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DIABETES INSIPIDUS
TABLE OF CONTENTS
DECLARATION………………………………………………………………………...ii
FACULTY GUIDED APPROVAL……………………………………………….…iii
ACKNOWLEDGEMENT…………………………………………………………….iv
LIST OF FIGURES……………………………………………………………………..vi
INTRODUCTION……………………………………………………………………….6
SIGNS AND SYMPTOMS…………………………………………………………..8
CAUSES………………………………………………………………………………….10
TYPES…………………………………………………………………………………….11
 NEPHROGENIC……………………………………………………………….11
 CENTRAL………………………………………………………………………..13
 GESTATIONAL………………………………………………………………..15
 DIPSOGENIC…………………………………………………………………..15
DIAGNOSIS…………………………………………………………………………….16
TREATMENT…………………………………………………………………………..18
REFERENCES………………………………………………………………………….
INTRODUCTION
Diabetes insipidus is a rare disorder that manifests itself when a
person's kidneys pass an abnormally large volume of urine.
It is an uncommon condition in which kidneys are unable to prevent the
excretion of water.
Diabetes insipidus affects about one in 25,000 people in the general
population. Adults are more likely to develop the condition but it can
occur at any age.
Diabetes insipidus (DI) is also defined as the passage of large volumes
(>3 L/24 hr) of dilute urine (< 300 mOsm/kg). People with diabetes
insipidus have normal blood glucose levels; however, their kidneys
cannot balance fluid in the body.
In people with diabetes insipidus, the kidneys can pass 3 to 20 quarts
of urine a day. As a result, a person with diabetes insipidus may feel the
need to drink large amounts of liquids.
The condition is caused by a hormonal abnormality and isn't related to
diabetes.The hormone vasopressin, also called antidiuretic hormone,
controls the fluid removal rate through urination. The hypothalamus, a
small gland located at the base of the brain, produces vasopressin. The
nearby pituitary gland stores the vasopressin and releases it into the
bloodstream when the body has a low fluid level. Vasopressin signals
the kidneys to absorb less fluid from the bloodstream, resulting in less
urine. When the body has extra fluid, the pituitary gland releases
smaller amounts of vasopressin, and sometimes none, so the kidneys
remove more fluid from the bloodstream and produce more urine. The
quantity of water retained in the body is closely controlled by several
mechanisms, one of the most important of which is a hormone (a
chemical secreted into the blood by an endocrine gland) secreted by
the posterior pituitary gland, a structure which lies deep within the
brain. This is called vasopressin or anti-diuretic hormone (ADH) because
its function is to control the loss of water as urine from the kidneys.
SIGNS AND SYMPTOMS
The main complication of diabetes insipidus is dehydration if fluid loss
is greater than liquid intake.
 Thirst(polydipsia)
 dry skin
 fatigue
 sluggishness
 dizziness
 confusion
 nausea
 bed wetting
 frequent urination
 headace
 weight loss
 slower than expected growth
 loss of appetite
 hyperthermia(high body temperature)
In extreme conditions, if fluid is not immediately available they will
drink from flower vases, lavatory cisterns, puddles or anywhere else.
In general affected children remain well but if they become
dehydrated they may seem obviously ill.
CAUSES
Diabetes insipidus occurs when your body can't regulate how it
handles fluids. Normally, your kidneys remove excess body fluids
from your bloodstream. This fluid waste is temporarily stored in your
bladder as urine, before you urinate. The volume and composition of
your body fluids remain balanced through a combination of oral
intake and excretion by the kidneys. The rate of fluid excreted by
your kidneys is greatly influenced by the production of anti-diuretic
hormone (ADH), also known as vasopressin.
Our body makes ADH in the hypothalamus and stores the hormone
in your pituitary gland, a small gland located in the base of your
brain. ADH is released into your bloodstream when your body starts
to become dehydrated. ADH then concentrates the urine by
triggering the kidney tubules to release water back into your
bloodstream rather than excreting as much water into your urine.
The increased loss of urine (polyuria) is reflected by a greatly
increased thirst and fluid intake (polydipsia) but eventually it may
become impossible to take in enough water and the person with this
condition will become dehydrated.
TYPES OF DIABETES INSIPIDUS
There are four types of diabetes insipidus :
1. NEPHROGENIC
 CONGENITAL NEPHROGENIC
 AQUIRED NEPHROGENIC
2. CENTRAL
3. GESTATIONAL
4. DIPSOGENIC
NEPHROGENIC DIABETESINSIPIDUS
The term nephrogenic refers to the kidneys. In nephrogenic diabetes
insipidus, ADH is still being released by your brain but your kidneys
become resistant to the effects of ADH. This means that ADH is not
able to work properly to allow your kidneys to concentrate your
urine.
