Abstract P179: Association Between Serum Metabolites and Carotid Atherosclerosis Among Japanese Men

Background: Complex metabolic pathways may exist for atherosclerosis. We examined metabolomic signatures that reflect mechanistic pathways associated with carotid atherosclerosis in apparently healthy men. Methods: A cross-sectional study was conducted in 675 Japanese men (46-83 years) from the SESS...

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Published inCirculation Vol. 149; no. Suppl_1; p. AP179
Main Authors Ganbaatar, Gantsetseg, Kadota, Aya, Okami, Yukiko, Whiley, Luke, Chan, Queenie, Barinas-Mitchell, Emma, Torii, Sayuki, Kondo, Keiko, Morino, Katsutaro, Hisamatsu, Takashi, Fujiyoshi, Akira, Sekikawa, Akira M, Ueshima, Hirotsugu, Miura, Katsuyuki
Format Journal Article
LanguageEnglish
Japanese
Published Hagerstown, MD Ovid Technologies (Wolters Kluwer Health) 19.03.2024
Lippincott Williams & Wilkins
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Online AccessGet full text
ISSN0009-7322
1524-4539
DOI10.1161/circ.149.suppl_1.p179

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Summary:Background: Complex metabolic pathways may exist for atherosclerosis. We examined metabolomic signatures that reflect mechanistic pathways associated with carotid atherosclerosis in apparently healthy men. Methods: A cross-sectional study was conducted in 675 Japanese men (46-83 years) from the SESSA Study (2010-2014). A total of 468 serum metabolites were quantified by liquid chromatography mass spectrometry. The mean intima-media thickness (IMT) and total number of plaques from carotid arteries were measured using B-mode ultrasound. All metabolites were standardized prior to the analysis. We used partial least square regression and variable importance projection (VIP) method to extract the principal metabolites most associated with the mean IMT and total number of plaques. We used a multivariable linear model for the log-mean IMT and a multivariable Poisson model for the total number of plaques to assess the association between individual extracted serum metabolites and carotid measures. Each metabolite multivariable model adjusted for age, body mass index, smoking and drinking status, medications for hypertension, diabetes and dyslipidemia, and systolic blood pressure, high- and low-density lipoprotein cholesterols and hemoglobin A1c. We used false discovery rate adjusted p-values to control for multiple testing. Results: The average mean IMT and total number of plaques were 0.80 mm (SD: 0.16) and 2.06 (range: 0-14), respectively. There were 191 metabolites with a VIP value of one or higher for mean IMT. None of these metabolites was significantly associated with the log-mean IMT. On the other hand, there were 209 metabolites with a VIP value of one or higher for the total number of plaques. Among them, SulfoHexCer(d18:2/24:0(OH)) and SulfoHexCer(d18:2/16:0(OH)) had an inverse association with the total number of plaques (Figure 1). Conclusion: We identified distinct metabolites associated with the total number of plaques. The results suggest an important role of sphingolipids in carotid plaque formation.
Bibliography:Author Disclosures: For author disclosure information, please visit the AHA Epidemiology and Prevention-Lifestyle and Cardiometabolic Health 2024 Scientific Sessions Online Program Planner and search for the abstract title.
ISSN:0009-7322
1524-4539
DOI:10.1161/circ.149.suppl_1.p179