Back to Search Start Over

Serum triglycerides in Alzheimer disease

Authors :
Dinesh Kumar Barupal
Rebecca Baillie
Andrew J. Saykin
Leslie M. Shaw
Tanner Y. Jacobson
Matthias Arnold
P. Murali Doraiswamy
Shannon L. Risacher
Kwangsik Nho
Rima Kaddurah-Daouk
Oliver Fiehn
Megan M. Bernath
Sudeepa Bhattacharyya
Michael W. Weiner
John Q. Trojanowski
Source :
Neurology
Publication Year :
2020
Publisher :
Ovid Technologies (Wolters Kluwer Health), 2020.

Abstract

ObjectiveTo investigate the association of triglyceride (TG) principal component scores with Alzheimer disease (AD) and the amyloid, tau, neurodegeneration, and cerebrovascular disease (A/T/N/V) biomarkers for AD.MethodsSerum levels of 84 TG species were measured with untargeted lipid profiling of 689 participants from the Alzheimer's Disease Neuroimaging Initiative cohort, including 190 cognitively normal older adults (CN), 339 with mild cognitive impairment (MCI), and 160 with AD. Principal component analysis with factor rotation was used for dimension reduction of TG species. Differences in principal components between diagnostic groups and associations between principal components and AD biomarkers (including CSF, MRI and [18F]fluorodeoxyglucose-PET) were assessed with a generalized linear model approach. In both cases, the Bonferroni method of adjustment was used to correct for multiple comparisons.ResultsThe 84 TGs yielded 9 principal components, 2 of which, consisting of long-chain, polyunsaturated fatty acid–containing TGs (PUTGs), were significantly associated with MCI and AD. Lower levels of PUTGs were observed in MCI and AD compared to CN. PUTG principal component scores were also significantly associated with hippocampal volume and entorhinal cortical thickness. In participants carrying the APOE ε4 allele, these principal components were significantly associated with CSF β-amyloid1–42 values and entorhinal cortical thickness.ConclusionThis study shows that PUTG component scores were significantly associated with diagnostic group and AD biomarkers, a finding that was more pronounced in APOE ε4 carriers. Replication in independent larger studies and longitudinal follow-up are warranted.

Details

ISSN :
1526632X and 00283878
Volume :
94
Database :
OpenAIRE
Journal :
Neurology
Accession number :
edsair.doi.dedup.....d6b0a3e0b4a2485cea7ba4ce9a603f2c