The association between tau PET and retrospective cortical thinning in clinically normal elderly.
The association between tau PET and retrospective cortical thinning in clinically normal elderly.
复制标题
Tau PET与临床正常老年人的回顾性皮质稀疏之间的关联。
DOI:
10.1016/j.neuroimage.2017.05.049
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发表时间:
2017-08-15
期刊:
影响因子:
5.7
通讯作者:
Schultz AP
中科院分区:
文献类型:
--
作者:
LaPoint MR;Chhatwal JP;Sepulcre J;Johnson KA;Sperling RA;Schultz AP
Tau pathology has been associated with neuronal loss at autopsy, but the temporal evolution of tau pathology and atrophy remains unclear. Here, we investigate the association between cross-sectional AV-1451-PET as a marker of tau pathology and cortical thickness cross-sectionally. We also investigated retrospective rates of cortical thinning over the three years preceding the AV-1451 scan in a clinically normal cohort of 103 older adults from the Harvard Aging Brain Study. Tau measurements were Geometric Transfer Matrix partial volume corrected standardized uptake value ratios (SUVRs) with a cerebellar gray reference region. Thirty-four FreeSurfer-defined cortical regions of interest (ROIs) were used for both thickness and AV-1451 in each hemisphere, with seven additional volumetric ROIs. We examined “local” relationships between AV-1451 and cortical thickness in the same ROI, as well as inferior temporal AV-1451 and all thickness ROIs. All models included baseline age and sex, both interacting with time in retrospective longitudinal models, as covariates. Cross-sectional models controlled for the number of days between the two scans. Cross-sectional local comparisons revealed significant associations between elevated AV-1451 and thinner cortical ROIs predominantly in temporal regions, while analyses associating inferior temporal AV-1451 with all cortical ROIs showed a widespread pattern of significant relationships, which was strongest in temporal and parietal cortices. In our retrospective longitudinal analyses, we saw significant relationships in temporal and parietal regions. Significant local relationships were seen in right superior temporal, middle temporal, temporal pole, and fusiform, as well as the left cuneus and banks of the left superior temporal sulcus. Significant relationships between inferior temporal AV-1451 and faster thinning were observed in right temporal regions (middle temporal and fusiform) and bilateral parahippocampal cortices. We observed significant negative relationships between local and inferior temporal AV-1451 signal and both cross-sectional cortical thickness and rates of thinning in lateral and medial temporal regions. This is an important early step toward elucidating the relationship between tau pathology and retrospective longitudinal atrophy in aging and preclinical AD.
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影响因子:
3.7
作者:
Dickerson, Bradford C.;Bakkour, Akram;Salat, David H.;Feczko, Eric;Pacheco, Jenni;Greve, Douglas N.;Grodstein, Fran;Wright, Christopher I.;Blacker, Deborah;Rosas, H. Diana;Sperling, Reisa A.;Atri, Alireza;Growdon, John H.;Hyman, Bradley T.;Morris, John C.;Fischl, Bruce;Buckner, Randy L.
通讯作者:
Buckner, Randy L.
影响因子:
9.9
作者:
Henneman, W. J. P.;Vrenken, H.;van der Flier, W. M.
通讯作者:
van der Flier, W. M.
影响因子:
5.7
作者:
Fischl, Bruce
通讯作者:
Fischl, Bruce
影响因子:
9.9
作者:
ARRIAGADA, PV;GROWDON, JH;HYMAN, BT
通讯作者:
HYMAN, BT
影响因子:
4.2
作者:
Alcolea, Daniel;Vilaplana, Eduard;Fortea, Juan
通讯作者:
Fortea, Juan