Diabetes insipidus overview: Difference between revisions

Jump to navigation Jump to search
 
(5 intermediate revisions by 3 users not shown)
Line 1: Line 1:
__NOTOC__
__NOTOC__
{{Diabetes insipidus}}
{{Diabetes insipidus}}
{{CMG}}{{AE}}{{DAMI}}
{{CMG}}; {{AE}} {{DAMI}}
==Overview==
==Overview==
Diabetes insipidus ([[DI]]) is a syndrome characterized by the excretion of abnormally large volumes of dilute urine. It can be classified into 3 fundamentally different types that must be distinguished for safe and effective management. They are: 1. [[Central diabetes insipidus|Central DI]] also called [[Neurogenic|neurogenic DI]], due to inadequate production and secretion of [[antidiuretic hormone]], [[arginine vasopressin]] ([[AVP]]), 2. [[Nephrogenic diabetes insipidus|Nephrogenic DI]] due to [[renal]] insensitivity to the [[antidiuretic effect]] of [[AVP]] and 3. Primary polydipsia also known as [[Psychogenic|psychogenic DI]], due to suppression of [[arginine vasopressin]] secretion by excessive fluid intake. Patients with [[DI]] typically present with excessive day and nighttime [[urination]], excessive drinking of fluids in order to compensate for the lost fluids in urine which may lead to [[Electrolyte imbalance|electrolyte imbalances]] such as [[Hyponatremia|hypo]]- or [[hypernatremia]]. The causes of Diabetes insipidus are unique to the type of the diabetes insipidus caused, and the treatment should be targeted at understanding the underlying cause of the [[disease]].
Diabetes insipidus ([[DI]]) is a syndrome characterized by the excretion of abnormally large volumes of dilute [[urine]]. It can be classified into three fundamentally different types that must be distinguished from one another in order to facilitate appropriate diagnosis and treatment. These are [[central DI]] (also called [[Neurogenic|neurogenic DI]]), which occurs due to inadequate production and secretion of [[antidiuretic hormone]], [[arginine vasopressin]] ([[AVP]]); [[Nephrogenic diabetes insipidus|nephrogenic DI]], which occurs due to [[renal]] insensitivity to the [[antidiuretic effect]] of [[AVP]]; and primary polydipsia (also known as [[Psychogenic|psychogenic DI]]), which occurs due to the suppression of [[arginine vasopressin]] secretion by excessive [[fluid intake]]. Patients with [[DI]] typically present with excessive day and nighttime [[urination]] and excessive fluid intake in order to compensate for the lost fluids in urine, which may lead to [[Electrolyte imbalance|electrolyte imbalances]] such as [[Hyponatremia|hypo]]- or [[hypernatremia]]. The causes of diabetes insipidus are unique to each variation of the disease, and a treatment plan should be targeted toward the underlying cause of the [[disease]].


==Historical Perspective==
==Historical Perspective==
The history of Diabetes Insipidus dates as far back as the early 1670s when Thomas Willis noted that there was a difference in the taste of [[urine]] produced by different patients who presented with [[polyuria]] and [[polydipsia]]. This marked the beginning of the research into the difference between the popularly known [[diabetes mellitus]] and [[diabetes insipidus]].
The history of diabetes insipidus dates back as the early 1670s when Thomas Willis noted that there was a difference in the taste of [[urine]] produced by different patients who presented with [[polyuria]] and [[polydipsia]]. This marked the beginning of the research into the difference between the popularly known [[diabetes mellitus]] and [[diabetes insipidus]].


==Classification==
==Classification==
Diabetes insipidus can be classified into 3: [[central diabetes insipidus|central]], [[nephrogenic diabetes insipidus|nephrogenic]], and [[psychogenic]] diabetes insipidus which is due to a defect in water balance leading to the excretion of large volumes of dilute urine ([[urine osmolality]] usually below 250 mosmol/kg). Some rarer types of diabetes insipidus include [[Gestational age|gestational]] diabetes insipidus which occurs only in [[pregnancy]], [[autoimmune]] diabetes insipidus caused by an autoimmune reaction and thirst related diabetes insipidus.
Diabetes insipidus can be classified into three types: [[central diabetes insipidus|Central]], [[nephrogenic diabetes insipidus|nephrogenic]], and [[psychogenic]] diabetes insipidus. Some rare types of diabetes insipidus include [[Gestational age|gestational]] diabetes insipidus which occurs only in [[pregnancy]]; [[autoimmune]] diabetes insipidus caused by an autoimmune reaction and thirst related diabetes insipidus.


