Skip to main content
Log in

Nierschade bij kinderen met een mononier

De KIMONO-studie

  • Artikelen
  • Published:
Tijdschrift voor Kindergeneeskunde

Samenvatting

Inleiding

Kinderen met een mononier hebben mogelijk een verhoogd risico op het ontwikkelen van hypertensie, (micro)albuminurie en chronische nierinsufficiëntie.Twee oorzaken hiervoor zouden glomerulaire hyperfiltratie en de hoge incidentie van congenitale afwijkingen van nieren en urinewegen (CAKUT) kunnen zijn. De KIMONO-studie inventariseert het bestaan van tekenen van nierschade op de kinderleeftijd in een groot cohort van kinderen met een mononier.

Patiënten en methoden

Tekenen van nierschade (hypertensie, microalbuminurie en antihypertensieve/antiproteïnurische medicatie) werden retrospectief geëvalueerd in 206 kinderen met een mononier (aangeboren: n=116; verworven: n=90). Vervolgens werd er een afzonderlijke analyse uitgevoerd voor kinderen met en zonder ipsilaterale CAKUT.

Resultaten

Op een gemiddelde leeftijd van 9,5 (standaarddeviatie 5,6) jaar waren tekenen van nierschade aanwezig bij 32% van de kinderen met een mononier. Het bestaan van tekenen voor nierschade was niet afhankelijk van het type mononier. Kinderen met ipsilaterale CAKUT hadden vaker tekenen van nierschade dan kinderen zonder ipsilaterale CAKUT (48% vs. 25%; p=0,03).

Discussie

Het KIMONO-studiecohort toont aan dat een aanzienlijk deel van de kinderen op jonge leeftijd één of meer tekenen heeft van nierschade. Deze resultaten suggereren een belangrijk risico op chronische nierinsufficiëntie op latere leeftijd. Het risico is extra duidelijk wanneer er CAKUT aanwezig is aan de zijde van de mononier. Wij benadrukken daarom de noodzaak tot poliklinisch vervolg van alle kinderen met een mononier.

Summary

Introduction

Children with a solitary functioning kidney (SFK) have a potential risk of developing hypertension, (micro)albuminuria and chronic kidney disease. This might be caused by glomerular hyperfiltration and the high incidence of congenital anomalies of the kidney and urinary tract (CAKUT). The KIMONO-study determines the incidence of renal injury in a large cohort of children with an SFK.

Methods

Markers for renal injury (hypertension, (micro)albuminuria and chronic kidney disease) were retrospectively evaluated in 206 children with different types of SFK (congenital: n=116; acquired: n=90). Additionally, children with ipsilateral CAKUT were stratified and analyzed separately.

Results

Renal injury occurred in 32% of the children with an SFK at a mean age of 9.5 (standard deviation 5.6) years. The incidence of renal injury was independent from SFK-type. Children with ipsilateral CAKUT more frequently showed renal injury than children without CAKUT (48% vs. 25%; p=0.03).

Discussion

The KIMONY-study cohort demonstrates that a substantial sample of children with an SFK show signs of renal injury at a young age. These results imply an important risk for chronic kidney disease in later life, which is even more pronounced in children with additional ipsilateral CAKUT.We therefore underline the need for clinical follow-up of this specific patient group.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Figuur 1:
Figuur 2:

Literatuur

  1. González E, Gutiérrez E, Morales E, et al. Factors influencing the progression of renal damage in patients with unilateral renal agenesis and remnant kidney. Kidney Int. 2005;68:263-70.

    Article  PubMed  Google Scholar 

  2. Argueso LR, Ritchey ML, Boyle ET Jr, et al. Prognosis of patients with unilateral renal agenesis. Pediatr Nephrol. 1992;6:412-6.

    Article  PubMed  CAS  Google Scholar 

  3. Argueso LR, Ritchey ML, Boyle ET Jr, et al. Prognosis of children with solitary kidney after unilateral nephrectomy. J Urol. 1992;148(2 Pt 2):747-51.

    PubMed  CAS  Google Scholar 

  4. Brenner BM, Garcia DL, Anderson S. Glomeruli and blood pressure. Less of one, more the other? Am J Hypertens. 1988;1(4 Pt 1):335-47.

