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
Causes of nephrogenic DI
Features
Investigation
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