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Dreyfuss, J.M.* ; Djordjilović, V.* ; Pan, H.* ; Bussberg, V.* ; MacDonald, A.M.* ; Narain, N.R.* ; Kiebish, M.A.* ; Blüher, M. ; Tseng, Y.H.* ; Lynes, M.D.*

ScreenDMT reveals DiHOMEs are replicably inversely associated with BMI and stimulate adipocyte calcium influx.

Comm. Biol. 7:996 (2024)
Postprint DOI PMC
Open Access Gold
Creative Commons Lizenzvertrag
Activating brown adipose tissue (BAT) improves systemic metabolism, making it a promising target for metabolic syndrome. BAT is activated by 12,13-dihydroxy-9Z-octadecenoic acid (12,13-diHOME), which we previously identified to be inversely associated with BMI and which directly improves metabolism in multiple tissues. Here we profile plasma lipidomics from 83 people and test which lipids' association with BMI replicates in a concordant direction using our novel tool ScreenDMT, whose power and validity we demonstrate via mathematical proofs and simulations. We find that the linoleic acid diols 12,13-diHOME and 9,10-diHOME are both replicably inversely associated with BMI and mechanistically activate calcium influx in mouse brown and white adipocytes in vitro, which implicates this signaling pathway and 9,10-diHOME as candidate therapeutic targets. ScreenDMT can be applied to test directional mediation, directional replication, and qualitative interactions, such as identifying biomarkers whose association is shared (replication) or opposite (qualitative interaction) across diverse populations.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Conjugated Linoleic-acid; Lipokine 12,13-dihome; Brown Fat; Mediation
Sprache englisch
Veröffentlichungsjahr 2024
HGF-Berichtsjahr 2024
ISSN (print) / ISBN 2399-3642
e-ISSN 2399-3642
Zeitschrift Communications Biology
Quellenangaben Band: 7, Heft: 1, Seiten: , Artikelnummer: 996 Supplement: ,
Verlag Springer
Verlagsort London
Begutachtungsstatus Peer reviewed
Institut(e) Helmholtz Institute for Metabolism, Obesity and Vascular Research (HI-MAG)
POF Topic(s) 30201 - Metabolic Health
Forschungsfeld(er) Helmholtz Diabetes Center
PSP-Element(e) G-506501-001
Förderungen NIH fellowships
US Army Medical Research
U.S. National Institutes of Health (NIH)
United States Department of Defense | U.S. Army (United States Army)
DOI 10.1038/s42003-024-06646-z
WOS ID 001291756700002
Scopus ID 85201359239
PubMed ID 39143411
Erfassungsdatum 2024-10-01
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