Serum levels of pigment epithelium-derived factor (PEDF) are positively associated with acanthosis nigricans in obese adolescents

Diabet Med. 2012 Jul;29(7):e117-20. doi: 10.1111/j.1464-5491.2012.03592.x.

Abstract

Introduction: Circulating pigment epithelium-derived factor, or serine protease inhibitor F1, is upregulated during adipogenesis, contributing to obesity-induced insulin resistance. Furthermore, pigment epithelium-derived factor is abundant in stage I melanosomes and has been reported to increase pigment granules and the appearance of mature melanosomes in retinal pigment epithelium. As acanthosis nigricans is a well-recognized clinical marker of insulin resistance, we hypothesized that increased pigment epithelium-derived factor might be associated with the generation of acanthosis nigricans.

Methods: Acanthosis nigricans, anthropometric measurements, circulating total PEDF and metabolic profiles were assessed in 28 obese adolescents in a hospital-based obesity clinic.

Results: Subjects with acanthosis nigricans (n = 10) showed greater plasma levels of pigment epithelium-derived factor (PEDF) than those without [geometric mean 23.55 (range 15.2-40.2) vs. 9.01 (range 5.5-18.7) μg/ml; P < 0.001]. Although pigment epithelium-derived factor was positively correlated with the homeostasis model assessment for insulin resistance (HOMA-IR) (r = 0.779, P < 0.001; 95% CI 0.573-0.892), as previously reported, for the same degree of insulin resistance, those with acanthosis nigricans exhibited a 2.1-fold (95%CI 2.0-2.3) higher level of pigment epithelium-derived factor.

Conclusions: While acanthosis nigricans is undoubtedly associated with insulin resistance, its appearance is not ubiquitous in patients at any given level of HOMA-IR. The higher levels of pigment epithelium-derived factor in those with acanthosis nigricans compared with those without, with similar levels of resistance, suggest that pigment epithelium-derived factor levels are associated with acanthosis nigricans.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acanthosis Nigricans / blood*
  • Acanthosis Nigricans / genetics
  • Adipogenesis / genetics
  • Adolescent
  • Biomarkers / blood
  • Blood Glucose / metabolism*
  • Body Mass Index
  • Eye Proteins / blood*
  • Eye Proteins / genetics
  • Female
  • Humans
  • Insulin Resistance
  • Male
  • Nerve Growth Factors / blood*
  • Nerve Growth Factors / genetics
  • Obesity / blood*
  • Obesity / complications
  • Serpins / blood*
  • Serpins / genetics
  • Up-Regulation
  • alpha 1-Antitrypsin / blood*
  • alpha 1-Antitrypsin / genetics

Substances

  • Biomarkers
  • Blood Glucose
  • Eye Proteins
  • Nerve Growth Factors
  • SERPINA1 protein, human
  • Serpins
  • alpha 1-Antitrypsin
  • pigment epithelium-derived factor