Correlations between APOE4 allele and regional amyloid and tau burdens in cognitively normal older individuals.
Correlations between APOE4 allele and regional amyloid and tau burdens in cognitively normal older individuals.
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DOI:
10.1038/s41598-022-18325-2
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发表时间:
2022-08-22
影响因子:
4.6
通讯作者:
Sepulcre, Jorge
中科院分区:
文献类型:
--
作者:
Hong, Yun Jeong;Kim, Chan-Mi;Lee, Jae Hong;Sepulcre, Jorge
The correlations between apolipoprotein epsilon 4 (APOE4) status and regional amyloid, tau, and cortical thickness in cognitively normal elderly are not fully understood. Our cross-sectional study aimed to compare regional amyloid/tau burden, and cortical thickness according to APOE4 carrier status and assess correlations between APOE4 and Alzheimer’s disease (AD)-related biomarker burdens. We analyzed 185 cognitively normal participants from the Alzheimer’s Disease Neuroimaging Initiative (ADNI) cohort. Participants aged 55–90 with normal cognitive function were divided into amyloid ß-positive (Aß+) APOE4 carriers (group 1, n = 27), Aß+ APOE4 non-carriers (group 2, n = 29), and Aß− normal controls (group 0, n = 129). We compared amyloid depositions, tau depositions, and cortical thickness among the three groups and assessed correlations between APOE4 existence and imaging biomarkers adjusted for age and sex. The participants in group 2 were older than those in the other groups. The regional amyloid/tau standardized uptake value ratios (SUVRs) did not differ between groups 1 and 2, but the amyloid/tau SUVRs in most regions were numerically higher after adjusting for age difference. APOE4 allele had robust correlations with increased amyloid burden in the fronto-temporo-parietal cortical areas after adjustment for age and sex, but it had weaker and mixed correlations with the regional tau burden and did not have significant correlation with cortical thickness. We identified that the presence of APOE4 allele might be more highly associated with amyloid deposition than with other AD-related biomarkers such as tau or cortical thickness in cognitively normal elderly.
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影响因子:
29
作者:
Therriault, Joseph;Benedet, Andrea L.;Rosa-Neto, Pedro
通讯作者:
Rosa-Neto, Pedro
影响因子:
9.9
作者:
Cummings, JL
通讯作者:
Cummings, JL
DOI:
10.1016/j.jalz.2019.07.011
发表时间:
2019-12
期刊:
Alzheimer's & dementia : the journal of the Alzheimer's Association
影响因子:
--
作者:
Williams OA;An Y;Armstrong NM;Shafer AT;Helphrey J;Kitner-Triolo M;Ferrucci L;Resnick SM
通讯作者:
Resnick SM
影响因子:
120.7
作者:
Jansen, Willemijn J.;Ossenkoppele, Rik;Knol, Dirk L.;Tijms, Betty M.;Scheltens, Philip;Verhey, Frans R. J.;Visser, Pieter Jelle
通讯作者:
Visser, Pieter Jelle
影响因子:
64.8
作者:
Shi Y;Yamada K;Liddelow SA;Smith ST;Zhao L;Luo W;Tsai RM;Spina S;Grinberg LT;Rojas JC;Gallardo G;Wang K;Roh J;Robinson G;Finn MB;Jiang H;Sullivan PM;Baufeld C;Wood MW;Sutphen C;McCue L;Xiong C;Del-Aguila JL;Morris JC;Cruchaga C;Alzheimer’s Disease Neuroimaging Initiative;Fagan AM;Miller BL;Boxer AL;Seeley WW;Butovsky O;Barres BA;Paul SM;Holtzman DM
通讯作者:
Holtzman DM