Characterization of Retinal Drusen in Subjects at High Genetic Risk of Developing Sporadic Alzheimer’s Disease: An Exploratory Analysis

• Published in: Journal of personalized medicine Vol. 12; no. 5; p. 847
• Main Authors: López-Cuenca, Inés, Salobrar-García, Elena, Gil-Salgado, Inés, Sánchez-Puebla, Lidia, Elvira-Hurtado, Lorena, Fernández-Albarral, José A., Ramírez-Toraño, Federico, Barabash, Ana, de Frutos-Lucas, Jaisalmer, Salazar, Juan J., Ramírez, José M., Ramírez, Ana I., de Hoz, Rosa
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 23.05.2022; MDPI
• Subjects: Age; Alzheimer's disease; Apolipoprotein E; Cardiovascular diseases; Classification; Diabetes; Diabetes mellitus; Diabetic retinopathy; Eye surgery; Glaucoma; Health risk assessment; Hypercholesterolemia; Hypertension; Isoforms; Macular degeneration; Neurodegeneration; Neurodegenerative diseases; Pathology; Perfusion; Precision medicine; Retina; Risk factors; Senile plaques; Thinning; Visual impairment; choroid; OCT; Alzheimer’s disease; ApoE ɛ4; retina; family history; AMD; diabetes mellitus; hypertension; hard drusen; hypercholesterolemia
• ISSN: 2075-4426; 2075-4426
• DOI: 10.3390/jpm12050847

Having a family history (FH+) of Alzheimer’s disease (AD) and being a carrier of at least one ɛ4 allele of the ApoE gene are two of the main risk factors for the development of AD. AD and age-related macular degeneration (AMD) share one of the main risk factors, such as age, and characteristics including the presence of deposits (Aβ plaques in AD and drusen in AMD); however, the role of apolipoprotein E isoforms in both pathologies is controversial. We analyzed and characterized retinal drusen by optical coherence tomography (OCT) in subjects, classifying them by their AD FH (FH- or FH+) and their allelic characterization of ApoE ɛ4 (ApoE ɛ4- or ApoE ɛ4+) and considering cardiovascular risk factors (hypercholesterolemia, hypertension, and diabetes mellitus). In addition, we analyzed the choroidal thickness by OCT and the area of the foveal avascular zone with OCTA. We did not find a relationship between a family history of AD or any of the ApoE isoforms and the presence or absence of drusen. Subjects with drusen show choroidal thinning compared to patients without drusen, and thinning could trigger changes in choroidal perfusion that may give rise to the deposits that generate drusen.