There are two form of nephrogenic –
Congenital nephrogenic diabetes insipidus
Congenital diabetes Insipidus is present from birth and is caused by
several genes that cause the kidneys of the foetus to form
improperly. Kidneys contain cells called nephrons which regulate
what water is passed by urine and what water is reabsorbed back
into the body. These nephrons react to the ADH released by the
hypothalamus, and if they are damaged, they can end up 'ignoring'
the ADH, leading to constant production of urine.
Deformations can occur in the body by the presence of several rogue
genes. This mutation can only be passed from unaffected mothers to
their sons. However, this very rarely happens, apparently affecting
just 1 in 250,000 births.
There is an even rarer gene mutation that can cause nephrogenic
diabetes insipidus in both males and females.
Acquired nephrogenic diabetes insipidus
Acquired diabetes insipidus occurs after birth as a result of an
outside factor damaging the kidneys and leading to the excessive
urination.
Lithium is used in some medications, particularly for bi-polar
disorder, and long term intake of lithium can cause damage to the
nephrons in the kidneys. Being taken off lithium however, can
restore normal kidney function if it is diagnosed early, so having
kidney function tests every three months is advised by the NHS if you
are on lithium containing medication.
Infections, blockages (such as kidney stones) or other forms of
damage to the kidney could lead to diabetes insipidus
CENTRAL DIABETES INSIPIDUS
Neurogenic diabetes Insipidus, or central and cranial diabetes
insipidus occurs when your brain produces or releases a reduced
amount of ADH. ADH usually helps your kidneys to concentrate your
urine. If less ADH is released, you will pass an increased volume of
dilute urine.
Cranial diabetes insipidus can occur if your hypothalamus or pituitary
gland is damaged. This causes a reduction in production and release
of ADH. The causes of cranial diabetes insipidus include:
 Head injury.
 Cancerous (malignant) or non-cancerous (benign) tumours of your
brain or pituitary gland.
 Surgery to your brain around the region of the pituitary gland and
hypothalamus.
 Idiopathic diabetes insipidus. In this condition the cells in your
hypothalamus become damaged and stop producing ADH. In
many cases, the damage is thought to be due to an autoimmune
problem. Normally, your body makes antibodies to fight infections
- for example, when you catch a cold or have a sore throat. These
antibodies help to kill the germs (bacteria or viruses) causing the
infection. In autoimmune diseases your body makes similar
antibodies (autoantibodies) that attack its normal cells. In this
case, the cells of your hypothalamus are attacked by
autoantibodies.
 Infections including encephalitis and meningitis.
 Some rare inherited conditions.
Cranial diabetes insipidus may just be a problem on its own.
However, sometimes it can occur with other problems because the
production of other hormones that are released by the pituitary
gland is also affected. If cranial diabetes insipidus is caused by a head
injury or surgery to your brain, it may only be a problem for a short
period of time, perhaps a few weeks.
Gestational diabetes insipidus
During pregnancy, the uterus produces vasopressinase which can
break down ADH. The nephrones in the kidneys do not receive the
'stop making urine' message and continue to produce it.
Usually Gestational diabetes insipidus will disappear after the
pregnancy.
Dipsogenic diabetes insipidus
Some cases of diabetes insipidus occur because of an issue with the
thirst function. Similar damage to the hypothalamus that causes
neurogenic diabetes insipidus can also result in a malfunction to the
thirst mechanism, resulting in thirst that won't go away. This will
lead to a constant need to drink, which in turn can lead to excessive
urination.
DIAGNONIS
Blood and urine tests
For example:
 To check the levels of sodium and potassium salts in your blood.
These can be high in diabetes insipidus.
 To check the level of sugar (glucose) in your blood and urine to
exclude diabetes mellitus.
A water deprivation test
This is a special test where you must not drink any water or other
fluids for a certain period of time (usually around 6-8 hours). The
volume of urine that you produce will be measured to see if there is
any change in the amount. If your body is working normally, the
amount of urine that you produce should reduce if you have not
drunk anything for a long time. However, if you have diabetes
insipidus, there will be little change in your urine production.