    PubMed  CAS  Google Scholar 

  5. Brenner BM, Lawler EV, Mackenzie HS. The hyperfiltration theory: a paradigm shift in nephrology. Kidney Int. 1996;49:1774-7.

    Article  PubMed  CAS  Google Scholar 

  6. Hostetter TH, Olson JL, Rennke HG, et al. Hyperfiltration in remnant nephrons: a potentially adverse response to renal ablation. Am J Physiol. 1981;241:F85-93.

    Google Scholar 

  7. Schreuder MF, Nauta J. Prenatal programming of nephron number and blood pressure. Kidney Int. 2007;72:265-8.

    Article  PubMed  CAS  Google Scholar 

  8. Keller G, Zimmer G, Mall G, et al. Nephron number in patients with primary hypertension. N Engl J Med. 2003;348:101-8.

    Article  PubMed  Google Scholar 

  9. Woolf AS, Hillman KA. Unilateral renal agenesis and the congenital solitary functioning kidney: developmental, genetic and clinical perspectives. BJU Int. 2007;99:17-21.

    Article  PubMed  CAS  Google Scholar 

  10. Abou Jaoude P, Dubourg L, Bacchetta J, et al. Congenital versus acquired solitary kidney: is the difference relevant? Nephrol Dial Transplant. 2011;26:2188-94.

    Article  PubMed  Google Scholar 

  11. Dursun H, Bayazit AK, Buyukcelik M, et al. Associated anomalies in children with congenital solitary functioning kidney. Pediatr Surg Int. 2005; 21:456-9.

    Article  PubMed  Google Scholar 

  12. Kaneyama K, Yamataka A, Satake S, et al. Associated urologic anomalies in children with solitary kidney. J Pediatr Surg. 2004;39:85-7.

    Article  PubMed  Google Scholar 

  13. Woolf AS. Renal hypoplasia and dysplasia: starting to put the puzzle together. J Am Soc Nephrol. 2006;17:2647-9.

    Article  PubMed  CAS  Google Scholar 

  14. Westland R, Schreuder MF, Bokenkamp A, et al. Renal injury in children with a solitary functioning kidney – the KIMONO study. Nephrol Dial Transplant. 2011;26:1533-41.

    Article  PubMed  Google Scholar 

  15. Lebowitz RL, Olbing H, Parkkulainen KV, et al. International system of radiographic grading of vesicoureteric reflux. International Reflux Study in Children. Pediatr Radiol. 1985;15:105-9.

    Article  CAS  Google Scholar 

  16. National High Blood Pressure Education Program Working Group on High Blood Pressure in Children and Adolescents. The fourth report on the diagnosis, evaluation, and treatment of high blood pressure in children and adolescents. Pediatrics. 2004;114(2 Suppl 4th Report):555-76.

    Article  Google Scholar 

  17. Hogg RJ, Portman RJ, Milliner D, et al. Evaluation and management of proteinuria and nephrotic syndrome in children: recommendations from a pediatric nephrology panel established at the National Kidney Foundation conference on proteinuria, albuminuria, risk, assessment, detection, and elimination (PARADE). Pediatrics. 2000;105: 1242-9.

    Google Scholar 

  18. Schwartz GJ, Brion LP, Spitzer A. The use of plasma creatinine concentration for estimating glomerular filtration rate in infants, children, and adolescents. Pediatr Clin North Am. 1987;34:571-90.

    PubMed  CAS  Google Scholar 

  19. Rosenbaum DM, Korngold E, Teele RL. Sonographic assessment of renal length in normal children. AJR Am J Roentgenol. 1984;142:467-9.

    PubMed  CAS  Google Scholar 

  20. Loftus WK, Gent RJ, LeQuesne GW, Metreweli C. Renal length in Chinese children: sonographic measurement and comparison with western data. J Clin Ultrasound. 1998;26:349-52.

    Article  PubMed  CAS  Google Scholar 

  21. Fehrman-Ekholm I, Elinder CG, Stenbeck M, et al. Kidney donors live longer. Transplantation. 1997;64:976-8.

    Article  PubMed  CAS  Google Scholar 

  22. Ibrahim HN, Foley R, Tan L, et al. Long-term consequences of kidney donation. N Engl J Med. 2009;360:459-69.

    Article  PubMed  CAS  Google Scholar 

  23. Okuda S, Motomura K, Sanai T, et al. Influence of age on deterioration of the remnant kidney in uninephrectomized rats. Clin Sci (Lond). 1987;72: 571-6.

