TY - JOUR
T1 - Retinal Optical Coherence Tomography Features Associated With Incident and Prevalent Parkinson Disease
AU - Wagner, Siegfried Karl
AU - Romero-Bascones, David
AU - Cortina-Borja, Mario
AU - Williamson, Dominic J.
AU - Struyven, Robbert R.
AU - Zhou, Yukun
AU - Patel, Salil
AU - Weil, Rimona S.
AU - Antoniades, Chrystalina A.
AU - Topol, Eric J.
AU - Korot, Edward
AU - Foster, Paul J.
AU - Balaskas, Konstantinos
AU - Ayala, Unai
AU - Barrenechea, Maitane
AU - Gabilondo, Iñigo
AU - Schapira, Anthony H.V.
AU - Khawaja, Anthony P.
AU - Patel, Praveen J.
AU - Rahi, Jugnoo S.
AU - Denniston, Alastair K.
AU - Petzold, Axel
AU - Keane, Pearse Andrew
AU - for UK Biobank Eye & Vision Consortium
N1 - Publisher Copyright:
© 2023 Lippincott Williams and Wilkins. All rights reserved.
PY - 2023/10/17
Y1 - 2023/10/17
N2 - Background and Objectives Cadaveric studies have shown disease-related neurodegeneration and other morphological abnormalities in the retina of individuals with Parkinson disease (PD); however, it remains unclear whether this can be reliably detected with in vivo imaging. We investigated inner retinal anatomy, measured using optical coherence tomography (OCT), in prevalent PD and subsequently assessed the association of these markers with the development of PD using a prospective research cohort. Methods This cross-sectional analysis used data from 2 studies. For the detection of retinal markers in prevalent PD, we used data from AlzEye, a retrospective cohort of 154,830 patients aged 40 years and older attending secondary care ophthalmic hospitals in London, United Kingdom, between 2008 and 2018. For the evaluation of retinal markers in incident PD, we used data from UK Biobank, a prospective population-based cohort where 67,311 volunteers aged 40–69 years were recruited between 2006 and 2010 and underwent retinal imaging. Macular retinal nerve fiber layer (mRNFL), ganglion cell–inner plexiform layer (GCIPL), and inner nuclear layer (INL) thicknesses were extracted from fovea-centered OCT. Linear mixed-effects models were fitted to examine the association between prevalent PD and retinal thicknesses. Hazard ratios for the association between time to PD diagnosis and retinal thicknesses were estimated using frailty models. Results Within the AlzEye cohort, there were 700 individuals with prevalent PD and 105,770 controls (mean age 65.5 ± 13.5 years, 51.7% female). Individuals with prevalent PD had thinner GCIPL (−2.12 μm, 95% CI −3.17 to −1.07, p = 8.2 × 10−5) and INL (−0.99 μm, 95% CI −1.52 to −0.47, p = 2.1 × 10−4). The UK Biobank included 50,405 participants (mean age 56.1 ± 8.2 years, 54.7% female), of whom 53 developed PD at a mean of 2,653 ± 851 days. Thinner GCIPL (hazard ratio [HR] 0.62 per SD increase, 95% CI 0.46–0.84, p = 0.002) and thinner INL (HR 0.70, 95% CI 0.51–0.96, p = 0.026) were also associated with incident PD. Discussion Individuals with PD have reduced thickness of the INL and GCIPL of the retina. Involvement of these layers several years before clinical presentation highlight a potential role for retinal imaging for at-risk stratification of PD.
AB - Background and Objectives Cadaveric studies have shown disease-related neurodegeneration and other morphological abnormalities in the retina of individuals with Parkinson disease (PD); however, it remains unclear whether this can be reliably detected with in vivo imaging. We investigated inner retinal anatomy, measured using optical coherence tomography (OCT), in prevalent PD and subsequently assessed the association of these markers with the development of PD using a prospective research cohort. Methods This cross-sectional analysis used data from 2 studies. For the detection of retinal markers in prevalent PD, we used data from AlzEye, a retrospective cohort of 154,830 patients aged 40 years and older attending secondary care ophthalmic hospitals in London, United Kingdom, between 2008 and 2018. For the evaluation of retinal markers in incident PD, we used data from UK Biobank, a prospective population-based cohort where 67,311 volunteers aged 40–69 years were recruited between 2006 and 2010 and underwent retinal imaging. Macular retinal nerve fiber layer (mRNFL), ganglion cell–inner plexiform layer (GCIPL), and inner nuclear layer (INL) thicknesses were extracted from fovea-centered OCT. Linear mixed-effects models were fitted to examine the association between prevalent PD and retinal thicknesses. Hazard ratios for the association between time to PD diagnosis and retinal thicknesses were estimated using frailty models. Results Within the AlzEye cohort, there were 700 individuals with prevalent PD and 105,770 controls (mean age 65.5 ± 13.5 years, 51.7% female). Individuals with prevalent PD had thinner GCIPL (−2.12 μm, 95% CI −3.17 to −1.07, p = 8.2 × 10−5) and INL (−0.99 μm, 95% CI −1.52 to −0.47, p = 2.1 × 10−4). The UK Biobank included 50,405 participants (mean age 56.1 ± 8.2 years, 54.7% female), of whom 53 developed PD at a mean of 2,653 ± 851 days. Thinner GCIPL (hazard ratio [HR] 0.62 per SD increase, 95% CI 0.46–0.84, p = 0.002) and thinner INL (HR 0.70, 95% CI 0.51–0.96, p = 0.026) were also associated with incident PD. Discussion Individuals with PD have reduced thickness of the INL and GCIPL of the retina. Involvement of these layers several years before clinical presentation highlight a potential role for retinal imaging for at-risk stratification of PD.
UR - https://www.scopus.com/pages/publications/85174642208
U2 - 10.1212/WNL.0000000000207727
DO - 10.1212/WNL.0000000000207727
M3 - Article
C2 - 37604659
AN - SCOPUS:85174642208
SN - 0028-3878
VL - 101
SP - e1581-e1593
JO - Neurology
JF - Neurology
IS - 16
ER -