Antidiuretic hormone test
After the period of fluid deprivation, you may then be given a
medicine that is similar to ADH. If you have cranial diabetes
insipidus, once you have been given this medicine, the amount of
urine that you produce should reduce. The medicine is replacing the
ADH that you are lacking. If you have nephrogenic diabetes insipidus,
you may have no, or only a small, response to the medicine.
Other tests
Other tests may sometimes be suggested to look for possible causes
of diabetes insipidus. For example, an MRI scan of your brain and
pituitary gland.
TREATMENT
Treatment of diabetes insipidus depends on what form of the
condition you have. Treatment options for the most common types
of diabetes insipidus include:
 Central diabetes insipidus. Because the cause of this form of
diabetes insipidus is a lack of anti-diuretic hormone (ADH),
treatment is usually with a synthetic hormone called
desmopressin. You can take desmopressin as a nasal spray, as oral
tablets or by injection.
The synthetic hormone will eliminate the increase in urination. For
most people with this form of the condition, desmopressin is safe
and effective. If the condition is caused by an abnormality in the
pituitary gland or hypothalamus (such as a tumor), your doctor will
first treat the abnormality.
Desmopressin should be considered a medication you take as
needed. This is because in most people, the deficiency of ADH is not
complete, and the amount made by the body can vary day to day.
Taking more desmopressin than needed can result in too much
water retention and low sodium levels in the blood. Symptoms of
low sodium include lethargy, headache, nausea and, in severe cases,
seizures.
In mild cases of central diabetes insipidus, you may need only to
increase your water intake.
 Nephrogenic diabetes insipidus. This condition is the result of
your kidneys not properly responding to ADH, so desmopressin is
not a treatment option. Instead, your doctor may prescribe a low-
salt diet to help reduce the amount of urine your kidneys make.
You'll also need to drink enough water to avoid dehydration.
The drug hydrochlorothiazide, used alone or with other medications,
may improve symptoms. Although hydrochlorothiazide is a diuretic
(usually used to increase urine output), in some cases it can reduce
urine output for people with nephrogenic diabetes insipidus.
If symptoms from nephrogenic diabetes insipidus are due to
medications you're taking, stopping these medicines may help;
however, don't stop taking any medication without first talking to
your doctor.
 Gestational diabetes insipidus. Treatment for most cases of
gestational diabetes insipidus is with the synthetic hormone
desmopressin. In rare cases, this form of the condition is caused
by an abnormality in the thirst mechanism. In these rare cases,
doctors don't prescribe desmopressin.

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Diabetes insipidus

  • 1. DIABETES INSIPIDUS TABLE OF CONTENTS DECLARATION………………………………………………………………………...ii FACULTY GUIDED APPROVAL……………………………………………….…iii ACKNOWLEDGEMENT…………………………………………………………….iv LIST OF FIGURES……………………………………………………………………..vi INTRODUCTION……………………………………………………………………….6 SIGNS AND SYMPTOMS…………………………………………………………..8 CAUSES………………………………………………………………………………….10 TYPES…………………………………………………………………………………….11  NEPHROGENIC……………………………………………………………….11  CENTRAL………………………………………………………………………..13  GESTATIONAL………………………………………………………………..15  DIPSOGENIC…………………………………………………………………..15 DIAGNOSIS…………………………………………………………………………….16 TREATMENT…………………………………………………………………………..18
  • 2. REFERENCES…………………………………………………………………………. INTRODUCTION Diabetes insipidus is a rare disorder that manifests itself when a person's kidneys pass an abnormally large volume of urine. It is an uncommon condition in which kidneys are unable to prevent the excretion of water. Diabetes insipidus affects about one in 25,000 people in the general population. Adults are more likely to develop the condition but it can occur at any age. Diabetes insipidus (DI) is also defined as the passage of large volumes (>3 L/24 hr) of dilute urine (< 300 mOsm/kg). People with diabetes insipidus have normal blood glucose levels; however, their kidneys cannot balance fluid in the body. In people with diabetes insipidus, the kidneys can pass 3 to 20 quarts of urine a day. As a result, a person with diabetes insipidus may feel the need to drink large amounts of liquids. The condition is caused by a hormonal abnormality and isn't related to diabetes.The hormone vasopressin, also called antidiuretic hormone, controls the fluid removal rate through urination. The hypothalamus, a
  • 3. small gland located at the base of the brain, produces vasopressin. The nearby pituitary gland stores the vasopressin and releases it into the bloodstream when the body has a low fluid level. Vasopressin signals the kidneys to absorb less fluid from the bloodstream, resulting in less urine. When the body has extra fluid, the pituitary gland releases smaller amounts of vasopressin, and sometimes none, so the kidneys remove more fluid from the bloodstream and produce more urine. The quantity of water retained in the body is closely controlled by several mechanisms, one of the most important of which is a hormone (a chemical secreted into the blood by an endocrine gland) secreted by the posterior pituitary gland, a structure which lies deep within the brain. This is called vasopressin or anti-diuretic hormone (ADH) because its function is to control the loss of water as urine from the kidneys.
