Symplicured

Endocrine

Addison's Disease

Also known as: Primary Adrenal Insufficiency (Addison's Disease)

Addison's disease occurs when the adrenal glands do not produce enough cortisol and often aldosterone. It is a rare but serious condition that requires lifelong hormone replacement.

Understanding Addison's Disease

Addison's disease affects approximately 1 in 10,000 people. In developed countries, autoimmune destruction accounts for 80-90% of cases. In developing countries, tuberculosis remains a leading cause.

The adrenal glands produce cortisol (essential for stress response, metabolism, and immune function) and aldosterone (regulating salt and water balance). Loss of these hormones is life-threatening without replacement.

Adrenal crisis can be triggered by illness, surgery, or missing medication — patients must carry emergency injection kits and medical alert identification.

Common Symptoms

People with Addison's Disease often experience the following symptoms.

Hyperpigmentation

Darkening of skin, particularly in creases, scars, and mucous membranes, from excess ACTH stimulating melanocytes.

Chronic Fatigue

Profound, progressive fatigue that worsens with activity and is not relieved by rest.

Salt Craving

Intense craving for salty foods from aldosterone deficiency and sodium loss.

Postural Hypotension

Dizziness upon standing due to low blood volume and impaired vascular tone.

Risk Factors

Certain factors may increase your likelihood of developing Addison's Disease.

Autoimmune conditions

Age 30-50

Female sex

Tuberculosis (in developing countries)

Treatment Options

Common approaches to managing addison's disease. Always consult a healthcare provider for personalized treatment.

Hydrocortisone Replacement

Oral hydrocortisone taken 2-3 times daily to mimic the natural cortisol circadian rhythm.

Fludrocortisone

Mineralocorticoid replacement for aldosterone deficiency, maintaining salt and water balance.

Stress Dosing

Doubling or tripling hydrocortisone during illness, injury, or surgery to prevent adrenal crisis.

Emergency Injection Kit

Injectable hydrocortisone for patients to carry for emergency use when oral medication cannot be taken.

How It's Diagnosed

Morning cortisol (low), ACTH (elevated in primary), ACTH stimulation test (inadequate cortisol response), and adrenal antibodies for autoimmune cause.

When to See a Doctor

Seek emergency care for adrenal crisis: severe weakness, confusion, low blood pressure, vomiting, and loss of consciousness. This is life-threatening without immediate treatment.

Prevention Strategies

Steps that may help reduce the risk of developing or worsening addison's disease.

No prevention for autoimmune Addison's

Always carry emergency steroid injection

Wear medical alert identification

Educate family on crisis management

Potential Complications

If left untreated or poorly managed, addison's disease may lead to:

  • Adrenal crisis (life-threatening)
  • Osteoporosis from over-replacement
  • Associated autoimmune conditions
  • Psychological impact

Frequently Asked Questions

Is Addison's disease life-threatening?

Without treatment, yes. With proper hormone replacement, most patients live normal lives. Adrenal crisis is the main danger.

Can Addison's be cured?

No. Lifelong hormone replacement is required. The autoimmune destruction is irreversible.

What triggers an adrenal crisis?

Illness, surgery, dehydration, missing medication, or any physical stress without adequate cortisol coverage.

Think you might have Addison's Disease?

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This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition.

Addison's Disease — Symptoms, Causes & Treatment | Symplicured | Symplicured