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

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 o...

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Veröffentlicht in:The journal of clinical endocrinology and metabolism 2014-11, Vol.99 (11), p.E2335-E2340
Hauptverfasser: Ng, Theodore W. K, Ooi, Esther M. M, Watts, Gerald F, Chan, Dick C, Weir, Jacquelyn M, Meikle, Peter J, Barrett, P. Hugh R
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container_end_page E2340
container_issue 11
container_start_page E2335
container_title The journal of clinical endocrinology and metabolism
container_volume 99
creator Ng, Theodore W. K
Ooi, Esther M. M
Watts, Gerald F
Chan, Dick C
Weir, Jacquelyn M
Meikle, Peter J
Barrett, P. Hugh R
description 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 GM3 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.
doi_str_mv 10.1210/jc.2014-1665
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K ; Ooi, Esther M. M ; Watts, Gerald F ; Chan, Dick C ; Weir, Jacquelyn M ; Meikle, Peter J ; Barrett, P. Hugh R</creator><creatorcontrib>Ng, Theodore W. K ; Ooi, Esther M. M ; Watts, Gerald F ; Chan, Dick C ; Weir, Jacquelyn M ; Meikle, Peter J ; Barrett, P. Hugh R</creatorcontrib><description>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 &lt; .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 GM3 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.</description><identifier>ISSN: 0021-972X</identifier><identifier>EISSN: 1945-7197</identifier><identifier>DOI: 10.1210/jc.2014-1665</identifier><identifier>PMID: 25140396</identifier><language>eng</language><publisher>United States: Endocrine Society</publisher><subject>Cardiovascular diseases ; Cholesterol ; Cross-Over Studies ; Dose-Response Relationship, Drug ; Double-Blind Method ; Fluorobenzenes - administration &amp; dosage ; Fluorobenzenes - pharmacology ; Gangliosides ; Humans ; Hydroxymethylglutaryl-CoA Reductase Inhibitors - administration &amp; dosage ; Hydroxymethylglutaryl-CoA Reductase Inhibitors - pharmacokinetics ; Lecithin ; Liquid chromatography ; Lysophosphatidylcholine ; Male ; Mass spectroscopy ; Metabolic syndrome ; Metabolic Syndrome - blood ; Middle Aged ; Phosphatidylcholine ; Phosphatidylethanolamine ; Phosphatidylglycerol ; Phosphatidylinositol ; Phosphatidylserine ; Phospholipids ; Phospholipids - blood ; Placebos ; Plasma ; Plasma levels ; Pyrimidines - administration &amp; dosage ; Pyrimidines - pharmacology ; Rosuvastatin Calcium ; Sphingolipids ; Sphingolipids - blood ; Sphingomyelin ; Statins ; Sulfonamides - administration &amp; dosage ; Sulfonamides - pharmacology</subject><ispartof>The journal of clinical endocrinology and metabolism, 2014-11, Vol.99 (11), p.E2335-E2340</ispartof><rights>Copyright © 2014 by the Endocrine Society</rights><rights>Copyright © 2014 by the Endocrine Society 2014</rights><rights>Copyright © 2014 by The Endocrine Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5441-e0bc89e532b0250720d6f19ae1b0fbf2e7e32a0d09cee08c5e44c49b78e91b403</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25140396$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ng, Theodore W. K</creatorcontrib><creatorcontrib>Ooi, Esther M. M</creatorcontrib><creatorcontrib>Watts, Gerald F</creatorcontrib><creatorcontrib>Chan, Dick C</creatorcontrib><creatorcontrib>Weir, Jacquelyn M</creatorcontrib><creatorcontrib>Meikle, Peter J</creatorcontrib><creatorcontrib>Barrett, P. Hugh R</creatorcontrib><title>Dose-Dependent Effects of Rosuvastatin on the Plasma Sphingolipidome and Phospholipidome in the Metabolic Syndrome</title><title>The journal of clinical endocrinology and metabolism</title><addtitle>J Clin Endocrinol Metab</addtitle><description>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 &lt; .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 GM3 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. 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Hugh R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dose-Dependent Effects of Rosuvastatin on the Plasma Sphingolipidome and Phospholipidome in the Metabolic Syndrome</atitle><jtitle>The journal of clinical endocrinology and metabolism</jtitle><addtitle>J Clin Endocrinol Metab</addtitle><date>2014-11</date><risdate>2014</risdate><volume>99</volume><issue>11</issue><spage>E2335</spage><epage>E2340</epage><pages>E2335-E2340</pages><issn>0021-972X</issn><eissn>1945-7197</eissn><abstract>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 &lt; .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 GM3 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.</abstract><cop>United States</cop><pub>Endocrine Society</pub><pmid>25140396</pmid><doi>10.1210/jc.2014-1665</doi><oa>free_for_read</oa></addata></record>
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subjects Cardiovascular diseases
Cholesterol
Cross-Over Studies
Dose-Response Relationship, Drug
Double-Blind Method
Fluorobenzenes - administration & dosage
Fluorobenzenes - pharmacology
Gangliosides
Humans
Hydroxymethylglutaryl-CoA Reductase Inhibitors - administration & dosage
Hydroxymethylglutaryl-CoA Reductase Inhibitors - pharmacokinetics
Lecithin
Liquid chromatography
Lysophosphatidylcholine
Male
Mass spectroscopy
Metabolic syndrome
Metabolic Syndrome - blood
Middle Aged
Phosphatidylcholine
Phosphatidylethanolamine
Phosphatidylglycerol
Phosphatidylinositol
Phosphatidylserine
Phospholipids
Phospholipids - blood
Placebos
Plasma
Plasma levels
Pyrimidines - administration & dosage
Pyrimidines - pharmacology
Rosuvastatin Calcium
Sphingolipids
Sphingolipids - blood
Sphingomyelin
Statins
Sulfonamides - administration & dosage
Sulfonamides - pharmacology
title Dose-Dependent Effects of Rosuvastatin on the Plasma Sphingolipidome and Phospholipidome in the Metabolic Syndrome
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