EDITOR--In their article on understanding oedema Diskin et al have overlooked an important body of work that challenges the traditional pathophysiological explanation for the development of oedema in the nephrotic syndrome secondary to renal disease.[1] Animal as well as several human studies have shown that sodium retention seems to occur as a primary phenomenon in the nephrotic syndrome as a result of increased sodium reabsorption in the collecting duct.[2-4] This in turn may be due to resistance to atrial natriuretic peptide.[5]
Hypoalbuminaemia and changes in transcapillary pressures, as well as volume regulating hormones and sodium retention, are mechanisms that do have a role in nephrotic, oedematous patients. Whether sodium retention is the dominant mechanism for the development of oedema remains uncertain. For clinicians it is not the oedema but the assessment of intravascular volume status (using clinical and laboratory data) in children with the nephrotic syndrome that remains an inexact science.
Nadeem E Moghal consultant paediatric nephrologist Department of Paediatric Nephrology, Royal Victoria Infirmary, Newcastle upon Tyne NE 1 4LP N.E.Moghal@newcasde.ac.uk
Competing interest: None declared.
[1] Diskin CJ, Stokes TJ, Dansby LM, Carter TB, Radcliff L, Thomas SG. Towards an understanding of oedema. BMJ 1999;318:1610-3. (12 June.)
[2] Ichikawa I, Rennke HG, Hoyer JR, Badr KF, Schor N, Troy JL, et al. Role for intrarenal mechanisms in the impaired salt excretion of experimental nephrotic syndrome. J Clin Invest 1983;71:91-103.
[3] Geers AB, Koomans HA, Roos JC, Boer P, Mees EJD. Functional relationships in the nephrotic syndrome. Kidney Int 1984;26:324-30.
[4] Bohlin AB, Berg U. Renal sodium handling in minimal change nephrotic syndrome. Arch Dis Child 1984;59:825-30.
[5] Perico N, Remuzzi G. Edema of the nephrotic syndrome: the role of the atrial peptide system. Am J Kidney Dis 1993;22:355-66.
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