Association between plasma PCSK9 and gamma-glutamyl transferase levels in diabetic patients

Atherosclerosis. 2010 Aug;211(2):700-2. doi: 10.1016/j.atherosclerosis.2010.04.015. Epub 2010 Apr 20.

Abstract

Background: Proprotein convertase subtilisin kexin type 9 (PCSK9) is a secreted proprotein convertase acting as a natural inhibitor of the low-density lipoprotein (LDL) receptor. Here, we prospectively investigated the relationship between the circulating levels of PCSK9 and metabolic parameters in 117 diabetic patients.

Results: Plasma PCSK9 level was significantly higher in type 2 than in type 1 diabetes (P=0.04), in diabetic patients under statins (P<10(-4)) and in those with macrovascular complications (P=0.002). Univariable regression analysis revealed that plasma PCSK9 level correlated positively with age (P=0.003), body mass index (P=0.04), systolic blood pressure (SBP) (P=0.01), gamma-glutamyl transferase (GGT) levels (P=0.0002) and statin treatment (P=0.001). In a multivariable linear regression analysis, PCSK9 correlated positively with GGT level (beta=21.91, P=0.0019) after adjustment for gender, age, type of diabetes, statin treatment, BMI, SBP and HbA1c.

Conclusion: PCSK9 level was independently associated with GGT level in diabetic patients, suggesting potential interaction between PCSK9 and liver function.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blood Pressure
  • Cholesterol / blood
  • Diabetes Mellitus, Type 1 / blood*
  • Diabetes Mellitus, Type 2 / blood*
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Gene Expression Regulation, Enzymologic*
  • Glycated Hemoglobin / biosynthesis
  • Humans
  • Male
  • Proprotein Convertase 9
  • Proprotein Convertases
  • Prospective Studies
  • Receptors, LDL / metabolism
  • Regression Analysis
  • Serine Endopeptidases / blood*
  • gamma-Glutamyltransferase / blood*

Substances

  • Glycated Hemoglobin A
  • Receptors, LDL
  • Cholesterol
  • gamma-Glutamyltransferase
  • PCSK9 protein, human
  • Proprotein Convertase 9
  • Proprotein Convertases
  • Serine Endopeptidases