| Literature DB >> 31133557 |
Mingxia Liu1, Cecilia Frej2, Carl D Langefeld3, Jasmin Divers3, Donald W Bowden4, J Jeffrey Carr5, Abraham K Gebre1, Jianzhao Xu4, Benny Larsson6, Björn Dahlbäck2, Barry I Freedman7, John S Parks8,4.
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, P = 0.01] and plasma apoM (OR = 0.10, P = 0.02), but not HDL apoM (P = 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.Entities:
Keywords: apolipoprotein M; apolipoproteins; atherosclerosis; clinical studies; ethnicity; high density lipoprotein; sphingosine-1-phosphate
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Year: 2019 PMID: 31133557 PMCID: PMC6672033 DOI: 10.1194/jlr.P089409
Source DB: PubMed Journal: J Lipid Res ISSN: 0022-2275 Impact factor: 5.922