Medial temporal lobe atrophy patterns in early-versus late-onset amnestic Alzheimer's disease

被引:0
作者
Wuestefeld, Anika [1 ]
Pichet Binette, Alexa [1 ]
van Westen, Danielle [2 ,3 ]
Strandberg, Olof [1 ]
Stomrud, Erik [1 ,4 ]
Mattsson-Carlgren, Niklas [1 ,5 ,6 ]
Janelidze, Shorena [1 ]
Smith, Ruben [1 ,4 ]
Palmqvist, Sebastian [1 ,4 ]
Baumeister, Hannah [7 ]
Berron, David [1 ,7 ]
Yushkevich, Paul A. [8 ]
Hansson, Oskar [1 ,4 ]
Spotorno, Nicola [1 ]
Wisse, Laura E. M. [2 ]
机构
[1] Lund Univ, Dept Clin Sci Malmo, Clin Memory Res Unit, Klin Gatan 28,Room C1103b, SE-22242 Lund, Sweden
[2] Lund Univ, Dept Diagnost Radiol, Clin Sci, Klin Gatan 13B, SE-22242 Lund, Sweden
[3] Skane Univ Hosp, Image & Funct, S-22242 Lund, Sweden
[4] Skane Univ Hosp, Memory Clin, S-20502 Malmo, Sweden
[5] Skane Univ Hosp, Dept Neurol, S-22242 Lund, Sweden
[6] Lund Univ, Wallenberg Ctr Mol Med, S-22184 Lund, Sweden
[7] German Ctr Neurodegenerat Dis DZNE, D-39120 Magdeburg, Germany
[8] Univ Penn, Dept Radiol, Penn Image Comp & Sci Lab PICSL, Philadelphia, PA 19104 USA
关键词
Tau-PET imaging; Amyloid-beta; MRI; Medial temporal lobe subregions; Aging; In vivo; Amnestic AD; Early-onset; Late-onset; Amygdala segmentation protocol; TPD-43; MEMORY; TAU; SEGMENTATION; BIOMARKERS; PET;
D O I
10.1186/s13195-024-01571-z
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BackgroundThe medial temporal lobe (MTL) is hypothesized to be relatively spared in early-onset Alzheimer's disease (EOAD). Yet, detailed examination of MTL subfields and drivers of atrophy in amnestic EOAD is lacking.MethodsBioFINDER-2 participants with memory impairment, abnormal amyloid-beta and tau-PET were included. Forty-one amnestic EOAD individuals <= 65 years and, as comparison, late-onset AD (aLOAD, >= 70 years, n = 154) and amyloid-beta-negative cognitively unimpaired controls were included. MTL subregions and biomarkers of (co-)pathologies were measured.ResultsAD groups showed smaller MTL subregions compared to controls. Atrophy patterns were similar across AD groups: aLOAD showed thinner entorhinal cortices than aEOAD; aEOAD showed thinner parietal regions than aLOAD. aEOAD showed lower white matter hyperintensities than aLOAD. No differences in MTL tau-PET or transactive response DNA binding protein 43-proxy positivity were found.ConclusionsWe found evidence for MTL atrophy in amnestic EOAD and overall similar levels to aLOAD of MTL tau pathology and co-pathologies.
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页数:12
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