Addison's disease

Overview

Addison’s disease - also known as primary adrenal insufficiency or hypoadrenalism - is a rare disorder of the adrenal glands.

The adrenal glands are two small glands that sit on top of the kidneys. They produce two essential hormones: cortisol and aldosterone.

The adrenal gland is damaged in Addison's disease, so it does not produce enough cortisol and aldosterone.

About 8,400 people in the UK have Addison's disease. It can affect people of any age, although it's most common between the ages of 30 and 50. It is also more common in women than men.

Early-stage symptoms of Addison’s disease are similar to other more common health conditions such as depression or flu. You may experience:

  • fatigue (lack of energy or motivation)
  • muscle weakness
  • low mood
  • loss of appetite and unintentional weight loss
  • increased thirst

Over time, these problems may become more severe and you may experience further symptoms, such as dizziness, fainting, cramps and exhaustion. You may also develop small areas of darkened skin, or darkened lips or gums.

Although these symptoms aren’t always caused by Addison’s disease, you should see your GP if you have them so they can be investigated.

Read more about the symptoms of Addison’s disease and diagnosing Addison’s disease.

Why it happens

The condition is usually the result of a problem with the immune system, which causes it to attack the outer later of the adrenal gland (the adrenal cortex), disrupting the production of the steroid hormones aldosterone and cortisol. It is not clear why this happens, but it is responsible for 70-90% of cases in the UK.

Other potential causes include conditions that can damage the adrenal glands, such as tuberculosis (TB), although this is uncommon in the UK.

Read more about the causes of Addison’s disease.

Treating Addison's disease

Addison’s disease is treated with medication to replace the missing hormones. You will need to take the medication for the rest of your life.

With treatment, symptoms of Addison's disease can largely be controlled. Most people with the condition have a normal lifespan and are able to live an active life, with few limitations.

However, many people with Addison's disease also find they must learn to manage bouts of fatigue and there may be associated health conditions, such as diabetes or an underactive thyroid.

People with Addison's disease must be constantly aware of the risk of a sudden worsening of symptoms, called an adrenal crisis. This can happen when the levels of cortisol in your body fall significantly.

An adrenal crisis is a medical emergency. If left untreated it can be fatal. If you or someone you know has Addison’s disease and is experiencing severe symptoms, dial 999 to request an ambulance.

Information about you

If you have Addison's disease, your clinical team will pass information about you on to the National Congenital Anomaly and Rare Diseases Registration Service (NCARDRS).

This helps scientists look for better ways to prevent and treat this condition. You can opt out of the register at any time.

Find out more about the register.

Symptoms

Addison's disease can be difficult to detect at first because early symptoms are similar to symptoms of many other health conditions.

The initial symptoms of Addison's disease include:

  • fatigue (lack of energy or motivation)
  • lethargy (abnormal drowsiness or tiredness)
  • muscle weakness
  • low mood (mild depression) or irritability
  • loss of appetite and unintentional weight loss
  • the need to urinate frequently
  • increased thirst
  • craving for salty foods

Dehydration can also be an early sign of Addison’s disease. It is caused by the lack of the hormone aldosterone in your body, which is used to regulate the balance of salt and water.

Later symptoms

Further symptoms of Addison’s disease tend to develop gradually over months or years. However, additional stress, caused by another illness or an accident, for example, may cause your symptoms to suddenly get worse.

You may go on to develop:

  • low blood pressure when you stand up, which can cause dizziness and fainting
  • feeling sick (nausea)
  • vomiting
  • diarrhoea
  • abdominal, joint or back pain
  • muscle cramps
  • chronic exhaustion, which may cause depression
  • brownish discolouration of the skin, lips and gums (hyperpigmentation), particularly in the creases on your palms, on scars or on pressure points, such as your knuckles or knees
  • a reduced libido (a lack of interest in sex), particularly in women

Some women may also have irregular periods or miss some periods completely. Children with Addison's disease may experience puberty later than usual.

Some people with Addison's disease also develop low blood sugar (hypoglycaemia). This can cause symptoms such as difficulty concentrating, confusion, anxiety and even unconsciousness (particularly in children).

If you're experiencing these symptoms of Addison's disease, see your GP so that they can diagnose or rule out the condition. These symptoms will usually improve with appropriate treatment.

Adrenal crisis

If Addison’s disease is left untreated, the levels of hormones produced by the adrenal gland gradually decrease in the body. This will cause the symptoms to get progressively worse and eventually lead to a life-threatening situation that is known as an adrenal or Addisonian crisis.

During an adrenal crisis the symptoms of Addison’s disease appear quickly and severely. This could happen when you're already experiencing initial symptoms or without any symptoms at all.

