Literature DB >> 28127122

Relation between proprotein convertase subtilisin/kexin type 9 and directly measured low-density lipoprotein cholesterol.

Kristen M Tecson1, Katherine S Panettiere-Kennedy1, Jane I Won1, Puja Garg1, Oluseun Olugbode1, Peter A McCullough1.   

Abstract

Proprotein convertase subtilisin/kexin type 9 (PCSK9) is a regulator of low-density lipoprotein cholesterol (LDL-C) receptor (LDL-R) recycling and, thus, is a determinant of plasma LDL-C concentration. We sought to determine the relation between serum concentrations of PCSK9 and LDL-C while considering a variety of influential variables, including treatment for dyslipidemia. Using a prospective lipid clinic registry, we evaluated clinical variables, the results of advanced lipid testing, and PCSK9 concentrations determined by immunoassay. We evaluated the relationship between directly measured LDL-C and PCSK9 in serum by performing a simple linear regression. Correlation analyses were performed to examine the relationships of PCSK9 to other clinical and laboratory values and to test for differences in median PCSK9 across patient groups. Factors identified as potential predictors were considered jointly in a multivariate model. For the 26 patients in the analyses, a relationship was not detected between LDL-C and PCSK9 (r = 0.009, P = 0.97); however, PCSK9 was correlated with C-peptide (r = 0.48; P = 0.01) and heart rate (r = 0.52; P = 0.006). Median PCSK9 values differed between statin users (284.0 ng/mL [quartile 1 = 241.0, quartile 3 = 468.0]) and nonusers (219.0 ng/mL [quartile 1 = 151.0, quartile 3 = 228.0]; P = 0.02). More investigation is needed to evaluate the relationship between LDL and PCSK9, as well as the determinants of PCSK9, a major factor regulating cholesterol concentrations.

Entities:  

Year:  2017        PMID: 28127122      PMCID: PMC5242103          DOI: 10.1080/08998280.2017.11929514

Source DB:  PubMed          Journal:  Proc (Bayl Univ Med Cent)        ISSN: 0899-8280


  14 in total

Review 1.  The PCSK9 decade.

Authors:  Gilles Lambert; Barbara Sjouke; Benjamin Choque; John J P Kastelein; G Kees Hovingh
Journal:  J Lipid Res       Date:  2012-07-17       Impact factor: 5.922

2.  The proprotein convertase (PC) PCSK9 is inactivated by furin and/or PC5/6A: functional consequences of natural mutations and post-translational modifications.

Authors:  Suzanne Benjannet; David Rhainds; Josée Hamelin; Nasha Nassoury; Nabil G Seidah
Journal:  J Biol Chem       Date:  2006-08-15       Impact factor: 5.157

Review 3.  Clinical aspects of PCSK9.

Authors:  Bertrand Cariou; Cédric Le May; Philippe Costet
Journal:  Atherosclerosis       Date:  2011-04-22       Impact factor: 5.162

4.  Validation of the Friedewald formula for the determination of low-density lipoprotein cholesterol compared with beta-quantification in a large population.

Authors:  André J Tremblay; Hugo Morrissette; Jean-Marc Gagné; Jean Bergeron; Claude Gagné; Patrick Couture
Journal:  Clin Biochem       Date:  2004-09       Impact factor: 3.281

5.  Genetic and metabolic determinants of plasma PCSK9 levels.

Authors:  Susan G Lakoski; Thomas A Lagace; Jonathan C Cohen; Jay D Horton; Helen H Hobbs
Journal:  J Clin Endocrinol Metab       Date:  2009-04-07       Impact factor: 5.958

6.  Atorvastatin increases human serum levels of proprotein convertase subtilisin/kexin type 9.

Authors:  Holly E Careskey; R Aleks Davis; William E Alborn; Jason S Troutt; Guoqing Cao; Robert J Konrad
Journal:  J Lipid Res       Date:  2007-11-21       Impact factor: 5.922

7.  Serum proprotein convertase subtilisin kexin type 9 is correlated directly with serum LDL cholesterol.

Authors:  William E Alborn; Guoqing Cao; Holly E Careskey; Yue-Wei Qian; Danise R Subramaniam; Julian Davies; Elaine M Conner; Robert J Konrad
Journal:  Clin Chem       Date:  2007-08-16       Impact factor: 8.327

8.  PCSK9 inhibition with evolocumab (AMG 145) in heterozygous familial hypercholesterolaemia (RUTHERFORD-2): a randomised, double-blind, placebo-controlled trial.

Authors:  Frederick J Raal; Evan A Stein; Robert Dufour; Traci Turner; Fernando Civeira; Lesley Burgess; Gisle Langslet; Russell Scott; Anders G Olsson; David Sullivan; G Kees Hovingh; Bertrand Cariou; Ioanna Gouni-Berthold; Ransi Somaratne; Ian Bridges; Rob Scott; Scott M Wasserman; Daniel Gaudet
Journal:  Lancet       Date:  2014-10-01       Impact factor: 79.321

9.  Elevated PCSK9 levels in untreated patients with heterozygous or homozygous familial hypercholesterolemia and the response to high-dose statin therapy.

Authors:  Frederick Raal; Vanessa Panz; Andrew Immelman; Gillian Pilcher
Journal:  J Am Heart Assoc       Date:  2013-04-24       Impact factor: 5.501

10.  ODYSSEY FH I and FH II: 78 week results with alirocumab treatment in 735 patients with heterozygous familial hypercholesterolaemia.

Authors:  John J P Kastelein; Henry N Ginsberg; Gisle Langslet; G Kees Hovingh; Richard Ceska; Robert Dufour; Dirk Blom; Fernando Civeira; Michel Krempf; Christelle Lorenzato; Jian Zhao; Robert Pordy; Marie T Baccara-Dinet; Daniel A Gipe; Mary Jane Geiger; Michel Farnier
Journal:  Eur Heart J       Date:  2015-09-01       Impact factor: 29.983

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  2 in total

Review 1.  Usefulness of alirocumab and evolocumab for the treatment of patients with diabetic dyslipidemia.

Authors:  Jun Zhang; Kristen M Tecson; Natalia A Rocha; Peter A McCullough
Journal:  Proc (Bayl Univ Med Cent)       Date:  2018-04-11

2.  Effects of increased body weight and short-term weight loss on serum PCSK9 levels - a prospective pilot study.

Authors:  Theodosios D Filippatos; Evangelos Liberopoulos; Maria Georgoula; Constantinos C Tellis; Alexandros D Tselepis; Moses Elisaf
Journal:  Arch Med Sci Atheroscler Dis       Date:  2017-10-05
  2 in total

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