Urinary netrin-1: A new biomarker for the early diagnosis of renal damage in obese children

Duygu Övünç Hacıhamdioğlu, Bülent Hacıhamdioğlu, Demet Altun, Tuba Müftüoğlu, Ferhan Karademir, Selami Süleymanoğlu

Research output: Contribution to journalArticlepeer-review

13 Citations (Scopus)

Abstract

Objective: Urinary netrin-1 is a new marker to demonstrate early tubular damage. The aim of this study was to determine whether urinary netrin-1 is increased in obese children. Methods: A total of 68 normoalbuminuric and normotensive obese patients and 65 controls were included in the study. Urine samples were collected for assessment of urinary phosphorus, sodium, potassium, creatinine, albumin, and netrin-1. Blood samples were collected for measurements of fasting glucose, insulin, lipid, phosphorus, sodium, potassium, and creatinine levels. Homeostatic model assessment insulin resistance index was calculated. Results: Gender and age were similar between obese and control groups (12.01±3.03 vs. 11.7±3.2 years, p=0.568 and 33 vs. 35 girls, p=0.543, respectively). Obese patients had significantly higher netrin-1 excretion than the controls (841.68±673.17 vs. 228.94±137.25 pg/mg creatinine, p=0.000). Urinary netrin-1 level was significantly higher in obese subjects with insulin resistance compared to those without insulin resistance (1142±1181 vs. 604.9±589.91 pg/mg creatinine, p=0.001). Conclusion: In normotensive and normoalbuminuric obese children, urinary netrin-1 level can increase before onset of albuminuria. Urinary netrin-1 excretion appears to be affected predominantly by insulin resistance and hyperinsulinemia. Urinary netrin-1 may be a new biomarker for determining early tubular injury in obese children.

Original languageEnglish
Pages (from-to)282-287
Number of pages6
JournalJCRPE Journal of Clinical Research in Pediatric Endocrinology
Volume8
Issue number3
DOIs
Publication statusPublished - Sept 2016
Externally publishedYes

Keywords

  • Children
  • Insulin resistance
  • Netrin-1
  • Obesity
  • Tubular dysfunction

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