Signs of an adrenal crisis include:

An adrenal crisis is a medical emergency. If left untreated it can be fatal. If you suspect you or someone you know with Addison’s disease is having an adrenal crisis, dial 999 to request an ambulance.

If an adrenal crisis is not treated, it can lead to a coma and death. There is also a risk your brain will not get enough oxygen if treatment is delayed, which can cause permanent disability.

Who can get it

Addison's disease develops when the outer layer of your adrenal glands (your adrenal cortex) is damaged, reducing the levels of hormones it produces.

Problems with the immune system

In the UK, a problem with the immune system is the most common cause of Addison's disease, accounting for 70-90% of cases.

The immune system is your body’s defence against infection and disease. If you're ill, your immune system produces antibodies (a special type of protein that destroys disease-carrying organisms and toxins). These antibodies attack the cause of the illness.

However, if you develop a problem with your immune system, it can start to attack your own healthy tissues and organs. This is known as an autoimmune disorder.

Addison’s disease can develop if your immune system attacks your adrenal glands and severely damages your adrenal cortex.

When 90% of the adrenal cortex is destroyed, your adrenal glands won't be able to produce enough of the steroid hormones cortisol and aldosterone. Once levels of these start decreasing, you'll experience symptoms of Addison’s disease.

It's not clear why some people develop this problem with their immune system, although it can run in families.

Genetics

Research has shown that some people with certain genes are more likely to develop autoimmune disorders.

It's not clear how these genes lead to Addison's disease and similar conditions, but it does mean your risk of developing Addison's disease is increased if you or a close family member have another autoimmune condition, such as:

  • vitiligo: a long-term condition that causes pale, white patches to develop on the skin
  • type 1 diabetes: a long-term condition caused by your body not producing insulin
  • hypothyroidism: an underactive thyroid gland

Other causes

Tuberculosis (TB) is the most common cause of Addison's disease worldwide, but is rare in the UK.

TB is a bacterial infection that mostly affects the lungs, but can also spread to other parts of your body. It can cause Addison’s disease if it damages your adrenal glands.

Other possible causes of Addison’s disease include:

  • infections: such as those that are linked to AIDS, or fungal infections
  • a haemorrhage: very heavy bleeding into the adrenal glands, sometimes associated with meningitis or other severe sepsis
  • cancer: if cancer cells from elsewhere in your body spread to your adrenal glands
  • amyloidosis: a disease where amyloid, a protein that is produced by the cells in your bone marrow, builds up in your adrenal glands and damages them
  • surgical removal of the adrenal glands (adrenalectomy), for example to remove a tumour
  • adrenoleukodystrophy (ALD) – a rare, life-limiting, inherited condition affecting the adrenal glands and nerve cells in the brain that most often affects young boys
  • certain treatments needed for Cushing's syndrome – a collection of symptoms caused by very high levels of cortisol in the body

Secondary adrenal insufficiency

The production of hormones from the adrenal gland can also be affected by damage to the pituitary gland – a pea-sized gland located below the brain that produces a hormone that stimulates the adrenal gland. This is called secondary adrenal insufficiency and is a separate condition to Addison's disease.

Secondary adrenal insufficiency can occur if your pituitary gland becomes damaged – for example, because of a tumour on the pituitary gland (pituitary adenoma).

Diagnosis

To help diagnose Addison’s disease, your GP will first ask about your symptoms and review your medical history.

They're also likely to ask if anyone in your family has an autoimmune disorder (a condition caused by a problem with their immune system).

Your GP will examine your skin for any evidence of brownish discolouration (hyperpigmentation), particularly in certain areas, such as:

  • where skin creases on your palm
  • in your elbow crease
  • on any scars
  • your lips and gums

However, hyperpigmentation doesn't occur in all cases of Addison’s disease.

You will also be tested for low blood pressure (hypotension); while you're lying down and again shortly after you stand up. This is to see whether you have postural or orthostatic hypotension (low blood pressure when you change position).

Blood tests

If Addison’s disease is suspected, blood tests will be carried out to measure the levels of sodium, potassium and cortisol in your body. A low sodium, high potassium or low cortisol level may indicate Addison’s disease.

You may need to see a hospital hormone specialist (endocrinologist) for your blood to be tested for the following:

  • a low level of the hormone aldosterone
  • a high level of adrenocorticotrophic hormone (ACTH)
  • a low level of glucose (sugar used for energy)
  • positive adrenal antibodies (antibodies designed to attack the adrenal gland)

Any of the above could be a sign of Addison’s disease.

Synacthen stimulation test

If cortisol in your blood is low, or your symptoms strongly suggest Addison’s disease, you'll need to have a synacthen stimulation test to confirm the diagnosis.

