Article
Urinary Extracellular Vesicles as a Source of NGAL for Diabetic Kidney Disease Evaluation in Children and Adolescents With Type 1 Diabetes Mellitus
Fecha
2021Registro en:
Ugarte F, Santapau D, Gallardo V, Garfias C, Yizmeyia´ n A, Villanueva S, Sepu´lveda C, Rocco J, Pasten C, Urquidi C, Cavada G, San Martin P, Cano F and Irarra´ zabal CE (2022) Urinary Extracellular Vesicles as a Source of NGAL for Diabetic Kidney Disease Evaluation in Children and Adolescents With Type 1 Diabetes Mellitus. Front. Endocrinol. 12:654269. doi: 10.3389/fendo.2021.654269
Autor
Ugarte, Francisca
Santapau, Daniela
Gallardo, Vivian
Garfias, Carolina
Yizmeyián, Anahí
Villanueva, Soledad
Sepúlveda, Carolina
Rocco, Jocelyn
Pasten, Consuelo
Urquidi, Cinthya
Cavada, Gabriel
San Martin, Pamela
Cano, Francisco
Irarrázabal, Carlos E.
Institución
Resumen
Background: Tubular damage has a role in Diabetic Kidney Disease (DKD). We evaluated
the early tubulointerstitial damage biomarkers in type-1 Diabetes Mellitus (T1DM) pediatric
participants and studied the correlation with classical DKD parameters.
Methods: Thirty-four T1DM and fifteen healthy participants were enrolled. Clinical and
biochemical parameters [Glomerular filtration Rate (GFR), microalbuminuria (MAU),
albumin/creatinine ratio (ACR), and glycated hemoglobin A1c (HbA1c)] were evaluated.
Neutrophil gelatinase-associated lipocalin (NGAL), Hypoxia-inducible Factor-1a (HIF-1a),
and Nuclear Factor of Activated T-cells-5 (NFAT5) levels were studied in the supernatant
(S) and the exosome-like extracellular vesicles (E) fraction from urine samples.
Results: In the T1DM, 12% had MAU >20 mg/L, 6% ACR >30 mg/g, and 88% had eGFR
>140 ml/min/1.72 m2
. NGAL in the S (NGAL-S) or E (NGAL-E) fraction was not detectable
in the control. The NGAL-E was more frequent (p = 0.040) and higher (p = 0.002) than
NGAL-S in T1DM. The T1DM participants with positive NGAL had higher age (p = 0.03),
T1DM evolution (p = 0.03), and serum creatinine (p = 0.003) than negative NGAL. The
NGAL-E correlated positively with tanner stage (p = 0.0036), the median levels of HbA1c
before enrollment (p = 0.045) and was independent of ACR, MAU, and HbA1c at the
enrollment. NFAT5 and HIF-1a levels were not detectable in T1DM or control.
Conclusion: Urinary exosome-like extracellular vesicles could be a new source of early
detection of tubular injury biomarkers of DKD in T1DM patients.