  • 4. SIGNS AND SYMPTOMS The main complication of diabetes insipidus is dehydration if fluid loss is greater than liquid intake.  Thirst(polydipsia)  dry skin  fatigue
  • 5.  sluggishness  dizziness  confusion  nausea  bed wetting  frequent urination  headace  weight loss  slower than expected growth  loss of appetite  hyperthermia(high body temperature) In extreme conditions, if fluid is not immediately available they will drink from flower vases, lavatory cisterns, puddles or anywhere else. In general affected children remain well but if they become dehydrated they may seem obviously ill.
  • 7. Diabetes insipidus occurs when your body can't regulate how it handles fluids. Normally, your kidneys remove excess body fluids from your bloodstream. This fluid waste is temporarily stored in your bladder as urine, before you urinate. The volume and composition of your body fluids remain balanced through a combination of oral intake and excretion by the kidneys. The rate of fluid excreted by your kidneys is greatly influenced by the production of anti-diuretic hormone (ADH), also known as vasopressin. Our body makes ADH in the hypothalamus and stores the hormone in your pituitary gland, a small gland located in the base of your brain. ADH is released into your bloodstream when your body starts to become dehydrated. ADH then concentrates the urine by triggering the kidney tubules to release water back into your bloodstream rather than excreting as much water into your urine. The increased loss of urine (polyuria) is reflected by a greatly increased thirst and fluid intake (polydipsia) but eventually it may become impossible to take in enough water and the person with this condition will become dehydrated. TYPES OF DIABETES INSIPIDUS
  • 8. There are four types of diabetes insipidus : 1. NEPHROGENIC  CONGENITAL NEPHROGENIC  AQUIRED NEPHROGENIC 2. CENTRAL 3. GESTATIONAL 4. DIPSOGENIC NEPHROGENIC DIABETESINSIPIDUS The term nephrogenic refers to the kidneys. In nephrogenic diabetes insipidus, ADH is still being released by your brain but your kidneys become resistant to the effects of ADH. This means that ADH is not able to work properly to allow your kidneys to concentrate your urine. There are two form of nephrogenic – Congenital nephrogenic diabetes insipidus Congenital diabetes Insipidus is present from birth and is caused by several genes that cause the kidneys of the foetus to form improperly. Kidneys contain cells called nephrons which regulate what water is passed by urine and what water is reabsorbed back into the body. These nephrons react to the ADH released by the hypothalamus, and if they are damaged, they can end up 'ignoring' the ADH, leading to constant production of urine.
  • 9. Deformations can occur in the body by the presence of several rogue genes. This mutation can only be passed from unaffected mothers to their sons. However, this very rarely happens, apparently affecting just 1 in 250,000 births. There is an even rarer gene mutation that can cause nephrogenic diabetes insipidus in both males and females. Acquired nephrogenic diabetes insipidus Acquired diabetes insipidus occurs after birth as a result of an outside factor damaging the kidneys and leading to the excessive urination. Lithium is used in some medications, particularly for bi-polar disorder, and long term intake of lithium can cause damage to the nephrons in the kidneys. Being taken off lithium however, can restore normal kidney function if it is diagnosed early, so having kidney function tests every three months is advised by the NHS if you are on lithium containing medication. Infections, blockages (such as kidney stones) or other forms of damage to the kidney could lead to diabetes insipidus
  • 10. CENTRAL DIABETES INSIPIDUS Neurogenic diabetes Insipidus, or central and cranial diabetes insipidus occurs when your brain produces or releases a reduced amount of ADH. ADH usually helps your kidneys to concentrate your urine. If less ADH is released, you will pass an increased volume of dilute urine. Cranial diabetes insipidus can occur if your hypothalamus or pituitary gland is damaged. This causes a reduction in production and release of ADH. The causes of cranial diabetes insipidus include:  Head injury.
