TY - JOUR
T1 - Retinal capillary microvessel morphology changes are associated with vascular damage and dysfunction in cerebral small vessel disease
AU - Wiseman, Stewart J
AU - Zhang, Jun-fang
AU - Gray, Calum
AU - Hamid, Charlene
AU - Valdés Hernández, Maria Del C
AU - Ballerini, Lucia
AU - Thrippleton, Michael J
AU - Manning, Cameron
AU - Stringer, Michael
AU - Sleight, Emilie
AU - Muñoz Maniega, Susana
AU - Morgan, Alasdair
AU - Cheng, Yajun
AU - Arteaga, Carmen
AU - Jaime Garcia, Dany
AU - Clancy, Una
AU - Doubal, Fergus N
AU - Dhillon, Baljean
AU - Macgillivray, Tom
AU - Wu, Yun-cheng
AU - Wardlaw, Joanna M
N1 - Funding Information:
The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This work is supported by: the UK Dementia Research Institute which receives its funding from DRI Ltd, funded by the UK MRC, Alzheimer’s Society and Alzheimer’s Research UK; the Fondation Leducq Network for the Study of Perivascular Spaces in Small Vessel Disease (16 CVD 05); Stroke Association ‘Small Vessel Disease-Spotlight on Symptoms (SVD-SOS)’(SAPG 19\100068; British Heart Foundation Edinburgh Centre for Research Excellence (RE/18/5/34216); The Row Fogo Charitable Trust Centre for Research into Aging and the Brain; Stroke Association Garfield Weston Foundation Senior Clinical Lectureship (F.N.D.) (TSALECT 2015/04); NHS Research Scotland (F.N.D.); Stroke Association Post-Doctoral Fellowship (S.J.W.) (SAPDF 18/100026); NHS Lothian Research and Development Office (MJT); European Union Horizon 2020, PHC-03–15, project No666881, ‘SVDs@Target’ (MS); Chief Scientist Office of Scotland Clinical Academic Fellowship (UC) (CAF/18/08); Stroke Association Princess Margaret Research Development Fellowship (UC) (2018); Medical Research Scotland studentship (AM) (PhD-1165–2017); MRC Doctoral Training Programme in Precision Medicine (CM) (MR/R01566X/1); Siemens Healthcare (AM and CM); Science and Technology Innovation 2030-“Brain Science and Brain-Like Intelligence Technology” Major Project (The China Brain Project) (No. 2021ZD0201905), Clinical Research Innovation Plan of Shanghai General Hospital (CTCCR-2018B03) and the National Natural Science Foundation of China (81971185, 82171243). The research MRI scanner is supported by the Scottish Funding Council through the Scottish Imaging Network, A Platform for Scientific Excellence (SINAPSE) Collaboration; the Wellcome Trust (104916/Z/14/Z), Dunhill Trust (R380R/1114), Edinburgh and Lothians Health Foundation (2012/17), Muir Maxwell Research Fund and the University of Edinburgh.
Publisher Copyright:
© The Author(s) 2022.
PY - 2022/10/27
Y1 - 2022/10/27
N2 - Cerebral small vessel disease (SVD) is a cause of stroke and dementia. Retinal capillary microvessels revealed by optical coherence tomography angiography (OCTA) are developmentally related to brain microvessels. We quantified retinal vessel density (VD) and branching complexity, investigating relationships with SVD lesions, white matter integrity on diffusion tensor imaging (DTI) and cerebrovascular reactivity (CVR) to CO2 in patients with minor stroke. We enrolled 123 patients (mean age 68.1 ± SD 9.9 years), 115 contributed retinal data. Right (R) and left (L) eyes are reported. After adjusting for age, eye disease, diabetes, blood pressure and image quality, lower VD remained associated with higher mean diffusivity (MD) (standardized β; R −0.16 [95%CI −0.32 to −0.01]) and lower CVR (L 0.17 [0.03 to 0.31] and R 0.19 [0.02 to 0.36]) in normal appearing white matter (NAWM). Sparser branching remained associated with sub-visible white matter damage shown by higher MD (R −0.24 [−0.08 to −0.40]), lower fractional anisotropy (FA) (L 0.17 [0.01 to 0.33]), and lower CVR (R 0.20 [0.02 to 0.38]) in NAWM. OCTA-derived metrics provide evidence of microvessel abnormalities that may underpin SVD lesions in the brain.
AB - Cerebral small vessel disease (SVD) is a cause of stroke and dementia. Retinal capillary microvessels revealed by optical coherence tomography angiography (OCTA) are developmentally related to brain microvessels. We quantified retinal vessel density (VD) and branching complexity, investigating relationships with SVD lesions, white matter integrity on diffusion tensor imaging (DTI) and cerebrovascular reactivity (CVR) to CO2 in patients with minor stroke. We enrolled 123 patients (mean age 68.1 ± SD 9.9 years), 115 contributed retinal data. Right (R) and left (L) eyes are reported. After adjusting for age, eye disease, diabetes, blood pressure and image quality, lower VD remained associated with higher mean diffusivity (MD) (standardized β; R −0.16 [95%CI −0.32 to −0.01]) and lower CVR (L 0.17 [0.03 to 0.31] and R 0.19 [0.02 to 0.36]) in normal appearing white matter (NAWM). Sparser branching remained associated with sub-visible white matter damage shown by higher MD (R −0.24 [−0.08 to −0.40]), lower fractional anisotropy (FA) (L 0.17 [0.01 to 0.33]), and lower CVR (R 0.20 [0.02 to 0.38]) in NAWM. OCTA-derived metrics provide evidence of microvessel abnormalities that may underpin SVD lesions in the brain.
U2 - 10.1177/0271678X221135658
DO - 10.1177/0271678X221135658
M3 - Article
SN - 1559-7016
JO - Journal of Cerebral Blood Flow and Metabolism
JF - Journal of Cerebral Blood Flow and Metabolism
ER -