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Ocular indicators of Alzheimer's: exploring disease in the retina

期刊

ACTA NEUROPATHOLOGICA
卷 132, 期 6, 页码 767-787

出版社

SPRINGER
DOI: 10.1007/s00401-016-1613-6

关键词

Alzheimer's disease; Amyloid-beta; Tauopathy; Retinal biomarkers; Ocular abnormalities; Neurodegenerative disease

资金

  1. NIA [R41AG044897]
  2. Saban Family Foundation
  3. Marciano Family Foundation

向作者/读者索取更多资源

Although historically perceived as a disorder confined to the brain, our understanding of Alzheimer's disease (AD) has expanded to include extra-cerebral manifestation, with mounting evidence of abnormalities in the eye. Among ocular tissues, the retina, a developmental outgrowth of the brain, is marked by an array of pathologies in patients suffering from AD, including nerve fiber layer thinning, degeneration of retinal ganglion cells, and changes to vascular parameters. While the hallmark pathological signs of AD, amyloid beta-protein (A beta) plaques and neurofibrillary tangles (NFT) comprising hyperphosphorylated tau (pTau) protein, have long been described in the brain, identification of these characteristic biomarkers in the retina has only recently been reported. In particular, A beta deposits were discovered in post-mortem retinas of advanced and early stage cases of AD, in stark contrast to non-AD controls. Subsequent studies have reported elevated A beta(42/40) peptides, morphologically diverse A beta plaques, and pTau in the retina. In line with the above findings, animal model studies have reported retinal A beta deposits and tauopathy, often correlated with local inflammation, retinal ganglion cell degeneration, and functional deficits. This review highlights the converging evidence that AD manifests in the eye, especially in the retina, which can be imaged directly and non-invasively. Visual dysfunction in AD patients, traditionally attributed to well-documented cerebral pathology, can now be reexamined as a direct outcome of retinal abnormalities. As we continue to study the disease in the brain, the emerging field of ocular AD warrants further investigation of how the retina may faithfully reflect the neurological disease. Indeed, detection of retinal AD pathology, particularly the early presenting amyloid biomarkers, using advanced high-resolution imaging techniques may allow large-scale screening and monitoring of at-risk populations.

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