Hemoglobin (Hb) is the special protein within the red blood cells that carries oxygen from the lungs to the rest of the body. Hemoglobin is what makes your blood look red in color.

Your hemoglobin type is inherited through family genes. The color of your hair, the color of your eyes, and your hemoglobin type are all examples of things that are determined by genes. You receive one gene for hemoglobin type from your mother and one from your father. Hemoglobin A or normal adult hemoglobin is the most common type.

Hemoglobinopathy is a term used to describe disorders caused by the presence of abnormal hemoglobin production in the blood.

Sickle cell trait occurs when a person inherits a normal hemoglobin gene (Hb A) from one parent, and a sickle hemoglobin gene (Hb S) from the other parent. 

This results in hemoglobin AS or sickle cell trait. A person with sickle cell trait may also be called a sickle cell carrier. Sickle cell trait is not a disease and usually does not affect one's health, but individuals with sickle cell trait can pass the sickle hemoglobin gene to their children.

A simple blood test called a hemoglobin electrophoresis will detect sickle cell trait. This test will tell if you are a carrier of the sickle cell trait or if you have the disease.

Your physician can give you the test or the test may be obtained at some hospitals, sickle cell centers, and health department clinics.

Sickle cell disease is a group of inherited blood disorders caused by the presence of hemoglobin S in red blood cells. The red cells change to a sickle (banana) shape and can clog blood vessels causing damage to the body's tissues and organs.

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Sickle cell anemia (Hb SS) is the most common type of sickle cell disease. There are other hemoglobin types such as hemoglobin C or hemoglobin E, that in combination with the gene for sickle hemoglobin can result in different forms of sickle cell disease (Hb SC, Hb SE, Hb S/beta thalassemia).

They are sickle cell trait and the various types of sickle cell disease.

You inherit the abnormal hemoglobin from your parents. You cannot catch it from someone else or pass it to another person like a cold or other infections. You are born with sickle cell hemoglobin and it is present for life. If you inherit only one sickle gene, you have sickle cell trait and will not develop the disease. If you inherit two sickle cell genes, you have sickle cell anemia.

Sickle cell anemia affects millions of people throughout the world. It is particularly common among people whose ancestors come from Africa; Spanish speaking regions (South America, Cuba, Central America); Saudi Arabia; India; and Mediterranean countries, such as Turkey, Greece, and Italy. 

In the United States, most people who have sickle cell disease are African American. In Missouri, the disease occurs in approximately 1 in every 400 African-American births, and approximately 1 in 12 African Americans carry the sickle cell trait.

Most states now perform a blood test for sickle cell disease on all newborn infants. Early diagnosis of sickle cell anemia is critical so that children who have the disease can receive proper treatment. Since May 1989, all babies born in Missouri are tested for sickle cell conditions through the Missouri Newborn Screening Program (MNSP). 

This test is performed at the same time and from the same blood samples as other routine newborn screening tests. If the test shows the presence of sickle hemoglobin, a second blood test is performed to confirm the diagnosis. These tests also tell whether the child carries the sickle cell trait.

A small blood sample is taken from the infant's heel, usually before the baby leaves the hospital. The blood sample will show whether the baby has sickle cell trait, sickle cell disease or any other abnormal hemoglobin.

When ONE parent has sickle cell trait and the other parent has normal hemoglobin the child may inherit:

• two normal hemoglobin genes, or
• one normal hemoglobin gene and one sickle cell gene.

With EACH pregnancy there is a:

• 50% chance that the baby will have normal red blood cells (AA).
• 50% chance that the baby will have sickle cell trait (AS).

When BOTH parents have sickle cell trait (AS), the child may inherit:

• two normal hemoglobin genes, or
• one normal hemoglobin gene and one sickle cell gene, or
• two sickle cell genes

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With EACH pregnancy there is a:

• 25% chance that the baby's red blood cells will be normal (AA).
• 50% chance that the baby will have sickle cell trait (AS).
• 25% chance that the baby will have sickle cell disease (SS).

Sickle shaped red blood cells tend to get stuck in narrow blood vessels blocking the flow of blood. This can cause damage to organs including the spleen, liver and kidneys. Other complications include pain episodes, lung problems and stroke.

People who are planning to become parents should know whether they are carriers of the sickle cell gene. If they are, they may want to seek genetic counseling to find out what the chances are that their child will have sickle cell trait or sickle cell anemia.

Your doctor can do a simple blood test called a hemoglobin electrophoresis. This test will tell if you are a carrier of the sickle cell trait or if you have the disease.

The California Newborn Screening Program tests newborns for sickle cell and other hemoglobinopathies.

Family members of infants identified with sickle cell conditions can be screened at county and city health departments, family planning clinics and hospitals.

Depends on whether or not you have a matched full sibling (you and your brother or sister have same parents).  There are several studies looking at different donors for bone marrow transplant, but only a transplant from a full sibling has been studied enough to be approved by most insurance companies.  If your sibling has sickle cell trait they can still be a donor.

There are some new therapies that have decreased the incidence of graft versus host disease (the stem cells from the donor attack the recipient of the transplant) that can cause a lot of problems including death.

The survival from a bone marrow transplant is very good, over 95% in some studies.  The cure is less, about 85% to 90%.  Which is still good.

Gene therapy looks very promising, but is still in the research phases.

Now with COVID19 studies are on hold in most cases.

So should you have a transplant?  

That is something you and your personal physician should discuss in detail.  It is a decision that generally has a good outcome, but has risk.

The short answer is: Yes.

In studies of the new therapies some of the subjects remained on hydroxyurea and did well.  It is not clear that they did better than those not taking hydroxyurea, but the studies were somewhat time limited so it is not clear how the new therapies will fair over a long period of time.

Clearly hydroxyurea turned out to be much more effective (especially in children) than anyone thought it would in the 1980’s when it was first used for sickle cell disease.  Hopefully these new therapies will also prove to be as effective as hydroxyurea.

Penicillin (or amoxicillin or erythromycin) was studied first in young children under 3 years old.  This study was stopped early as there were deaths in the arm of the study that was randomized to the placebo compared to penicillin.  Penicillin taken twice a day reduced mortality from pneumococcal infections by 95%.  This was before there was a vaccine for pneumococcal disease.  Even now with the vaccine, young children should be taking penicillin or erythromycin if they are allergic.  Neither the vaccine nor the penicillin will be 100% effective in preventing disease as there are strains of pneumococcus that are not in the vaccine and there are infections by other bacteria that could be slowed by penicillin or other antibiotics used as prophylaxis.

Remember, neither treats an infection.  They can slow the infection down to give you time to get medical attention.

Should you stop antibiotic prophylaxis? 

 If you have S beta + thalassemia then most doctors would tell you to stop by the age of five…

First know what your sickle cell status is and what your partner’s sickle cell status is.

• If one has sickle cell trait and the other does not, then you can have a child with trait, but not with disease.
• If you both have sickle cell trait (or are a carrier for a hemoglobin that with hemoglobin S can cause disease, like C trait) then if you both have S trait you have a 25% chance of having a child with sickle cell disease with each pregnancy.

Prenatal testing for sickle cell disease can be done early.

You can have amniocentesis which can be diagnostic for Hemoglobinopathy like sickle cell disease (15 to 18 week’s gestation).

Even earlier in the pregnancy you can have Chorionic villus sampling is done 10 to 12 week’s of gestational age.

There are some laboratories that can test the mothers blood (a venous blood draw) for some kinds of disease (like trisomy 21, Down’s Syndrome), it is not generally available for sickle cell disease.