APOE- ε 4 is not associated with pure-tone hearing thresholds, visual acuity or cognition, cross-sectionally or over 3 years of follow up in the Canadian Longitudinal Study on Aging

被引:0
作者
Mick, Paul [1 ]
Kabir, Rasel [2 ]
Karunatilake, Malshi [3 ]
Pichora-Fuller, M. Kathleen [4 ]
Young, Terry-Lyn [5 ]
Sosero, Yuri [6 ]
Gan-or, Ziv [6 ]
Wittich, Walter [7 ]
Phillips, Natalie A. [8 ]
机构
[1] Univ Saskatchewan, Coll Med, Dept Surg, Saskatoon, SK, Canada
[2] Saskatchewan Hlth Author, Saskatoon, SK, Canada
[3] Univ Alberta, Coll Hlth Sci, Dept Ophthalmol & Visual Sci, Edmonton, AB, Canada
[4] Univ Toronto, Fac Arts & Sci, Dept Psychol, Toronto, ON, Canada
[5] Mem Univ Newfoundland, Fac Med, St John, NF, Canada
[6] McGill Univ, Fac Med & Hlth Sci, Dept Human Genet, Montreal, PQ, Canada
[7] Univ Montreal, Ecole Optometrie, Montreal, PQ, Canada
[8] Concordia Univ, Fac Arts & Sci, Dept Psychol, Montreal, PQ, Canada
基金
加拿大健康研究院; 加拿大创新基金会;
关键词
Apolipoprotein E; APOE; Hearing; Vision; Cognition; CLSA; APOLIPOPROTEIN-E GENOTYPE; ALZHEIMERS-DISEASE; OLD-AGE; E GENE; HEALTHY; RISK; MEMORY; DECLINE; POLYMORPHISMS; PERFORMANCE;
D O I
10.1016/j.neurobiolaging.2024.01.006
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Introduction: Hearing loss and diminished visual acuity are associated with poorer cognition, but the underlying mechanisms are not understood. The apolipoprotein ( APOE ) e4 allelic variant may drive the associations. We tested whether APOE -e4 allele count (0, 1, or 2) was associated with declines in memory, executive function, pure -tone hearing threshold averages, and pinhole -corrected visual acuity among participants in the Canadian Longitudinal Study on Aging (CLSA). Methods: Multivariable linear mixed regression models were utilized to assess associations between APOE -e4 allele count and each of the outcome variables. For each main effects model, interactions between APOE -e4 and sex and age group (45-54-, 55-64-, 65-74-, and 75-85 years) respectively, were analyzed. Results: Significant associations were not observed in main effects models. Models including APOE- e4 * age (but not APOE- e4 * sex) interaction terms better fit the data compared to main effects models. In age group -stratified models, however, there were minimal differences in effect estimates according to allele count. Conclusion: APOE -e4 allele count does not appear to be a common cause of sensory -cognitive associations in this large cohort.
引用
收藏
页码:72 / 82
页数:11
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