4.6 Article

Heart fatty acid binding protein and Aβ-associated Alzheimer's neurodegeneration

期刊

MOLECULAR NEURODEGENERATION
卷 8, 期 -, 页码 -

出版社

BIOMED CENTRAL LTD
DOI: 10.1186/1750-1326-8-39

关键词

Alzheimer's disease; Fatty acids; Lipids; Amyloid; Tau; Brain atrophy

资金

  1. National Institutes of Health [R01AG031224, K01AG029218, K02 NS067427, T32 EB005970]
  2. Research Council of Norway [183782/V50]
  3. South East Norway Health Authority [2010-074]
  4. Alzheimer's Disease Neuroimaging Initiative (ADNI) (National Institutes of Health) [U01 AG024904]
  5. National Institute on Aging
  6. National Institute of Biomedical Imaging and Bioengineering
  7. Alzheimer's Association
  8. Alzheimer's Drug Discovery Foundation
  9. BioClinica, Inc.
  10. Biogen Idec Inc.
  11. Bristol-Myers Squibb Company
  12. Eisai Inc.
  13. Elan Pharmaceuticals, Inc.
  14. Eli Lilly and Company
  15. F. Hoffmann-La Roche Ltd
  16. Genentech, Inc.
  17. GE Healthcare
  18. Innogenetics, N.V.
  19. IXICO Ltd.
  20. Janssen Alzheimer Immunotherapy Research & Development, LLC.
  21. Johnson & Johnson Pharmaceutical Research & Development LLC.
  22. Medpace, Inc.
  23. Merck Co., Inc.
  24. Meso Scale Diagnostics, LLC.
  25. NeuroRx Research
  26. Novartis Pharmaceuticals Corporation
  27. Pfizer Inc.
  28. Piramal Imaging
  29. Servier
  30. Synarc Inc.
  31. Takeda Pharmaceutical Company
  32. Canadian Institutes of Health Research
  33. Northern California Institute for Research and Education
  34. NIH [P30 AG010129, K01 AG030514]

向作者/读者索取更多资源

Background: Epidemiological and molecular findings suggest a relationship between Alzheimer's disease (AD) and dyslipidemia, although the nature of this association is not well understood. Results: Using linear mixed effects models, we investigated the relationship between CSF levels of heart fatty acid binding protein (HFABP), a lipid binding protein involved with fatty acid metabolism and lipid transport, amyloid beta (A beta), phospho-tau, and longitudinal MRI-based measures of brain atrophy among 295 non-demented and demented older individuals. Across all participants, we found a significant association of CSF HFABP with longitudinal atrophy of the entorhinal cortex and other AD-vulnerable neuroanatomic regions. However, we found that the relationship between CSF HABP and brain atrophy was significant only among those with low CSF A beta(1-42) and occurred irrespective of phospho-tau(181p) status. Conclusions: Our findings indicate that A beta associated volume loss occurs in the presence of elevated HFABP irrespective of phospho-tau. This implicates a potentially important role for fatty acid binding proteins in Alzheimer's disease neurodegeneration.

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