Relationship of plasma apolipoprotein M with proprotein convertase subtilisin-kexin type 9 levels in non-diabetic subjects

Summary, in English

Purpose: Apolipoprotein M (apoM) retards atherosclerosis development in murine models, and may be regulated by pathways involved in LDL metabolism. Proprotein convertase subtilisin-kexin type 9 (PCSK9) plays a key role in LDL receptor processing. We determined the extent to which plasma apoM is related to PCSK9 levels in subjects with varying degrees of obesity. Methods: We sought correlations between plasma apoM and PCSK9, measured using recently developed ELISAs, in 79 non-diabetic subjects. Results: ApoM and PCSK9 levels were both correlated positively with total cholesterol, non-HDL cholesterol, LDL cholesterol and apoB (P < 0.05 to P < 0.001). ApoM correlated positively with PCSK9 in lean individuals (n = 37, r = 0.337, P = 0.041), but not in overweight subjects (n = 32, r = 0.125, P = 0.50) and in obese subjects (n = 10, r = -0.055, P = 0.88). Conclusions: The PCSK9 pathway may contribute to plasma apoM regulation in humans. The influence of PCSK9 on circulating apoM appears to be modified by adiposity. (C) 2010 Elsevier Ireland Ltd. All rights reserved.

• Författare: Paul J. W. H. Kappelle; Gilles Lambert; Björn Dahlbäck; Lars Bo Nielsen; Robin P. F. Dullaart
• Avdelning/ar: Klinisk kemi, Malmö
• Publiceringsår: 2011
• Språk: Engelska
• Sidor: 492-494
• Publikation/Tidskrift/Serie: Atherosclerosis
• Volym: 214
• Issue: 2
• Länkar: http://dx.doi.org/10.1016/j.atherosclerosis.2010.10.041
• Dokumenttyp: Artikel i tidskrift
• Förlag: Elsevier
• Ämne: Cardiac and Cardiovascular Systems
• Nyckelord: Apolipoprotein M; Apolipoprotein B; LDL cholesterol; Obesity; PCSK9
• Status: Published
• Forskningsgrupp: Clinical Chemistry, Malmö
• ISBN/ISSN/Övrigt: ISSN: 1879-1484