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. 2019;72(1):45-53.
doi: 10.3233/JAD-190538.

Race, APOEɛ4, and Long-Term Cognitive Trajectories in a Biracial Population Sample

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Race, APOEɛ4, and Long-Term Cognitive Trajectories in a Biracial Population Sample

Kumar B Rajan et al. J Alzheimers Dis. 2019.

Abstract

Background: The association of the APOEɛ4 allele with incident Alzheimer's dementia is higher among European Americans (EAs) than African Americans (AAs), but similar for the rate of cognitive decline.

Objective: To examine the racial differences in the association of the APOEɛ4 allele with incident Alzheimer's dementia and cognitive decline.

Methods: Using a population-based sample of 5,117 older adults (66% AAs and 63% females), we identified cognitive trajectory groups from a latent class mixed model and examined the association of the APOEɛ4 allele with these groups.

Results: The frequency of the APOEɛ4 allele was higher among AAs than EAs (37% versus 26%). Four cognitive trajectories were identified: slow, mild, moderate, and rapid. Overall, AAs had a lower baseline global cognition than EAs, and a higher proportion had rapid (7% versus 5%) and moderate (20% versus 15%) decline, but similar mild (44% versus 46%), and lesser slow (29% versus 34%) decline compared to EAs. Additionally, 25% of AAs (13% of EAs) with mild and 5% (<1% of EAs) with slow decline were diagnosed with incident Alzheimer's dementia. The APOEɛ4 allele was associated with higher odds of rapid and moderate decline compared to slow decline among AAs and EAs, but not with mild decline.

Conclusions: AAs had lower cognitive levels and were more likely to meet the cognitive threshold for Alzheimer's dementia among mild and slow decliners, explaining the attenuated association of the ɛ4 allele with incident Alzheimer's dementia among AAs.

Keywords: Alzheimer’s disease; Apolipoproteins E; cognitive aging; race relations.

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Figures

Fig. 1.
Fig. 1.
Predicted 10-year course of cognitive decline in four severity categories among African Americans and European Americans. The solid line shows rapid decliners, dashed line shows moderate decliners, dotted line shows mild decliners, and dotted and dashed line shows slow decliners. The bold dashed line is average level of global cognitive function among those developing incident Alzheimer’s dementia.

References

    1. Dixon RA, de Frias CM (2004) The Victoria Longitudinal Study: From characterizing cognitive aging to illustrating changes in memory compensation. Aging Neuropsychol Cogn 11, 346–376.
    1. Berg S (1996) Aging, behavior, and terminal decline In: Birren JE, Schaie KW, eds. Handbook of the psychology of aging. Academic Press, New York.
    1. Daviglus ML, Bell CC, Berrettini W, Bowen PE, Connolly ES Jr, Cox NJ, Dunbar-Jacob JM, Granieri EC, Hunt G, McGarry K, Patel D, Potosky AL, Sanders-Bush E, Silberberg D, Trevisan M (2010) National Institutes of Health State-of-the-Science Conference Statement: Preventing Alzheimer’s Disease and Cognitive Decline. NIH Consens State Sci Statements 27, 1–30. - PubMed
    1. Colby SL, Ortman JM (2015) Projections of the size and composition of the US Population: 2014 to 2060, 25–1143.
    1. Rajan KB, Weuve J, Barnes LL, Wilson RS, Evans DA (2019) Prevalence and incidence of clinically diagnosed Alzheimer’s disease dementia from 1994 to 2012 in a population study. Alzheimers Dement 15, 1–7. - PMC - PubMed

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