4.7 Article

Cortical microstructural correlates of astrocytosis in autosomal-dominant Alzheimer disease

期刊

NEUROLOGY
卷 94, 期 19, 页码 E2026-E2036

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1212/WNL.0000000000009405

关键词

-

资金

  1. Swedish Research Council [2017-02965, 2017-06086, K2014-61x-05817]
  2. Swedish Foundation for Strategic Research (SSF) [RB13-0192]
  3. Knut and Alice Wallenberg Foundation
  4. Stockholm County Council-Karolinska Institutet regional agreement on medical training and clinical research (ALF grant)
  5. GE Healthcare
  6. Swedish Brain Foundation
  7. Alzheimer Foundation in Sweden
  8. Dementia Association
  9. Swedish Brain Power
  10. EU FP7 large-scale integrating project INMiND (uni-muenster.de/INMiND)
  11. Foundation for Old Servants
  12. Karolinska Institutet's Foundation for Aging Research
  13. Gun and Bertil Stohne's Foundation
  14. Ahlen Foundation
  15. Ake Wiberg Foundation
  16. Departament de Salut de laGeneralitat de Catalunya, Pla estrategic de recerca i innovacio en salut (PERIS) 2016-2020 [SLT006/17/95]
  17. Loo and Hans Osterman's Foundation

向作者/读者索取更多资源

ObjectiveTo study the macrostructural and microstructural MRI correlates of brain astrocytosis, measured with C-11-deuterium-L-deprenyl (C-11-DED)-PET, in familial autosomal-dominant Alzheimer disease (ADAD).MethodsThe total sample (n = 31) comprised ADAD mutation carriers (n = 10 presymptomatic, 39.2 10.6 years old; n = 3 symptomatic, 55.5 2.0 years old) and noncarriers (n = 18, 44.0 +/- 13.7 years old) belonging to families with mutations in either the presenilin-1 or amyloid precursor protein genes. All participants underwent structural and diffusion MRI and neuropsychological assessment, and 20 participants (6 presymptomatic and 3 symptomatic mutation carriers and 11 noncarriers) also underwent C-11-DED-PET.ResultsVertex-wise interaction analyses revealed a differential relationship between carriers and noncarriers in the association between C-11-DED binding and estimated years to onset (EYO) and between cortical mean diffusivity (MD) and EYO. These differences were due to higher C-11-DED binding in presymptomatic carriers, with lower binding in symptomatic carriers compared to noncarriers, and to lower cortical MD in presymptomatic carriers, with higher MD in symptomatic carriers compared to noncarriers. Using a vertex-wise local correlation approach, C-11-DED binding was negatively correlated with cortical MD and positively correlated with cortical thickness.ConclusionsOur proof-of-concept study is the first to show that microstructural and macrostructural changes can reflect underlying neuroinflammatory mechanisms in early stages of Alzheimer disease (AD). The findings support a role for neuroinflammation in AD pathogenesis, with potential implications for the correct interpretation of neuroimaging biomarkers as surrogate endpoints in clinical trials.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据