Systemic lupus erythematosus
What is systemic lupus erythematosus?
Lupus erythematosus (LE) is a group of diverse persistent autoimmune inflammatory diseases. Systemic lupus erythematosus (SLE) affects several organs (such as skin, joints and kidneys) and blood tests reveal circulating autoantibodies. The clinical features of SLE are highly variable and may overlap with other diseases and conditions. Skin involvement or cutaneous lupus (CLE) affects 80% of patients with SLE.
What causes systemic lupus erythematosus?
Factors leading to SLE include:
- Genetic predisposition, incuding haplotype HLA-B8, -DR3
- Exposure to sunlight
- Viral infection, particularly Epstein-Barr virus
- Toxins such as cigarette smoke
- Drugs in drug-induced LE
- Emotional upset
The manifestations of SLE are due to loss of regulation of the patient's immune system.
- Nuclear proteins are not processed properly.
- Nuclear debris accumulates within the cell.
- This leads to production of autoantibodies against nuclear proteins.
- Immune complexes are not removed.
- The complement system is activated.
- Inflammation leads to cell and/or tissue injury.
Who gets systemic lupus erythematosus?
SLE can affect males and females of any age. Every year about 2 to 7 new cases are diagnosed in a population of 100,000 people. SLE is much more common in females than males, and onset is most often between the ages of 15 and 45 years.
Autoantibodies can be present in people that have no manifestation of the disease.
Cutaneous features of SLE
About 80% of patients with SLE have skin involvement (cutaneous LE) and it is the first sign of SLE in about one quarter of them. It can present as LE-specific or LE-nonspecific manifestations. LE-specific lesions tend to be induced or aggravated by exposure to ultraviolet radiation and are localised in sun-exposed sites such as face, neck, V of neck and upper back.
Specific cutaneous SLE
Cutaneous lupus (CLE) has specific acute, subacute and chronic manifestations described in the table below. Typically, SLE presents with acute CLE. About half of patients with subacute CLE develop mild SLE but only 5% of patients with chronic CLE to have SLE, ie these are usually skin problems without involvement of other organs.
|Acute CLE||Subacute CLE||Chronic CLE|
Nonspecific cutaneous SLE
Nonspecific cutaneous SLE refers to features relating to underlying illness rather than an autoimmune attack. These features may occur in other autoimmune or connective tissue diseases.
- Nail fold capillary telangiectasia
- Raynaud phenomenon (white fingers and toes on exposure to the cold)
- Vasculopathy of tips of digits (occlusion of small blood vessels by thrombus)
- Diffuse hair thinning without brittle hair
- Urticaria, which may be neutrophilic on biopsy
- Cutaneous vasculitis: palpable purpura or urticarial vasculitis
- Livedo reticularis (a network pattern of blood vessels) in 20–30% patients with SLE
- Papular mucinosis (deposits of mucin in skin)
- Calcinosis cutis (deposits of calcium in skin)
Nonspecific cutaneous lupus erythematosus
What are the systemic features of systemic lupus erythematosus?
Numerous systemic features may occur in SLE and can result in critical illness. Specific involvement of various organs is described in the table below.
|General||Tiredness, malaise, chronic pain, fever with flares|
|Joints||Arthritis or synovitis causing swelling, pain and morning stiffness|
|Lungs||Pleurisy or pleural effusions|
|Heart||Pericarditis or pericardial effusions|
|Kidneys||Protein, casts in urine, glomerulonephritis|
|Brain||Seizures, psychosis, confusion|
|Nervous system||Mononeuritis multiplex, myelitis, peripheral neuropathy|
|Blood||Reduced numbers of red cells, white cells and platelets|
How is systemic lupus erythematosus diagnosed?
SLE can be difficult to diagnose at times because of the great variety of presentations of the disease, and the presence of similar symptoms in people that do not have the disease. Several attempts have been made to help clinicians reach the diagnosis, including the American College of Rheumatology criteria for the classification of SLE (revised in 1997). In 2012, the criteria were revised by the Systemic Lupus International Collaborating Clinics (SLICC).
