It has been suggested that Autoimmune adrenalitis be merged into this article or section. (Discuss)
Classification and external resources
Addison’s disease (also chronic adrenal insufficiency, hypocortisolism, and hypocorticism) is a rare, chronic endocrine disorder wherein the adrenal glands produce insufficient steroid hormones (glucocorticoids and often mineralocorticoids).. Lifelong, continuous treatment with steroid replacement therapy is required, with regular follow-up treatment and monitoring for other health problems.
It is generally diagnosed via blood tests and medical imaging. Treatment involves replacing the absent hormones (oral hydrocortisone and fludrocortisone).
Addison’s disease is named after Dr. Thomas Addison, the British physician who first described the condition in On the Constitutional and Local Effects of Disease of the Suprarenal Capsules (1849). The adjective “Addisonian” describes features of the condition, and patients suffering Addison’s disease. While Addison’s six patients in 1855 all had adrenal tuberculosis, the term “Addison’s disease” does not imply an underlying disease process.
• 1 Signs and symptoms
o 1.1 Symptoms
o 1.2 Clinical signs
o 1.3 Addisonian crisis
• 2 Causes
o 2.1 Adrenal dysgenesis
o 2.2 Impaired steroidogenesis
o 2.3 Adrenal destruction
• 3 Diagnosis
o 3.1 Suggestive features
o 3.2 Testing
• 4 Treatment
o 4.1 Maintenance
o 4.2 Crisis
• 5 Epidemiology
• 6 Prognosis
• 7 Famous Addisonians
• 8 In other animals
• 9 See also
• 10 References
• 11 External links
Signs and symptoms
The symptoms of Addison’s disease develop insidiously, and it may take some time to be recognized. The most common symptoms are fatigue, lightheadedness upon standing or while upright, muscle weakness, fever, weight loss, difficulty in standing up, anxiety, nausea, vomiting, diarrhea, headache, sweating, changes in mood and personality, joint and muscle pains. Some have marked cravings for salt or salty foods due to the urinary losses of sodium. Affected individuals may note increased tanning since adrenal insufficiency is manifested in the skin primarily by hyperpigmentation.:501
The negative feedback loop for glucocorticoids. Because primary hypocortisolism is manifested as a deficiency in glucocorticoid release from the adrenal cortex, increased ACTH will be released by the pituitary in order to trigger release of the absent glucocorticoid; it is because of this overstimulation of ACTH that bronzing of the skin occurs. In secondary or tertiary hypocortisolism, there is a deficiency of either CRH or ACTH release by the hypothalamus or pituitary gland, respectively. The former will manifest as no ACTH release while the latter will manifest as physiologic (normal) ACTH release; neither will cause an overproduction of ACTH.
On examination, the following may be noticed:
• Low blood pressure that falls further when standing (orthostatic hypotension)
• In long-standing Addison’s Disease, the pinna of the ear may become calcified
• Most people with primary Addison’s have darkening (hyperpigmentation) of the skin, including areas not exposed to the sun; characteristic sites are skin creases (e.g. of the hands), nipple, and the inside of the cheek (buccal mucosa), also old scars may darken. This occurs because melanocyte-stimulating hormone (MSH) and adrenocorticotropic hormone (ACTH) share the same precursor molecule, Pro-opiomelanocortin (POMC). After production in anterior pituitary gland, POMC gets cleaved into Gamma-MSH, ACTH and Beta-lipotropin. The subunit ACTH undergoes further cleavage to produce Alpha-MSH, the most important MSH for skin pigmentation. In secondary and tertiary forms of Addison’s, skin darkening does not occur.
• Medical conditions such as type I diabetes, autoimmune thyroid disease (Hashimoto’s thyroiditis and goiter) and vitiligo often occur together with Addison’s (often in the setting of Autoimmune polyendocrine syndrome). Hence, symptoms and signs of any of the former conditions may also be present in the individual with Addison’s. The occurrence of Addison’s Disease in someone who also has Hashimoto’s thyroiditis is called Schmidt syndrome.
An “Addisonian crisis” or “adrenal crisis” is a constellation of symptoms that indicate severe adrenal insufficiency. This may be the result of either previously undiagnosed Addison’s disease, a disease process suddenly affecting adrenal function (such as adrenal hemorrhage), or an intercurrent problem (e.g. infection, trauma) in someone known to have Addison’s disease. It is a medical emergency and potentially life-threatening situation requiring immediate emergency treatment.
Characteristic symptoms are:
• Sudden penetrating pain in the legs, lower back or abdomen
• Severe vomiting and diarrhea, resulting in dehydration
• Low blood pressure
• Syncope (loss of consciousness and ability to stand)
• Confusion, psychosis, slurred speech
• Severe lethargy
Causes of adrenal insufficiency can be grouped by the way they cause the adrenals to produce insufficient cortisol. These are adrenal dysgenesis (the gland has not formed adequately during development), impaired steroidogenesis (the gland is present but is biochemically unable to produce cortisol) or adrenal destruction (disease processes leading to the gland being damaged).
