Increased microRNA-146a levels in plasma of patients with newly diagnosed type 2 diabetes mellitus

PLoS One. 2013 Sep 2;8(9):e73272. doi: 10.1371/journal.pone.0073272. eCollection 2013.

Abstract

Background: MicroRNAs (miRNAs), a class of small non-coding RNAs, are thought to serve as crucial regulators of gene expression. Dysregulated expression of miRNAs has been described in various diseases and may contribute to related pathologic processes. Our aim was to examine circulating miRNA-146a levels in newly diagnosed type 2 diabetes mellitus (new-T2DM) patients from a Chinese Han population.

Methodology/principal findings: Circulating miRNA-146a was extracted from plasma samples of 90 new-T2DM patients and 90 age- and sex-matched controls. Quantitative PCR assessment revealed that circulating miRNA-146a levels were significantly elevated in new-T2DM patients compared with controls. Participants in the highest tertile of circulating miRNA-146a levels showed a notably higher risk for new-T2DM (crude OR 4.333, 95% CI, 1.935 to 9.705, P = 0.001) than persons in the lowest tertile. Controlling for known risk factors and some biochemical indicators did not attenuate the aforementioned association. In addition, receiver operating characteristic (ROC) curves generated for miRNA-146a revealed an area under the curve (AUC) of 0.725 (95% CI, 0.651 to 0.799, P < 0.001). Moreover, higher circulating miRNA-146a levels were significantly associated with higher plasma heme oxygenase-1 (HO-1) concentrations (β coefficient = 0.131, P < 0.001) and lower HOMA-beta (β coefficient = -0.153, P = 0.015).

Conclusions/significance: We found that circulating miRNA-146a levels were significantly elevated in new-T2DM patients compared with healthy controls. Whether expression of circulating miRNA-146a holds predictive value for T2DM warrants further investigations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Asian People
  • Case-Control Studies
  • Diabetes Mellitus, Type 2 / blood*
  • Diabetes Mellitus, Type 2 / diagnosis*
  • Diabetes Mellitus, Type 2 / enzymology
  • Diabetes Mellitus, Type 2 / genetics
  • Disease Susceptibility
  • Female
  • Heme Oxygenase-1 / blood
  • Humans
  • Male
  • MicroRNAs / blood*
  • Middle Aged
  • ROC Curve

Substances

  • MIRN146 microRNA, human
  • MicroRNAs
  • Heme Oxygenase-1

Grants and funding

This work was funded by the National Science and Technology Support Program (2012BAI02B02) of China and the National Natural Science Foundation of China (NSFC 81072291). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.