Sickle cell disease is an inherited blood disorder characterized by defective hemoglobin (a protein in red blood cells that carries oxygen to the tissues of the body).
Sickle cell disease inhibits the ability of hemoglobin in red blood cells to carry oxygen. Cells containing normal hemoglobin are smooth, disk-shaped, and flexible, like doughnuts without holes, so they can move through the vessels in our bodies easily. Cells containing sickle cell hemoglobin are stiff and sticky and form into the shape of a sickle or crescent, like the letter C, when they lose their oxygen. These sickle cells tend to cluster together, and cannot easily move through the blood vessels. The cluster causes a blockage in small arteries or capillaries and stops the movement of healthy, normal oxygen-carrying blood. This blockage is what causes the painful and damaging complications of sickle cell disease.
Sickle cells only live for about 10 to 20 days, while normal red blood cells can live up to 120 days. Also, sickle cells risk being destroyed by the spleen because of their shape and stiffness. The spleen is an organ that helps filter the blood of infections. Sickled cells get stuck in this filter and die. Due to the decreased number of healthy red blood cells circulating in the body, a person with sickle cell disease is chronically anemic. The spleen also suffers damage from the sickled cells blocking healthy oxygen carrying cells and typically infarcts in the first few years of life. Without a normal functioning spleen, these individuals are more at risk for infections. Infants and young children are at risk for life-threatening infections.
The most common variations of the sickle cell gene include the following:
Sickle cell trait. The person is carrying a single defective gene. Some of their hemoglobin is the destructive HbS, but they also have some normal hemoglobin, HbA. This is referred to as HbAS. People with sickle cell trait are usually without symptoms of the disease. Mild anemia may occur and red cells tend to be small. Under intense, stressful conditions, exhaustion, hypoxia (low oxygen), and/or severe infection, the sickling of the defective hemoglobin may occur and result in some complications associated with the sickle cell disease. Most people with the sickle cell trait lead normal lives.
Sickle cell anemia. The person has most or all of the normal hemoglobin (HbA) replaced with the sickle hemoglobin (HbS). This is referred to as HbSS. It is the most common and most severe form of the sickle cell variations. These people suffer from a variety of complications due to the shape and thickness of the sickled cells. Severe and chronic anemia is also a common characteristic for people with HbSS.
Sickle cell--hemoglobin SC disease. The person has one copy of both HbS and HbC. This is often referred to as HbSC. Hemoglobin C causes abnormal red blood cells, called target cells, to develop. Having just some hemoglobin C and normal hemoglobin, a person will usually not have any symptoms of anemia, but can develop anemia and eye and hip complications later in life. However, if a person has both HbS and HbC, some mild to moderate anemia occurs. These people often suffer some of the complications associated with HbSS, sickle cell disease, but to a milder degree. Vaso-occlusive crises (the flow of blood is blocked because the sickled cells have become stuck in the blood vessels), organ damage from repeated sickling and anemia, and high risk for infection are all similar traits for HbSS and HbSC.
Sickle cell--hemoglobin E disease. This variation is similar to sickle cell-C disease except that an element has been replaced in the hemoglobin molecule. This variation is most often also seen in Southeast Asian populations. Some people with hemoglobin E disease are without symptoms. However, under certain conditions, such as exhaustion, hypoxia, severe infection, and/or iron deficiency, some mild to moderate anemia may occur.
Hemoglobin S-beta-thalassemia. This involves an inheritance of both the thalassemia and sickle cell genes. The disorder produces symptoms of moderate anemia and many of the same conditions associated with sickle cell disease. While this disorder more often has milder symptoms than sickle cell disease, it may also produce exacerbations as severe as those of sickle cell disease.
All forms of sickle cell disease can exhibit the complications associated with the disease.
Sickle cell disease primarily affects those of African descent and Hispanics of Caribbean ancestry, but the trait has also been found in those with Middle Eastern, Indian, Latin American, American Indian, and Mediterranean heritage.
It has been estimated that 90,000 to 100,000 people in the U.S. are affected by sickle cell anemia and that approximately 3 million people have the sickle cell trait. Approximately one in 12 African-Americans has sickle cell trait. Millions worldwide suffer complications from sickle cell disease.
Sickle cell is an inherited disease caused by a genetic mutation. Genes are found on structures in the cells of our body called chromosomes. There are normally 46 total, or 23 pairs, of chromosomes in each cell of our body. The 11th pair of chromosomes contains a gene responsible for normal hemoglobin production.
A mutation or error in this gene is what causes sickle cell disease. This mutation is thought to have originated in areas of the world where malaria was common, since people with sickle trait tolerate malaria better and have a reproductive advantage in areas with malaria. The sickle trait actually protects them from the parasite that causes malaria, which is carried by mosquitoes. Malaria is most often seen in Africa and in the Mediterranean area of Europe.
Sickle cell is a genetic disease. A person will be born with sickle cell disease only if two HbS genes are inherited—one from the mother and one from the father. A person who has only one HbS gene is healthy and said to be a "carrier" of the disease. They may also be described as having sickle cell trait. A carrier has an increased chance to have a child with sickle cell disease if he or she has a child with someone who also has a sickle cell gene. This type of inheritance is called autosomal recessive.
Autosomal means that the gene is on one of the first 22 pairs of chromosomes that do not determine gender, so that males and females are equally affected by the disease.
Recessive means that two copies of the gene, one inherited from each parent, are necessary to have the condition.