All causes in this category are genetic, and generally very rare. These include mutations to the SF1 transcription factor, congenital adrenal hypoplasia (AHC) due to DAX-1 gene mutations and mutations to the ACTH receptor gene (or related genes, such as in the Triple A or Allgrove syndrome). DAX-1 mutations may cluster in a syndrome with glycerol kinase deficiency with a number of other symptoms when DAX-1 is deleted together with a number of other genes.
To form cortisol, the adrenal gland requires cholesterol, which is then converted biochemically into steroid hormones. Interruptions in the delivery of cholesterol include Smith-Lemli-Opitz syndrome and abetalipoproteinemia.
Of the synthesis problems, congenital adrenal hyperplasia is the most common (in various forms: 21-hydroxylase, 17α-hydroxylase, 11β-hydroxylase and 3β-hydroxysteroid dehydrogenase), lipoid CAH due to deficiency of StAR and mitochondrial DNA mutations. Some medications interfere with steroid synthesis enzymes (e.g. ketoconazole), while others accelerate the normal breakdown of hormones by the liver (e.g. rifampicin, phenytoin).
Autoimmune adrenalitis is the most common cause of Addison’s disease in the industrialized world. Autoimmune destruction of the adrenal cortex is cause by an immune reaction against the enzyme 21-hydroxylase (a phenomenon first described in 1992). This may be isolated or in the context of autoimmune polyendocrine syndrome (APS type 1 or 2), in which other hormone-producing organs such as the thyroid and pancreas may also be affected..
Adrenal destruction is also a feature of adrenoleukodystrophy (ALD), and when the adrenal glands are involved in metastasis (seeding of cancer cells from elsewhere in the body, especially lung), hemorrhage (e.g. in Waterhouse-Friderichsen syndrome or antiphospholipid syndrome), particular infections (tuberculosis, histoplasmosis, coccidioidomycosis), deposition of abnormal protein in amyloidosis.
Routine investigations may show:
• Hypoglycemia, low blood sugar (worse in children due to loss of glucocorticoid’s glucogenic effects)
• Hyponatraemia (low blood sodium levels), due both to a deficiency in Aldosterone (a mineralocorticoid) dependant Sodium retention and also the effect of Corticotropin-releasing hormone to stimulate secretion of ADH
• Hyperkalemia (raised blood potassium levels), due to loss of production of the hormone aldosterone
• Eosinophilia and lymphocytosis (increased number of eosinophils or lymphocytes, two types of white blood cells)
• Metabolic acidosis (increased blood acidity), also due to loss of the hormone aldosterone because sodium reabsorption in the distal tubule is linked with acid/hydrogen ion (H+) secretion. Low levels of aldosterone stimulation of the renal distal tubule leads to sodium wasting in the urine and H+ retention in the serum.
In suspected cases of Addison’s disease, one needs to demonstrate that adrenal hormone levels are low even after appropriate stimulation (called the ACTH stimulation test) with synthetic pituitary ACTH hormone tetracosactide . Two tests are performed, the short and the long test.
The short test compares blood cortisol levels before and after 250 micrograms of tetracosactide (IM/IV) is given. If, one hour later, plasma cortisol exceeds 170 nmol/L and has risen by at least 330 nmol/L to at least 690 nmol/L, adrenal failure is excluded. If the short test is abnormal, the long test is used to differentiate between primary adrenal failure and secondary adrenocortical failure.
The long test uses 1 mg tetracosactide (IM). Blood is taken 1, 4, 8, and 24 hours later. Normal plasma cortisol level should reach 1000 nmol/L by 4 hours. In primary Addison’s disease, the cortisol level is reduced at all stages whereas in secondary corticoadrenal insufficiency, a delayed but normal response is seen.
Other tests that may be performed to distinguish between various causes of hypoadrenalism are renin and adrenocorticotropic hormone levels, as well as medical imaging – usually in the form of ultrasound, computed tomography or magnetic resonance imaging (MRI).
Adrenoleukodystrophy, and the milder form, adrenomyeloneuropathy, cause adrenal insufficiency combined with neurological symptoms. These diseases are estimated to be the cause of adrenal insufficiency in approximately 35% of male patients with idiopathic Addison’s disease and should be considered in the differential diagnosis of any male with adrenal insufficiency. Diagnosis is made by a blood test to detect very long chain fatty acids (VLCFA).
