Literature DB >> 21492858

Plasma non-cholesterol sterols in primary hypobetalipoproteinemia.

Davide Noto1, Angelo B Cefalù, Giacoma Barraco, Francesca Fayer, Mariangela Minà, Pin Yue, Patrizia Tarugi, Gustav Schonfeld, Maurizio R Averna.   

Abstract

Primary hypobetalipoproteinemia (pHBL) is characterized by plasma cholesterol levels <5th percentile of a population distribution. Plasma non-cholesterol sterols (NCS) are markers of cholesterol liver synthesis and intestinal absorption. Plasma NCS were measured in 111 pHBL subjects, 108 low cholesterol (LC) and 253 normal cholesterol (NC) controls to gain information on cholesterol metabolism in pHBL, and to assess whether NCS measurements may aid in distinguishing pHBL from LC controls. pHBL subjects compared with LC controls were characterized by increased cholesterol absorption (campesterol/TC) while the synthesis (lathosterol/TC) was not increased. The analysis of pHBL subjects divided by gene defect showed a high campesterol/TC ratio in familial HBL (FHBL) carriers of apolipoproteinB (ApoB) truncations longer than ApoB48 and in FHBL without known gene defect ("not linked"). One not linked kindred was characterized by an increase of the 7-dehydrocholesterol/latho ratio. In a discriminant analysis plasma NCS did not improve the power of TC levels to distinguish FHBL from LC controls. In conclusion, increased cholesterol absorption was found in FHBL subjects harbouring truncations of ApoB>ApoB48, and FHBL harbouring as yet unknown molecular defects. Not linked FHBL kindred are not homogeneous in terms of plasma NCS levels. NCS cannot replace genetic HBL analysis.
Copyright © 2011 Elsevier Ireland Ltd. All rights reserved.

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Year:  2011        PMID: 21492858     DOI: 10.1016/j.atherosclerosis.2010.10.050

Source DB:  PubMed          Journal:  Atherosclerosis        ISSN: 0021-9150            Impact factor:   5.162


  2 in total

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Journal:  Nutr Rev       Date:  2018-10-01       Impact factor: 7.110

2.  Mutations in the ANGPTL3 gene and familial combined hypolipidemia: a clinical and biochemical characterization.

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Journal:  J Clin Endocrinol Metab       Date:  2012-06-01       Impact factor: 5.958

  2 in total

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