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Circulating lipids are related to longitudinal changes of ATN biomarkers for Alzheimer's disease.

Journal articles  - Journal Article
Kim, JP; Nho, K; Wang, T; Huynh, K; Arnold, M; Risacher, SL; Bice, PJ; Han, X; Kristal, BS; Blach, C; Baillie, R; Kastenmüller, G; Meikle, PJ ...
Published in: Mol Psychiatry
September 2026

Investigating the relationship of circulating lipidome profiles with cross-sectional and longitudinal changes of central Alzheimer's disease (AD) biomarkers, including amyloid/tau/neurodegeneration (A/T/N), can provide a holistic view between the lipidome and AD pathophysiology. In this study, we quantified a total of 749 plasma lipid species at baseline using liquid chromatography-mass spectrometry and performed cross-sectional and longitudinal association analysis of plasma lipidome profiles with longitudinal A/T/N biomarkers for AD in the Alzheimer's Disease Neuroimaging Initiative cohort (N = 1395). We identified several lipid species, classes, and network modules of correlated lipids that were significantly associated with cross-sectional and longitudinal changes of A/T/N biomarkers. Notably, we identified lysoalkylphosphatidylcholine (LPC(O)) as associated with cross-sectional "A/N" biomarkers at the lipid species, class, and module levels. Also, Phosphatidylethanolamine (PE) ethers were associated with A/T/N biomarkers in the species level and with "N" biomarkers in the class and module levels. GM3 ganglioside showed association with cross-sectional and longitudinal changes of "N" biomarkers at the species and class levels. Furthermore, 20 lipid species, out of all 57 species identified as associated with "less severe" AD biomarkers, contained docosahexaenoic acid (DHA), indicating that the previously reported beneficial effects of DHA on AD were significant at the central biomarker level. In conclusion, our approach linking peripheral metabolic changes with brain metabolic, structural, and functional states strengthens evidence from previous studies that were performed using only clinical AD diagnosis. Importantly, our study also enabled identification of novel lipids that play potential roles in progression of AD pathophysiology, suggesting dysregulation of lipid metabolic pathways as precursors to AD development and progression.

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Published In

Mol Psychiatry

DOI

EISSN

1476-5578

Publication Date

September 2026

Volume

31

Issue

9

Start / End Page

5395 / 5408

Location

England

Related Subject Headings

  • tau Proteins
  • Psychiatry
  • Phosphatidylethanolamines
  • Male
  • Longitudinal Studies
  • Lipids
  • Lipidomics
  • Lipid Metabolism
  • Humans
  • Female
 

Citation

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ICMJE
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Kim, J. P., Nho, K., Wang, T., Huynh, K., Arnold, M., Risacher, S. L., … Alzheimer’s Disease Metabolomics Consortium (ADMC). (2026). Circulating lipids are related to longitudinal changes of ATN biomarkers for Alzheimer's disease. Mol Psychiatry, 31(9), 5395–5408. https://doi.org/10.1038/s41380-026-03626-z
Kim, Jun Pyo, Kwangsik Nho, Tingting Wang, Kevin Huynh, Matthias Arnold, Shannon L. Risacher, Paula J. Bice, et al. “Circulating lipids are related to longitudinal changes of ATN biomarkers for Alzheimer's disease.Mol Psychiatry 31, no. 9 (September 2026): 5395–5408. https://doi.org/10.1038/s41380-026-03626-z.
Kim JP, Nho K, Wang T, Huynh K, Arnold M, Risacher SL, et al. Circulating lipids are related to longitudinal changes of ATN biomarkers for Alzheimer's disease. Mol Psychiatry. 2026 Sep;31(9):5395–408.
Kim, Jun Pyo, et al. “Circulating lipids are related to longitudinal changes of ATN biomarkers for Alzheimer's disease.Mol Psychiatry, vol. 31, no. 9, Sept. 2026, pp. 5395–408. Pubmed, doi:10.1038/s41380-026-03626-z.
Kim JP, Nho K, Wang T, Huynh K, Arnold M, Risacher SL, Bice PJ, Han X, Kristal BS, Blach C, Baillie R, Kastenmüller G, Meikle PJ, Saykin AJ, Kaddurah-Daouk R, Alzheimer’s Disease Neuroimaging Initiative, Alzheimer’s Disease Metabolomics Consortium (ADMC). Circulating lipids are related to longitudinal changes of ATN biomarkers for Alzheimer's disease. Mol Psychiatry. 2026 Sep;31(9):5395–5408.

Published In

Mol Psychiatry

DOI

EISSN

1476-5578

Publication Date

September 2026

Volume

31

Issue

9

Start / End Page

5395 / 5408

Location

England

Related Subject Headings

  • tau Proteins
  • Psychiatry
  • Phosphatidylethanolamines
  • Male
  • Longitudinal Studies
  • Lipids
  • Lipidomics
  • Lipid Metabolism
  • Humans
  • Female