==Pathophysiology==
==Pathophysiology==
The [[posterior pituitary]] consists of [[Paraventricular nucleus|paraventricular]] and the [[Supraoptic nucleus|supra-optic]] nuclei that synthesizes [[oxytocin]] and [[arginine vasopressin]] respectively. In [[Central diabetes insipidus|Central DI]], there is an absence of [[vasopressin]] which is responsive to the exogenous administration of [[desmopressin]]. On the contrary, in [[Nephrogenic diabetes insipidus|nephrogenic DI]], [[solute]] excretion and all [[filtration]] functions of the [[kidney]] are normal but [[urine]] is [[hypotonic]] and there is a characteristic resistance to the [[antidiuretic]] effects of both [[endogenous]] and [[exogenous]] administration of [[vasopressin]]. More than 55 different [[genetic]] [[mutations]] resulting in a defective [[prohormone]] and a deficiency of [[AVP]] have been identified in familial [[Diabetes insipidus|central diabetes]]. Many conditions have been associated with the development of [[diabetes insipidus]] such as [[Wolfram syndrome]] also known as DIDMOAD, [[Langerhans cell histiocytosis]] (LCH), [[Sickle-cell disease|sickle cell disease]], [[amyloidosis]] etc.
The [[posterior pituitary]] consists of [[Paraventricular nucleus|paraventricular]] and the [[Supraoptic nucleus|supra-optic]] nuclei that synthesizes [[oxytocin]] and [[arginine vasopressin]] respectively. In [[Central diabetes insipidus|Central DI]], there is an absence of [[vasopressin]] which is responsive to the exogenous administration of [[desmopressin]]. On the contrary, in [[Nephrogenic diabetes insipidus|nephrogenic DI]], [[solute]] excretion and all [[filtration]] functions of the [[kidney]] are normal but [[urine]] is [[hypotonic]] and there is a characteristic resistance to the [[antidiuretic]] effects of both [[endogenous]] and [[exogenous]] administration of [[vasopressin]]. More than 55 different [[genetic]] [[mutations]] resulting in a defective [[prohormone]] and a deficiency of [[AVP]] have been identified in familial [[Diabetes insipidus|central diabetes]]. Many conditions have been associated with the development of [[diabetes insipidus]] such as [[Wolfram syndrome]] also known as DIDMOAD, [[Langerhans cell histiocytosis]] ([[Langerhans cell histiocytosis|LCH]]), [[Sickle-cell disease|sickle cell disease]] and [[amyloidosis]].


==Causes==
==Causes==
Line 26: Line 26:


==Risk Factors==
==Risk Factors==
The risk factors in the development of diabetes insipidus vary depending on the type of DI caused. There are a few risk factors in the development of [[Central diabetes insipidus|central DI]] which include [[genetic mutations]], [[Pituitary disease|pituitary disorders]], [[hypothalamic]] injury, head [[tumors]]. The most potent risk factor in the development of [[nephrogenic diabetes insipidus]] is [[lithium]] use as [[lithium]] has a very narrow [[therapeutic index]] of 0.4-0.8. Excessive water intake has been identified to be the only risk factor associated with psychogenic DI and [[pregnancy]] for gestational DI.
The [[risk factors]] in the development of diabetes insipidus vary depending on the type of DI caused. There are a few [[risk factors]] in the development of [[Central diabetes insipidus|central DI]] which include [[genetic mutations]], [[Pituitary disease|pituitary disorders]], [[hypothalamic]] injury, head [[tumors]]. The most potent [[risk factor]] in the development of [[nephrogenic diabetes insipidus]] is [[lithium]] use; as [[lithium]] has a very narrow [[therapeutic index]] of 0.4-0.8 mmol/L . Excessive water intake has been identified to be the only [[risk factor]] associated with psychogenic DI; also [[pregnancy]] is the for gestational DI.


