Prognostic value of microRNA-495-3p, adiponectin, and cardiometabolic index in type 2 diabetic nephropathy

Xu-Chun Xu1, He-Jing Fang2, Hua-Ying Huang3

  • 1Department of Nephrology, Jinhua Municipal Central Hospital, Jinhua 321000, Zhejiang Province, China. xuchunxu099@163.com.

PubMed
Abstract

Insights

Low miR-495-3p and high adiponectin (ADPN) and cardiometabolic index (CMI) levels predict poor prognosis in type 2 diabetic nephropathy (T2DN). These biomarkers offer potential for early risk prediction and improved clinical management of T2DN.

Area of Science:

  • Biochemistry
  • Nephrology
  • Endocrinology

Background:

  • Type 2 diabetic nephropathy (T2DN) is a severe diabetes complication with challenging prognosis prediction.
  • MicroRNAs (e.g., miR-495-3p), adiponectin (ADPN), and cardiometabolic index (CMI) are potential biomarkers for metabolic and renal diseases.
  • The combined predictive value of miR-495-3p, ADPN, and CMI for T2DN prognosis requires further investigation.

Purpose of the Study:

  • To investigate serum levels of miR-495-3p, ADPN, and CMI in T2DN patients.
  • To evaluate the prognostic value of these biomarkers in T2DN.

Main Methods:

  • Serum samples from 98 T2DN patients and 49 controls were analyzed for miR-495-3p, ADPN, and CMI.
  • Patients were followed for 6 months to assess prognosis.
  • Multivariate logistic regression and ROC curve analyses were employed to determine predictive values.

Main Results:

  • T2DN patients showed lower miR-495-3p and higher ADPN and CMI levels than controls (P < 0.05).
  • Poor prognosis was associated with even lower miR-495-3p and higher ADPN and CMI levels (P < 0.05).
  • miR-495-3p, ADPN, and CMI, along with liver enzymes and kidney function markers, independently predicted prognosis (P < 0.05).

Conclusions:

  • Decreased miR-495-3p and elevated ADPN and CMI levels are associated with T2DN and poor prognosis.
  • These biomarkers demonstrate potential for T2DN risk stratification and clinical management.
  • Further research can validate these findings for routine clinical application.