Metachromatic leukodystrophy

Metachromatic leukodystrophy
Classification and external resources
Sulfatide
ICD-10	E75.2
ICD-9	330.0
OMIM	250100
DiseasesDB	8080
eMedicine	ped/2893
MeSH	D007966

Metachromatic leukodystrophy (MLD, also called Arylsulfatase A deficiency) is a lysosomal storage disease which is commonly listed in the family of leukodystrophies. Leukodystrophies affect the growth and/or development of myelin, the fatty covering which acts as an insulator around nerve fibers throughout the central and peripheral nervous systems. It involves sulfatide accumulation.

Causes

MLD is directly caused by a deficiency of the enzyme arylsulfatase A and is usually characterized by enzyme activity which is less than 10% of human controls. Without this enzyme, sulfatides build up in many tissues of the body, eventually destroying the myelin sheath of the nervous system. The myelin sheath is a fatty covering that protects nerve fibers. Without it, the nerves in the brain (central nervous system - CNS) and the peripheral nerves (peripheral nervous system - PNS) which control, among other things the muscles related to mobility, cease to function properly.

A recent study contended sulfatide is not completely responsible for MLD because it is non toxic. It has been suggested lysosulfatide, sulfatide which has had its acyl group removed, plays a role because of its cytotoxic properties in vitro.

Genetics

MLD has an autosomal recessive inheritance pattern. The inheritance probabilities per birth are as follows:

• If both parents are carriers:
  • 25% (1 in 4) children will have the disorder
  • 50% (2 in 4) children will be carriers (but unaffected)
  • 25% (1 in 4) children will be free of MLD - unaffected child that is not a carrier

• If one parent is affected and one is free of MLD:
  • 0% (0) children will have the disorder - only one parent is affected, other parent always gives normal gene
  • 100% (4 in 4) children will be carriers (but unaffected)

• If one parent is a carrier and the other is free of MLD:
  • 50% (2 in 4) children will be carriers (but unaffected)
  • 50% (2 in 4) children will be free of MLD - unaffected child that is not a carrier

In addition to these frequencies there is a 'pseudo'-deficiency that affects 7% of the population. People with the pseudo deficiency do not have any MLD problems unless they also have carrier or affected status. Pseudo-deficiency tests as low enzyme levels but sulfatide is processed normally so MLD symptoms do not exist.

For further information, see recessive gene and dominance relationship. Also, consult the MLD genetics page at the MLD Foundation.

Symptoms and forms

Like many other genetic disorders that affect lipid metabolism, there are several forms of MLD, which are late infantile, juvenile, and adult.

• In the late infantile form, which is the most common form of MLD (50-60%), affected children begin having difficulty walking after the first year of life, usually at 15–24 months. Symptoms include muscle wasting and weakness, muscle rigidity, developmental delays, progressive loss of vision leading to blindness, convulsions, impaired swallowing, paralysis, and dementia. Children may become comatose. Untreated, most children with this form of MLD die by age 5, often much sooner.

• Children with the juvenile form of MLD (onset between 3 and 10 years of age) usually begin with impaired school performance, mental deterioration, and dementia and then develop symptoms similar to the late infantile form but with slower progression. Age of death is variable, but normally within 10 to 15 years of symptom onset although some juveniles can live for several decades or longer after onset.

• The adult form commonly begins after age 16 as a psychiatric disorder or progressive dementia. Adult-onset MLD progresses more slowly than the late infantile and juvenile forms, with a protracted course of a decade or more.

Palliative care can help with many of the symptoms and usually improves quality and longevity of life.

Carriers have low enzyme levels compared to their family population ("normal" levels vary from family to family) but even low enzyme levels are adequate to process the body's sulfatide.

Treatment

There is no cure for MLD, and no standard treatment. It is a terminal illness. Children with advanced juvenile or adult onset, and late infantile patients displaying symptoms have treatment limited to pain and symptom management. Presymptomatic late infantile MLD patients, as well as those with juvenile or adult MLD that are either presymptomatic or displaying mild to moderate symptoms, have the option of bone marrow transplantation (including stem cell transplantation), which is under investigation to see if it may slow down progression of disease, or stop its progression in the central nervous system. However, results in the peripheral nervous system have been less dramatic, and the long-term results of these therapies have been mixed.

Several treatment options for the future are currently being investigated. These include gene therapy, enzyme replacement therapy (ERT), substrate reduction therapy (SRT), and potentially enzyme enhancement therapy (EET).

A team of international researchers and foundations organized in 2008 to form an International MLD Registry to create and manage a shared repository of knowledge, including the natural history of MLD. This consortium consists of scientific, academic and industry resources. This registry never became operational.

