TY - JOUR
T1 - Changes of the retinal and choroidal vasculature in cerebral small vessel disease
AU - Geerling, Clara F.
AU - Terheyden, Jan H.
AU - Langner, S. Magdalena
AU - Kindler, Christine
AU - Keil, Vera C.
AU - Turski, Christopher A.
AU - Turski, Gabrielle N.
AU - Wintergerst, Maximillian W. M.
AU - Petzold, Gabor C.
AU - Finger, Robert P.
N1 - Funding Information: Open Access funding enabled and organized by Projekt DEAL. This research was supported by funding of the German Scholars Organization/Else Kröner Fresenius Stiftung (GSO/EKFS 16) to RPF and BONFOR GEROK Program, Faculty of Medicine, University of Bonn, Grant No O-137.0028 to MWMW. Funding Information: CFG, JHT, SML, CAT, GNT: Heidelberg Engineering, Optos, Carl Zeiss Meditec, CenterVue (devices). CK, VCK: none. MWMW: Heidelberg Engineering, Optos, Carl Zeiss Meditec, CenterVue (devices), DigiSight Technologies (travel support) Heine Optotechnik (research funding), Heine Optotechnik (research funding, devices, travel reimbursement, consultant), D-EYE Srl (devices), Eyenuk Inc. (free analysis), ASKIN & CO GmbH (travel reimbursement, honoraria), Berlin-Chemie AG (grant, travel reimbursements). GCP: Bayer, Boehringer, Pfizer und BMS (sponsoring). RPF: Bayer, Novartis, Santen, Opthea, Novelion, Santhera, Inositec, Alimera and RetinaImplant, Allergan, Boehringer Ingelheim (consultant); Bayer, Ellex, Alimera (research funding); Heidelberg Engineering, Optos, Carl Zeiss Meditec, CenterVue (devices). Publisher Copyright: © 2022, The Author(s).
PY - 2022/12/1
Y1 - 2022/12/1
N2 - Cerebral small vessel disease (CSVD) is associated with changes in the retinal vasculature which can be assessed non-invasively with much higher resolution than the cerebral vasculature. To detect changes at a microvascular level, we used optical coherence tomography angiography which resolves retinal and choroidal vasculature. Participants with CSVD and controls were included. White matter lesions were determined on magnetic resonance imaging (MRI). The retinal and choroidal vasculature were quantified using swept-source optical coherence tomography angiography. Data were analysed using linear regression. We included 30 participants (18 females; patients, n = 20; controls, n = 10) with a mean age of 61 ± 10 years. Patients had a higher mean white matter lesion index and number of lesions than controls (p ≤ 0.002). The intraindividual deviation of choriocapillaris reflectivity differed significantly between age-matched patients (0.234 ± 0.012) and controls (0.247 ± 0.011; p = 0.029). Skeleton density of the deep retinal capillaries was significantly associated with the number of lesions on MRI (β = − 5.3 × 108, 95%-confidence interval [− 10.3 × 108; − 0.2 × 108]) when controlling for age. The choroidal microvasculature and the deep retinal vascular plexus, as quantified by optical coherence tomography angiography, are significantly altered in CSVD. The value of these findings in diagnosing or monitoring CSVD need to be assessed in future studies.
AB - Cerebral small vessel disease (CSVD) is associated with changes in the retinal vasculature which can be assessed non-invasively with much higher resolution than the cerebral vasculature. To detect changes at a microvascular level, we used optical coherence tomography angiography which resolves retinal and choroidal vasculature. Participants with CSVD and controls were included. White matter lesions were determined on magnetic resonance imaging (MRI). The retinal and choroidal vasculature were quantified using swept-source optical coherence tomography angiography. Data were analysed using linear regression. We included 30 participants (18 females; patients, n = 20; controls, n = 10) with a mean age of 61 ± 10 years. Patients had a higher mean white matter lesion index and number of lesions than controls (p ≤ 0.002). The intraindividual deviation of choriocapillaris reflectivity differed significantly between age-matched patients (0.234 ± 0.012) and controls (0.247 ± 0.011; p = 0.029). Skeleton density of the deep retinal capillaries was significantly associated with the number of lesions on MRI (β = − 5.3 × 108, 95%-confidence interval [− 10.3 × 108; − 0.2 × 108]) when controlling for age. The choroidal microvasculature and the deep retinal vascular plexus, as quantified by optical coherence tomography angiography, are significantly altered in CSVD. The value of these findings in diagnosing or monitoring CSVD need to be assessed in future studies.
UR - http://www.scopus.com/inward/record.url?scp=85125976094&partnerID=8YFLogxK
U2 - https://doi.org/10.1038/s41598-022-07638-x
DO - https://doi.org/10.1038/s41598-022-07638-x
M3 - Article
C2 - 35256658
SN - 2045-2322
VL - 12
JO - Scientific Reports
JF - Scientific Reports
IS - 1
M1 - 3660
ER -