Genetic Variation Underlying Traumatic Brain injury (TBI) and Late Onset Alzheimer's Disease (LOAD)
Technical Report,15 Sep 2016,14 Sep 2017
Trustees of Columbia University New York United States
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Age-related changes in memory function are not uniform even in the absence of dementia and contributing factors are unclear. Characterization of non-disease associated cognitive changes is crucial to gain a more complete understanding of brain aging. Episodic memory was investigated in 13,979 ethnically diverse elderly ages 72 to 85 years with two to 15 years of follow-up, and with known dementia status, age, education and APOE genotypes at baseline. Adjusted trajectories of episodic memory performance over time were estimated using Latent Class Mixed Models. We also calculated the age-specific annual incidence rates of dementia in the non-demented elderly n10,659. Two major episodic memory trajectories were estimated within each of the study groups 1 Stables - consisting of individuals exhibiting a constant or improved memory function overtime and 2 Decliners - consisting of individuals with a decline in memory performance overtime. Compared with the individuals in the Stable trajectory, Decliners were more likely women, older, less educated, from non-White ancestry population and APOE-4 carriers. The highest annual incident rates of dementia were observed in the oldest age group 85 years old, among those of Caribbean-Hispanics ancestry and among Decliners who exhibited rates of incident dementia five times higher than those with Stable trajectories rates 15 per 100 person per year versus 3 per 100 person-per year. Episodic memory can be preserved over time among elderly regardless of ethnic group. Age, gender, education and APOE genotype influence the maintenance of episodic memory over time. Declining memory over time is one of the strongest predictors of incident dementia.
- Medicine and Medical Research
- Genetic Engineering and Molecular Biology