Research Towards Effective Therapies and Clinical Trials

Bone Marrow and Stem Cell Transplant Therapies

• Several trials are underway to continue to improve the effectiveness and reduce the risks of bone marrow and stem cell transplants. Cord blood transplants and reduced preparative routines are being studied.
• Families are cautioned that there are unregulated hucksters usually operating in Central or South America, or China that would be happy to take your money and have you believe stem cell infusions will "cure" MLD. These claims are false.

Gene therapy

• Two different approaches to gene therapy are currently being researched for MLD.
  • Italian researchers at the San Raffaele Telethon Institute are testing a novel approach combining gene therapy with a stem cell transplant. Recruiting for the Italian Phase I/II Clinical Trial formally started on March 24, 2010 after approval from the Italian Authorities. The trial is testing the efficacy and safety of of an autologous (using the patient's own cells) hematopoietic stem cell transplant (HSCT) after genetic modification to deliver a super-therapeutic (over-expressing) ARSA enzyme to the nervous system by the route of the blood cells. Using the patient's own stem cells with genetic correction should reduce or eliminate the complications of graft vs. host disease and provide a long term solution to proper ARSA expression in MLD patients. Bench and animal tests showed positive results.
    • Inclusion criteria are pre-symptomatic late infantiles and both pre- and early-symptomatic juveniles. See details on inclusion criteria and the trial protocol here.
    • The trial is single center in Milano, Italy. All costs to be paid by the researchers. This is a 3 year study. Five patients have been enrolled, four have completed the transplant, and recruiting is still underway. It is too early to determine efficacy.(Current January 2012)
  • A French group is exploring a direct injection into the brain. They anticipate starting clinical trials in 2012 (current as of January 2012)

Enzyme replacement therapy (ERT)

• Shire Human Genetic Therapies (Shire HGT), a division of Shire PLC of the UK, is now recruiting for their clinical trial for their intrathecal HGT-1110 product . (current January 2012)
  • Additional clinical trial information, including inclusion criteria, can be found on the MLD Foundation website here.
  • The clinical trial is a 40 week multi-site European study of 15 children with 5 children to be in a placebo control group.
  • HGT-1110 has orphan product status in both Europe and the United States.
• Shire suspended development of the the Metazyme intravenous ERT product in 2010. It was in clinical trial when it was acquired from Zymenex in 2008 (subsequently renamed HGT-1111 by Shire) after it was shown to not have sufficient efficacy by a Phase I/II clinical trial in Europe. The initial study completed September 2008 and the extension study completed October 2010 with the cessation of product supply to trial participants.

Substrate reduction therapy

• Zacharon Pharmaceuticals from San Diego is initiating a drug discovery program for MLD. This program is based on using assays which measure sulfatide accumulation in cultured fibroblasts as a means to discover and develop small molecule drugs for MLD. (This approach differs from other approaches which have measured enzyme activity to discover effective drugs.) As of July 2011, Zacharon has begun adapting the assays it developed for other lysosomal storage diseases so that they can be employed to discover and develop drugs for MLD.(current January 2012)
• The Cooper Health System (New Jersey) sponsored a clinical trial underway to determine the safety and efficacy of a Vitamin K antagonist (Warfarin) in treating Metachromatic Leukodystrophy (MLD) in 2009. No results are known to have been published. (current January 2011)

Research & Clinical Trial updates provided by the MLD Foundation''

See also

MLD Specific Organizations:

• MLD Foundation

Leukodystrophy & Lysosomal Disease Organizations:

• Australian Leukodystrophy Support Group (Australia)
• Bethany's Hope (Canada)
• ELA, The European Leukodystrophy Association
• The Evanosky Foundation
• Hide & Seek Foundation for Lysosomal Disease Research
• The Myelin Project
• New Zealand Organisation for Rare Disorders
• The Stennis Foundation

External links

• Some portions of this article are courtesy of the public domain text available at the National Institute of Neurological Disorders and Stroke
• Further information regarding MLD, treatments, genetics, and current research projects, can be found at:
  • The Evanosky Foundation
  • MLD Foundation
    • MLD-101 ... A layperson's guide to MLD
    • Updates on current MLD research & clinical trials
    • Contact other families and support
  • The Stennis Foundation
• Zacharon Pharmaceuticals
• Shire HGT drug development pipeline
• 2008 eMedicine article about MLD by Ikeda & Moore of UCLA and Steiner of OHSU
• NIH/GeneReviews at NIH/UW GeneTests overview of MLD written by Arvan Fluharty of UCLA (updated August 2011)
• OMIM entries on ARSA Deficiency