TY - JOUR
T1 - Macular ganglion cell complex and peripapillary retinal nerve fiber layer thinning in patients with type-1 gaucher disease
AU - Weill, Yishay
AU - Zimran, Ari
AU - Zadok, David
AU - Wasser, Lauren M.
AU - Revel-Vilk, Shoshana
AU - Hanhart, Joel
AU - Dinur, Tama
AU - Arkadir, David
AU - Becker-Cohen, Michal
N1 - Publisher Copyright:
© 2020 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2020/10/1
Y1 - 2020/10/1
N2 - Type-1 Gaucher disease (GD1) is considered to be non-neuronopathic however recent evidence of neurological involvement continues to accumulate. There is limited evidence of retinal abnormalities in GD1. The purpose of this study was to evaluate the retinal findings of patients with GD1. Thirty GD1 individuals and 30 healthy volunteers between the ages 40–75 years were prospectively enrolled. Macular and optic nerve optical coherence tomography (OCT) scans of both eyes of each patient were performed and thickness maps were compared between groups. Patients with a known neurodegenerative disease, glaucoma, high myopia and previous intraocular surgeries were excluded. It was shown that patients with GD1 presented with higher incidence of abnormal pRNFL OCT scan and showed significantly thinner areas of pRNFL and macular ganglion cell complex (GCC) when compared to a healthy control population. Changes in retinal thickness were not associated with GD1 genotype, treatment status, disease monitoring biomarker (lyso-Gb1) and severity score index (Zimran SSI). Further investigations are needed to determine whether these findings possess functional visual implications and if retinal thinning may serve as biomarker for the development of future neurodegenerative disease in this population.
AB - Type-1 Gaucher disease (GD1) is considered to be non-neuronopathic however recent evidence of neurological involvement continues to accumulate. There is limited evidence of retinal abnormalities in GD1. The purpose of this study was to evaluate the retinal findings of patients with GD1. Thirty GD1 individuals and 30 healthy volunteers between the ages 40–75 years were prospectively enrolled. Macular and optic nerve optical coherence tomography (OCT) scans of both eyes of each patient were performed and thickness maps were compared between groups. Patients with a known neurodegenerative disease, glaucoma, high myopia and previous intraocular surgeries were excluded. It was shown that patients with GD1 presented with higher incidence of abnormal pRNFL OCT scan and showed significantly thinner areas of pRNFL and macular ganglion cell complex (GCC) when compared to a healthy control population. Changes in retinal thickness were not associated with GD1 genotype, treatment status, disease monitoring biomarker (lyso-Gb1) and severity score index (Zimran SSI). Further investigations are needed to determine whether these findings possess functional visual implications and if retinal thinning may serve as biomarker for the development of future neurodegenerative disease in this population.
KW - Ganglion cell complex
KW - Gaucher disease
KW - Neurodegenerative disorder
KW - Optical coherence tomography
KW - Retinal ganglion cells
KW - Retinal nerve fiber layer
KW - Retinal thinning
UR - http://www.scopus.com/inward/record.url?scp=85091998078&partnerID=8YFLogxK
U2 - 10.3390/ijms21197027
DO - 10.3390/ijms21197027
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C2 - 32987733
AN - SCOPUS:85091998078
SN - 1661-6596
VL - 21
SP - 1
EP - 9
JO - International Journal of Molecular Sciences
JF - International Journal of Molecular Sciences
IS - 19
M1 - 7027
ER -