In Vivo Characterization of Retinal Microvascular Impairment in Age Related Memory Loss

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In Vivo Characterization of Retinal Microvascular Impairment in Age Related Memory Loss Hong Jiang, MD, PhD Assistant Professor Bascom Palmer Eye Institute Department of Neurology Evelyn F. McKnight Brain Institute University of Miami, Miller School of Medicine Miami, FL Bascom Palmer E Y E I N S T I T U T E

Thomas Sydenham Father of English Medicine A man is as old as his arteries. Vascular Aging (1624-1689) Leonard A). J R Coll Physicians Lond 1990; 24:141 143. De Meyer T et al., Ageing Res Rev 2011; 10:297 303. Franklin SS. J Hypertens 2002; 20:1693 1696

The vasculatures in the eye and cerebral cortex have the same main blood supply, which is the internal carotid artery (ICA) Cited from Atlas of Ocular Blood Flow

Eye is the Window of the Brain Retina is the extension of brain. Eye and brain are in similar constricted environment. Retinal and cerebral small vessels share similar: embryological origin Anatomical features Blood-retinal barrier The transparent ocular media enables noninvasive visualization and analysis in vivo: Neurodegeneration Microvascular dysfunction

Optic Disk Fovea Fundus Photo

Retinal Microvascular Abnormalities large scale epidemiologic study Atherosclerosis Risk in Communities Study (ARIC) Strong link between the presence of retinal vascular abnormalites and both clinical (stroke) and subclinical (white matter lesions) detected on MRI With and without diabetes and hypertension The Rotterdam Study Larger venular calibers associated with an increased risk of vascular dementia After adjustment of stroke and cardiovascular risk factors Cardiovascular Health Study Total number of retinal signs reversely correlated with the executive function and gait speed After adjustment of vascular risk factors Yatsuya H. et al.,.stroke 2010; 41: 1349 1355 Wong TY et al., Lancet 2001; 358: 1134 1140 Cheung N. et al., Brain. 2010; 133: 1987 1993. Kawasaki R. et al., Stroke. 2010; 41: 1826 1828 De Jong FJ et al., Neurology, 2011. 76. 816 821 Dae Hyun Kim et al. Stroke. 2011;42:1589-1595

Observable retinal microvessels in the eye ncpm

Advanced Ophthalmic Imaging Lab Extended infrastructure of McKnight Brain Institute Novel non-invasive imaging modalities Retinal Function Imager (RFI) quantitative analysis of microcirculation (pre-capillary arteriole, post-capillary venule) Optic coherence tomography angiography (OCTA) depth resolved microvascular network Ultrahigh resolution optic coherence tomography (UHR-OCT) tomographic intraretinal thickness analysis Polarization sensitive optic coherence tomography (PS-OCT) Micro-structural integrity of retinal nerve fiber layer

Retinal Function Imager (RFI) A retinal function imager (RFI, Optical Imaging Ltd, Rehovot, Israel) was used to capture reflectance changes as a function of time under stroboscopic illumination. Digital camera Flash unit and PC Hemoglobin in red blood cells was used as an intrinsic motion-contrast agent in the generation of: Blood flow velocity maps Microvascular network Fundus Camera Jiang et al. Microvasc. Res. 2013;85:134-137. Jiang et al. Microvasc Res. 2013 Epub ahead of print Izhaky et al. Jpn. J. Ophthalmol. 2009;53:345-351. Landa et al. Int. Ophthalmol. 2010;32:211-215 9

RFI blood flow measurement Blood flow-velocity visualization Automatic Quantification (mm/sec) Movie from a series of 8 mages Field of view : 20 degree Image size 4.6 x 4.6 mm 2 1024 x 1024 pixels (mm/sec)

