The differences between nephrotic and nephritic syndrome are easily forgotten. At the most basic level, remember that nephrotic syndrome involves the loss of a lot of protein, whereas nephritic syndrome involves the loss of a lot of blood.
Nephrotic syndrome
Proteinuria (>3.5g in 24hrs)
++++ Protein
Urine looks frothy
Tip: Nephrotic & Protein both have an “O” which may help you remember!
Hypoalbuminaemia
Albumin is lost in the urine.
Gaps in podocytes allow proteins to leak into the urine.
Oedema
Albumin is lost in the urine.
Hypoalbuminemia results in decreased intravascular oncotic pressure.
As a result, fluid moves out of the intravascular compartment and into the surrounding tissues causing oedema.
Hyperlipidemia
Due to hypoalbuminaemia, the liver compensates and increases production, however, this has the side effect of also increasing the production of lipids, hence causing hyperlipidaemia.
Nephritic syndrome
Haematuria
+++ Blood – microscopic or macroscopic haematuria
Red cell casts – distinguishing feature, form in nephrons and indicate glomerular damage
Haematuria occurs due to podocytes developing large pores which allows blood and protein to escape into the urine.
Proteinuria
++ Protein (small amount)
Hypertension
Usually only mild
Low urine volume <300ml/day
Due to reduced renal function.
Differential diagnosis of Nephrotic and Nephritic syndrome
Nephrotic or nephritic syndrome can be caused by multiple disease processes. First deciding between nephritic and nephrotic syndrome is a useful starting point for your differential diagnosis. This is because each is associated with a particular subset of diseases. Below is just a quick overview of which diseases are associated with which syndrome, for more details read the Glomerulonephritis article.
Nephrotic syndrome – associated diseases
Primary causes
Minimal change glomerulonephritis
Focal segmental glomerulosclerosis
Membranous glomerulonephritis
Secondary causes
SLE
Hep B and C
HIV
Diabetes mellitus
Malignancy
Nephritic syndrome – associated diseases
Post-streptococcal glomerulonephritis – appears weeks after upper respiratory tract infection (URTI)
IgA nephropathy – appears within a day or two after a URTI
Rapidly progressive glomerulonephritis (crescentic glomerulonephritis)
- Goodpasture’s syndrome – anti-GBM antibodies against basal membrane antigens
- Vasculitic disorder – Wegener’s granulomatosis / Microscopic Polyangiitis / Churg Strauss disease
Membranoproliferative glomerulonephritis – primary or secondary to SLE / Hepatitis B/C
Henoch-Schönlein purpura – systemic vasculitis – deposition of IgA in the skin and kidneys
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