Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2021 Oct 24;10(21):4899.
doi: 10.3390/jcm10214899.

The Usefulness of Urinary Periostin, Cytokeratin-18, and Endoglin for Diagnosing Renal Fibrosis in Children with Congenital Obstructive Nephropathy

Affiliations

The Usefulness of Urinary Periostin, Cytokeratin-18, and Endoglin for Diagnosing Renal Fibrosis in Children with Congenital Obstructive Nephropathy

Agnieszka Turczyn et al. J Clin Med. .

Abstract

Congenital obstructive nephropathy (CON) leads to renal fibrosis and chronic kidney disease. The aim of the study was to investigate the predictive value of urinary endoglin, periostin, cytokeratin-18, and transforming growth factor-β1 (TGF-β1) for assessing the severity of renal fibrosis in 81 children with CON and 60 controls. Children were divided into three subgroups: severe, moderate scars, and borderline lesions based on 99mTc-ethylenedicysteine scintigraphy results. Periostin, periostin/Cr, and cytokeratin-18 levels were significantly higher in the study group compared to the controls. Children with severe scars had significantly higher urinary periostin/Cr levels than those with borderline lesions. In multivariate analysis, only periostin and cytokeratin-18 were independently related to the presence of severe and moderate scars, and periostin was independently related to borderline lesions. However, periostin did not differentiate advanced scars from borderline lesions. In ROC analysis, periostin and periostin/Cr demonstrated better diagnostic profiles for detection of advanced scars than TGF-β1 and cytokeratin-18 (AUC 0.849; 0.810 vs. 0.630; 0.611, respectively) and periostin for detecting borderline lesions than endoglin and periostin/Cr (AUC 0.777 vs. 0.661; 0.658, respectively). In conclusion, periostin seems to be a promising, non-invasive marker for assessing renal fibrosis in children with CON. CK-18 and TGF-β1 demonstrated low utility, and endoglin was not useful for diagnosing advanced scars.

Keywords: children; congenital obstructive nephropathy; cytokeratin-18; endoglin; periostin; renal fibrosis; transforming growth factor-β1.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Study flow diagram. CAKUT—congenital anomalies of the kidney and urinary tract; UTI—urinary tract infection; UPJO—ureteropelvic junction obstruction; UVJO—ureterovesical junction obstruction; PUV—posterior urethral valves.

Similar articles

Cited by

References

    1. Harambat J., van Stralen K.J., Kim J.J., Tizard E.J. Epidemiology of chronic kidney disease in children. Pediatr. Nephrol. 2012;27:363–373. doi: 10.1007/s00467-011-1939-1. - DOI - PMC - PubMed
    1. Chevalier R.L. Prognostic factors and biomarkers of congenital obstructive nephropathy. Pediatr. Nephrol. 2015;31:1411–1420. doi: 10.1007/s00467-015-3291-3. - DOI - PubMed
    1. Chevalier R.L., Thornhill B.A., Forbes M.S., Kiley S.C. Mechanisms of renal injury and progression of renal disease in congenital obstructive nephropathy. Pediatr. Nephrol. 2009;25:687–697. doi: 10.1007/s00467-009-1316-5. - DOI - PubMed
    1. Zieg J., Blahova K., Seeman T., Bronsky J., Dvorakova H., Pechova M., Janda J., Matousovic K. Urinary transforming growth factor-β1 in children with obstructive uropathy. Nephrology. 2011;16:595–598. doi: 10.1111/j.1440-1797.2011.01459.x. - DOI - PubMed
    1. Misseri R., Rink R.C., Meldrum D.R., Meldrum K.K. Inflammatory mediators and growth factors in obstructive renal injury. J. Surg. Res. 2004;119:149–159. doi: 10.1016/j.jss.2004.02.016. - DOI - PubMed