Adipose and Plasma microRNAs miR-221 and 222 Associate with Obesity, Insulin Resistance, and New Onset Diabetes after Peritoneal Dialysis

Nutrients. 2022 Nov 18;14(22):4889. doi: 10.3390/nu14224889.

Abstract

Background: The correlation between microRNA, obesity, and glycemic intolerance in patients on peritoneal dialysis (PD) is unknown. We aimed to measure the adipose and plasma miR-221 and -222 levels, and to evaluate their association with adiposity, glucose intolerance, and new onset diabetes mellitus (NODM) after the commencement of PD.

Methods: We prospectively recruited incident adult PD patients. miR-221 and -222 were measured from adipose tissue and plasma obtained during PD catheter insertion. These patients were followed for 24 months, and the outcomes were changes in adiposity, insulin resistance, and NODM after PD.

Results: One hundred and sixty-five patients were recruited. Patients with pre-existing DM had higher adipose miR-221 (1.1 ± 1.2 vs. 0.7 ± 0.9-fold, p = 0.02) and -222 (1.9 ± 2.0 vs. 1.2 ± 1.3-fold, p = 0.01). High adipose miR-221 and -222 levels were associated with a greater increase in waist circumference (miR-221: beta 1.82, 95% CI 0.57-3.07, p = 0.005; miR-222: beta 1.35, 95% CI 0.08-2.63, p = 0.038), Homeostatic Model Assessment for Insulin Resistance (HOMA) index (miR-221: beta 8.16, 95% CI 2.80-13.53, p = 0.003; miR-222: beta 6.59, 95% CI 1.13-12.05, p = 0.018), and insulin requirements (miR-221: beta 0.05, 95% CI 0.006-0.09, p = 0.02; miR-222: beta 0.06, 95% CI 0.02-0.11, p = 0.002) after PD. The plasma miR-222 level predicted the onset of NODM (OR 8.25, 95% CI 1.35-50.5, p = 0.02).

Conclusion: miR-221 and -222 are associated with the progression of obesity, insulin resistance, and NODM after PD.

Keywords: adipose miRNA; diabetes mellitus; insulin resistance; obesity; peritoneal dialysis.

MeSH terms

  • Adipose Tissue / chemistry
  • Adult
  • Diabetes Mellitus* / blood
  • Diabetes Mellitus* / genetics
  • Humans
  • Insulin Resistance* / genetics
  • MicroRNAs* / blood
  • MicroRNAs* / genetics
  • Obesity* / blood
  • Obesity* / genetics
  • Peritoneal Dialysis* / adverse effects
  • Renal Insufficiency / therapy

Substances

  • MicroRNAs
  • MIRN221 microRNA, human
  • MIRN222 microRNA, human

Grants and funding

This study was supported in part by the Hong Kong Society of Nephrology Research Grant, the Richard Yu Chinese University of Hong Kong (CUHK) PD Research Fund, and CUHK research accounts 6905134 and 8601286. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.