Diabetes insipidus

From WikiMD's Food, Medicine & Wellness Encyclopedia

Diabetes insipidus is a rare, chronic endocrine condition characterized by excessive thirst (polydipsia) and excessive urination (polyuria), specifically the excretion of abnormally large volumes of dilute urine. This condition is not related to diabetes mellitus, a disorder of insulin deficiency or resistance, despite sharing the common name diabetes, derived from the Greek word for siphon.[1]

Arginine vasopressin3d

Classification[edit | edit source]

Diabetes insipidus can be categorized into four types:[2] Central Diabetes Insipidus: Arises from a deficiency of vasopressin, also known as antidiuretic hormone (ADH), caused by damage to the hypothalamus or pituitary gland. Nephrogenic Diabetes Insipidus: Occurs when the kidneys are unable to respond to vasopressin. Gestational Diabetes Insipidus: Occurs only during pregnancy and the postpartum period. In some cases, an enzyme made by the placenta—vasopressinase—destroys the mother's vasopressin. Dipsogenic Diabetes insipidus: Results from a defect in thirst sensation, leading to chronic fluid intake that suppresses vasopressin secretion.

Main symptoms of diabetes hi

Symptoms and Signs[edit | edit source]

The primary symptoms of diabetes insipidus are excessive thirst and the production of large volumes of dilute urine. These symptoms may lead to dehydration, dry skin, rapid heart rate (tachycardia), low blood pressure (hypotension), and fatigue. Without treatment, severe dehydration and electrolyte imbalance can develop, which are serious medical conditions.[3]

Diagnosis[edit | edit source]

Diagnosis typically involves clinical evaluation, urine and blood tests, a water deprivation test, and sometimes a magnetic resonance imaging (MRI) scan to identify potential damage to the hypothalamus or pituitary gland.[4]

Treatment[edit | edit source]

Treatment involves addressing the underlying cause, if possible, and replacing the deficient hormone. Synthetic vasopressin, or desmopressin, can be taken as a nasal spray, oral tablet, or injection to replace the missing vasopressin in central diabetes insipidus. For nephrogenic diabetes insipidus, treatment may involve a low-salt diet to reduce the amount of urine the kidneys make, and certain diuretics to help the kidneys reduce fluid accumulation.[5] Adequate hydration is crucial in all forms of diabetes insipidus.

Prognosis[edit | edit source]

The prognosis for patients with diabetes insipidus largely depends on the underlying cause. If the condition is managed appropriately, individuals can lead normal lives. However, if left untreated, diabetes insipidus can cause severe dehydration and other complications.[6]

Epidemiology[edit | edit source]

Diabetes insipidus is a rare condition. Its incidence is estimated to be 1 in 25,000 individuals. It affects males and females equally, and can occur at any age.[7]

See also[edit | edit source]

References[edit | edit source]

Diabetes insipidus Resources
Doctor showing form.jpg

Translate to: East Asian 中文, 日本, 한국어, South Asian हिन्दी, Urdu, বাংলা, తెలుగు, தமிழ், ಕನ್ನಡ,
Southeast Asian Indonesian, Vietnamese, Thai, မြန်မာဘာသာ, European español, Deutsch, français, русский, português do Brasil, Italian, polski


Health science - Medicine - Nephrology - edit
Diseases of the glomerulus
Lupus nephritis | Post-infectious glomerulonephritis | Minimal change disease | Focal segmental glomerulosclerosis | Diabetic nephropathy
Diseases of the proximal convoluted tubules
Fanconi syndrome (Type II renal tubular acidosis) | renal cell carcinoma
Diseases of the distal convoluted tubules
pseudohypoaldosteronism (Type IV renal tubular acidosis)
Diseases of the collecting duct
Type I renal tubular acidosis
Tumours of the kidney
renal cell carcinoma | Wilms' tumour (children)
Diseases of the renal vasculature
renal artery stenosis | vasculitis | atheroembolic disease
Tubulointerstitial diseases of the kidney
Drug-induced interstitial nephritis | Obstructive nephropathy | Radiation nephritis | Reflux nephropathy | Sarcoidosis
Genetic diseases of the kidney/syndromes associated with kidney dysfunction
Alport syndrome | Polycystic kidney disease | Wilms' tumour (children)

von Hippel-Lindau syndrome | Hereditary papillary renal carcinoma | Birt-Hogg-Dube syndrome | Hereditary renal carcinoma

Genetic diseases of the kidney/syndromes associated with kidney dysfunction

Chronic Kidney Disease

Anemia in CKD | Causes of CKD | CKD Overview | CKD Tests and Diagnosis | Diabetic Kidney Disease | Eating Right for CKD | High Blood Pressure and Kidney Disease | Managing CKD | Mineral and Bone Disorder in CKD | Nutrition for Advanced CKD in Adults | Preventing CKD | Quick Reference on UACR & GFR

Kidney Failure

Eating and Nutrition for Hemodialysis | Financial Help for Treatment of Kidney Failure | Hemodialysis | Kidney Failure | Kidney Transplant | Peritoneal Dialysis

Other Kidney Topics

Acquired Cystic Kidney Disease | Amyloidosis and Kidney Disease | Diabetes Insipidus | Ectopic Kidney | Glomerular Diseases | Goodpasture Syndrome | Henoch-Schönlein Purpura | IgA Nephropathy | Kidney Dysplasia | Kidney Infection (Pyelonephritis) | Kidney Stones | Lupus Nephritis | Medullary Sponge Kidney | Nephrotic Syndrome in Adults | Pain Medicine and Kidney Damage | Polycystic Kidney Disease (PKD) | Renal Artery Stenosis | Renal Tubular Acidosis | Simple Kidney Cysts | Solitary Kidney | Your Kidneys and How They Work | Your Urinary Tract and How It Works

Wiki.png

Navigation: Wellness - Encyclopedia - Health topics - Disease Index‏‎ - Drugs - World Directory - Gray's Anatomy - Keto diet - Recipes

Search WikiMD


Ad.Tired of being Overweight? Try W8MD's physician weight loss program.
Semaglutide (Ozempic / Wegovy and Tirzepatide (Mounjaro) available.
Advertise on WikiMD

WikiMD is not a substitute for professional medical advice. See full disclaimer.

Credits:Most images are courtesy of Wikimedia commons, and templates Wikipedia, licensed under CC BY SA or similar.

Contributors: Admin, Prab R. Tumpati, MD