==Screening==
==Screening==
Line 32: Line 32:


==Natural History, Complications and Prognosis==
==Natural History, Complications and Prognosis==
Diabetes insipidus if left untreated results in an elevation in serum sodium and [[osmolality]]. The [[hyperosmolarity]] seen in these patients may also present with [[neurologic]] symptoms such as [[confusion]], [[altered mental status]], [[seizures]], [[coma]] and death. The two major complications of diabetes insipidus are [[dehydration]] and [[electrolyte imbalance]]. Some [[research]] also demonstrates that there is decrease in [[bone mineral density]] seen in patients with diabetes insipidus. However the mechanism of development is not clearly understood neither is the treatment clearly accounted for because treatment of diabetes insipidus does not reverse the disorder.
Diabetes insipidus if left untreated results in an elevation in serum [[sodium]] and [[osmolality]]. The [[hyperosmolarity]] seen in these patients may also present with [[neurologic]] symptoms such as [[confusion]], [[altered mental status]], [[seizures]], [[coma]] and death. The two major complications of diabetes insipidus are [[dehydration]] and [[electrolyte imbalance]]. Some [[research]] also demonstrates that there is decrease in [[bone mineral density]] seen in patients with diabetes insipidus. However the mechanism of development is not clearly understood neither is the treatment clearly accounted for because treatment of diabetes insipidus does not reverse the disorder.


==Diagnosis==
==Diagnosis==


===History and Symptoms===
===History and Symptoms===
Clinical examination may provide important clues to possible underlying diagnoses. The age at which symptoms develop together with the pattern of fluid intake, may influence subsequent investigation of diabetes insipidus. The primary symptoms are persistent [[polyuria]] and [[polydipsia]], and young children may have severe [[dehydration]], [[vomiting]], [[constipation]], [[fever]], [[irritability]], [[sleep disturbance]], [[failure to thrive]] and [[growth retardation]].
[[Clinical examination]] may provide important clues to possible underlying diagnoses. The age at which symptoms develop together with the pattern of fluid intake, may influence subsequent investigation of diabetes insipidus. The primary symptoms are persistent [[polyuria]] and [[polydipsia]], and young children may have severe [[dehydration]], [[vomiting]], [[constipation]], [[fever]], [[irritability]], [[sleep disturbance]], [[failure to thrive]] and [[growth retardation]].


===Physical Examination===
===Physical Examination===
Line 43: Line 43:


===Laboratory Findings===
===Laboratory Findings===
There are a couple of laboratory investigations that can be carried out in order to diagnose diabetes insipidus. Some of them include plasma sodium and urine osmolality, measurement of urine output, plasma and urine ADH measurement.
There are a couple of laboratory investigations that can be carried out in order to diagnose diabetes insipidus. Some of them include [[Sodium|plasma sodium]] and [[Urine osmolality|urine osmolality,]] measurement of [[urine output]], plasma and urine [[ADH]] measurement.


===Electrocardiogram===
===Electrocardiogram===
Line 49: Line 49:


===Chest X Ray===
===Chest X Ray===
There are no electrocardiogram findings associated with diabetes insipidus.
There are no chest X ray findings associated with diabetes insipidus.


===CT===
===CT===
Line 58: Line 58:


===Echocardiography or Ultrasound===
===Echocardiography or Ultrasound===
There are no Echocardiography or Ultrasound findings associated with diabetes insipidus.
There are no echocardiography or ultrasound findings associated with diabetes insipidus.


===Other Imaging Findings===
===Other Imaging Findings===
Line 68: Line 68:
==Treatment==
==Treatment==
===Medical Therapy===
===Medical Therapy===
The hallmark symptoms of both central and nephrogenic diabetes insipidus (DI) are polyuria, nocturia, and polydipsia due to a concentrating defect. Treatment of central diabetes insipidus is primarily aimed at decreasing the urine output, usually by increasing the activity of antidiuretic hormone (ADH, also called arginine vasopressin or AVP). However, nephrogenic diabetes insipidus (DI) results from resistance of the kidney to the actions of antidiuretic hormone(ADH). As a result, patients with this disorder are not likely to have a good response to hormone administration (as DDAVP) or to drugs that increase either the renal response to ADH or ADH secretion and so other treatment options must be explored.
The hallmark [[symptoms]] of both central and [[nephrogenic diabetes insipidus]] (DI) are [[polyuria]], [[nocturia]], and [[polydipsia]] due to a concentrating defect. Treatment of central diabetes insipidus is primarily aimed at decreasing the urine output, usually by increasing the activity of [[antidiuretic hormone]] ([[ADH]], also called [[arginine vasopressin]] or [[AVP]]). However, [[nephrogenic diabetes insipidus]] (DI) results from resistance of the [[kidney]] to the actions of [[antidiuretic hormone]]([[ADH]]). As a result, patients with this disorder are not likely to have a good response to [[hormone]] administration (as [[DDAVP]]) or to [[drugs]] that increase either the renal response to [[ADH]] or [[ADH]] secretion and so other treatment options must be explored.