In this couple, there is a risk of having:
Children with sickle cell disease = S S (one in four, or 25 percent)
Children who are carriers of the gene like their parents = A S S A (two in four, or 50 percent have sickle cell trait)
Children who do not get the gene from either parent: A A (one in four, or 25 percent)
For parents who are each carriers of a sickle cell gene, there is a one in four, or a 25 percent chance with each subsequent pregnancy, for another child to be born with sickle cell disease. This means that there is a three out of four, or a 75 percent chance, that another child will not have sickle cell disease. There is a 50 percent chance that a child will be born with sickle cell trait, like the parents.
The following is a list of symptoms and complications associated with sickle cell disease. However, each individual may experience symptoms differently. Symptoms and complications may include, but are not limited to, the following:
Anemia. This is the most common symptom of all the sickle cell diseases. In sickle cell disease, red blood cells are produced but then become deformed into the sickle shape, which causes red blood cells to lose their oxygen carrying capacity. This sickle shape makes the cells stiff and sticky causing them to become stuck in the vessels, destroyed by the spleen, or simply die because of their abnormal function. The decrease in red blood cells causes anemia. Severe anemia can make the person's ability to carry oxygen to the tissues more difficult, possibly causing them to be pale, dizzy, short of breath, and tired. Healing and normal growth and development may be delayed because of chronic anemia.
Pain crisis, or sickle crisis. This occurs when the flow of blood is blocked to an area because the sickled cells have become stuck in the blood vessel. These are also called vaso-occlusive crises. The pain can occur anywhere, but most often occurs in the chest, arms, and legs. Painful swelling of the fingers and toes, called dactylitis, can occur in infants and children younger than age 3. Any interruption in blood flow to the body can result in pain, swelling, and possible death of the surrounding tissue not receiving adequate blood and oxygen.
Acute chest syndrome. This occurs when sickling is in the chest. This can be a life-threatening complication of sickle cell disease. It often occurs suddenly, when the body is under stress from infection, fever, or dehydration. The sickled cells stick together and block the flow of oxygen in the tiny vessels in the lungs. It resembles pneumonia and can include fever, pain, and a violent cough. Multiple episodes of acute chest syndrome can cause permanent lung damage. Damage to the blood vessels in the lungs can lead to high blood pressures in the lungs (pulmonary hypertension).
Splenic sequestration (pooling). Crises are a result of sickle cells pooling in the spleen. This can cause a sudden drop in hemoglobin and can be life-threatening if not treated promptly. The spleen can also become enlarged and painful from the increase in blood volume. After repeated episodes of splenic sequestration, the spleen becomes scarred, and permanently damaged. Most children, by age 8, do not have a functioning spleen either from surgical removal, or from repeated episodes of splenic sequestration. The risk of infection is a major concern of children without a functioning spleen. Infection is the major cause of death in children younger than age 5 in this population.
Stroke. This is another sudden and severe complication of people with sickle cell disease. The misshapen cells can block the major blood vessels that supply the brain with oxygen. Any interruption in the flow of blood and oxygen to the brain can result in devastating neurological impairment. Having had one stroke from sickle cell anemia, a person is more likely to have a second and third stroke.
Jaundice, or yellowing of the skin, eyes, and mouth. Jaundice is a common sign and symptom of sickle disease. Sickle cells do not live as long as normal red blood cells and, therefore, they are dying more rapidly than the liver can filter them out. Bilirubin (which causes the yellow color) from these broken down cells builds up in the system causing jaundice.
Priapism. A painful obstruction of the penis by sickle cells. If not promptly treated, it can result in impotence.
Any and all major organs are affected by sickle cell disease. The liver, heart, kidneys, gallbladder, eyes, bones, and joints can suffer damage from the abnormal function of the sickle cells and their inability to flow through the small blood vessels correctly. Problems may include the following:
Kidney damage and loss of body water in the urine
Multiple organ failure
The symptoms of sickle cell disease may resemble other blood disorders or medical problems. Always consult your doctor for a diagnosis.
In addition to a complete medical history and physical examination, diagnostic procedures for sickle cell disease may include blood tests and other evaluation procedures. Many states provide routine newborn screening blood tests in order to begin proper treatment as soon as possible. Early diagnosis is essential in providing proper preventive treatment for some of the devastating complications of the disease.
Hemoglobin electrophoresis is a blood test that can determine if a person is a carrier of a specific sickle cell trait, or has any of the diseases associated with the sickle cell gene.
Specific treatment for sickle cell disease will be determined by your doctor based on:
Your age, overall health, and medical history
Extent of the disease
Your tolerance for specific medications, procedures, or therapies
Expectations for the course of the disease
Your opinion or preference
Early diagnosis and prevention of complications is critical in sickle cell disease treatment. The objectives of treatment are to prevent organ damage including strokes, prevent infection, and treat symptoms. Treatment may include:
Pain medications. This is for sickle cell crises.
Drinking plenty of water daily (eight to 10 glasses). This is to prevent and treat pain crises. In some situations, intravenous fluids may be required.
Blood transfusions. Blood transfusions may be used for anemia and to prevent stroke. Transfusions are also used to dilute the HbS with normal hemoglobin to treat chronic pain, acute chest syndrome, splenic sequestration, and other emergencies.
Vaccinations and antibiotics. These are used to prevent infections.
Folic acid. Folic acid will help prevent severe anemia.
Hydroxyurea. Hydroxyurea is a medication that has recently been found to help reduce the frequency of pain crises and acute chest syndrome. It may also help decrease the need for frequent blood transfusions. The long-term effects of the medication, however, are unknown.
Regular eye exams. These are done to screen for associated retinopathy.
Bone marrow transplant. Bone marrow transplants have been effective in curing some people with sickle cell disease; the decision to undergo this procedure is based on the severity of the disease and ability to find a suitable bone marrow donor. These decisions need to be discussed with your doctor and are only done at centers that specialize in stem cell transplantation.