Retinal capillary microvessel morphology changes are associated with vascular damage and dysfunction in cerebral small vessel disease

Author:

Wiseman Stewart J123ORCID,Zhang Jun-Fang4,Gray Calum3ORCID,Hamid Charlene13,Valdés Hernández Maria del C12,Ballerini Lucia12,Thrippleton Michael J123,Manning Cameron1,Stringer Michael123ORCID,Sleight Emilie12,Muñoz Maniega Susana1,Morgan Alasdair1,Cheng Yajun15,Arteaga Carmen1ORCID,Jaime Garcia Dany1,Clancy Una1,Doubal Fergus N1,Dhillon Baljean16,MacGillivray Tom13,Wu Yun-Cheng4,Wardlaw Joanna M123ORCID

Affiliation:

1. Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK

2. UK Dementia Research Institute, University of Edinburgh, Edinburgh, UK

3. Edinburgh Imaging Facilities, Edinburgh Imaging, University of Edinburgh, UK

4. Department of Neurology, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China

5. Department of Neurology, West China Hospital, Sichuan University, Chengdu, China

6. NHS Lothian Princess Alexandra Eye Pavilion, UK

Abstract

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.

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine,Neurology (clinical),Neurology

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