    CAS  Google Scholar 

  24. Wikstad I, Celsi G, Larsson L, et al. Kidney function in adults born with unilateral renal agenesis or nephrectomized in childhood. Pediatr Nephrol. 1988;2:177-82.

    Article  PubMed  CAS  Google Scholar 

  25. Provoost AP, Brenner BM. Long-term follow-up of humans with single kidneys: the need for longitudinal studies to assess true changes in renal function. Curr Opin Nephrol Hypertens. 1993;2:521-6.

    Article  PubMed  CAS  Google Scholar 

  26. Wilson BE, Davies P, Shah K, et al. Renal length and inulin clearance in the radiologically normal single kidney. Pediatr Nephrol. 2003;18:1147-51.

    Article  PubMed  Google Scholar 

  27. Vu KH, Van Dyck M, Daniels H, Proesmans W. Renal outcome of children with one functioning kidney from birth. A study of 99 patients and a review of the literature. Eur J Pediatr. 2008;167: 885-90.

    Article  PubMed  Google Scholar 

  28. Hegde S, Coulthard MG. Renal agenesis and unilateral nephrectomy: what are the risks of living with a single kidney? Pediatr Nephrol. 2009;24: 439-46.

    Article  PubMed  Google Scholar 

  29. Aslam M,Watson AR. Unilateral multicystic dysplastic kidney: long term outcomes. Arch Dis Child. 2006;91:820-3.

    Article  PubMed  CAS  Google Scholar 

  30. Wasilewska A, Zoch-Zwierz W, Jadeszko I, et al. Assessment of serum cystatin C in children with congenital solitary kidney. Pediatr Nephrol. 2006; 21:688-93.

    Article  PubMed  Google Scholar 

  31. Seeman T, Patzer L, John U, et al. Blood pressure, renal function, and proteinuria in children with unilateral renal agenesis. Kidney Blood Press Res. 2006;29:210-5.

    Article  PubMed  Google Scholar 

  32. Mei-Zahav M, Korzets Z, Cohen I, et al. Ambulatory blood pressure monitoring in children with a solitary kidney – a comparison between unilateral renal agenesis and uninephrectomy. Blood Press Monit. 2001;6:263-7.

    Article  PubMed  CAS  Google Scholar 

  33. Schreuder MF, Langemeijer ME, Bokenkamp A, et al. Hypertension and microalbuminuria in children with congenital solitary kidneys. J Paediatr Child Health. 2008;44:363-8.

    Article  PubMed  Google Scholar 

  34. Dursun H, Bayazit AK, Cengiz N, et al. Ambulatory blood pressure monitoring and renal functions in children with a solitary kidney. Pediatr Nephrol. 2007;22:559-64.

    Article  PubMed  Google Scholar 

  35. Robitaille P, Mongeau JG, Lortie L, Sinnassamy P. Long-term follow-up of patients who underwent unilateral nephrectomy in childhood. Lancet. 1985;1:1297-9.

    Article  PubMed  CAS  Google Scholar 

  36. Beeman SC, Zhang M, Gubhaju L, et al. Measuring glomerular number and size in perfused kidneys using MRI. Am J Physiol Renal Physiol. 2011;300: F1454-7.

    Article  Google Scholar 

  37. Sanna-Cherchi S, Ravani P, Corbani V, et al. Renal outcome in patients with congenital anomalies of the kidney and urinary tract. Kidney Int. 2009;76: 528-33.

    Article  PubMed  Google Scholar 

  38. Chevalier RL. When is one kidney not enough? Kidney Int. 2009;76:475-7.

    Article  PubMed  Google Scholar 

  39. Corbani V, Ghiggeri GM, Sanna-Cherchi S. Congenital solitary functioning kidneys: which ones warrant follow-up into adult life? Nephrol Dial Transplant. 2011;26:1458-60.

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Rik Westland.

Additional information

Alle auteurs verklaren geen conflicterende belangen te hebben.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Westland, R., Bökenkamp, A., van Wijk, J. et al. Nierschade bij kinderen met een mononier. TIJDSCHR. KINDERGENEESKUNDE 80, 129–136 (2012). https://doi.org/10.1007/s12456-012-0037-z

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12456-012-0037-z

Navigation