Antiphospholipid syndrome is an immune disorder in which abnormal antibodies are linked to abnormal blood clots in veins and arteries. It mostly affects the legs, but clots may also form in the kidneys, lungs, and other organs.

It may lead to complications in pregnancy, such as recurring pregnancy loss and preterm births.

Antiphospholipid syndrome (APS) is also known as Antiphospholipid Antibody Syndrome, Hughes syndrome, or sticky blood.

The abnormal antibodies attack fats that contain phosphorous, known as phospholipids. Heart valve abnormalities are common in people with APS, and up to one in three cases of stroke under the age of 50 years may be due to it.

In the legs, APS can lead to deep vein thrombosis (DVT). If a clot develops in the brain, there is a serious risk of stroke.

There is no cure for APS, but current treatments can significantly reduce the risk of developing blood clots.

Most people with APS who receive treatment can lead normal, healthy lives, but, rarely, a person with the syndrome will continue to develop clots.

According to the APS Foundation of America, between 1 and 5 percent of people in the United States are thought to have APS. It is responsible for 15 to 20 percent of all cases of DVT and pulmonary embolism, or blood clots on the lung. It affects women three to five more often than men.

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Antiphospholipid syndrome affects blood consistency.

Signs and symptoms of antiphospholipid syndrome depend mainly on where the clots travel to, and where they form.

A clot or embolus, which is a traveling clot, can result in:

  • DVT: A clot forms in one of the large veins, usually in the arm or leg, and it partially or completely blocks circulation. If a DVT blood clot moves into the lungs, a life-threatening condition known as a pulmonary embolism (PE) can result.
  • Pulmonary embolism (PE): An embolus, or traveling clot, appears in one part of the body, circulates throughout the body, and then blocks blood flowing through a vessel in another part of the body. In PE, an embolus blocks an artery that feeds the lungs.
  • Complications of pregnancy: These include recurring miscarriages, preterm delivery, and preeclampsia, or high blood pressure during pregnancy.
  • Ischemic stroke: A blood clot interrupts blood flow to a part of the brain, cutting off the supply of oxygen and glucose. Brain cell death and brain damage can results. Around 75 percent of all stroke cases are ischemic.

Less common signs and symptoms include:

  • headaches or migraines
  • dementia and seizures, if a clot blocks blood flow to parts of the brain
  • livedo reticularis, a lace-like purplish rash on the knees and wrists

Around 30 percent of people with APS have heart valve abnormalities. In many cases, the mitral valve thickens, or develops extra mass, causing blood to leak back into one of the heart’s chambers. Some patients may have problems with the aortic valve.

Levels of platelets can drop. Platelets are the blood cells that are needed for normal clotting. This can lead to episodes of bleeding, for examples nosebleeds, or bleeding gums. Some people may experience bleeding into the skin, causing small red spots to appear.

In very rare cases, a person may develop:

Symptoms tend to appear between the ages of 20 and 50 years, but sometimes they develop during childhood.

Catastrophic antiphospholipid syndrome

Catastrophic antiphospholipid syndrome (CAPS) is a type of “thrombotic storm,” in which multiple clots suddenly form. It affects a small minority of patients with APS, progressively damaging several organs.

Blood clots abruptly develop all over the body, resulting in multiple organ failure. Why it happens is unclear.

Symptoms vary, depending on which organs are affected, but they include:

  • abdominal pain
  • confusion
  • edema, or swelling, in the ankles, feet, or hands
  • fits, or seizures
  • progressive breathlessness
  • tiredness
  • coma
  • death

Symptoms tend to appear suddenly and get worse rapidly.

CAPS is a medical emergency and the patient will need intensive care as soon as possible, so that the body’s functions can be maintained while high-dose anticoagulants are administered.

Research suggests that around 46 percent of patients with catastrophic antiphospholipid syndrome do not survive the initial event, and there is a risk of a repeat event at some time, even with medical care.

A doctor will usually prescribe medication to thin the blood, to reduce the chance of clotting. The patient will normally need this medication for the rest of their life.

Possible combinations include aspirin with warfarin, or Coumadin, or possibly heparin. If warfarin does not work, the dose may be increased or heparin may be added.

The clotting action of anticoagulants can sometimes lead to a hemorrhage, or excessive bleeding.

