Effects of circulating member B of the family with sequence similarity 3 on the risk of developing metabolic syndrome and its components: A 5-year prospective study

J Diabetes Investig. 2018 Jul;9(4):782-788. doi: 10.1111/jdi.12780. Epub 2018 Jan 3.

Abstract

Aims/introduction: Member B of the family with sequence similarity 3 (FAM3B), also known as pancreatic-derived factor, is mainly synthesized and secreted by islet β-cells, and plays a role in abnormal metabolism of glucose and lipids. However, the prospective association of FAM3B with metabolic disorders remains unclear. The present study aimed to reveal the predictive relationship between pancreas-specific cytokine and metabolic syndrome (MetS).

Materials and methods: A total of 210 adults (88 men and 122 women) without MetS, aged between 40 and 65 years, were recruited and received a comprehensive health examination. Baseline serum FAM3B levels were determined by sandwich enzyme-linked immunosorbent assay. Subsequently, all participants underwent a follow-up examination after 5 years. MetS was identified in accordance with the International Diabetes Federation criteria.

Results: During follow up, 35.7% participants developed MetS. In comparison with the non-MetS group, participants with MetS had an increased serum FAM3B at baseline (21.85 ng/mL [19.38, 24.17 ng/mL] vs 28.56 ng/mL [25.32, 38.10 ng/mL], P < 0.001). Moreover, serum FAM3B was significantly associated with variations in fasting plasma insulin (r = -0.306, P < 0.001), homeostasis model assessment of β-cell function (r = -0.328, P < 0.001) and homeostasis model assessment of insulin resistance (r = -0.191, P = 0.006). Furthermore, a positive correlation between baseline FAM3B and the incidence of MetS was observed, even after multivariable adjustment (relative risk 1.23 [1.15, 1.31], P < 0.001). Furthermore, the optimal cut-off values of FAM3B was 23.98 ng/mL for predicting MetS based on the Youden Index.

Conclusions: Elevated circulating FAM3B might be considered as a predictor of newly-onset MetS and its progression.

Keywords: Member B of the family with sequence similarity 3; Metabolic syndrome; Prospective study.

MeSH terms

  • Adult
  • Aged
  • Cytokines / blood*
  • Female
  • Humans
  • Insulin / blood
  • Male
  • Metabolic Syndrome / blood*
  • Metabolic Syndrome / diagnosis*
  • Metabolic Syndrome / epidemiology
  • Middle Aged
  • Neoplasm Proteins / blood*
  • Prospective Studies
  • Risk Factors
  • Sensitivity and Specificity

Substances

  • Cytokines
  • FAM3B protein, human
  • Insulin
  • Neoplasm Proteins