02280nas a2200265 4500000000100000008004100001100002000042700001600062700001200078700001200090700001200102700001300114700001200127700001800139700001200157700001400169700001500183700001600198245010700214250001500321300001000336490000600346520161100352020005101963 2014 d1 aLindley Richard1 aDe Silva D.1 aWang J.1 aWong T.1 aWong M.1 aBaker M.1 aHand P.1 aRochtchina E.1 aLiew G.1 aHankey G.1 aWardlaw J.1 aMitchell P.00aDiffering associations of white matter lesions and lacunar infarction with retinal microvascular signs a2012/09/20 a921-50 v93 a

BACKGROUND: White matter lesions (WML) and lacunar infarcts (LI) are believed to have microvascular etiologies but the exact microvascular changes occurring in each is unclear. AIM: Using the retina as a proxy, we assessed retinal microvascular changes in WML and LI. METHODS: We prospectively recruited 1211 acute stroke patients. Four subgroups were identified from neuroimaging: WML alone, LI alone, both WML and LI, neither WML nor LI. Masked retinal photographs identified retinopathy and retinal arteriolar wall signs and measured retinal vascular caliber. RESULTS: Compared with 448 controls with neither WML nor LI, 384 patients with only WML were more likely to have retinopathy [odds ratio (OR) 1.5, 95% confidence interval (CI) 1.1 to 2.1] and enhanced arteriolar light reflex (OR 1.6, 95% CI 1.1 to 2.3); 200 patients with only LI were more likely to have arteriolar narrowing (OR 1.6, 95% CI 1.1 to 2.3) and enhanced arteriolar light reflex (OR 1.6, 95% CI 1.0 to 2.4); and 179 patients with both WML and LI were more likely to have arteriovenous nicking (OR 1.7, 95% CI 1.1 to 2.6), enhanced arteriolar light reflex (OR 2.0, 95% CI 1.3 to 3.2) and wider venules (OR 2.3, 95% CI 1.4 to 3.6). All analyses were adjusted for age, gender, study site and cardiovascular risk factors. CONCLUSION: Both WML and LI were associated with retinal microvascular signs, supporting a microvascular etiology. Differing patterns of association suggest different mechanisms may predominate, e.g. greater endothelial permeability in WML, and ischemia associated with arteriolar wall disease in LI.

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