Evidence map›Paper›PMID 41940830›Full record

ArticleJournal of Alzheimer's disease : JAD2026

Plasma lipid trajectories improve prediction of future Alzheimer's disease.

Haotian Zou, Tingting Wang, Kevin Huynh, Peter J Meikle, Rima Kaddurah-Daouk, Sheng Luo, Alzheimer's Disease Neuroimaging Initiative, Alzheimer's Disease Metabolomics Consortium

Abstract read
In one paragraph

Article in Journal of Alzheimer's disease : JAD, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Haotian ZouDepartment of Biostatistics & Bioinformatics, Duke University, Durham, NC, USA.ORCID 0000-0002-3595-8716
Tingting WangBaker Heart and Diabetes Institute, Melbourne, Victoria, Australia.
Kevin HuynhBaker Heart and Diabetes Institute, Melbourne, Victoria, Australia.
Peter J MeikleBaker Heart and Diabetes Institute, Melbourne, Victoria, Australia.
Rima Kaddurah-DaoukDepartment of Psychiatry and Behavioral Sciences, Duke Institute for Brain Sciences, Durham, NC, USA.
Sheng LuoDepartment of Biostatistics & Bioinformatics, Duke University, Durham, NC, USA.
Alzheimer's Disease Neuroimaging Initiative
Alzheimer's Disease Metabolomics Consortium

Funding

Alzheimer's Disease Neuroimaging Initiative - SupplementU01AG024904 · NIA · NORTHERN CALIFORNIA INSTITUTE RES &EDUC · PI WEINER, MICHAEL W · 2004 to 2015
$121.0M
Project 4 - Mechanistic studies on the role of the gut microbiome in models for Alzheimer's diseaseU19AG063744 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI Rima F Kaddurah-Daouk · 2019 to 2026
$54.1M
Research Education Component CoreP30AG072958 · NIA · DUKE UNIVERSITY · PI GWENN A GARDEN, Heather E. Whitson · 2021 to 2026
$24.1M
Metabolomic Signatures for Disease Sub-classification and Target Prioritization in AMP-ADU01AG061359 · NIA · DUKE UNIVERSITY · PI KADDURAH-DAOUK, RIMA F, KASTENMULLER, GABI · 2018 to 2022
$10.0M
Metabolic Signatures Underlying Vascular Risk Factors for Alzheimer-type DementiasRF1AG051550 · NIA · DUKE UNIVERSITY · PI KADDURAH-DAOUK, RIMA F, KLING, MITCHEL ALLAN · 2015 to 2016
$6.3M
Metabolic Networks and Pathways Predictive of Sex Differences in AD Risk and Responsiveness to TreatmentRF1AG059093 · NIA · DUKE UNIVERSITY · PI BRINTON, ROBERTA EILEEN, CHANG, RUI · 2018 to 2018
$5.9M
Metabolic Networks and Pathways in Alzheimer's DiseaseR01AG046171 · NIA · DUKE UNIVERSITY · PI KADDURAH-DAOUK, RIMA F · 2014 to 2017
$4.4M
Gut Liver Brain Biochemical Axis in Alzheimer's DiseaseRF1AG058942 · NIA · DUKE UNIVERSITY · PI KADDURAH-DAOUK, RIMA F, VAN DUIJN, CORNELIA MARJA · 2018 to 2018
$3.4M
Metabolic age to define influences of the lipidome on brain aging in Alzheimer's diseaseR01AG081322 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI Matthias Arnold, Rima F Kaddurah-Daouk · 2023 to 2026
$2.6M
Integrative modeling and dynamic prediction of Alzheimer's diseaseR01AG064803 · NIA · DUKE UNIVERSITY · PI LUO, SHENG · 2020 to 2024
$2.3M
Integrative modeling and dynamic prediction of Alzheimer's diseaseR56AG064803 · NIA · DUKE UNIVERSITY · PI LUO, SHENG · 2019 to 2019
$483k
NIA NIH HHS P30 AG072958NIA NIH HHS R01 AG046171NIA NIH HHS R01 AG064803NIA NIH HHS R01 AG081322NIA NIH HHS R56 AG064803NIA NIH HHS RF1 AG051550NIA NIH HHS RF1 AG058942NIA NIH HHS RF1 AG059093NIA NIH HHS U01 AG024904NIA NIH HHS U01 AG061359NIA NIH HHS U19 AG063744
6 · The paper itself

Abstract

BackgroundEarly identification of individuals at elevated risk for Alzheimer's disease (AD) is critical for prevention. Blood-based biomarkers offer scalable alternatives to cerebrospinal fluid and imaging, but the prognostic value of longitudinal plasma lipid trajectories remains unclear.ObjectiveTo evaluate whether multi-year plasma lipid trajectories improve prediction of AD conversion beyond demographic, clinical, genetic, and neuropsychological measures.MethodsWe studied 1150 cognitively normal or mildly impaired Alzheimer's Disease Neuroimaging Initiative participants; 329 progressed to AD dementia over a mean follow-up of 2.3 years. Plasma lipidomics quantified 749 lipid species by high-resolution LC-MS. Trajectories were summarized using functional principal component analysis and related to time to conversion using covariate-adjusted Cox proportional hazards models. Predictive performance was assessed by concordance index and likelihood-ratio tests.ResultsCross-sectional lipid profiles modestly improved prediction beyond demographic and clinical covariates, and longitudinal lipid trajectories yielded small additional gains. Ether-linked triglycerides showed the strongest longitudinal associations with conversion, with TG(O-50:1) [NL-18:1] exhibiting the most robust signal. Neuropsychological measures provided substantially stronger discrimination, and lipid trajectories added limited value once cognitive information was included. Nevertheless, longitudinal lipid changes contributed consistent improvements in models without neuropsychological predictors, supporting their role as complementary blood-based markers in settings where standardized cognitive assessments are unavailable or impractical.ConclusionsPlasma lipid trajectories capture biologically relevant metabolic change associated with AD progression and provide complementary predictive information. Longitudinal lipidomic profiling may support early risk stratification and cohort enrichment when cognitive assessments are unavailable.

Indexed as

Alzheimer DiseaseLipidsAgedAged, 80 and overBiomarkersDisease ProgressionFemaleHumansLipidomicsLongitudinal StudiesMaleNeuropsychological TestsPredictive Value of TestsBiomarkersLipidsAlzheimer’s diseaseAlzheimer’s Disease Neuroimaging Initiativecognitive declinefunctional principal component analysislipid metabolismsurvival analysis

Identifiers

PMID41940830
PMCPMC13110075

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.