Adrenoleukodystrophy (ALD) | Diagnosis & Treatment

How is adrenoleukodystrophy diagnosed?

Early diagnosis of cerebral ALD is critical, because there is a narrow window in which the condition can be treated. Once the disease progresses, there is no way to replace the lost myelin or reverse the neurological damage already done.

Diagnostic testing

Without a family history, most women aren’t aware they are carriers of ALD. As a result, their sons are often misdiagnosed and their symptoms are easily mistaken for behavior or developmental issues.

When a clinician suspects ALD, they will perform two tests — a magnetic resonance imaging (MRI) scan to determine whether there is damage to the brain tissue and a blood test to measure the concentration of very long chain fatty acids, which are elevated in males with ALD.

Genetic testing

Genetic testing can identify the defective gene that causes ALD. It also can accurately identify other members of the family who have ALD — females who are carriers and boys who aren’t yet exhibiting symptoms.

Newborn screening

A newborn screening test, which was added to the United States Recommended Uniform Newborn Screening Panel in 2016 but currently is available in only a handful of states, detects elevated very long chain fatty acid levels in the blood, a clear indicator of ALD. With newborn screening, boys at risk can be identified and treated early.

What are the treatment options for ALD?

Stem cell transplant

The only effective treatment option for cerebral ALD is a stem cell transplant, a procedure in which the patient receives blood stem cells from a genetically matched donor. The purpose is to provide healthy stem cells that produce the protein lacking in boys with ALD.

Prior to the stem cell transplant, there is an intensive process to prepare for treatment. This involves using chemotherapy to prepare the body to receive the donor cells. Although a donor stem cell transplant has been shown to halt the progression of ALD, it has its own set of challenges and risks:

  • It can be difficult to find a donor match that has a similar or identical genetic makeup
  • There is a high risk of infection, because the immune system is strongly inhibited to allow the recipient’s body to accept the transplanted new stem cells.
  • Following transplant, the condition continues to progress for six to 18 months, so early treatment is crucial.
  • For symptomatic boys, a transplant can in some cases be associated with a rapidly advanced condition.

Gene therapy for ALD

Gene therapy is being studied as a potential treatment for cerebral ALD. A clinical trial at the Dana-Farber/Boston Children's Cancer and Blood Disorders Center uses an experimental approach for asymptomatic ALD boys. Their own blood stem cells are removed, treated in the laboratory with a vector, which is a non-infectious virus that is used to get the gene that makes the ALD protein (ABCD1 gene) into the cell. The cells containing the vector, carrying the new gene, are then given back to the patient by an intravenous (IV) infusion. When these new cells grow, divide and make new cells in the body, they will have the ABCD1 gene and be able to break down the very long chain fatty acids that cause the serious neurological symptoms of ALD.

While still experimental, the advantage of this approach is that there is no need to look for a donor, so there is no risk of the transplant fighting the body (called “graft-versus-host disease”), and therefore no need for powerful immunosuppression drugs.

Learn more about the Gene Therapy Program.