Central diabetes insipidus

Not to be confused with Nephrogenic diabetes insipidus.
Neurogenic diabetes insipidus
Other names: central diabetes insipidus;
pituitary diabetes insipidus;
neurohypophyseal diabetes insipidus;
cranial diabetes insipidus;
neurogenic diabetes insipidus
Hyperintense signal of posterior pituitary on image could not be detected, lack of this bright spot is typical of central diabetes insipidus.
SymptomsIncrease thirst, polyuria and dehydration.

Central diabetes insipidus, also called neurogenic diabetes insipidus, is a type of diabetes insipidus due to a lack of vasopressin (ADH) production in the brain. Vasopressin acts to increase the volume of blood (intravascularly), and decrease the volume of urine produced. Therefore, a lack of it causes increased urine production and volume depletion.

It is also known as neurohypophyseal diabetes insipidus,[1][2] referring to the posterior pituitary (neurohypophysis), which is supplied by the hypothalamus in the brain. This condition has only polyuria in common with diabetes. Although not mutually exclusive, with most typical cases, the name diabetes insipidus is a misleading misnomer.[3] A better name might be "hypothalamic-neurohypophyseal ADH deficiency".

Signs and symptoms

Increased thirst, polyuria and dehydration with metabolic encephalopathy.

Unknown

In at least 25% of cases (the most commonly occurring classification), neurogenic diabetes insipidus is of unknown cause, meaning that the lack of vasopressin production arose from an unknown cause.[4] It is also due to damage of the hypothalamus, pituitary stalk, posterior pituitary, and can arise from head trauma.

Acquired

The lack of vasopressin production usually results from some sort of damage to the pituitary gland. It may be due to damage to the brain caused by:

Vasopressin is released by the posterior pituitary, but unlike most other pituitary hormones, vasopressin is produced in the hypothalamus. Neurogenic diabetes insipidus can be a failure of production at the hypothalamus, or a failure of release at the pituitary.[5]

Genetic

The most rare form of central DI is familial neurogenic diabetes insipidus. This form of DI is due to an inherited mutation of the arginine vasopressin-neurophysin II (AVP-NPII) gene, inherited in an autosomal dominant manner. At one point, only 45 families worldwide were known to possess this genetic trait.[6] It is now more widely recognized, although the precise number of people affected with this form of DI is unknown at the present time.

There is also an X-linked familial form.Wolfram Syndrome (also called DIDMOAD) is characterised by DI, diabetes mellitus nerve deafness and optic atrophy.

Cause

The cause of this condition,Central diabetes insipidus is due to partial or complete deficiency of the antidiuretic hormone, arginine vasopressin [7]

Diagnosis

In many respects, the diagnosis of central diabetes insipidus begins as a diagnosis of exclusion. Specifically, other more common causes of polyuria and polydipsia are ruled out. Common rule outs include: diabetes mellitus, chronic kidney disease, hypokalemia, hypercalcemia, and psychogenic polydipsia. Once these conditions have been ruled out a water deprivation test is employed to confirm the diagnosis of CDI.

Treatment

The disorder is treated with vasopressin analogs such as desmopressin. Nonetheless, many times desmopressin alone is not enough to bring under control all the symptoms, and another intervention must be implemented.

See also

References

  1. ↑ Chitturi S, Harris M, Thomsett MJ, et al. (December 2008). "Utility of AVP gene testing in familial neurohypophyseal diabetes insipidus". Clin. Endocrinol. 69 (6): 926–30. doi:10.1111/j.1365-2265.2008.03303.x. PMID 18494865. S2CID 22350358.
  2. ↑ Lee YW, Lee KW, Ryu JW, et al. (2008). "Mutation of Glu78 of the AVP-NPII gene impairs neurophysin as a carrier protein for arginine vasopressin in a family with neurohypophyseal diabetes insipidus". Ann. Clin. Lab. Sci. 38 (1): 12–4. PMID 18316776. Archived from the original on 2019-12-13. Retrieved 2022-04-09.
  3. ↑ "The Pathogenesis of Diabetes Insipidus". Journal of the American Medical Association. 49 (6): 499. 1907. doi:10.1001/jama.1907.02530060049004. Archived from the original on 2022-07-02. Retrieved 2022-04-09.
  4. 1 2 3 4 "Diabetes Inspidus". Library of the National Medical Society. 2008. {{cite journal}}: Cite journal requires |journal= (help) http://www.medical-library.org/journals4a/diabetes_insipidus.htm Archived 2012-02-22 at the Wayback Machine
  5. ↑ "Central Diabetes Insipidus: Pituitary Gland Disorders: Merck Manual Home Health Handbook". Archived from the original on 2011-11-02. Retrieved 2009-04-04.
  6. ↑ "Familial Neurogenic Diabetes Insipidus: a disease caused by a traffic jam?". The Diabetes Insipidus Foundation. 2006. {{cite journal}}: Cite journal requires |journal= (help) http://diabetesinsipidus.org/4di_familial.htm Archived 2009-04-29 at the Wayback Machine
  7. ↑ "Central Diabetes Insipidus". NORD (National Organization for Rare Disorders). Archived from the original on 21 February 2017. Retrieved 2 July 2022.
Classification
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