Association of sickle cell trait with measures of cognitive function and dementia in African Americans
Year: 2019
Type: article
Abstract: The incidence and prevalence of cognitive decline and dementia are significantly higher among African Americans compared with non-Hispanic Whites. The aim of this study was to determine whether inheritance of the sickle cell trait (SCT) i.e. heterozygosity for the sickle cell mutation increases the risk of cognitive decline or dementia Among African Americans. We studied African American participants enrolled in the Atherosclerosis Risk in Communities study. SCT genotype at baseline and outcome data from cognitive assessments at visits 2, 4 and 5, and an MRI performed at visit 5 were analyzed for the association between SCT and risk of cognitive impairment and/or dementia. There was no significant difference in risk factors profile between participants with SCT (N = 176) and those without SCT (N = 2532). SCT was not independently associated with a higher prevalence of global or domain-specific cognitive impairment at baseline or with more rapid cognitive decline. Participants with SCT had slightly lower incidence of dementia (HR = 0.63 [0.38, 1.05]). On the other hand, SCT seems to interact with the apolipoprotein E ε4 risk allele resulting in poor performance on digit symbol substitution test at baseline (z-score = −0.08, Pinteraction = 0.05) and over time (z-score = −0.12, Pinteraction = 0.04); and with diabetes mellitus leading to a moderately increased risk of dementia (HR = 2.06 [0.89, 4.78], Pinteraction = 0.01). SCT was not an independent risk factor for prevalence or incidence of cognitive decline or dementia, although it may interact with and modify other putative risk factors for cognitive decline and dementia.
Source: eNeurologicalSci
Language: English
Subfield: Psychiatry and Mental health
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $1,400
Funders: U.S. Department of Health and Human Services, American Society of Hematology, National Institutes of Health, National Heart, Lung, and Blood Institute, National Human Genome Research Institute, National Institute of Environmental Health Sciences, National Center for Research Resources, National Center for Advancing Translational Sciences
Awards: G1114307781, G1360749331, G1712314342, G1788514665, G1823732541, G2195207551, GWA for Gene-Environment Interaction Effects Influencing CHD, G3973572274, G400646947, G4149753725, G4290615481, G4516765154, ARIC Neurocognitive Study (ARIC-NCS) Renewal UNC 4 of 5, G4747441672, G4790942633, G506570908, G5352314984, G536099884, G5364873420, Genome-Wide Association for Loci Influencing CHD and Other Heart, Lung and Blood, G5622977475, G5770678025, G583528397, G5928944960, G6060132884, Duke - UNC Clinical Hematology and Transfusion Research Career Development Progra, G6739173425, ARIC Neurocognitive Study (ARIC-NCS) Renewal 2 of 5, ARIC Neurocognitive Study (ARIC-NCS), G6837735701, G6978868085, G7155745631, G7535686976, G7861490744, G8738262636, G8937114048, From GWAS loci to blood pressure genes, variants & mechanisms - Renewal, G931818222
OpenAlex ID: W2963535823
