TDP-43-associated atrophy in brains with and without frontotemporal lobar degeneration

被引:10
作者
Buciuc, Marina [1 ]
Martin, Peter R. [2 ]
Tosakulwong, Nirubol [2 ]
Murray, Melissa E. [3 ]
Petrucelli, Leonard [3 ]
Senjem, Matthew L. [4 ]
Spychalla, Anthony J. [4 ]
Knopman, David S. [1 ]
Boeve, Bradley F. [1 ]
Petersen, Ronald C. [1 ]
Parisi, Joseph E. [5 ]
Reichard, R. Ross [5 ]
Dickson, Dennis W. [3 ]
Jack, Clifford R., Jr. [4 ]
Whitwell, Jennifer L. [4 ]
Josephs, Keith A. [1 ]
机构
[1] Mayo Clin, Dept Neurol, 200 1st St NW, Rochester, MN 55905 USA
[2] Mayo Clin, Dept Quantitat Hlth Sci, 200 1st St NW, Rochester, MN 55905 USA
[3] Mayo Clin, Dept Neurosci, 4500 San Pablo Rd S, Jacksonville, FL 32224 USA
[4] Mayo Clin, Dept Radiol, 200 1st St NW, Rochester, MN 55905 USA
[5] Mayo Clin, Dept Lab Med & Pathol, 200 1st St NW, Rochester, MN 55905 USA
基金
美国国家卫生研究院;
关键词
Alzheimer's disease; TDP-43; MRI; LATE; Old age FTLD; ALZHEIMERS-DISEASE; NEUROPATHOLOGIC ASSESSMENT; TDP-43; IMMUNOREACTIVITY; HIPPOCAMPAL SCLEROSIS; HEXANUCLEOTIDE REPEAT; NATIONAL INSTITUTE; DEFINED SUBTYPES; DEMENTIA; PATHOLOGY; TAU;
D O I
10.1016/j.nicl.2022.102954
中图分类号
R445 [影像诊断学];
学科分类号
100207 ;
摘要
Transactive response DNA-binding protein of similar to 43 kDa (TDP-43), a primary pathologic substrate in tau-negative frontotemporal lobar degeneration (FTLD), is also often found in the brains of elderly individuals without FTLD and is a key player in the process of neurodegeneration in brains with and without FTLD. It is unknown how rates and trajectories of TDP-43-associated brain atrophy compare between these two groups. Additionally, non-FTLD TDP-43 inclusions are not homogeneous and can be divided into two morphologic types: type- a and neurofibrillary tangle-associated type-beta. Therefore, we explored whether neurodegeneration also varies due to the morphologic type. In this longitudinal retrospective study of 293 patients with 843 MRI scans spanning over similar to 10 years, we used a Bayesian hierarchical linear model to quantify similarities and differences between the non-FTLD TDP-43 (type-alpha/type-beta) and FTLD-TDP (n = 68) in both regional volume at various timepoints before death and annualized rate of atrophy. Since Alzheimer's disease (AD) is a frequent co-pathology in non-FTLD TDP-43, we further divided types alpha/beta based on presence/absence of intermediate-high likelihood AD: AD-TDP type-beta (n = 90), AD-TDP type- a (n = 104), and Pure-TDP (n = 31, all type-alpha). FTLD-TDP was associated with faster atrophy rates in the inferior temporal lobe and temporal pole compared to all non-FTLD TDP-43 groups. The atrophy rate in the frontal lobe was modulated by age with younger FTLD-TDP having the fastest rates. Older FTLD-TDP showed a limbic predominant pattern of neurodegeneration. AD-TDP type- a showed faster rates of hippocampal atrophy and smaller volumes of amygdala, temporal pole, and inferior temporal lobe compared to AD-TDP type-beta. Pure-TDP was associated with slowest rates and less atrophy in all brain regions. The results suggest that there are differences and similarities in longitudinal brain volume loss between FTLD-TDP and non-FTLD TDP-43. Within FTLD-TDP age plays a role in which brain regions are the most affected. Additionally, brain atrophy regional rates also vary by non-FTLD TDP-43 type.
引用
收藏
页数:12
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