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Top-down lipidomics of low density lipoprotein reveal altered lipid profiles in advanced chronic kidney disease.
Reis, Ana; Rudnitskaya, Alisa; Chariyavilaskul, Pajaree; Dhaun, Neeraj; Melville, Vanessa; Goddard, Jane; Webb, David J; Pitt, Andrew R; Spickett, Corinne M.
Afiliação
  • Reis A; School of Life and Health Sciences, Aston University, Birmingham, UK.
  • Rudnitskaya A; Centro de Estudios do Ambiente e do Mar (CESAM), Department of Chemistry, Universidade de Aveiro, Portugal.
  • Chariyavilaskul P; Clinical Pharmacology Unit, British Heart Foundation Centre of Research Excellence, Queen's Medical Research Institute, University of Edinburgh, Edinburgh, UK.
  • Dhaun N; Clinical Pharmacology Unit, British Heart Foundation Centre of Research Excellence, Queen's Medical Research Institute, University of Edinburgh, Edinburgh, UK Department of Renal Medicine, Royal Infirmary of Edinburgh, Edinburgh, UK.
  • Melville V; Clinical Pharmacology Unit, British Heart Foundation Centre of Research Excellence, Queen's Medical Research Institute, University of Edinburgh, Edinburgh, UK.
  • Goddard J; Department of Renal Medicine, Royal Infirmary of Edinburgh, Edinburgh, UK.
  • Webb DJ; Clinical Pharmacology Unit, British Heart Foundation Centre of Research Excellence, Queen's Medical Research Institute, University of Edinburgh, Edinburgh, UK.
  • Pitt AR; School of Life and Health Sciences, Aston University, Birmingham, UK.
  • Spickett CM; School of Life and Health Sciences, Aston University, Birmingham, UK.
J Lipid Res ; 56(2): 413-22, 2015 Feb.
Article em En | MEDLINE | ID: mdl-25424003
ABSTRACT
This study compared the molecular lipidomic profile of LDL in patients with nondiabetic advanced renal disease and no evidence of CVD to that of age-matched controls, with the hypothesis that it would reveal proatherogenic lipid alterations. LDL was isolated from 10 normocholesterolemic patients with stage 4/5 renal disease and 10 controls, and lipids were analyzed by accurate mass LC/MS. Top-down lipidomics analysis and manual examination of the data identified 352 lipid species, and automated comparative analysis demonstrated alterations in lipid profile in disease. The total lipid and cholesterol content was unchanged, but levels of triacylglycerides and N-acyltaurines were significantly increased, while phosphatidylcholines, plasmenyl ethanolamines, sulfatides, ceramides, and cholesterol sulfate were significantly decreased in chronic kidney disease (CKD) patients. Chemometric analysis of individual lipid species showed very good discrimination of control and disease sample despite the small cohorts and identified individual unsaturated phospholipids and triglycerides mainly responsible for the discrimination. These findings illustrate the point that although the clinical biochemistry parameters may not appear abnormal, there may be important underlying lipidomic changes that contribute to disease pathology. The lipidomic profile of CKD LDL offers potential for new biomarkers and novel insights into lipid metabolism and cardiovascular risk in this disease.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Insuficiência Renal Crônica / Lipídeos / Lipoproteínas LDL Tipo de estudo: Etiology_studies / Guideline / Prognostic_studies / Risk_factors_studies Limite: Adult / Humans / Male / Middle aged Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Insuficiência Renal Crônica / Lipídeos / Lipoproteínas LDL Tipo de estudo: Etiology_studies / Guideline / Prognostic_studies / Risk_factors_studies Limite: Adult / Humans / Male / Middle aged Idioma: En Ano de publicação: 2015 Tipo de documento: Article