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

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Authors: Jun Pyo Kim, Kwangsik T. Nho, Tingting Wang, Kevin Huynh, Matthias Arnold, Shannon L. Risacher, Paula J. Bice, Xianlin Han, Bruce S. Kristal, Colette Blach, Rebecca Baillie, Gabi Kastenmüller
+88 more Peter J. Meikle, Andrew J. Saykin, Rima F Kaddurah-Daouk, for the Alzheimer’s Disease Neuroimaging Initiative, Michael Weiner, Paul Aisen, Ronald Petersen, Clifford R. Jack, William Jagust, Susan Landau, Monica Rivera-Mindt, Ozioma Okonkwo, Leslie M. Shaw, Edward B. Lee, Arthur W. Toga, Laurel Beckett, Danielle Harvey, Robert C. Green, Andrew J. Saykin, Kwangsik Nho, Richard J. Perrin, Duygu Tosun, Nick C. Fox, Paul Thompson, Charles DeCarli, Robert A. Koeppe, Gil Rabinovici, John Morris, Nigel J. Cairns, Tatiana M. Foroud, Shannon L. Risacher, Rima Kaddurah-Daouk, Neil Buckholtz, John K. Hsiao, Laurie Ryan, Susan Molchan, Alexandra Kueider‐Paisley, P Murali Doraiswamy, Colette Blach, Arthur Moseley, Siamak Mahmoudiandehkhordi, Kathleen Welsh-Balmer, Brenda Plassman, Andrew J. Saykin, Shannon L. Risacher, Gabi Kastenmüller, Matthias Arnold, Rebecca Baillie, Rob Knight, Pieter Dorrestein, JB Brewer, E D Mayer, Jennifer Labus, Pierre Baldi, Arpana Gupta, Oliver Fiehn, DINESH BARUPAL, Peter Meikle, Sarkis Mazmanian, Dan Rader, Leslie Shaw, Cornelia van Duijn, Najaf Amin, Alejo Nevado-Holgado, David Bennett, R R Krishnan, Ali Keshavarzian, Robin Vogt, Arfan Ikram, Thomas Hankemeier, Ines Thiele, Cory Funk, Priyanka Baloni, Wei Jia, David Wishart, Roberta Brinton, Lindsay Farrer, Rhoda Au, Wendy Qiu, Peter Würtz, Therese Koal, Anna Greenwood, Jan Krumsiek, Karsten Suhre, J P Newman, Ivan Hernandez, Tatiana Foroud, F K Sacks
Cited by: 1
References: 67

Abstract

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. G M3 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.

Fields of Study & Subjects

Fatty Acid Research and Health Metabolomics and Mass Spectrometry Studies Alzheimer's disease research and treatments

Publication details

Journal / source
Molecular Psychiatry
Publisher
Springer Science and Business Media LLC
Volume
31
Issue
9
Pages
5395–5408
Publication date
16 June 2026
Language
EN