  • 11.  Cancerous (malignant) or non-cancerous (benign) tumours of your brain or pituitary gland.  Surgery to your brain around the region of the pituitary gland and hypothalamus.  Idiopathic diabetes insipidus. In this condition the cells in your hypothalamus become damaged and stop producing ADH. In many cases, the damage is thought to be due to an autoimmune problem. Normally, your body makes antibodies to fight infections - for example, when you catch a cold or have a sore throat. These antibodies help to kill the germs (bacteria or viruses) causing the infection. In autoimmune diseases your body makes similar antibodies (autoantibodies) that attack its normal cells. In this case, the cells of your hypothalamus are attacked by autoantibodies.  Infections including encephalitis and meningitis.  Some rare inherited conditions. Cranial diabetes insipidus may just be a problem on its own. However, sometimes it can occur with other problems because the production of other hormones that are released by the pituitary gland is also affected. If cranial diabetes insipidus is caused by a head injury or surgery to your brain, it may only be a problem for a short period of time, perhaps a few weeks.
  • 12. Gestational diabetes insipidus During pregnancy, the uterus produces vasopressinase which can break down ADH. The nephrones in the kidneys do not receive the 'stop making urine' message and continue to produce it. Usually Gestational diabetes insipidus will disappear after the pregnancy. Dipsogenic diabetes insipidus Some cases of diabetes insipidus occur because of an issue with the thirst function. Similar damage to the hypothalamus that causes neurogenic diabetes insipidus can also result in a malfunction to the thirst mechanism, resulting in thirst that won't go away. This will lead to a constant need to drink, which in turn can lead to excessive urination.
  • 13. DIAGNONIS Blood and urine tests For example:  To check the levels of sodium and potassium salts in your blood. These can be high in diabetes insipidus.  To check the level of sugar (glucose) in your blood and urine to exclude diabetes mellitus. A water deprivation test This is a special test where you must not drink any water or other fluids for a certain period of time (usually around 6-8 hours). The volume of urine that you produce will be measured to see if there is any change in the amount. If your body is working normally, the amount of urine that you produce should reduce if you have not drunk anything for a long time. However, if you have diabetes insipidus, there will be little change in your urine production. Antidiuretic hormone test After the period of fluid deprivation, you may then be given a medicine that is similar to ADH. If you have cranial diabetes insipidus, once you have been given this medicine, the amount of urine that you produce should reduce. The medicine is replacing the ADH that you are lacking. If you have nephrogenic diabetes insipidus, you may have no, or only a small, response to the medicine.
  • 14. Other tests Other tests may sometimes be suggested to look for possible causes of diabetes insipidus. For example, an MRI scan of your brain and pituitary gland.
  • 15. TREATMENT Treatment of diabetes insipidus depends on what form of the condition you have. Treatment options for the most common types of diabetes insipidus include:  Central diabetes insipidus. Because the cause of this form of diabetes insipidus is a lack of anti-diuretic hormone (ADH), treatment is usually with a synthetic hormone called desmopressin. You can take desmopressin as a nasal spray, as oral tablets or by injection. The synthetic hormone will eliminate the increase in urination. For most people with this form of the condition, desmopressin is safe and effective. If the condition is caused by an abnormality in the pituitary gland or hypothalamus (such as a tumor), your doctor will first treat the abnormality. Desmopressin should be considered a medication you take as needed. This is because in most people, the deficiency of ADH is not complete, and the amount made by the body can vary day to day. Taking more desmopressin than needed can result in too much water retention and low sodium levels in the blood. Symptoms of low sodium include lethargy, headache, nausea and, in severe cases, seizures. In mild cases of central diabetes insipidus, you may need only to increase your water intake.
  • 16.  Nephrogenic diabetes insipidus. This condition is the result of your kidneys not properly responding to ADH, so desmopressin is not a treatment option. Instead, your doctor may prescribe a low- salt diet to help reduce the amount of urine your kidneys make. You'll also need to drink enough water to avoid dehydration. The drug hydrochlorothiazide, used alone or with other medications, may improve symptoms. Although hydrochlorothiazide is a diuretic (usually used to increase urine output), in some cases it can reduce urine output for people with nephrogenic diabetes insipidus. If symptoms from nephrogenic diabetes insipidus are due to medications you're taking, stopping these medicines may help; however, don't stop taking any medication without first talking to your doctor.  Gestational diabetes insipidus. Treatment for most cases of gestational diabetes insipidus is with the synthetic hormone desmopressin. In rare cases, this form of the condition is caused by an abnormality in the thirst mechanism. In these rare cases, doctors don't prescribe desmopressin.