MicroRNAs miR-29a-3p and miR-192-5p: promising urinary biomarkers for kidney function loss

Cristine Dieter1,2,3, Eliandra Girardi1, Marcia Puñales4

  • 1Hospital de Clínicas de Porto Alegre Serviço de Endocrinologia Porto Alegre RG Brasil Serviço de Endocrinologia, Hospital de Clínicas de Porto Alegre, Porto Alegre, RG, Brasil.

Abstract

Insights

Higher levels of miR-29a-3p and miR-192-5p were found in patients with diabetic kidney disease (DKD). These microRNAs may serve as biomarkers for DKD in type 1 diabetes mellitus (T1DM).

Area of Science:

  • Biochemistry
  • Molecular Biology
  • Nephrology

Background:

  • Diabetic kidney disease (DKD) is a major complication of type 1 diabetes mellitus (T1DM).
  • Identifying reliable biomarkers for DKD is crucial for early diagnosis and management.
  • MicroRNAs (miRNAs) have emerged as potential diagnostic and prognostic indicators in various diseases.

Purpose of the Study:

  • To evaluate the urinary expression levels of miR-29a-3p and miR-192-5p.
  • To compare miRNA expression between T1DM patients with and without DKD.
  • To investigate the correlation between miRNA expression and indicators of kidney function.

Main Methods:

  • The study included 29 T1DM patients, categorized into non-DKD and DKD groups.
  • Urinary miRNA expression was quantified using quantitative polymerase chain reaction (qPCR).
  • Statistical analyses were performed to compare groups and assess correlations.

Main Results:

  • Urinary miR-29a-3p levels were significantly higher in patients with DKD compared to those without.
  • Urinary miR-192-5p levels were elevated in patients with moderate DKD.
  • Both miRNAs showed negative correlations with estimated glomerular filtration rate (eGFR) and positive correlations with creatinine levels.

Conclusions:

  • Differential expression of miR-29a-3p and miR-192-5p suggests their involvement in DKD pathogenesis.
  • These miRNAs hold promise as potential non-invasive biomarkers for detecting DKD in T1DM patients.
  • Further research is warranted to validate their clinical utility.