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Nephrotic syndrome

Nephrotic syndrome is a disorder where the kidneys have been damaged, causing them to leak protein from the blood into the urine. It is a fairly benign disease when it occurs in childhood, but may lead on to chronic renal failure, especially in adults, or be a sign of an underlying serious disease such as systemic lupus erythematosus or a malignancy. more...

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Signs and symptoms

  • The most common sign is excess fluid in the body. This may take several forms:
    • Puffiness around the eyes, characteristically in the morning.
    • Edema over the legs which is pitting (i.e. leaves a little pit when the fluid is pressed out, which resolves over a few seconds).
    • Fluid in the pleural cavity causing pleural effusion.
    • Fluid in the peritoneal cavity causing ascites.
  • Thrombosis
  • High levels of cholesterol (hypercholesterolemia)
  • Renal failure
  • Hypertension (rarely)
  • Some patients may notice foamy urine, due to a lowering of the specific gravity by the high amount of proteinuria. (Actual urinary complaints such as hematuria, or oliguria are uncommon, and seen often in nephritic syndrome.)
  • Hypoalbuminemia

Diagnosis

Other causes of edema are congestive heart failure and cirrhosis. High urine levels of protein can readily be detected with a dipstick. The best way to make a diagnosis is to quantify the amount of protein in a 24-hour urine sample or a random albumin to creatinine ratio (ACR). A diagnosis of nephrotic syndrome requires more than 3.5 grams of proteinuria per 1.73 square metre surface area in adults. Additional components of the nephrotic syndrome include hypercholesterolemia and low serum albumin levels.

Pathogenesis

The glomeruli of the kidneys are the parts that normally filter the blood. They consist of capillaries that are fenestrated (leaky, due to little holes called fenestrae or windows) and that allow fluid, salts, and other small solutes to flow through, but normally not proteins.

In nephrotic syndrome, the glomeruli become damaged due to diabetes, glomerulonephritis, or even prolonged hypertension (high blood pressure) so that small proteins, such as albumin can pass through the kidneys into urine.

Nephrotic syndrome is characterised by proteinuria (detectable protein in the urine), and low albumin levels in blood plasma. As a compensation, the liver begins to make more of all its proteins, and levels of large proteins (such as alpha 2-macroglobulin) increase.

Edema usually occurs due to salt and water retention by the diseased kidneys as well as sometimes due to the reduced colloid oncotic pressure (because of reduced albumin in the plasma). Cholesterol levels are also increased, and though the mechanism isn't fully understood, it is thought to be due to the increased synthesis of lipoproteins in the liver. There is an increased tendency for thrombosis (up to 25%), perhaps due to urinary loss of inhibitors of clotting such as antithrombin III.

Similar loss of immunoglobulins increases the risks of infections and relevant immunisation is recommended against pneumococcus, Haemophilus influenzae, and meningococcus.

Read more at Wikipedia.org


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Hypoalbuminaemia and transcapillary pressures have role in nephrotic syndrome - Statistical Data Included
From British Medical Journal, 9/25/99 by Nadeen E Moghal

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.

COPYRIGHT 1999 British Medical Association
COPYRIGHT 2000 Gale Group

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