Your GP may refer you to an endocrinology unit (a unit that specialises in the study of hormones) for the test. How urgently you're referred depends on how severe your symptoms are.

Synacthen is a man-made (synthetic) copy of the adrenocorticotrophic hormone (ACTH). ACTH is naturally produced by the pituitary gland (a pea-sized gland below the brain) to encourage the adrenal glands to release the hormones cortisol and aldosterone.

When synacthen is administered, the adrenal glands should respond in the same way as they would to ACTH, and release cortisol and other steroid hormones into the blood.

A blood sample will be taken and tested for cortisol, before an injection of synacthen is given into your arm. After 30 and 60 minutes, a further blood sample will be taken for cortisol measurement.

If the ACTH level is high, but the cortisol and aldosterone levels are low, it's usually confirmation of Addison’s disease.

Thyroid function test

Your thyroid gland may also be tested to see if it's working properly.

Your thyroid gland is found in your neck. It produces hormones that control your body's growth and metabolism.

People with Addison’s disease often have an underactive thyroid gland (hypothyroidism), where the thyroid gland does not produce enough hormones.

By testing the levels of certain hormones in your blood, your endocrinologist (a specialist in hormone conditions) can determine whether you have hypothyroidism.

Scans

In some cases, your specialist may refer you for a scan of your adrenal glands – this could be a computerised tomography (CT) scan or a magnetic resonance imaging (MRI) scan.

Diagnosis during an adrenal crisis

If Addison’s disease is left untreated, it eventually leads to an adrenal crisis. This is where the symptoms of Addison’s disease appear quickly and severely.

During an adrenal crisis, there's not enough time to perform a synacthen stimulation test to confirm Addison’s disease.

If possible, blood will be taken and tested for any of the abnormalities listed above. While you're waiting for the results, treatment may be started with steroid injections, and fluids containing salt and glucose.

Read more about how Addison’s disease is treated.

Driving

If you're diagnosed with Addison's disease and have a bus, coach or lorry licence, it's your legal obligation to inform the Driver and Vehicle Licensing Agency (DVLA).

Read about driving and Addison's disease on the GOV.UK website.

Treatment

If you have Addison’s disease, you'll need to take daily medication to replace the lost hormones. This should help you to live an active life, although many people find they still need to manage their fatigue.

Sometimes, the underlying causes of Addison’s disease can be treated. For example, tuberculosis (TB) is treated with a course of antibiotics over a period of at least six months.

However, most cases are caused by a problem with the immune system that can't be cured.

Medication for Addison’s disease

Treatment usually involves corticosteroid (steroid) replacement therapy for life. Corticosteroid medication is used to replace the hormones cortisol and aldosterone that your body no longer produces. It's usually taken in tablet form 2 or 3 times a day.

A medication called hydrocortisone is usually used to replace the cortisol. Other possible medicines are prednisolone or dexamethasone, although these are less commonly used.

Aldosterone is replaced with a medication called fludrocortisone. Your GP may also ask you to add extra salt to your daily diet, although if you're taking enough fludrocortisone medicine this may not be necessary. Unlike most people, if you feel the urge to eat something salty, then you should eat it.

Some people take dehydroepiandrosterone (DHEA) to improve their stamina or libido (sex drive). It's not available on prescription as it's a classed as a food supplement, but it's available to buy from pharmacies or health food shops.

If you experience symptoms that you believe may benefit from DHEA, speak to your GP. They can arrange blood tests and recommend the correct dose for you.

In general, the medicines used for Addison's disease do not have side effects, unless your dose is too high. If you take a higher dose than necessary for a long time, there's a risk of problems such as weakened bones (osteoporosis), mood swings and difficulty sleeping (insomnia).

Living with Addison’s disease

Many people with Addison's disease find that taking their medication enables them to continue with their normal diet and exercise routines.

However, bouts of fatigue are also common, and it can take some time to learn how to manage these periods of low energy.

Some people find that needing to take regular doses of medication is restrictive and affects their daily life or emotional health. Missing a dose of medication, or taking it late, can also lead to exhaustion or insomnia.

Some people can develop associated health conditions, such as diabetes or an underactive thyroid, which require extra treatment and management.

You'll usually need to have appointments with an endocrinologist every 6 to 12 months so they can review your progress and adjust your medication dose, if necessary. Your GP can provide support and repeat prescriptions in between these visits.

