Atherosclerosis
Volume 209, Issue 1 , Pages 39-41, March 2010

An alternative pathway of reverse cholesterol transport: The oxysterol 27-hydroxycholesterol

  • Oliver Weingärtner

      Affiliations

    • Klinik für Innere Medizin III, Kardiologie, Angiologie und Internistische Intensivmedizin, Universitätsklinikum des Saarlandes, D-66421 Homburg/Saar, Germany
    • Corresponding Author InformationCorresponding author at: Klinik für Innere Medizin III, Universitätsklinikum des Saarlandes, D-66421 Homburg/Saar, Germany. Tel.: +49 6841 1621333; fax: +49 6841 1621331.
  • ,
  • Ulrich Laufs

      Affiliations

    • Klinik für Innere Medizin III, Kardiologie, Angiologie und Internistische Intensivmedizin, Universitätsklinikum des Saarlandes, D-66421 Homburg/Saar, Germany
  • ,
  • Michael Böhm

      Affiliations

    • Klinik für Innere Medizin III, Kardiologie, Angiologie und Internistische Intensivmedizin, Universitätsklinikum des Saarlandes, D-66421 Homburg/Saar, Germany
  • ,
  • Dieter Lütjohann

      Affiliations

    • Institut für klinische Chemie und Pharmakologie, Universitätsklinikum Bonn, D-53105 Bonn, Germany

Received 4 May 2009; received in revised form 7 September 2009; accepted 9 September 2009. published online 05 October 2009.

Abstract 

Reverse cholesterol transport, although not well understood, is an important mechanism in the pathophysiology of atherosclerosis. Macrophages can eliminate some cholesterol from atherosclerotic lesions by an oxidative mechanism involving sterol 27-hydroxylase. Patients with inherited “cerebrotendinous xanthomatosis” lack sterol 27-hydroxylase (CYP27A1) and develop severe premature atherosclerosis despite normal serum cholesterol concentrations. Thus, it has been speculated that sterol 27-hydroxylase is an anti-atherosclerotic enzyme. Here, we report the case of a 25-year-old patient who presented to our emergency room with an acute non-ST elevation myocardial infarction due to severe coronary heart disease. Lipid analysis revealed dramatically increased 27-hydroxycholesterol and low high-density lipoprotein (HDL)-cholesterol levels. Previous reports suggest that 27-hydroxylase is upregulated to protect peripheral cells from severe cholesterol accumulation, especially in cases of ineffective reverse cholesterol transport due to low HDL-cholesterol levels. Our findings indicate that oxysterols could play an important and so far underestimated role in reverse cholesterol transport.

Keywords: Reverse cholesterol transport, Atherosclerosis, HDL-cholesterol, Oxysterols

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PII: S0021-9150(09)00728-X

doi:10.1016/j.atherosclerosis.2009.09.015

Atherosclerosis
Volume 209, Issue 1 , Pages 39-41, March 2010