Interaction between KLOTHO-VS Heterozygosity and APOE ε4 Allele Predicts Rate of Cognitive Decline in Late-Onset Alzheimer's Disease

被引:2
作者
Chen, Xi Richard [1 ]
Shao, Yongzhao J. [2 ,3 ]
Sadowski, Martin [4 ,5 ,6 ]
机构
[1] Univ Rochester, Sch Med & Dent, Rochester, NY 14642 USA
[2] NYU Grossman Sch Med, Dept Populat Hlth, New York, NY 10016 USA
[3] NYU Grossman Sch Med, Dept Environm Med, New York, NY 10016 USA
[4] NYU Grossman Sch Med, Dept Neurol, New York, NY 10016 USA
[5] NYU Grossman Sch Med, Dept Psychiat, New York, NY 10016 USA
[6] NYU Grossman Sch Med, Dept Biochem & Mol Pharmacol, New York, NY 10016 USA
关键词
Alzheimer's disease; KLOTHO; APOE; cognitive decline; aging; BRAIN TAU DEPOSITION; SEX; ASSOCIATION; RISK; IMPAIRMENT; DEMENTIA; DEFICITS; RESERVE; MODEL; MICE;
D O I
10.3390/genes14040917
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
KLOTHO-VS heterozygosity (KL-VShet+) promotes longevity and protects against cognitive decline in aging. To determine whether KL-VShet+ mitigates Alzheimer's disease (AD) progression, we used longitudinal linear-mixed models to compare the rate of change in multiple cognitive measures in AD patients stratified by APOE epsilon 4 carrier status. We aggregated data on 665 participants (208 KL-VShet-/epsilon 4-, 307 KL-VShet-/epsilon 4+, 66 KL-VShet+/epsilon 4-, and 84 KL-VShet+/epsilon 4+) from two prospective cohorts, the National Alzheimer's Coordinating Center and the Alzheimer's Disease Neuroimaging Initiative. All participants were initially diagnosed with mild cognitive impairment, later developed AD dementia during the study, and had at least three subsequent visits. KL-VShet+ conferred slower cognitive decline in epsilon 4 non-carriers (+0.287 MMSE points/year, p = 0.001; -0.104 CDR-SB points/year, p = 0.026; -0.042 ADCOMS points/year, p < 0.001) but not in epsilon 4 carriers who generally had faster rates of decline than non-carriers. Stratified analyses showed that the protective effect of KL-VShet+ was particularly prominent in male participants, those who were older than the median baseline age of 76 years, or those who had an education level of at least 16 years. For the first time, our study provides evidence that KL-VShet+ status has a protective effect on AD progression and interacts with the epsilon 4 allele.
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页数:17
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