22nd June 2023

Renal Tubular Acidosis (RTA)

Type 1 Renal Tubular Acidosis

Type 1 RTA, also known as distal RTA, is caused by the failure of acid secretion of the alpha intercalated cells in the distal tubule. As a result, patients will have a urine pH >5.5, an inappropriate finding considering there is usually evidence of acidosis systemically with bicarbonate levels usually <15 mmol/L. Biochemistry will also show evidence of hypokalaemia, hypercalciuria and decreased citrate excretion with a normal anion gap metabolic acidosis. Hypokalaemia in these patients is driven by secondary hyperaldosteronism.

In a subset of patients with distal RTA, the inability to acidify urine is present without evidence of systemic acidosis. This is termed incomplete distal RTA.

Patients with distal RTA – due to alkalised urine, hypercalciuria and low urinary citrate – are prone to urinary stone formation and nephrocalcinosis, which in itself can cause distal RTA. They also undergo bone demineralisation causing rickets in children and osteomalacia in adults.

Causes for distal RTA include:

• Autoimmune disease – classically Sjogren’s syndrome but can also be seen with hypergammaglobulinemia or SLE.
• Chronic obstructive uropathy
• Cirrhosis
• Drugs – commonly associated medications include amphotericin B, ifosfamide and lithium.
• Hereditary – mutation of kidney band 3 anion transport protein is associated with distal RTA. It can be transmitted in both autosomal dominant and recessive fashions.
• Renal transplantation
• Sickle cell anaemia

Treatment of distal RTA is with sodium bicarbonate supplementation. The repletion of bicarbonate and sodium will lead to a reversal of secondary hyperaldosteronism and the resolution of hypokalaemia. In some cases, potassium citrate can be given to increase potassium levels, as well as reduce the risk of exacerbating stone disease (which can be an associated risk of using sodium bicarbonate or sodium citrate).

Type 2 Renal Tubular Acidosis

Whilst distal RTA is due to an inability to clear hydrogen ions, proximal RTA (otherwise known as Type 2 RTA) derives from a failure in reabsorbing bicarbonate, leading to bicarbonate wasting in urine and subsequent systemic acidaemia. As the distal intercalated cells are still functioning, the urine is still able to acidify, meaning the same levels of urine alkalisation are not seen in proximal RTA that are seen in distal RTA.
Causes of proximal RTA include primary causes such as Fanconi’s syndrome or Lowe syndrome, familial causes such as cystinosis (abnormal accumulation of cystine crystals throughout the body) or Wilson’s disease, or acquired disorders such as amyloidosis, multiple myeloma, and exposures to heavy metals, ifosfamide or acetazolamide.

Fanconi’s syndrome refers to a generalised dysfunction of the proximal tubules, leading to inadequate reabsorption of multiple electrolytes, including glucose, phosphate, and bicarbonate. Due to the loss of phosphate, patients with Fanconi’s are at high risk of bone demineralisation causing osteomalacia in adults and rickets in children.

Causes of Fanconi’s syndrome can be inherited (either as a primary idiopathic cause or secondary to another process such as cystinosis, tyrosinaemia or Wilson’s disease), or acquired from intrinsic renal diseases such as interstitial nephritis, acute tubular nephrosis, Sjogren’s syndrome, myeloma, or amyloidosis. Drugs such as cisplatin, ifosfamide, sodium valproate, tenofovir and aminoglycoside antibiotics such as gentamicin can also cause Fanconi’s syndrome.

Management in Fanconi’s syndrome involves treatment of the metabolic acidosis with alkali such as bicarbonate or citrate, replacement of lost electrolytes and treatment of underlying cause if present.

Type 4 Renal Tubular Acidosis

Type 4 Renal Tubular Acidosis is noteworthy as the only RTA which causes a high rather than a low potassium. Type 4 RTA results from either a deficiency or lack of response to aldosterone on the distal tubule. As a result of the reduced excretion of potassium and hydrogen ions from this disturbance in aldosterone, a hyperkalaemic, normal anion gap metabolic acidosis can be seen. The hyperkalaemia also feeds back to affect the proximal tubule by reducing the amount of ammonia (NH₃) synthesised, leading to a further inability to excrete acid.

Type 4 RTA can be picked up on routine testing in patients with hyperkalaemia
Causes include:

• Medication – e.g. NSAIDs, ACE inhibitors and ARBs, ciclosporin and potassium sparing diuretics such as spironolactone and eplerenone.
• Primary hypoaldosteronism – commonly primary adrenal insufficiency but also includes congenital adrenal hyperplasia.
• Secondary hypoaldosteronism – stemming from diseases of the pituitary and hypothalamus, likely also affecting the adrenals.
• Hyporeninaemic hypoaldosteronism – commonly caused by diabetic nephropathy or chronic interstitial nephritis.
• Pseudohypoaldosteronism – genetic resistance to aldosterone that mimics hypoaldosteronism.

Management of Type 4 RTA involves treatment of the hyperkalaemia with dietary restriction and diuresis as required. If the underlying cause can be treated (such as primary adrenal insufficiency), this should be done. Some patients may also benefit from mineralocorticoid replacement, with careful monitoring for exacerbation of hypertension or oedema.

Type 3 Renal Tubular Acidosis

Amongst a series of rare disorders, type 3 renal tubular acidosis is rarer still. This is a mixed renal tubular acidosis involving the proximal and distal tubule and can be associated with congenital type II carbonic anhydrase deficiency. Information on type 3 renal tubular acidosis is limited to case reports and is highly unlikely to come up in an MRCP examination.