Failing to take your medication could lead to a serious condition called an adrenal crisis, so you must:

  • remember to collect your repeat prescriptions
  • keep spare medication as necessary – for example, in the car or at work, and always carry some spare medication with you
  • take your medication every day at the right time
  • pack extra medication if you're going away – usually double what you would normally need, plus your injection kit (see below)
  • carry your medication in your hand luggage if you are travelling by plane, with a note from your doctor explaining why it is necessary
  • carry a steroid emergency card or download one onto your mobile phone

You could also inform close friends or colleagues of your condition. Tell them about the signs of adrenal crisis and what they should do if you experience one.

NHS steroid emergency card

If you have Addison's disease, you'll need to take steroids on a long-term basis, so you should keep a steroid emergency card with you at all times.

The card will make healthcare professionals aware you're taking steroids if you're admitted to hospital in an emergency. This means they'll be able to make sure you get any treatment you need appropriately and quickly.

The card describes the steps that need to be taken in an emergency. It also has a QR code that links to further specialist advice. You can download and carry it with you, or you could use the image of the card as a screensaver on your mobile phone to show healthcare teams in an emergency.

Medical alert bracelets

It's also a good idea to wear a medical alert bracelet or necklace that informs people you have Addison's disease.

After a serious accident, such as a car crash, a healthy person produces more cortisol. This helps you cope with the stressful situation and additional strain on your body that results from serious injury. As your body cannot produce cortisol, you'll need a hydrocortisone injection to replace it and prevent an adrenal crisis.

Wearing a medical alert bracelet will inform any medical staff treating you about your condition and what medication you require.

Medical alert bracelets or necklaces are pieces of jewellery engraved with your medical condition and an emergency contact number. They are available from a number of retailers. Ask your GP if there's one they recommend, or go to the MedicAlert website.

If you need to stay in hospital, the healthcare professionals responsible for your care will also need to know you need steroid replacement medication throughout your stay. It's important to note that this advice still applies even if you're not supposed to eat or drink (nil by mouth) for any reason.

Adjusting your medication

At certain times, your medication may need to be adjusted to account for any additional strain on your body. For example, you may need to increase the dosage of your medication if you experience any of the following:

  • an illness or infection - particularly if you have a high temperature of 38 or above
  • an accident, such as a car crash
  • an operation, dental or medical procedure (e.g. tooth filling, endoscopy)
  • strenuous exercise which is not usually part of your daily life
  • Severe emotional or psychological stress, such as grief

This will help your body cope with the additional stress. Your endocrinologist will monitor your dosage and advise about any changes.

Over time, as you get used to the condition and learn what can trigger your symptoms, you may learn how to adjust your medication yourself. However, always consult your GP or specialist if you're unsure.

Sick day rules

Your endocrinologist can advise you on "sick day rules". This is when you increase your medicine dose to keep you well during periods of stress, illness or injury. If you do not increase your dose at these times, you may experience an adrenal crisis. Extra doses help your body to respond.

The ADSHG advises you always to have 3 months' supply available of your essential steroid medicine. This is in case you need to increase your dose to follow your sick day rules, or to cover if there is a shortage of your medicine.

Emergency treatment

You and a partner or family member may be trained to administer an injection of hydrocortisone in an emergency.

This could be necessary if you go into shock after an injury, or if you experience vomiting or diarrhoea and are unable to keep down oral medication. This may occur if you're pregnant and have morning sickness. Your endocrinologist will discuss with you when an injection might be necessary.

If you need to administer emergency hydrocortisone, always call your GP immediately afterwards. Check what out-of-hours services are available in your local area, in case the emergency is outside normal working hours.

You can also register yourself with your local ambulance service, so they have a record of your requirement for a steroid injection or tablets, if you need their assistance.

Treating adrenal crisis

Adrenal crisis, or Addisonian crisis, needs urgent medical attention.

If you or someone you know with Addison's disease is having an adrenal crisis, they will need a hydrocortisone injection immediately, either injected by themselves or by a person who is with them.

Then call 999 for an ambulance, saying it's an "adrenal crisis" or "Addisonian crisis".

Signs of an adrenal crisis include:

  • severe dehydration
  • pale, cold, clammy skin
  • sweating
  • rapid, shallow breathing
  • dizziness
  • low blood pressure (hypotension)
  • severe vomiting and diarrhoea
  • abdominal pain or paininthe side
  • fatigue and severe muscle weakness
  • headache
  • severe drowsiness or loss of consciousness

In hospital, you'll be given lots of fluid through a vein in your arm to rehydrate you. This will contain a mixture of salts and sugars (sodium, glucose and dextrose) to replace what your body is lacking. You'll also be injected with hydrocortisone to replace the missing cortisol hormone.

Any underlying causes of the adrenal crisis, such as an infection, will also be treated.



The information on this page has been adapted by NHS Wales from original content supplied by NHS UK NHS website nhs.uk
Last Updated: 05/07/2023 13:29:27