Serum LBP Is Associated with Insulin Resistance in Women with PCOS

PLoS One. 2016 Jan 22;11(1):e0145337. doi: 10.1371/journal.pone.0145337. eCollection 2016.

Abstract

Introduction: Lipopolysaccharide-binding protein (LBP) is closely associated with many metabolic disorders. However, no study has been done to explore the relationship between LBP and polycystic ovary syndrome (PCOS). The objective of this study was to investigate whether the serum LBP level is elevated and associated with insulin resistance (IR) in PCOS.

Participants and design: In this cross-sectional study, 117 PCOS patients and 121 age-matched controls were recruited. Hyperinsulinemic-euglycemic clamp was performed with an expression of M value for insulin sensitivity. Fasting serum samples were collected to detect LBP, lipids, insulin, sex hormones and high sensitive C reactive protein (hs-CRP). Pearson's correlation and multiple linear regression was used to analyze the associations between M value and LBP level.

Settings: The study was performed in a clinical research center.

Results: Compared with controls, PCOS subjects had a significantly higher LBP concentration (33.03±14.59 vs. 24.35±10.31 μg/ml, p<0.001), and lower M value (8.21±3.06 vs. 12.31±1.72 mg/min/kg, p<0.001). Both in lean and overweight/obese individuals, serum LBP level was higher in PCOS subjects than that in controls. M value was negatively correlated with body mass index (BMI), fasting serum insulin, triglycerides, low-density lipoprotein cholesterol (LDL-c), free testosterone, high sensitive C reactive protein (hs-CRP) and LBP, whereas positively correlated with high-density lipoprotein cholesterol (HDL-c) and sex hormone binding globulin (SHBG). Serum LBP level was associated with M value after adjusting for BMI, fasting serum insulin, SHBG, as well as hs-CRP.

Conclusion: Serum LBP level significantly is elevated in PCOS, and is independently associated with IR in PCOS.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute-Phase Proteins
  • Adult
  • Body Mass Index
  • Carrier Proteins / blood*
  • Case-Control Studies
  • Cross-Sectional Studies
  • Female
  • Humans
  • Insulin Resistance*
  • Linear Models
  • Membrane Glycoproteins / blood*
  • Obesity / blood
  • Obesity / physiopathology
  • Overweight / blood
  • Polycystic Ovary Syndrome / blood*
  • Polycystic Ovary Syndrome / physiopathology

Substances

  • Acute-Phase Proteins
  • Carrier Proteins
  • Membrane Glycoproteins
  • lipopolysaccharide-binding protein

Grants and funding

This work was supported by National Natural Science Foundation of China, Grants 81170751 and 81370954 (to QFL), and the National Key Clinical Specialties Construction Program of China. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.