Longitudinal Imaging of the Foveal Cone Mosaic in CNGA3-Associated Achromatopsia

被引:1
|
作者
Katta, Mohamed [1 ,2 ]
Georgiou, Michalis [1 ]
Singh, Navjit [1 ]
Kalitzeos, Angelos [1 ,2 ]
Dubra, Alfredo [3 ]
Carroll, Joseph [4 ]
Michaelides, Michel [1 ,2 ]
机构
[1] UCL, UCL Inst Ophthalmol, London, England
[2] Moorfields Eye Hosp NHS Fdn Trust, London, England
[3] Stanford Univ, Dept Ophthalmol, Palo Alto, CA USA
[4] Med Coll Wisconsin, Dept Ophthalmol & Visual Sci, Milwaukee, WI USA
基金
英国惠康基金; 美国国家卫生研究院;
关键词
adaptive optics; inherited retinal disease (IRD); CNGA3; achromatopsia (ACHM); cone dysfunction; RETINAL STRUCTURE; DENSITY; PHOTORECEPTORS; RELIABILITY; IDENTIFICATION; REPEATABILITY;
D O I
10.1167/iovs.65.12.6
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
PURPOSE . The purpose of this study was to assess the natural history of the foveal cone mosaic in CNGA3-associated achromatopsia (ACHM). METHODS . Thirteen eyes from 10 genetically confirmed patients underwent longitudinal imaging with optical coherence tomography (OCT) and non-confocal split detection adaptive optics scanning light ophthalmoscopy (AOSLO). OCT scans assessed outer nuclear layer (ONL) thickness, foveal ellipsoid zone (EZ) disruption, and foveal hypoplasia. AOSLO images were analyzed to calculate peak foveal cone density (PCD) and mean inter-cell distance (ICD) between cones. Mixed effects models were used to analyze the rate of annual change of PCD and ICD. RESULTS . Mean (+/- SD) age at visits was 29 +/- 10 years, with a follow-up of 2.6 +/- 1 years. There was no change in ONL thickness, degree of EZ disruption, or foveal hypoplasia over the follow-up period. We also observed a stable foveal cone mosaic using AOSLO imaging, with no significant change in PCD or ICD. Mean PCD was 15,346 cones/mm2 at the mean age of 29 years old (cf. 64,000-324,000 cones/mm2 in previously reported healthy controls), with a mean rate of change of -117.79 cones/mm2 (0.8%) per year, P = 0.130. Mean ICD at the mean age was 13.82 mu m, with a rate of change of 0.17 mu m per year, P = 0.83. CONCLUSIONS . CNGA3-associated ACHM displays stable foveal cone structure over time with a similar rate of change to CNGB3-associated ACHM (2% decline per year). The stable PCD, small cohort, and large variability within the cohort means significant age associations were not detected.
引用
收藏
页数:9
相关论文
共 50 条
  • [1] Characterization of Retinal Structure in CNGA3-associated Achromatopsia
    Georgiou, Michalis
    Langlo, Christopher S.
    Kalitzeos, Angelos
    Hirji, Nashila
    Kumaran, Neruban
    Dubra, Alfredo
    Carroll, Joseph
    Michaelides, Michel
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2018, 59 (09)
  • [2] Uniparental isodisomy of chromosome 2 in CNGA3-associated achromatopsia
    Kohl, Susanne
    Baumann, Britta
    Mayer, Anja-Kathrin
    Wissinger, Bernd
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2017, 58 (08)
  • [3] Longitudinal Imaging of Foveal Cone Structure in Congenital Achromatopsia
    Langlo, Christopher S.
    Collison, Frederick T.
    Summerfelt, Phyllis
    White, Carol
    Dubra, Alfredo
    Hauswirth, William W.
    Fishman, Gerald A.
    Carroll, Joseph
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2015, 56 (07)
  • [4] CNGA3-associated autosomal recessive achromatopsia caused by uniparental isodisomy of chromosome 2
    Kohl, S.
    Baumann, B.
    Mayer, A. K.
    Wissinger, B.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2018, 26 : 191 - 191
  • [5] Adaptive Optics Retinal Imaging in CNGA3-Associated Achromatopsia: Retinal Characterization, Interocular Symmetry, and Intrafamilial Variability
    Georgiou, Michalis
    Litts, Katie M.
    Kalitzeos, Angelos
    Langlo, Christopher S.
    Kane, Thomas
    Singh, Navjit
    Kassilian, Melissa
    Hirji, Nashila
    Kumaran, Neruban
    Dubra, Alfredo
    Carroll, Joseph
    Michaelides, Michel
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2019, 60 (01) : 383 - 396
  • [6] Longitudinal imaging of the parafoveal cone mosaic in congenital achromatopsia
    Chen, Nickolas
    Litts, Katie M.
    Nikezic, Danica
    Langlo, Christopher S.
    Higgins, Brian P.
    Lam, Byron L.
    Collison, Fred
    Pennesi, Mark E.
    Kay, Christine Nichols
    Tarima, Sergey
    Carroll, Joseph
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2024, 65 (07)
  • [7] REPEATABILITY AND LONGITUDINAL ASSESSMENT OF FOVEAL CONE STRUCTURE IN CNGB3-ASSOCIATED ACHROMATOPSIA
    Langlo, Christopher S.
    Erker, Laura R.
    Parker, Maria
    Patterson, Emily J.
    Higgins, Brian P.
    Summerfelt, Phyllis
    Razeen, Moataz M.
    Collison, Frederick T.
    Fishman, Gerald A.
    Kay, Christine N.
    Zhang, Jing
    Weleber, Richard G.
    Yang, Paul
    Pennesi, Mark E.
    Lam, Byron L.
    Chulay, Jeffrey D.
    Dubra, Alfredo
    Hauswirth, William W.
    Wilson, David J.
    Carroll, Joseph
    RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES, 2017, 37 (10): : 1956 - 1966
  • [8] Paternal Uniparental Isodisomy of Chromosome 2 in a Patient with CNGA3-Associated Autosomal Recessive Achromatopsia
    Kohl, Susanne
    Baumann, Britta
    Dassie, Francesca
    Mayer, Anja K.
    Solaki, Maria
    Reuter, Peggy
    Kuehlewein, Laura
    Wissinger, Bernd
    Maffei, Pietro
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2021, 22 (15)
  • [9] Intraobserver Repeatability and Interobserver Reproducibility of Foveal Cone Density Measurements in CNGA3- and CNGB3-Associated Achromatopsia
    Georgiou, Michalis
    Litts, Katie M.
    Singh, Navjit
    Kane, Thomas
    Patterson, Emily J.
    Hirji, Nashila
    Kalitzeos, Angelos
    Dubra, Alfredo
    Michaelides, Michel
    Carroll, Joseph
    TRANSLATIONAL VISION SCIENCE & TECHNOLOGY, 2020, 9 (07): : 1 - 10
  • [10] Residual Foveal Cone Structure in CNGB3-Associated Achromatopsia
    Langlo, Christopher S.
    Patterson, Emily J.
    Higgins, Brian P.
    Summerfelt, Phyllis
    Razeen, Moataz M.
    Erker, Laura R.
    Parker, Maria
    Collison, Frederick T.
    Fishman, Gerald A.
    Kay, Christine N.
    Zhang, Jing
    Weleber, Richard G.
    Yang, Paul
    Wilson, David J.
    Pennesi, Mark E.
    Lam, Byron L.
    Chiang, John
    Chulay, Jeffrey D.
    Dubra, Alfredo
    Hauswirth, William W.
    Carroll, Joseph
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2016, 57 (10) : 3984 - 3995