===Surgery===
===Surgery===

Latest revision as of 13:06, 27 September 2017

Diabetes insipidus Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Diabetes insipidus from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

Diagnostic study of choice

History and Symptoms

Physical Examination

Laboratory Findings

Electrocardiogram

X-Ray

CT scan

MRI

Echocardiography or Ultrasound

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Surgery

Primary Prevention

Secondary Prevention

Cost-Effectiveness of Therapy

Future or Investigational Therapies

Case Studies

Case #1

Diabetes insipidus overview On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Diabetes insipidus overview

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Diabetes insipidus overview

CDC on Diabetes insipidus overview

Diabetes insipidus overview in the news

Blogs on Diabetes insipidus overview

Directions to Hospitals Treating Diabetes insipidus

Risk calculators and risk factors for Diabetes insipidus overview

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Omodamola Aje B.Sc, M.D. [2]

Overview

Diabetes insipidus (DI) is a syndrome characterized by the excretion of abnormally large volumes of dilute urine. It can be classified into three fundamentally different types that must be distinguished from one another in order to facilitate appropriate diagnosis and treatment. These are central DI (also called neurogenic DI), which occurs due to inadequate production and secretion of antidiuretic hormone, arginine vasopressin (AVP); nephrogenic DI, which occurs due to renal insensitivity to the antidiuretic effect of AVP; and primary polydipsia (also known as psychogenic DI), which occurs due to the suppression of arginine vasopressin secretion by excessive fluid intake. Patients with DI typically present with excessive day and nighttime urination and excessive fluid intake in order to compensate for the lost fluids in urine, which may lead to electrolyte imbalances such as hypo- or hypernatremia. The causes of diabetes insipidus are unique to each variation of the disease, and a treatment plan should be targeted toward the underlying cause of the disease.

Historical Perspective

The history of diabetes insipidus dates back as the early 1670s when Thomas Willis noted that there was a difference in the taste of urine produced by different patients who presented with polyuria and polydipsia. This marked the beginning of the research into the difference between the popularly known diabetes mellitus and diabetes insipidus.

Classification

Diabetes insipidus can be classified into three types: Central, nephrogenic, and psychogenic diabetes insipidus. Some rare types of diabetes insipidus include gestational diabetes insipidus which occurs only in pregnancy; autoimmune diabetes insipidus caused by an autoimmune reaction and thirst related diabetes insipidus.

Pathophysiology

The posterior pituitary consists of paraventricular and the supra-optic nuclei that synthesizes oxytocin and arginine vasopressin respectively. In Central DI, there is an absence of vasopressin which is responsive to the exogenous administration of desmopressin. On the contrary, in nephrogenic DI, solute excretion and all filtration functions of the kidney are normal but urine is hypotonic and there is a characteristic resistance to the antidiuretic effects of both endogenous and exogenous administration of vasopressin. More than 55 different genetic mutations resulting in a defective prohormone and a deficiency of AVP have been identified in familial central diabetes. Many conditions have been associated with the development of diabetes insipidus such as Wolfram syndrome also known as DIDMOAD, Langerhans cell histiocytosis (LCH), sickle cell disease and amyloidosis.

Causes

Diabetes insipidus is caused by a variety of factors. The causes for each subtype of diabetes insipidus is classically different. It is important to identify these underlying causes of the various forms in order to appropriately diagnose and treat each type.

Differentiating Diabetes insipidus from other Diseases

Diabetes insipidus must be differentiated from other diseases that cause polyuria which is defined as a urine output exceeding 3 L/day in adults and 2 L/m2/day in children, increased frequency or nocturia and polydipsia. It is important to know that levels of hypo or hypernatremia is not sufficient to describe the underlying cause of diabetes insipidus.

