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Corneal Nerve and Brain Imaging in Mild Cognitive Impairment and Dementia

BACKGROUND: Visual rating of medial temporal lobe atrophy (MTA) is an accepted structural neuroimaging marker of Alzheimer’s disease. Corneal confocal microscopy (CCM) is a non-invasive ophthalmic technique that detects neuronal loss in peripheral and central neurodegenerative disorders. OBJECTIVE:...

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Detalles Bibliográficos
Autores principales: Al-Janahi, Eiman, Ponirakis, Georgios, Al Hamad, Hanadi, Vattoth, Surjith, Elsotouhy, Ahmed, Petropoulos, Ioannis N., Khan, Adnan, Gad, Hoda, Chandran, Mani, Sankaranarayanan, Anoop, Ramadan, Marwan, Elorrabi, Marwa, Gadelseed, Masharig, Tosino, Rhia, Gawhale, Priya V., Arasn, Anjum, Alobaidi, Maryam, Khan, Shafi, Manikoth, Pravija, Hamdi, Yasmin, Osman, Susan, Nadukkandiyil, Navas, AlSulaiti, Essa, Thodi, Noushad, Almuhannadi, Hamad, Mahfoud, Ziyad R., Own, Ahmed, Shuaib, Ashfaq, Malik, Rayaz A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7683060/
https://www.ncbi.nlm.nih.gov/pubmed/32925064
http://dx.doi.org/10.3233/JAD-200678
Descripción
Sumario:BACKGROUND: Visual rating of medial temporal lobe atrophy (MTA) is an accepted structural neuroimaging marker of Alzheimer’s disease. Corneal confocal microscopy (CCM) is a non-invasive ophthalmic technique that detects neuronal loss in peripheral and central neurodegenerative disorders. OBJECTIVE: To determine the diagnostic accuracy of CCM for mild cognitive impairment (MCI) and dementia compared to medial temporal lobe atrophy (MTA) rating on MRI. METHODS: Subjects aged 60–85 with no cognitive impairment (NCI), MCI, and dementia based on the ICD-10 criteria were recruited. Subjects underwent cognitive screening, CCM, and MTA rating on MRI. RESULTS: 182 subjects with NCI (n = 36), MCI (n = 80), and dementia (n = 66), including AD (n = 19, 28.8%), VaD (n = 13, 19.7%), and mixed AD (n = 34, 51.5%) were studied. CCM showed a progressive reduction in corneal nerve fiber density (CNFD, fibers/mm(2)) (32.0±7.5 versus 24.5±9.6 and 20.8±9.3, p < 0.0001), branch density (CNBD, branches/mm(2)) (90.9±46.5 versus 59.3±35.7 and 53.9±38.7, p < 0.0001), and fiber length (CNFL, mm/mm(2)) (22.9±6.1 versus 17.2±6.5 and 15.8±7.4, p < 0.0001) in subjects with MCI and dementia compared to NCI. The area under the ROC curve (95% CI) for the diagnostic accuracy of CNFD, CNBD, CNFL compared to MTA-right and MTA-left for MCI was 78% (67–90%), 82% (72–92%), 86% (77–95%) versus 53% (36–69%) and 40% (25–55%), respectively, and for dementia it was 85% (76–94%), 84% (75–93%), 85% (76–94%) versus 86% (76–96%) and 82% (72–92%), respectively. CONCLUSION: The diagnostic accuracy of CCM, a non-invasive ophthalmic biomarker of neurodegeneration, was high and comparable with MTA rating for dementia but was superior to MTA rating for MCI.