Hereditary angioedema and acquired angioedema (acquired C1 inhibitor deficiency) are caused by deficiency or dysfunction of C1 inhibitor, a protein that regulates the classical complement activation pathway (see Complement System). Diagnosis is by measurement of complement levels. C1 inhibitor is used to treat acute attacks. Prophylaxis is with attenuated androgens, which increase C1 inhibitor levels.
C1 inhibitor deficiency or dysfunction results in increased levels of bradykinin because C1 inhibitor also inhibits activated factor X11a and activated kallikrein, which are required for the generation of bradykinin, in the kinin system pathway.
Hereditary angioedema has 2 types:
Inheritance is autosomal dominant. Clinical presentation is usually during childhood or adolescence.
Acquired C1 inhibitor deficiency :
C1 inhibitor deficiency may be acquired when
Clinical presentation is usually at an older age, when patients have an associated disorder.
In all forms of hereditary and acquired angioedema, attacks can be precipitated by mild trauma (eg, dental work, tongue piercing), viral illness, cold exposure, pregnancy, or ingestion of certain foods or may be aggravated by emotional stress.
Symptoms and Signs
Symptoms and signs are similar to those of other forms of bradykinin-mediated angioedema, with asymmetric and mildly painful swelling that often involves the face, lips, and/or tongue. Swelling may also occur on the back of hands or feet or on the genitals. The GI tract is often involved, with manifestations that suggest intestinal obstruction, including nausea, vomiting, and colicky discomfort. Pruritus, urticaria, and bronchospasm do not occur, but laryngeal edema may be present, causing stridor (and sometimes death).
Swelling resolves within about 1 to 3 days of onset. In hereditary angioedema, symptoms resolve as complement components are consumed.
Levels of C4, C1 inhibitor, and C1q (a component of C1) are measured. Low levels of C4 (and C2, if measured) and decreased C1 inhibitor function confirm hereditary angioedema or acquired C1 inhibitor deficiency. Other findings include
If angioedema is not accompanied by urticaria and recurs without any clear cause, clinicians should suspect hereditary angioedema or acquired C1 inhibitor deficiency. If family members have it, they should suspect hereditary angioedema.
Acute attacks are treated with purified human C1 inhibitor, ecallantide, or icatibant (not available in the US). If none of these drugs is available, fresh frozen plasma or, in the European Union, tranexamic acid has been used. A recombinant form of C1 inhibitor (recombinant human C1 esterase inhibitor [rhC1INH], or conestat alfa) is available in Europe.
If the airways are affected, securing an airway is the highest priority. Epinephrine may provide transient benefit in acute attacks when airways are involved. However, the benefit may not be sufficient or may be temporary; then endotracheal intubation may be necessary. Corticosteroids and antihistamines are not effective. Analgesics, antiemetics, and fluid replacement can be used to relieve symptoms.
For long-term prophylaxis, attenuated androgens (eg, stanozolol 2 mg po tid, danazol 200 mg po tid) are used to stimulate hepatic C1 inhibitor synthesis. This treatment may be less effective for the acquired form. C1 inhibitor is effective but expensive.
Short-term prophylaxis is indicated before high-risk procedures (eg, dental or airway procedures) if C1 inhibitor is not available to treat an acute attack. Patients are usually given attenuated androgens 5 days before the procedure until 2 days afterward. If C1 inhibitor is available, some experts advocate giving it 1 h before high-risk procedures rather than attenuated androgens for short-term prophylaxis.
Last full review/revision March 2014 by Peter J. Delves, PhD
Content last modified March 2014