MRCEM Notes

Diabetes insipidus

Diabetes insipidus (DI) is a condition characterised by either a deficiency of antidiuretic hormone, ADH, (cranial DI) or an insensitivity to antidiuretic hormone (nephrogenic DI).

Causes of cranial DI
  • idiopathic
  • post head injury
  • pituitary surgery
  • craniopharyngiomas
  • histiocytosis X
  • DIDMOAD is the association of cranial Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy and Deafness (also known as Wolfram's syndrome)

Causes of nephrogenic DI
  • genetic: the more common form affects the vasopression (ADH) receptor, the less common form results from a mutation in the gene that encodes the aquaporin 2 channel
  • electrolytes: hypercalcaemia, hypokalaemia
  • drugs: demeclocycline, lithium
  • tubulo-interstitial disease: obstruction, sickle-cell, pyelonephritis

Features
  • polyuria
  • polydipsia

Investigation
  • high plasma osmolality, low urine osmolality
  • water deprivation test
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