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Nephrotic syndrome complicated by idiopathic central diabetes insipidus

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Abstract

Background

There is ongoing discussion regarding the mechanisms underlying edema formation in nephrotic syndrome (NS). Many studies published in the last decade reported that primary renal sodium retention was a major factor in edema formation. However, many of the factors influencing edema formation in NS remain unclear, including the role of arginine vasopressin (AVP).

Case-Diagnosis/Treatment

We report a 12-year-old boy with steroid-dependent NS complicated by idiopathic central diabetes insipidus (CDI). He did not develop edema during his first relapse of NS after developing CDI, despite having hypoalbuminemia. He had polydipsia, polyuria, low urine osmolality, and a low serum arginine AVP level. His fractional excretion of sodium was only slightly low. Endocrinological testing and magnetic resonance imaging revealed idiopathic CDI. After starting desmopressin therapy, he developed edema when his NS relapsed.

Conclusions

This is the first known reported case of NS in a patient with CDI. The findings suggest that appropriate AVP secretion in response to an increase in serum osmolality caused by renal sodium retention is necessary for excess extracellular fluid accumulation in NS. Further investigation is needed to more fully understand the role of AVP in edema formation in NS.

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References

  1. Siddall EC, Radhakrishnan J (2012) The pathophysiology of edema formation in the nephrotic syndrome. Kidney Int 82:635–642

    Article  PubMed  CAS  Google Scholar 

  2. Lourdel S, Loffing J, Favre G, Paulais M, Nissant A, Fakitsas P, Créminon C, Féraille E, Verrey F, Teulon J, Doucet A, Deschênes G (2005) Hyperaldosteronemia and activation of the epithelial sodium channel are not required for sodium retention in puromycin-induced nephrosis. J Am Soc Nephrol 16:3642–3650

    Article  PubMed  CAS  Google Scholar 

  3. Kim SW, Wang W, Neisen J, Praetorius J, Kwon TH, Knepper MA, Frøkiaer J, Nielsen S (2004) Increased expression and apical targeting of renal ENaC subunits in puromycin aminonucleoside-induced nephrotic syndrome in rats. Am J Physiol Renal Physiol 286:F922–F935

    Article  PubMed  CAS  Google Scholar 

  4. Di Iorgi N, Napoli F, Allegri AE, Olivieri I, Bertelli E, Gallizia A, Rossi A, Maghnie M (2012) Diabetes insipidus—diagnosis and management. Horm Res Paediatr 77:69–84

    Article  PubMed  CAS  Google Scholar 

  5. Rascher W, Tulassay T (1987) Hormonal regulation of water metabolism in children with nephrotic syndrome. Kidney Int Suppl 21:S83–S89

    PubMed  CAS  Google Scholar 

  6. Richards GE, Thomsett MJ, Bostin BA, Dimeglio LA, Shulman DI, Draznin M (2011) Natural history of idiopathic diabetes insipidus. J Pediatr 159:566–570

    Article  PubMed  Google Scholar 

  7. Svenningsen P, Bistrup C, Friis UG, Bertog M, Haerteis S, Krueger B, Stubbe J, Jensen ON, Thiesson HC, Uhrenholt TR, Jespersen B, Jensen BL, Korbmacher C, Skøtt O (2009) Plasmin in nephrotic urine activates the epithelial sodium channel. J Am Soc Nephrol 20:299–310

    Article  PubMed Central  PubMed  CAS  Google Scholar 

  8. Andersen RF, Buhl KB, Jensen BL, Svenningsen P, Rittig S (2013) Remission of nephrotic syndrome diminishes urinary plasmin content and abolishes activation of ENaC. Pediatr Nephrol 28:1227–1234

    Article  PubMed  Google Scholar 

  9. Deschênes G, Doucet A (2000) Collecting duct Na+/K+-ATPase activity is correlated with urinary sodium excretion in rat nephrotic syndromes. J Am Soc Nephrol 11:604–615

    PubMed  Google Scholar 

  10. Besse-Eshmann V, Klisic J, Nief V, Le Hir M, Kaissling B, Ambühl PM (2002) Regulation of the proximal tubular sodium/proton exchanger NHE3 in rats with puromycin aminonucleoside (PAN)-induced nephrotic syndrome. J Am Soc Nephrol 13:2199–2206

    Article  CAS  Google Scholar 

  11. Ryo HJ, Summer SN, Niederberger M, Kim JK, Schrier RW (1995) Arginine vasopressin gene expression in rats with puromycin-induced nephrotic syndrome. Am J Kidney Dis 25:58–62

    Article  Google Scholar 

  12. Balanescu S, Kopp P, Gaskill NG, Schindler C, Rutishauser J (2011) Correlation of plasma Copeptin and vasopressin concentration in hypo-, iso-, and hyperosmolar states. J Clin Endocrinol Metab 96:1046–1052

    Article  PubMed  CAS  Google Scholar 

  13. Snyder PM (2002) The epithelial Na + channel: cell surface insertion and retrieval in Na + homeostasis and hypertension. Endocr Rev 23:258–275

    Article  PubMed  CAS  Google Scholar 

  14. Mironova E, Bugaj V, Roos KP, Kohan DE, Stockand D (2012) Aldosterone-independent regulation of the epithelial Na + channel (ENac) by vasopressin in adrenalectomized mice. Proc Natl Acad Sci U S A 109:10095–10100

    Article  PubMed Central  PubMed  Google Scholar 

  15. Okada T, Sakaguchi T, Hatamura I, Saji F, Negi S, Otani H, Muragaki Y, Kawachi H, Shigematsu T (2009) Tolvaptan, a selective oral vasopressin V2 receptor antagonist, ameliorates podocyte injury in puromycin aminonucleoside nephrotic rats. Clin Exp Nephrol 13:438–446

    Article  PubMed  CAS  Google Scholar 

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Acknowledgements

We are grateful to Dr. Kaede Yanagita for her useful comments on this manuscript.

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Correspondence to Takao Konomoto.

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Konomoto, T., Tanaka, E., Imamura, H. et al. Nephrotic syndrome complicated by idiopathic central diabetes insipidus. Pediatr Nephrol 29, 927–930 (2014). https://doi.org/10.1007/s00467-013-2728-9

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  • DOI: https://doi.org/10.1007/s00467-013-2728-9

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