Retinal ganglion cell–inner plexiform layer thickness is nonlinearly associated with cognitive impairment in the community‐dwelling elderly

Abstract Introduction Thinning of optical coherence tomography–measured retinal nerve fiber layer thickness and ganglion cell–inner plexiform layer (GC‐IPL) thickness has been found in patients with Alzheimer's disease. However, the association of these retinal markers and cognition in nondemen...

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Main Authors: Yao‐Lin Liu, Yi‐Ting Hsieh, Ta‐Fu Chen, Jeng‐Min Chiou, Min‐Kuang Tsai, Jen‐Hau Chen, Yen‐Ching Chen
Format: Article
Language:English
Published: Wiley 2019-12-01
Series:Alzheimer’s & Dementia: Diagnosis, Assessment & Disease Monitoring
Subjects:
Online Access:https://doi.org/10.1016/j.dadm.2018.10.006
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spelling doaj-0bf736a99d8d454689b56cd447755f522020-11-25T03:59:48ZengWileyAlzheimer’s & Dementia: Diagnosis, Assessment & Disease Monitoring2352-87292019-12-01111192710.1016/j.dadm.2018.10.006Retinal ganglion cell–inner plexiform layer thickness is nonlinearly associated with cognitive impairment in the community‐dwelling elderlyYao‐Lin Liu0Yi‐Ting Hsieh1Ta‐Fu Chen2Jeng‐Min Chiou3Min‐Kuang Tsai4Jen‐Hau Chen5Yen‐Ching Chen6Department of OphthalmologyFar Eastern Memorial HospitalNew Taipei CityTaiwanDepartment of OphthalmologyNational Taiwan University HospitalTaipeiTaiwanDepartment of NeurologyNational Taiwan University HospitalTaipeiTaiwanInstitute of Statistical ScienceAcademia SinicaTaipeiTaiwanInstitute of Epidemiology and Preventive Medicine, College of Public Health, National Taiwan UniversityTaipeiTaiwanDepartment of Geriatrics and GerontologyNational Taiwan University HospitalTaipeiTaiwanInstitute of Epidemiology and Preventive Medicine, College of Public Health, National Taiwan UniversityTaipeiTaiwanAbstract Introduction Thinning of optical coherence tomography–measured retinal nerve fiber layer thickness and ganglion cell–inner plexiform layer (GC‐IPL) thickness has been found in patients with Alzheimer's disease. However, the association of these retinal markers and cognition in nondemented elders may not be linear. Methods This cross‐sectional study included 227 community‐dwelling elders (age 65+ years). Multivariable regression analyses were performed to investigate the association between retinal nerve fiber layer/GC‐IPL and global/domain‐specific cognition. Results The performance of global cognition decreased as mean GC‐IPL of bilateral eyes deviated from the sample mean (77.5 μm) (quadratic GC‐IPL: β = –0.49 × 10−2; 95% confidence interval: −0.74 × 10−2 to −0.23 × 10−2). Similar associations were also found for logical memory. No significant association was observed between retinal nerve fiber layer and cognition. Discussion Either thinning or thickening of GC‐IPL was associated with poor cognition in nondemented elderly (a U‐shaped association). GC‐IPL may serve as a noninvasive preclinical predictor of Alzheimer's disease.https://doi.org/10.1016/j.dadm.2018.10.006RetinaAlzheimer's diseaseBiomarkersPreclinical ADCognitive impairmentOptical coherence tomography
collection DOAJ
language English
format Article
sources DOAJ
author Yao‐Lin Liu
Yi‐Ting Hsieh
Ta‐Fu Chen
Jeng‐Min Chiou
Min‐Kuang Tsai
Jen‐Hau Chen
Yen‐Ching Chen
spellingShingle Yao‐Lin Liu
Yi‐Ting Hsieh
Ta‐Fu Chen
Jeng‐Min Chiou
Min‐Kuang Tsai
Jen‐Hau Chen
Yen‐Ching Chen
Retinal ganglion cell–inner plexiform layer thickness is nonlinearly associated with cognitive impairment in the community‐dwelling elderly
Alzheimer’s & Dementia: Diagnosis, Assessment & Disease Monitoring
Retina
Alzheimer's disease
Biomarkers
Preclinical AD
Cognitive impairment
Optical coherence tomography
author_facet Yao‐Lin Liu
Yi‐Ting Hsieh
Ta‐Fu Chen
Jeng‐Min Chiou
Min‐Kuang Tsai
Jen‐Hau Chen
Yen‐Ching Chen
author_sort Yao‐Lin Liu
title Retinal ganglion cell–inner plexiform layer thickness is nonlinearly associated with cognitive impairment in the community‐dwelling elderly
title_short Retinal ganglion cell–inner plexiform layer thickness is nonlinearly associated with cognitive impairment in the community‐dwelling elderly
title_full Retinal ganglion cell–inner plexiform layer thickness is nonlinearly associated with cognitive impairment in the community‐dwelling elderly
title_fullStr Retinal ganglion cell–inner plexiform layer thickness is nonlinearly associated with cognitive impairment in the community‐dwelling elderly
title_full_unstemmed Retinal ganglion cell–inner plexiform layer thickness is nonlinearly associated with cognitive impairment in the community‐dwelling elderly
title_sort retinal ganglion cell–inner plexiform layer thickness is nonlinearly associated with cognitive impairment in the community‐dwelling elderly
publisher Wiley
series Alzheimer’s & Dementia: Diagnosis, Assessment & Disease Monitoring
issn 2352-8729
publishDate 2019-12-01
description Abstract Introduction Thinning of optical coherence tomography–measured retinal nerve fiber layer thickness and ganglion cell–inner plexiform layer (GC‐IPL) thickness has been found in patients with Alzheimer's disease. However, the association of these retinal markers and cognition in nondemented elders may not be linear. Methods This cross‐sectional study included 227 community‐dwelling elders (age 65+ years). Multivariable regression analyses were performed to investigate the association between retinal nerve fiber layer/GC‐IPL and global/domain‐specific cognition. Results The performance of global cognition decreased as mean GC‐IPL of bilateral eyes deviated from the sample mean (77.5 μm) (quadratic GC‐IPL: β = –0.49 × 10−2; 95% confidence interval: −0.74 × 10−2 to −0.23 × 10−2). Similar associations were also found for logical memory. No significant association was observed between retinal nerve fiber layer and cognition. Discussion Either thinning or thickening of GC‐IPL was associated with poor cognition in nondemented elderly (a U‐shaped association). GC‐IPL may serve as a noninvasive preclinical predictor of Alzheimer's disease.
topic Retina
Alzheimer's disease
Biomarkers
Preclinical AD
Cognitive impairment
Optical coherence tomography
url https://doi.org/10.1016/j.dadm.2018.10.006
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