Epidemiology and Demographics

The prevalence of diabetes insipidus is estimated to be 3:100,000 individuals worldwide. The prevalence and incidence of both central and nephrogenic DI does not vary by gender. Similarly, no significant racial predilection in prevalence among ethnic groups have been found.

With both central and nephrogenic DI, inherited causes account for approximately 1-2% of all cases. An incidence of about 1 in 20 million births for nephrogenic DI caused by AQP2 mutations has been documented.

Risk Factors

The risk factors in the development of diabetes insipidus vary depending on the type of DI caused. There are a few risk factors in the development of central DI which include genetic mutations, pituitary disorders, hypothalamic injury, head tumors. The most potent risk factor in the development of nephrogenic diabetes insipidus is lithium use; as lithium has a very narrow therapeutic index of 0.4-0.8 mmol/L . Excessive water intake has been identified to be the only risk factor associated with psychogenic DI; also pregnancy is the for gestational DI.

Screening

According to the USPSTF screening for diabetes insipidus is not recommended.

Natural History, Complications and Prognosis

Diabetes insipidus if left untreated results in an elevation in serum sodium and osmolality. The hyperosmolarity seen in these patients may also present with neurologic symptoms such as confusion, altered mental status, seizures, coma and death. The two major complications of diabetes insipidus are dehydration and electrolyte imbalance. Some research also demonstrates that there is decrease in bone mineral density seen in patients with diabetes insipidus. However the mechanism of development is not clearly understood neither is the treatment clearly accounted for because treatment of diabetes insipidus does not reverse the disorder.

Diagnosis

History and Symptoms

Clinical examination may provide important clues to possible underlying diagnoses. The age at which symptoms develop together with the pattern of fluid intake, may influence subsequent investigation of diabetes insipidus. The primary symptoms are persistent polyuria and polydipsia, and young children may have severe dehydration, vomiting, constipation, fever, irritability, sleep disturbance, failure to thrive and growth retardation.

Physical Examination

Depending on the time of presentation, patients with diabetes insipidus usually appear generally weak without any focal neurologic findings. However, physical examination of patients with diabetes is usually remarkable for signs of dehydration, such as tachycardia, tachypnea, hypotension, and dry mucus membranes.

Laboratory Findings

There are a couple of laboratory investigations that can be carried out in order to diagnose diabetes insipidus. Some of them include plasma sodium and urine osmolality, measurement of urine output, plasma and urine ADH measurement.

Electrocardiogram

There are no electrocardiogram findings associated with diabetes insipidus.

Chest X Ray

There are no chest X ray findings associated with diabetes insipidus.

CT

There are no CT scan findings associated with diabetes insipidus.

MRI

There are no MRI findings associated with diabetes insipidus.

Echocardiography or Ultrasound

There are no echocardiography or ultrasound findings associated with diabetes insipidus.

Other Imaging Findings

There are no other imaging findings associated with diabetes insipidus.

Other Diagnostic Studies

There are no other diagnostic studies recommended for diabetes insipidus.

Treatment

Medical Therapy

The hallmark symptoms of both central and nephrogenic diabetes insipidus (DI) are polyuria, nocturia, and polydipsia due to a concentrating defect. Treatment of central diabetes insipidus is primarily aimed at decreasing the urine output, usually by increasing the activity of antidiuretic hormone (ADH, also called arginine vasopressin or AVP). However, nephrogenic diabetes insipidus (DI) results from resistance of the kidney to the actions of antidiuretic hormone(ADH). As a result, patients with this disorder are not likely to have a good response to hormone administration (as DDAVP) or to drugs that increase either the renal response to ADH or ADH secretion and so other treatment options must be explored.

Surgery

Surgical intervention is not recommended for the management of diabetes insipidus.

Primary Prevention

Majority of the cause of diabetes insipidus are idiopathic. However, for the ones in which the causes are known, prevention of the causes can help in avoiding diabetes insipidus.

Secondary Prevention

The secondary prevention of diabetes insipidus is same as its primary prevention.

Cost-Effectiveness of Therapy

Future or Investigational Therapies

Case Studies

Case #1

References

Template:WH Template:WS