TY - JOUR
T1 - Longitudinal changes in the macula and optic nerve in familial dysautonomia
AU - Kfir, Jonathan
AU - Wu, Mengfei
AU - Liu, Mengling
AU - Raju, Leela
AU - Schuman, Joel S.
AU - Ishikawa, Hiroshi
AU - Vanegas, Isabel M.
AU - Mendoza-Santiesteban, Carlos E.
AU - Palma, Jose Alberto
AU - Norcliffe-Kaufmann, Lucy
AU - Morgenstein, Barr
AU - Kaufmann, Horacio
AU - Wollstein, Gadi
N1 - Publisher Copyright:
© 2020, Springer-Verlag GmbH Germany, part of Springer Nature.
PY - 2021/4
Y1 - 2021/4
N2 - Objective: Familial Dysautonomia (FD) disease, lacks a useful biomarker for clinical monitoring. In this longitudinal study we characterized the structural changes in the macula, peripapillary and the optic nerve head (ONH) regions in subjects with FD. Methods: Data was consecutively collected from subjects attending the FD clinic between 2012 and 2019. All subjects were imaged with spectral-domain Optical Coherence Tomography (OCT). Global and sectoral measurements of mean retinal nerve fiber layer (RNFL) and macular ganglion cell and inner plexiform layer (GCIPL) thickness, and ONH parameters of rim area, average cup-to-disc (C:D) ratio, and cup volume were used for the analysis. The best fit models (linear, quadratic and broken stick linear model) were used to describe the longitudinal change in each of the parameters. Results: 91 subjects (149 eyes) with FD of ages 5–56 years were included in the analysis. The rate of change for average RNFL and average GCIPL thicknesses were significant before reaching a plateau at the age of 26.2 for RNFL and 24.8 for GCIPL (− 0.861 µm/year (95% CI − 1.026, − 0.693) and − 0.553 µm/year (95% CI − 0.645, − 0.461), respectively). Significant linear rate of progression was noted for all ONH parameters, except for a subset of subjects (24%), with no cupping that did not show progression in any of the ONH parameters. Conclusions: The rapidly declining RNFL and GCIPL can explain the progressive visual impairment previously reported in these subjects. Among all structural parameters, ONH parameters might be most suitable for longitudinal follow-up, in eyes with a measurable cup.
AB - Objective: Familial Dysautonomia (FD) disease, lacks a useful biomarker for clinical monitoring. In this longitudinal study we characterized the structural changes in the macula, peripapillary and the optic nerve head (ONH) regions in subjects with FD. Methods: Data was consecutively collected from subjects attending the FD clinic between 2012 and 2019. All subjects were imaged with spectral-domain Optical Coherence Tomography (OCT). Global and sectoral measurements of mean retinal nerve fiber layer (RNFL) and macular ganglion cell and inner plexiform layer (GCIPL) thickness, and ONH parameters of rim area, average cup-to-disc (C:D) ratio, and cup volume were used for the analysis. The best fit models (linear, quadratic and broken stick linear model) were used to describe the longitudinal change in each of the parameters. Results: 91 subjects (149 eyes) with FD of ages 5–56 years were included in the analysis. The rate of change for average RNFL and average GCIPL thicknesses were significant before reaching a plateau at the age of 26.2 for RNFL and 24.8 for GCIPL (− 0.861 µm/year (95% CI − 1.026, − 0.693) and − 0.553 µm/year (95% CI − 0.645, − 0.461), respectively). Significant linear rate of progression was noted for all ONH parameters, except for a subset of subjects (24%), with no cupping that did not show progression in any of the ONH parameters. Conclusions: The rapidly declining RNFL and GCIPL can explain the progressive visual impairment previously reported in these subjects. Among all structural parameters, ONH parameters might be most suitable for longitudinal follow-up, in eyes with a measurable cup.
KW - Familial dysautonomia
KW - Hereditary optic neuropathy
KW - Optical coherance tomography
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U2 - 10.1007/s00415-020-10298-4
DO - 10.1007/s00415-020-10298-4
M3 - Article
C2 - 33180192
AN - SCOPUS:85095878054
SN - 0340-5354
VL - 268
SP - 1402
EP - 1409
JO - Journal of Neurology
JF - Journal of Neurology
IS - 4
ER -