Using the SLICC criteria, SLE is diagnosed if the patient has either of the following over time:
- 4 criteria including ≥1 clinical criterion and ≥1 immunological criterion
- Biopsy-proven lupus nephritis and antinuclear antibodies or anti-double-stranded DNA antibodies
These criteria depend on history, clinical examination, exclusion of other causes of the symptoms, and the results of investigations—including blood tests and biopsy of affected tissue. Four of the 17 SLICC criteria relate to the skin.
|Clinical criteria||Immunologic criteria|
* SLICC Systemic Lupus International Collaborating Clinics; ANA antinuclear antibody; anti-dsDNA anti–double-stranded DNA
Cutaneous Lupus Erythematosus Disease Area and Severity Index (CLASI)
The Cutaneous Lupus Erythematosus Disease Area and Severity Index (CLASI) was developed in an attempt to classify the severity of CLE.  A score of activity and damage due to the disease is calculated in each of 12 anatomical locations (refer to original published paper for details).
Total activity score is made up of:
- Degree of redness (0–3) and scale (0–2)
- Mucous membrane involvement (0–1)
- Recent hair loss (0–1), nonscarring alopecia (0–3)
Total damage score is made up of:
- The degree of dyspigmentation (0–2), and scarring (0–2)
- Persistence of dyspigmentation more than 12 months doubles the dyspigmentation score
- Scalp scarring (0,3,4,5,6)
Patients with SLE often undergo skin biopsy.
- Acute CLE: nonspecific dermatitis.
- Subacute CLE: features of lupus noted in epidermis and superficial dermis
- Chronic discoid CLE: typical features of lupus with atrophy and scarring
- Direct immunofluorescence is positive in sun-protected normal skin in SLE
Multiple autoantibodies are typically present in SLE, often in high titre (see immunologic criteria above). Relating to skin disease in SLE:
- About 70% of patients with subacute CLE have positive extractable nuclear antibodies anti-Ro (also called anti-SSA) and/or anti-La (also called anti-SSB).
- Anti Ro/La is also associated with Sjogren syndrome and neonatal lupus.
- Low serum complement in SLE has been associated with urticarial vasculitis and renal disease.
- Antiphospholipid antibodies are associated with livedo reticularis, thrombosis and pregnancy complications (antiphospholipid syndrome).
- Anti-annexin 1 antibodies may be a diagnostic marker for discoid CLE
Patients with SLE should also have renal, liver and thyroid function and markers of inflammation performed, such as C-reactive protein (CRP), immunoglobulins and rheumatoid factor.
Photoprovocation tests are sometimes carried out to confirm that a skin eruption is precipitated by exposure to particular wavelengths of ultraviolet or visible radiation.
Other tests depend on which organ is affected. They may, for example, include:
- Urine tests for hyaline casts, creatinine, protein and blood
- Blood pressure
- Chest X-ray, ultrasound, CT and MRI scans
- Electrocardiograph (ECG) and echocardiograph
- Nerve and muscle testing
- Ophthalmological examination
- Endoscopy of the gastrointestinal tract
- Kidney biopsy
What is the treatment for systemic lupus erythematosus?
The following measures are important to reduce the chance of flares and organ damage.
- Careful protection from sun exposure using clothing, accessories and SPF 50+ broad-spectrum sunscreens. Sunscreens alone are not adequate.
- Smoking cessation
- Rest when needed
Intermittent courses of potent topical corticosteroids are important in the treatment of CLE. They should be applied accurately to the skin lesions.
Treatment of SLE depends on which are the predominant organs involved in the disease. Typically, any of the following drugs may be used alone or in combination.
- Systemic corticosteroids such as prednisone or prednisolone. These are the mainstay of treatment in a seriously ill patient with acute LE.
- Hydroxychloroquine and other antimalarials—response rates are about 80% in CLE.
- Methotrexate—best response in subacute CLE and discoid CLE
- Immunosuppressives such as azathioprine, mycophenolate and cyclophosphamide
- Intravenous immunoglobulin
- Aspirin is recommended for antiphospholipid syndrome.
- Targeted biologic therapies under evaluation for SLE include belimumab and off-label rituximab, abatacept, tociluzimab and eculizumab.
CLE is also sometimes treated with:
What is the outlook for systemic lupus erythematosus?
SLE leads to chronic illness with flares and periods of remissions. In some patients, all signs of active disease resolve in time.