C1 esterase Inhibitor
This is a test that measures the concentration of an inhibitor of complement in the blood.
How the test is performed
Blood is drawn from a vein, usually on the inside of the elbow or the back of the hand. The puncture site is cleaned with antiseptic, and an elastic band is placed around the upper arm to apply pressure and restrict blood flow through the vein. This causes veins below the band to fill with blood.
A needle is inserted into the vein, and the blood is collected in an air-tight vial or a syringe. During the procedure, the band is removed to restore circulation. Once the blood has been collected, the needle is removed, and the puncture site is covered to stop any bleeding.
The sample is then sent to the laboratory where the quantity of C1 inhibiting factor is measured.
How to prepare for the test
There are no special preparations.
For a child, it may be helpful to explain how the test will feel, and even practice or demonstrate on a doll. The more familiar your child is with what will happen to them, and the purpose of the test, the less anxiety they will feel.
How the test will feel
When the needle is inserted to draw blood, some people feel moderate pain, while others feel only a prick or stinging sensation. Afterward, there may be some throbbing.
Why the test is performed
Complement activity (CH50, CH100, terminal complement component, or individual complement proteins) is measured to determine if complement is involved in the development of a number of diseases. Complement activity is also measured to monitor severity of a disease or determine efficiency of treatment.
Patients with hereditary angioedema are often depleted of C1 esterase inhibitor.
C1 esterase inhibitor: 16 to 33 mg/dl (160 to 330 mg/L)
Note: mg/dl = milligrams per deciliter
What abnormal results mean
Increased complement activity may be seen in:
- ulcerative colitis
Decreased complement activity may be seen in:
- hereditary angioedema
- bacterial infections (especially Neisseria)
- lupus nephritis
- kidney transplant rejection
- systemic lupus erythematosus
What the risks are
- excessive bleeding
- fainting or feeling light-headed
- hematoma (blood accumulating under the skin)
- infection (a slight risk any time the skin is broken)
- multiple punctures to locate veins
Complement is a group of proteins in the blood that facilitate immunological and inflammatory responses. The “complement cascade” is a series of reactions that take place in the blood.
There are 9 major components of complement, labeled C1 through C9. The cascade can be started in several ways, especially by antigen-antibody complexes. The end-product of the cascade is the “membrane attack unit” (also called terminal complement component), which creates holes in the membrane, or surface, of attacking bacteria, thereby killing them.
CH50 or CH100 are tests for the activity of the complement system. There are also a number of side products of the complement cascade that attract white blood cells and increase the efficiency of certain types of white blood cells to engulf and destroy bacteria.
Some bacteria don’t need antibodies to set off the complement cascade. When they are exposed to fresh blood serum, complement is activated by an “alternative pathway”. C3, one of the major components of the complement cascade, binds (attaches) to these bacteria directly to eliminate them.
Bound C3, or some modified form of C3, forms a stable unit with other members of the complement cascade to form the membrane attack unit.
Typically, other tests that are more specific for the suspected disease are performed first.
by Simon D. Mitin, M.D.
All ArmMed Media material is provided for information only and is neither advice nor a substitute for proper medical care. Consult a qualified healthcare professional who understands your particular history for individual concerns.