Plasma apoM and S1P levels are inversely associated with mortality in African Americans with type 2 diabetes mellitus.

Mingxia Liu, Cecilia Frej, Carl D Langefeld, Jasmin Divers, Donald W Bowden, J Jeffrey Carr, Abraham K Gebre, Jianzhao Xu, Benny Larsson, Björn Dahlbäck, Barry I Freedman, John S Parks

Journal: Journal of lipid research 2020;60(8):1425-1431

PMID: 31133557

Abstract

apoM is a minor HDL apolipoprotein and carrier for sphingosine-1-phosphate (S1P). HDL apoM and S1P concentrations are inversely associated with atherosclerosis progression in rodents. We evaluated associations between plasma concentrations of S1P, plasma concentrations of apoM, and HDL apoM levels with prevalent subclinical atherosclerosis and mortality in the African American-Diabetes Heart Study participants (N = 545). Associations between plasma S1P, plasma apoM, and HDL apoM with subclinical atherosclerosis and mortality were assessed using multivariate parametric, nonparametric, and Cox proportional hazards models. At baseline, participants' median (25th percentile, 75th percentile) age was 55 (49, 62) years old and their coronary artery calcium (CAC) mass score was 26.5 (0.0, 346.5). Plasma S1P, plasma apoM, and HDL apoM were not associated with CAC. After 64 (57.6, 70.3) months of follow-up, 81 deaths were recorded. Higher concentrations of plasma S1P [odds ratio (OR) = 0.14, = 0.01] and plasma apoM (OR = 0.10, = 0.02), but not HDL apoM ( = 0.89), were associated with lower mortality after adjusting for age, sex, statin use, CAC, kidney function, and albuminuria. We conclude that plasma S1P and apoM concentrations are inversely and independently associated with mortality, but not CAC, in African Americans with type 2 diabetes after accounting for conventional risk factors.

Copyright © 2019 Liu et al.

Address: Section on Molecular Medicine, Department of Internal Medicine, Wake Forest School of Medicine, Winston-Salem, NC.; Department of Translational Medicine Skåne University Hospital, Lund University, Malmö, Sweden.; Division of Public Health Sciences, Department of Biostatistics and Data Science Wake Forest School of Medicine, Winston-Salem, NC.; Department of Biochemistry, Wake Forest School of Medicine, Winston-Salem, NC.; Department of Radiology Vanderbilt University Medical Center, Nashville, TN.; Department of Clinical Chemistry Skåne University Hospital, Lund, Sweden.; Section on Nephrology, Department of Internal Medicine, Wake Forest School of Medicine, Winston-Salem, NC [email protected] [email protected].; Section on Molecular Medicine, Department of Internal Medicine, Wake Forest School of Medicine, Winston-Salem, NC [email protected] [email protected].
Bant logo

© Copyright 2026, Nutrition Evidence

NED wishes to thank the following organisations for their support:

We use cookies to improve your experience and analyze site traffic with Google Analytics. By continuing to use our site, you agree to our use of cookies. Learn more.