Predictive value of PLA2R antibody in nephrotic syndrome

  • Research type

    Research Study

  • Full title

    Prospective study of phospholipase A(2) receptor antibody testing as a predictor of membranous nephropathy in patients with nephrotic syndrome undergoing renal biopsy

  • IRAS ID

    124130

  • Contact name

    Matthew MJ Edey

  • Contact email

    matthew.edey@hey.nhs.uk

  • Sponsor organisation

    Hull & East Yorkshire Hospitals NHS Trust

  • Research summary

    Nephrotic syndrome is a kidney disease in which the filtering parts of the kidney become damaged and allow protein to leak out of the blood into the urine. The daily loss of protein can be quite substantial. This results in fluid retention and can require long-term treatment with steroids and other medications. In order to decide which treatments can be offered to a patient with nephrotic syndrome, it is necessary at present to perform a kidney biopsy to make a specific diagnosis. There is a small risk of bleeding associated with a kidney biopsy, which can be severe.

    The most common type of nephrotic syndrome in adults is known as “Membranous Nephropathy”. It can be difficult to predict the course of membranous nephropathy at presentation. Some patients will progress to kidney failure and dialysis, and some others will recover spontaneously. Current recommendations are to avoid potentially toxic treatments for the first six months after diagnosis, and to observe the patient for progression of the disease.

    Recently membranous nephropathy, but not other types of nephrotic syndrome, has been associated with a particular antibody in the blood (called “PLA2R”). We would like to see how accurate in predicting membranous nephropathy this blood test is, if it is taken at the same time as a kidney biopsy for nephrotic syndrome. If it proves very accurate, it might be possible for some people with nephrotic syndrome to be diagnosed on the basis of a blood test only. They would then only require a biopsy if their condition had progressed after 6 months of observation.

  • REC name

    London - Camden & Kings Cross Research Ethics Committee

  • REC reference

    13/LO/1324

  • Date of REC Opinion

    16 Aug 2013

  • REC opinion

    Favourable Opinion