Urinary biomarkers of latent inflammation and fibrosis in children with vesicoureteral reflux.


Journal

International urology and nephrology
ISSN: 1573-2584
Titre abrégé: Int Urol Nephrol
Pays: Netherlands
ID NLM: 0262521

Informations de publication

Date de publication:
Apr 2020
Historique:
received: 07 08 2019
accepted: 05 12 2019
pubmed: 14 12 2019
medline: 27 1 2021
entrez: 14 12 2019
Statut: ppublish

Résumé

To investigate the urinary levels of TGF-β1, VEGF, and MCP-1 as potential biomarkers of latent inflammation and fibrosis in the kidney before and 6 months after correction of vesicoureteral reflux (VUR) in children. A total of 88 patients (mean age 26 months) with VUR were divided into three groups: group A-patients with grades II-III VUR, conservative treatment; group B-patients with grades III-V VUR, endoscopic correction of VUR; group C-patients with grades III-V VUR, ureteral reimplantation after failed endoscopic correction. Control group included 20 healthy children. Biomarker levels were measured by ELISA. At admission, TGF-β1 was close to control in all study groups, VEGF increased with severity of the disease, and MCP-1 increased in group C. Six months after correction of VUR, despite clinical and laboratory improvement, TGF-β1 and MCP-1 increased while VEGF decreased compared to the admission values in all groups; no amelioration of renal scarring was detected either by The results support our hypothesis that successful correction of VUR is not sufficient to stop or reduce the latent inflammatory and fibrotic processes that have already started in the kidney regardless of the reflux grade and treatment option. Measuring the urinary levels of TGF-β1, VEGF, and MCP-1 may aid in the development of non-invasive, pathophysiologically relevant approach to diagnosis and monitoring of kidney injury and fibrosis in children with VUR.

Identifiants

pubmed: 31832877
doi: 10.1007/s11255-019-02357-1
pii: 10.1007/s11255-019-02357-1
doi:

Substances chimiques

Biomarkers 0
CCL2 protein, human 0
Chemokine CCL2 0
Transforming Growth Factor beta1 0
Vascular Endothelial Growth Factor A 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

603-610

Références

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Auteurs

Olga Morozova (O)

Department of Pathophysiology, Sechenov First Moscow State Medical University (Sechenov University), Moscow, Russia.

Dmitry Morozov (D)

Department of Pediatric Surgery, Sechenov First Moscow State Medical University (Sechenov University), Moscow, Russia.

Dmitri Pervouchine (D)

Center for Data-Intensive Biomedicine and Biotechnology, Skolkovo Institute of Science and Technology, Moscow, Russia.

Yulia Einav (Y)

Holon Institute of Technology, Holon, Israel.

Darya Lakomova (D)

Department of Pediatric Surgery, Saratov State Medical University n. a. V. I. Razumovsky, Saratov, Russia.

Natalya Zakharova (N)

Research Institute for Fundamental and Clinical Uronephrology, Saratov State Medical University n. a. V. I. Razumovsky, Saratov, Russia.

Lubov Severgina (L)

Department of Pathological Anatomy, Sechenov First Moscow State Medical University (Sechenov University), Moscow, Russia.

Larisa Maltseva (L)

Department of Pathophysiology, Sechenov First Moscow State Medical University (Sechenov University), Moscow, Russia.

Ivan Budnik (I)

Department of Pathophysiology, Sechenov First Moscow State Medical University (Sechenov University), Moscow, Russia. budnik.ivan@gmail.com.

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