TY - JOUR
T1 - The ARIC-PET amyloid imaging study
T2 - Brain amyloid differences by age, race, sex, and APOE
AU - Gottesman, Rebecca F.
AU - Schneider, Andrea L.C.
AU - Zhou, Yun
AU - Chen, Xueqi
AU - Green, Edward
AU - Gupta, Naresh
AU - Knopman, David S.
AU - Mintz, Akiva
AU - Rahmim, Arman
AU - Sharrett, A. Richey
AU - Wagenknecht, Lynne E.
AU - Wong, Dean F.
AU - Mosley, Thomas H.
N1 - Publisher Copyright:
© 2016 American Academy of Neurology.
PY - 2016/8/2
Y1 - 2016/8/2
N2 - Objective: To evaluate differences in amyloid deposition in a community-based cohort without dementia by age, sex, race, education, and APOE ϵ4 allele status. Methods: Recruited from the longitudinal Atherosclerosis Risk in Communities study, 329 participants without dementia, ages 67-88 years, were imaged using florbetapir PET at 3 US community sites (Washington County, Maryland; Forsyth County, North Carolina; and Jackson, Mississippi). Standardized uptake value ratios (SUVRs) were calculated; global cortical SUVR >1.2 was evaluated as the primary outcome. Age, race, sex, education level, and number of APOE ϵ4 alleles were evaluated in multivariable models including vascular risk factors, brain white matter hyperintensity and total intracranial volume, and cognitive status. Results: A total of 141 of the participants (43%) were black. In multivariable models, odds of elevated SUVR was increased in participants with increasing age (odds ratio [OR] 1.63, 95% confidence interval [CI] 1.01-2.65 per 10 years of age) and black race (OR 2.08, 95% CI 1.23-3.51) but did not differ by educational level. Each ϵ4 allele was associated with increased odds of elevated SUVR (OR 2.65, 95% CI 1.61-4.39). Conclusions: In this community-based cohort without dementia, florbetapir uptake is associated with older age and APOE genotype. Black race was associated with higher SUVR, after adjusting for demographics, vascular risk factors, cognitive status, white matter hyperintensity volume, and APOE genotype, with effect sizes nearing those seen for APOE ϵ4. Replication of these findings is needed in other cohorts, and reasons for and consequences of these observed differences by race warrant further study.
AB - Objective: To evaluate differences in amyloid deposition in a community-based cohort without dementia by age, sex, race, education, and APOE ϵ4 allele status. Methods: Recruited from the longitudinal Atherosclerosis Risk in Communities study, 329 participants without dementia, ages 67-88 years, were imaged using florbetapir PET at 3 US community sites (Washington County, Maryland; Forsyth County, North Carolina; and Jackson, Mississippi). Standardized uptake value ratios (SUVRs) were calculated; global cortical SUVR >1.2 was evaluated as the primary outcome. Age, race, sex, education level, and number of APOE ϵ4 alleles were evaluated in multivariable models including vascular risk factors, brain white matter hyperintensity and total intracranial volume, and cognitive status. Results: A total of 141 of the participants (43%) were black. In multivariable models, odds of elevated SUVR was increased in participants with increasing age (odds ratio [OR] 1.63, 95% confidence interval [CI] 1.01-2.65 per 10 years of age) and black race (OR 2.08, 95% CI 1.23-3.51) but did not differ by educational level. Each ϵ4 allele was associated with increased odds of elevated SUVR (OR 2.65, 95% CI 1.61-4.39). Conclusions: In this community-based cohort without dementia, florbetapir uptake is associated with older age and APOE genotype. Black race was associated with higher SUVR, after adjusting for demographics, vascular risk factors, cognitive status, white matter hyperintensity volume, and APOE genotype, with effect sizes nearing those seen for APOE ϵ4. Replication of these findings is needed in other cohorts, and reasons for and consequences of these observed differences by race warrant further study.
UR - http://www.scopus.com/inward/record.url?scp=84982994428&partnerID=8YFLogxK
U2 - 10.1212/WNL.0000000000002914
DO - 10.1212/WNL.0000000000002914
M3 - Article
C2 - 27371485
AN - SCOPUS:84982994428
SN - 0028-3878
VL - 87
SP - 473
EP - 480
JO - Neurology
JF - Neurology
IS - 5
ER -