Patients should seek medical help at once if they experience:

  • blood in feces, urine, or vomit
  • coughing up blood
  • nosebleeds lasting longer than 10 minutes
  • severe bruising

Patients who experience thrombosis will normally need to take heparin and warfarin. When the thrombosis clears, they will continue with warfarin.

Treatment in pregnancy

A woman with a diagnosis with APS should plan for pregnancy from before conception. Treatment will start at the beginning of pregnancy and finish after delivery.

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It is important to monitor the blood, especially during pregnancy.

In an unplanned pregnancy, the effectiveness of treatment may be reduced as it will not begin until several weeks after conception.

Treatment will normally be aspirin, heparin, or both, depending on previous clots of pregnancy complications. Warfarin can cause birth defects, and it is not used during pregnancy.

If the patient does not respond to this treatment, intravenous immunoglobulin infusions and corticosteroids, such as prednisone, may be prescribed.

If, by the third trimester, there are no problems, the heparin treatment may stop, but the aspirin treatment may have to continue until the end of the pregnancy.

Regular blood tests will need to continue to ensure the blood can still clot enough to stop bleeding if the patient bruises or cuts herself.

A doctor will test for antiphospholipid syndrome if the patient has at least one episode of thrombosis or a pregnancy loss.

A blood test will show whether a person has abnormal antibodies.

Sometimes harmless antiphospholipid antibodies may develop for limited periods, because of an infection or some medication, so a second test will be needed to confirm the result.

If blood tests reveal abnormal antibodies, the doctor will assess the patient’s medical history to determine whether previous symptoms may have been caused by antiphospholipid syndrome.

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A blood clot can be life-threatening.

APS is an autoimmune disorder. An autoimmune disorder causes antibodies to attack good cells by mistake.

In APS, the person’s immune system produces antibodies called antiphospholipid antibodies.

These abnormal antibodies attack proteins and fats in the blood, and specifically phospholipids.

Phospholipids are cell membrane substances that play a role in the blood-clotting process.

If the antibodies attack the phospholipids, this can increase the risk of developing blood clots.

Blood clotting is what prevents people from bleeding too much after, for example, an injury.

The fats and proteins that are attacked are thought to be important in maintaining blood consistency.

The blood becomes sticky, significantly increasing the risk of developing blood clots.

People with antiphospholipid syndrome produce antibodies that attack either the phospholipids or the blood proteins that bind to the phospholipids.

There are two main types of APS:

  • Primary antiphospholipid syndrome: It is not linked to any other disease or condition but develops in isolation
  • Secondary antiphospholipid syndrome: It develops along with another autoimmune disorder, such as lupus

Why autoimmune disorders happen is unclear, and it is also unclear why some people with abnormal antibodies never develop symptoms.

A combination of genetic and environmental factors appears to be involved.

Genetics factors appear to affect the likelihood of having APS. If a family member has the syndrome, the individual will have a higher risk of developing it themselves.

Other risk factors include:

  • lupus, Sjogren’s syndrome, or another autoimmune disorder
  • hepatitis C, syphilis, cytomegalovirus (CMV), the parvovirus B19 and some other infections
  • some medications, including hydralazine, used to treat hypertension, and some anti-epileptic drugs

Some people have the antibodies but do not develop signs or symptoms. However, certain triggers can cause the condition to develop in these people.

Triggers include:

Young and middle-aged women are more likely to develop APS, but it can affect either gender and at any age.

A patient with APS needs to take all possible measures to lower the risk of developing blood clots.

This includes:

  • not smoking
  • maintaining a healthy bodyweight
  • remaining physically active

It is important to follow a healthful diet with plenty of fruit and vegetables and low fat and sugar.

The APS Foundation of American advises people with APS to:

  • maintain the same diet as before diagnosis, unless the doctor instructs otherwise
  • avoid “bingeing” and crash diets
  • limit intake of foods that are rich in vitamin K to one serving a day, for example, one cup of raw, or half a cup of cooked spinach, turnip greens, cucumber peel, broccoli, Brussels sprouts, green scallion, cabbage, and mustard greens.
  • avoid parsley, kale, seaweed, and green tea

People who use warfarin need to maintain a stable intake of vitamin K. Patients should not make any dietary changes or use any supplements of new medications without first consulting their physician.