitelliform macular dystrophy
    B. Wabbels
    M. N. Preising
    U. Kretschmann
    A. Demmler
    B. Lorenz
    [J]. Graefe's Archive for Clinical and Experimental Ophthalmology, 2006, 244 : 1453 - 1466