Sickle cell trait and risk of cognitive impairment in African-Americans: The REGARDS cohort

dc.contributor.authorCahill, Christina R.
dc.contributor.authorLeach, Justin M.
dc.contributor.authorMcClure, Leslie A.
dc.contributor.authorIrvin, Marguerite Ryan
dc.contributor.authorZakai, Neil A.
dc.contributor.authorNaik, Rakhi
dc.contributor.authorUnverzagt, Frederick
dc.contributor.authorWadley, Virginia G.
dc.contributor.authorHyacinth, Hyacinth I.
dc.contributor.authorManly, Jennifer
dc.contributor.authorJudd, Suzanne E.
dc.contributor.authorWinkler, Cheryl
dc.contributor.authorCushman, Mary
dc.contributor.departmentPsychiatry, School of Medicineen_US
dc.date.accessioned2019-09-03T18:00:47Z
dc.date.available2019-09-03T18:00:47Z
dc.date.issued2019-05-24
dc.description.abstractBackground: Sickle cell anemia may be associated with cognitive dysfunction, and some complications of sickle cell anemia might affect those with sickle cell trait (SCT), so we hypothesized that SCT is a risk factor for cognitive impairment. Methods: The Reasons for Geographic and Racial Differences in Stroke (REGARDS) study enrolled a national cohort of 30,239 white and black Americans from 2003 to 7, who are followed every 6 months. Baseline and annual global cognitive function testing used the Six-Item Screener (SIS), a validated instrument (scores range 0-6; ≤ 4 indicates cognitive impairment). Participants with baseline cognitive impairment and whites were excluded. Logistic regression was used to calculate the association of SCT with incident cognitive impairment, adjusted for risk factors. Linear mixed models assessed multivariable-adjusted change in test scores on a biennially administered 3-test battery measuring learning, memory, and semantic and phonemic fluency. Findings: Among 7743 participants followed for a median of 7·1 years, 85 of 583 participants with SCT (14·6%) developed incident cognitive impairment compared to 902 of 7160 (12·6%) without SCT. In univariate analysis, the odds ratio (OR) of incident cognitive impairment was 1·18 (95% CI: 0·93, 1·51) for those with SCT vs. those without. Adjustment did not impact the OR. There was no difference in change on 3-test battery scores by SCT status (all p > 0·11). Interpretation: In this prospective cohort study of black Americans, SCT was not associated with incident cognitive impairment or decline in test scores of learning, memory and executive function. Funding: National Institutes of Health, American Society of Hematology.en_US
dc.identifier.citationCahill, C. R., Leach, J. M., McClure, L. A., Irvin, M. R., Zakai, N. A., Naik, R., … Cushman, M. (2019). Sickle cell trait and risk of cognitive impairment in African-Americans: The REGARDS cohort. EClinicalMedicine, 11, 27–33. doi:10.1016/j.eclinm.2019.05.003en_US
dc.identifier.urihttps://hdl.handle.net/1805/20750
dc.language.isoen_USen_US
dc.publisherElsevieren_US
dc.relation.isversionof10.1016/j.eclinm.2019.05.003en_US
dc.relation.journalEClinicalMedicineen_US
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
dc.sourcePMCen_US
dc.subjectSickle cell traiten_US
dc.subjectCognitive dysfunctionen_US
dc.subjectCognitionen_US
dc.subjectProspective studiesen_US
dc.subjectRisk factorsen_US
dc.subjectEpidemiologyen_US
dc.titleSickle cell trait and risk of cognitive impairment in African-Americans: The REGARDS cohorten_US
dc.typeArticleen_US
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