Treatment for Addison’s disease involves replacing the missing cortisol, sometimes in the form of hydrocortisone tablets, or prednisone tablets in a dosing regimen that mimics the physiological concentrations of cortisol. Alternatively one quarter as much prednisolone may be used for equal glucocorticoid effect as hydrocortisone. Treatment must usually be continued for life. In addition, many patients require fludrocortisone as replacement for the missing aldosterone. Caution must be exercised when the person with Addison’s disease becomes unwell with infection, has surgery or other trauma, or becomes pregnant. In such instances, their replacement glucocorticoids, whether in the form of hydrocortisone, prednisone, prednisolone, or other equivalent, often need to be increased. Inability to take oral medication may prompt hospital attendance to receive steroids intravenously. People with Addison’s are often advised to carry information on them (e.g. in the form of a MedicAlert bracelet) for the attention of emergency medical services personnel who might need to attend to their needs.
Standard therapy involves intravenous injections of glucocorticoids and large volumes of intravenous saline solution with dextrose, a type of sugar. This treatment usually brings rapid improvement. When the patient can take fluids and medications by mouth, the amount of glucocorticoids is decreased until a maintenance dose is reached. If aldosterone is deficient, maintenance therapy also includes oral doses of fludrocortisone acetate. 
The frequency rate of Addison’s disease in the human population is sometimes estimated at roughly 1 in 100,000. Some research and information sites put the number closer to 40-60 cases per 1 million population. (1/25,000-1/16,600) (Determining accurate numbers for Addison’s is problematic at best and some incidence figures are thought to be underestimates.) Addison’s can afflict persons of any age, gender, or ethnicity, but it typically presents in adults between 30 and 50 years of age. Research has shown no significant predispositions based on ethnicity.
With proper medication, patients can expect to live a healthy and normal life.
A person with adrenal insufficiency should always carry identification stating their condition in case of an emergency. The card should alert emergency personnel about the need to inject 100 mg of cortisol if its bearer is found severely injured or unable to answer questions. The card should also include the doctor’s name and telephone number and the name and telephone number of the nearest relative to be notified. When traveling, a needle, syringe, and an injectable form of cortisol should be carried for emergencies. A person with Addison’s disease also should know how to increase medication during periods of stress or mild upper respiratory infections. Immediate medical attention is needed when severe infections, vomiting, or diarrhea occur, as these conditions can precipitate an Addisonian crisis. A patient who is vomiting may require injections of hydrocortisone, since oral hydrocortisone supplements cannot be adequately metabolised.
United States president John F. Kennedy (1961-63), probably the single most famous case of Addison’s Disease
• United States President John F. Kennedy was one of the best-known Addison’s disease sufferers. He was possibly one of the first Addisonians to survive major surgery. There was substantial secrecy surrounding his health during his years as president, and the 25th amendment to the U.S. constitution was introduced at least in part as a result of this secrecy.
• Eunice Kennedy Shriver, one of John F. Kennedy’s sisters, was believed to have Addison’s disease as well.
• Popular singer Helen Reddy.
• Scientist Eugene Merle Shoemaker, co-discoverer of the Comet Shoemaker-Levy 9.
• French Carmelite nun and religious writer Blessed Elizabeth of the Trinity
• American artist Ferdinand Louis Schlemmer died from Addison’s disease.
• Some have suggested that Jane Austen was an avant la lettre case, but others have disputed this.
• According to Dr. Carl Abbott, a Canadian medical researcher, Charles Dickens may also have been affected.
• Osama bin-Laden may be an Addisonian. Lawrence Wright noted that bin-Laden manifests all the key symptoms, such as “low blood pressure, weight loss, muscle fatigue, stomach irritability, sharp back pains, dehydration, and an abnormal craving for salt”. Bin-Laden is known to have consumed large amounts of the drug Sulbutiamine to treat his symptoms.
In other animals
Main article: Addison’s disease in canines
The condition has been diagnosed in all breeds of dogs. In general, it is underdiagnosed, and one must clinically suspect it as an underlying disorder for many presenting complaints. Females are overrepresented, and the disease often appears in middle age (4–7 years), although any age or gender may be affected. Genetic continuity between dogs and humans helps to explain the occurrence of Addison’s disease in both species.
Hypoadrenocorticism is treated with fludrocortisone or a monthly injection called Percorten V (desoxycorticosterone pivlate (DOCP)) and prednisone. Routine blood work is necessary in the initial stages until a maintenance dose is established.
Most of the medications used in the therapy of hypoadrenocorticism cause excessive thirst and urination, making it important to provide enough drinking water.
If the owner knows about an upcoming stressful situation (shows, traveling etc.), patients generally need an increased dose of prednisone to help deal with the added stress. Avoidance of stress is important for dogs with hypoadrenocorticism.
• ACTH stimulation test
• Cushing’s syndrome
• Addison’s disease in canines