Proteinuria

Authored by , Reviewed by Prof Cathy Jackson on

This page has been archived. It has not been updated since 11/12/2017. External links and references may no longer work.
If the filters in our kidneys are damaged, increased amounts of albumin and other larger proteins from our blood can pass through and escape into the urine.

This abnormal amount of protein in the urine is known as proteinuria.

The level and type of proteinuria (whether the urinary proteins are albumin only - albuminuria - or include other proteins) are a good indicator of the extent of kidney damage. Proteinuria is also a sign that someone is at risk of developing progressive deterioration of kidney function. Even small degrees of albuminuria/proteinuria are also associated with an increased risk of the development of heart and blood vessel disease.

Many diseases can cause inflammation of the kidney filters, a condition which is also known as glomerulonephritis. Other processes that can damage the kidney filters and cause proteinuria include diabetes, high blood pressure (hypertension), and some other forms of kidney diseases.

The National Institute for Health and Care Excellence (NICE) in the UK recommends that anybody at risk of developing chronic kidney disease (CKD), or with reduced kidney function, should have their urine tested to determine the amount of protein in it.

To test for kidney problems, your doctor may do an initial dipstick test on a sample of your urine. If your doctor suspects you may have CKD or reduced kidney function then a urine sample (preferably the first urine specimen of the day) will be sent to the local laboratory to be tested. This is the only way to identify small quantities of albumin and to measure the amount of protein present.

You may be asked to repeat the sample, particularly if the first one was not from early in the morning, because there are other factors which may cause a small increase in the amount of albumin.

Large amounts of protein in your urine may cause it to look foamy in the toilet. Also, the loss of protein from your body means your blood can no longer soak up enough fluid, and you may notice swelling in your hands, feet, abdomen, or face. These are signs of very large protein loss. This is called nephrotic syndrome.

Most people who have proteinuria will not notice any abnormal signs or symptoms related to this. Laboratory testing is the only way to find out how much protein you have in your urine.

NICE has suggested that the following people should be offered a urine test for proteinuria:

  • People with kidney function known to be less than 60% of normal.
  • People with diabetes.
  • People with high blood pressure (hypertension).
  • People with heart and blood vessel (cardiovascular) disease (coronary heart disease, chronic heart failure, peripheral arterial disease and cerebral vascular disease).
  • People with complex diseases which may involve the kidneys - for example, systemic lupus erythematosus (this is a disease where a person's immune system attacks and injures the body's own organs and tissues).
  • People with a family history of kidney failure or a family history of inherited kidney disease.
  • People found to have blood in their urine.

People who are at increased risk of developing kidney disease should have this test annually as a minimum or as part of their routine check-ups by the doctor. The exact frequency should depend on the clinical situation (level of risk) of the patient. It is important that people with CKD and diabetes should have a test for proteinuria as part of their regular reviews.

If proteinuria is confirmed, your doctor will do other tests and examinations to find out the cause. This may include referral to a kidney (renal) specialist (nephrologist) who will help to develop your kidney care plan. Your treatment may include:

  • Medicines.
  • Lifestyle changes such as losing excess weight, exercising and stopping smoking.
  • Sometimes changes in your diet.

If you have diabetes, high blood pressure or both, the first goal of treatment will be to control your blood glucose and blood pressure.

Further reading and references

  • ; NICE Clinical Guidelines (July 2014)

  • ; NICE Clinical Guideline (Mar 2013)

  • ; NICE Clinical Guideline (June 2015).

  • ; Clinical Manifestation and Management of ADPKD in Western Countries. Kidney Dis (Basel). 2016 Oct2(3):120-127. Epub 2016 Oct 6.

  • ; Edinburgh Renal Unit

  • ; Routine blood tests 1: why do we test for urea and electrolytes? Nursing Times 110: 5, 19-21, 2014.

  • ; Chronic kidney disease: identification and management in primary care. Pragmat Obs Res. 2016 Aug 177:21-32. eCollection 2016.

  • ; Establishing the presence or absence of chronic kidney disease: Uses and limitations of formulas estimating the glomerular filtration rate. World J Methodol. 2017 Sep 267(3):73-92. doi: 10.5662/wjm.v7.i3.73. eCollection 2017 Sep 26.

2 years i had the TUU and reimplatation. since then i have not seen the consultant who performed the surgery but have had 2 kidney scans (nuclear dye injection to show drainage) the first one pre-op...

matt90357
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