Dose-Dependent Effects of Rosuvastatin on the Plasma Sphingolipidome and Phospholipidome in the Metabolic Syndrome

被引:62
作者
Ng, Theodore W. K. [1 ,3 ]
Ooi, Esther M. M. [1 ]
Watts, Gerald F. [1 ]
Chan, Dick C. [1 ]
Weir, Jacquelyn M. [3 ]
Meikle, Peter J. [3 ]
Barrett, P. Hugh R. [1 ,2 ]
机构
[1] Sch Med & Pharmacol, Metab Res Ctr, Perth, WA, Australia
[2] Fac Engn, Perth, WA, Australia
[3] Baker IDI Heart & Diabet Inst, Metabol Lab, Melbourne, Vic 3004, Australia
基金
英国医学研究理事会;
关键词
LOW-DENSITY-LIPOPROTEIN; SPHINGOMYELIN; CERAMIDES; LDL; CHOLESTEROL; HYDROLYZE; KINETICS; PROTEIN; RISK;
D O I
10.1210/jc.2014-1665
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context: Statins are effective cholesterol- lowering agents that reduce cardiovascular disease risk but also have pleiotropic effects that may extend to other lipid classes. Objective: The purpose of this article was to investigate, in a post hoc analysis, the dose-dependent effects of rosuvastatin on plasma sphingolipids and phospholipids in men with the metabolic syndrome. Methods: Subjects (n = 12) were studied in a randomized, double-blind, triple-crossover trial of a 5-week treatment period with placebo or rosuvastatin (10 or 40 mg/day) with 2-week washouts between treatments. Plasma sphingolipid profiling was determined by liquid chromatography electrospray ionization-tandem mass spectrometry. Results: Rosuvastatin at 10 mg/d (R10) and 40 mg/d (R40) significantly (all P <.001 unless stated otherwise) lowered plasma cholesterol (-34% and -42% [% change with R10 and with R40, respectively]), low-density lipoprotein cholesterol (-49% and -57%) and triglyceride (-24%, P =.03 and -42%) concentrations. Compared with placebo, R10 and R40 significantly decreased the plasma levels of total sphingolipids including those of ceramide (-33% and -37%), sphingomyelin (-27% and -31%), monohexosylceramide (-40% and -47%), dihexosylceramide (-31% and -34%), and trihexosylceramide (-29% and -31%), and GM(3) gangliosides (-29% and -26%), lysophosphatidylcholine (-32% and -37%), alkylphosphatidylcholine (-19% and -19%), phosphatidylcholine (-17% and -19%), alkenylphosphatidylcholine (plasmalogen) (-20% and -22%), alkylphosphatidylethanolamine (-20%, P =.008 and -24%, P =.02), alkenylphosphatidylethanolamine (plasmalogen) (-24%, P =.003 and -23%, P =.007), phosphatidylglycerol (-24%, P =.07, -31%, P =.046), and phosphatidylinositol (-34% and -40%). No significant changes were found with phosphatidylethanolamine and phosphatidylserine. Significant dose effects were found with the majority of the plasma sphingolipids, whereas only phosphatidylcholine, lysophosphatidylcholine, alkylphosphatidylcholine, alkenylphosphatidylcholine (plasmalogen), and phosphatidylinositol had significant dose effects. Similar changes were found with plasma sphingolipids when results were normalized to the total phosphatidylcholine concentration. Conclusions: Rosuvastatin dose-dependently lowers plasma sphingolipids and phospholipids, independent of low-density lipoprotein lowering, in men with the metabolic syndrome.
引用
收藏
页码:E2335 / E2340
页数:6
相关论文
共 30 条
  • [1] Arimoto I, 1998, J LIPID RES, V39, P143
  • [2] Bergheanu SC, 2008, CURR MED RES OPIN, V24, P2477, DOI [10.1185/03007990802321709, 10.1185/03007990802321709 ]
  • [3] Ceramides as modulators of cellular and whole-body metabolism
    Bikman, Benjamin T.
    Summers, Scott A.
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2011, 121 (11) : 4222 - 4230
  • [4] Sphingomyelin inhibits the lecithin-cholesterol acyltransferase reaction with reconstituted high density lipoproteins by decreasing enzyme binding
    Bolin, DJ
    Jonas, A
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (32) : 19152 - 19158
  • [5] Ceramides Contained in LDL Are Elevated in Type 2 Diabetes and Promote Inflammation and Skeletal Muscle Insulin Resistance
    Boon, James
    Hoy, Andrew J.
    Stark, Romana
    Brown, Russell D.
    Meex, Ruth C.
    Henstridge, Darren C.
    Schenk, Simon
    Meikle, Peter J.
    Horowitz, Jeffrey F.
    Kingwell, Bronwyn A.
    Bruce, Clinton R.
    Watt, Matthew J.
    [J]. DIABETES, 2013, 62 (02) : 401 - 410
  • [6] Executive summary of the Third Report of the National Cholesterol Education Program (NCEP) expert panel on detection, evaluation, and treatment of high blood cholesterol in adults (Adult Treatment Panel III)
    Cleeman, JI
    Grundy, SM
    Becker, D
    Clark, LT
    Cooper, RS
    Denke, MA
    Howard, WJ
    Hunninghake, DB
    Illingworth, DR
    Luepker, RV
    McBride, P
    McKenney, JM
    Pasternak, RC
    Stone, NJ
    Van Horn, L
    Brewer, HB
    Ernst, ND
    Gordon, D
    Levy, D
    Rifkind, B
    Rossouw, JE
    Savage, P
    Haffner, SM
    Orloff, DG
    Proschan, MA
    Schwartz, JS
    Sempos, CT
    Shero, ST
    Murray, EZ
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 285 (19): : 2486 - 2497
  • [7] Link between plasma ceramides, inflammation and insulin resistance: association with serum IL-6 concentration in patients with coronary heart disease
    de Mello, V. D. F.
    Lankinen, M.
    Schwab, U.
    Kolehmainen, M.
    Lehto, S.
    Seppanen-Laakso, T.
    Oresic, M.
    Pulkkinen, L.
    Uusitupa, M.
    Erkkila, A. T.
    [J]. DIABETOLOGIA, 2009, 52 (12) : 2612 - 2615
  • [8] Reduction of low-density lipoprotein cholesterol in patients with coronary heart disease and metabolic syndrome: analysis of the Treating to New Targets study
    Deedwania, Prakash
    Barter, Philip
    Carmena, Rafael
    Fruchart, Jean-Charles
    Grundy, Scott M.
    Haffner, Steven
    Kastelein, John J. P.
    LaRosa, John C.
    Schachner, Holly
    Shepherd, James
    Waters, David D.
    [J]. LANCET, 2006, 368 (9539) : 919 - 928
  • [9] Prevalence of the metabolic syndrome among US adults - Findings from the Third National Health and Nutrition Examination Survey
    Ford, ES
    Giles, WH
    Dietz, WH
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2002, 287 (03): : 356 - 359
  • [10] Plasma Ceramides Are Elevated in Obese Subjects With Type 2 Diabetes and Correlate With the Severity of Insulin Resistance
    Haus, Jacob M.
    Kashyap, Sangeeta R.
    Kasumov, Takhar
    Zhang, Renliang
    Kelly, Karen R.
    DeFronzo, Ralph. A.
    Kirwan, John P.
    [J]. DIABETES, 2009, 58 (02) : 337 - 343