Aging of Retinal Microcirculation Retinal Blood Flow Velocity in Arterioles Retinal Blood Flow Velocity in Venules Arterolar Blood Flow Velocity (mm/s) 9.0 8.0 7.0 6.0 5.0 4.0 3.0 2.0 Normal Linear (Normal) 1.0 r = -0.34 r = 0.51 0.0 40 50 60 70 80 90 Age (years) MCI Linear (MCI) Venular Blood Flow Velocity (mm/s) 9.0 Normal MCI 8.0 7.0 Linear (Normal) Linear (MCI) 6.0 5.0 4.0 3.0 2.0 1.0 R² = 0.0062 R² = 0.004 0.0 40 50 60 70 80 90 Age (years) N = 28 (Normal = 14, MCI= 13)

Optic Coherence Tomography Angiography (OCTA) http://www.zeiss.com/meditec/en_de/c/oct angiography.html

OCTA for Quantitative Analysis of Microvascular Network in Intra-retinal Layers

Aging of Retinal Microvessels Retinal Superficial Capillary Plexus Retinal Deep Capillary Plexus Microvessel Density (Dbox) 1.81 Normal MCI Linear (Normal) Linear (MCI) 1.79 1.77 1.75 1.73 1.71 1.69 1.67 1.65 R² = 0.2547 R² = 0.0097 1.63 40 50 60 70 80 90 Age (years) Microvessel Density (Dbox) Normal MCI 1.81 Linear (Normal) Linear (MCI) 1.79 1.77 1.75 1.73 1.71 1.69 1.67 1.65 r = -0.41 r = -0.36 1.63 40 50 60 70 80 90 Age (Years) N = 31 (Normal = 18, MCI = 13)

Aging of Retinal Microvessels A Superficial B Deep Normal C Dbox = 1.768 Dbox = 1.762 D MCI Dbox = 1.741 Dbox = 1.760

Optic Coherence Tomography (OCT) of the Human Retina Retinal segmentation on SD-OCT Correlation of anatomy with OCT for the human retina Galetta SL et al., Neurol Neuroimmunol Neuroinflamm 2015 23;2(4):e135

RNFL thickness in patients with MCI, mild, moderate, severe AD and control subjects Liu D et al. BMC Neurol 2015;15:14

Ultrahigh Resolution OCT (UHR-OCT) Axial resolution = ~ 3 µm, automated segmentation of 6 intraretinal layers

Cross-Sectional Retinal Segmented Tomographic Thickness Maps of Intraretinal Layers Ultrahigh resolution OCT (UHR-OCT, axial resolution = ~3 µm) Fully-automated 3D segmentation software

Aging of Retinal Neurons Retinal Nerve Fiber Layer (RNFL) Retinal Ganglion Cells (GCL) Foveal RNFL Thickness (um) 50 Normal MCI 45 Linear (Normal) Linear (MCI) 40 35 30 25 R² = 0.1049 R² = 0.2418 20 40 50 60 70 80 90 GCIP Thickness (um) 90 Normal MCI 85 80 Linear (Normal) Linear (MCI) 75 70 65 60 55 50 45 R² = 0.0585 R² = 0.1754 40 40 50 60 70 80 90 100 Age (years) Age (years) N = 28 (Normal = 18, MCI = 10)

Summary Vascular aging is evident in retinal microcirculation and capillary network. More profound vascular aging in MCI patients is apparent. Non-invasive novel ophthalmic imaging is promising in studying the role of vascular aging in cognitive decline. Future longitudinal studies with large sample size are needed.

Critical question: which happens first? Cognitive aging Aging Our main hypothesis predicts that impairment initially occurs with the microvessel network and microcirculation, followed by cognitive aging and the loss of RNFL/GCL structure.

Acknowledgement Evelyn F. McKnight Brain Institute Department of Neurology Clinton B. Wright, MD Xiaoyan Sun, MD PhD Ms. Maria Carolina Mendoza- Puccini Bascom Palmer Eye Institute Jianhua Wang, MD PhD Ye Yang, MD Yantao Wei, MD PhD Dongyi Qu, MD PhD Liang Hu, MD Philip Rosenfeld, MD PhD Luiz Roisman, MD Giovanni Gregori, PhD Byron Lam, MD

NANOS pilot grant UM RSA 2015-41 NIH Center Grant P30 Research to Prevent Blindness Department of Defense