A test of lens opacity as an indicator of preclinical Alzheimer Disease

被引:17
作者
Bei, Ling [1 ]
Shui, Ying-Bo [1 ]
Bai, Fang [1 ]
Nelson, Suzanne K. [1 ]
Van Stavern, Gregory P. [1 ]
Beebe, David C. [1 ,2 ]
机构
[1] Washington Univ, Sch Med, Dept Ophthalmol & Visual Sci, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Cell Biol & Physiol, St Louis, MO 63110 USA
关键词
Lens opacity; Cataract; Scheimpflug imaging; Alzheimer Disease biomarkers; Preclinical Alzheimer Disease; MILD COGNITIVE IMPAIRMENT; CSF BIOMARKERS; CELL DEGENERATION; LONGITUDINAL DATA; GRADING SYSTEM; BETA; CATARACTS; EYES; ABSENCE; PEOPLE;
D O I
10.1016/j.exer.2015.03.010
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Previous studies reported that characteristic lens opacities were present in Alzheimer Disease (AD) patients postmortem. We therefore determined whether cataract grade or lens opacity is related to the risk of Alzheimer dementia in participants who have biomarkers that predict a high risk of developing the disease. AD biomarker status was determined by positron emission tomography-Pittsburgh compound B (PET-PiB) imaging and cerebrospinal fluid (CSF) levels of A beta(42). Cognitively normal participants with a clinical dementia rating of zero (CDR = 0; N = 40) or with slight evidence of dementia (CDR = 0.5; N = 2) were recruited from longitudinal studies of memory and aging at the Washington University Knight Alzheimer's Disease Research Center. The age, sex, race, cataract type and cataract grade of all participants were recorded and an objective measure of lens light scattering was obtained for each eye using a Scheimpflug camera. Twenty-seven participants had no biomarkers of Alzheimer dementia and were CDR = 0. Fifteen participants had biomarkers indicating increased risk of AD, two of which were CDR = 0.5. Participants who were biomarker positive were older than those who were biomarker negative. Biomarker positive participants had more advanced cataracts and increased cortical light scattering, none of which reached statistical significance after adjustment for age. We conclude that cataract grade or lens opacity is unlikely to provide a non-invasive measure of the risk of developing Alzheimer dementia. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:117 / 123
页数:7
相关论文
共 43 条
[1]  
Albert PS, 1999, STAT MED, V18, P1707, DOI 10.1002/(SICI)1097-0258(19990715)18:13<1707::AID-SIM138>3.0.CO
[2]  
2-H
[3]  
Augusteyn RC, 2007, MOL VIS, V13, P252
[4]  
Bassnett S, 1997, INVEST OPHTH VIS SCI, V38, P1678
[5]   Lens organelle degradation [J].
Bassnett, S .
EXPERIMENTAL EYE RESEARCH, 2002, 74 (01) :1-6
[6]   CSF markers for incipient Alzheimer's disease [J].
Blennow, K ;
Hampel, H .
LANCET NEUROLOGY, 2003, 2 (10) :605-613
[7]   RELIABILITY OF THE WASHINGTON-UNIVERSITY CLINICAL DEMENTIA RATING [J].
BURKE, WJ ;
MILLER, JP ;
RUBIN, EH ;
MORRIS, JC ;
COBEN, LA ;
DUCHEK, J ;
WITTELS, IG ;
BERG, L .
ARCHIVES OF NEUROLOGY, 1988, 45 (01) :31-32
[8]   LENS OPACITIES CLASSIFICATION SYSTEM-II (LOCS-II) [J].
CHYLACK, LT ;
LESKE, MC ;
MCCARTHY, D ;
KHU, P ;
KASHIWAGI, T ;
SPERDUTO, R .
ARCHIVES OF OPHTHALMOLOGY, 1989, 107 (07) :991-997
[9]  
Fotiou DF, 2007, AGING CLIN EXP RES, V19, P364
[10]   Oxidative stress increases production of beta-amyloid precursor protein and beta-amyloid (A beta) in mammalian lenses, and A beta has toxic effects on lens epithelial cells [J].
Frederikse, PH ;
Garland, D ;
Zigler, JS ;
Piatigorsky, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (17) :10169-10174