The Natural History of Metachromatic Leukodystrophy

Metachromatic Leukodystrophy Clinical Trial

— NH-US  

Official title:

The Natural History of Metachromatic Leukodystrophy

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT00639132
• Other study ID #: STUDY19020318
• Status: Active, not recruiting
• Start date: January 2012
• Est. completion date: January 2030

Study information

• Verified date: June 2023
• Source: University of Pittsburgh
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

There have not been longitudinal studies which track patients' neurologically or developmentally in a systematic manner. By simultaneously tracking patients' neurodevelopment along with neuroimaging and neurophysiologic studies it becomes much easier to draw conclusions on the differential effects of the disease process and any available treatments that patients might receive. In addition, many of the gene mutations, which cause MLD have not been linked to the age of onset or the expected disease course.

Description:

Metachromatic leukodystrophy (MLD), an autosomal recessively inherited lysosomal storage disorder, causes a deficiency of arylsulfatase A. This results in accumulation of sulfated glycolipids (sulphatide) within lysosomes of myelin forming cells in the central and peripheral nervous system and to a lesser extent in lysosomes of cells comprising the liver, kidneys, and gallbladder. The disease is characterized by progressive demyelination with wide variability in clinical onset and severity. Depending upon the age at onset and disease progression, MLD may be classified as late infantile (6 months to 4 years), early juvenile (4 to 6 years), late juvenile (6 to 16 years), and adult (>16 years). In the late infantile and early juvenile forms, blindness, gait disturbances, loss of speech, loss of hearing, and quadriparesis are common signs. In older children and adults the disease may present with gait disturbances, mental regression, and behavioral abnormalities. Disease progression, also variable, results in death within a few years to several decades; however, disease progression among affected siblings seems to follow a similar course, unlike many other leukodystrophies. Bone marrow transplantation (BMT) has been the only partially effective treatment reported for MLD. BMT has been shown to halt disease progression when asymptomatic patients achieve engraftment prior to the age at which symptoms occurred in an affected, symptomatic sibling. Despite stabilization of the clinical course when receiving BMT before symptoms, patients' neurophysiologic test abnormalities persist. The clinical implication of this finding has not been further researched. Patients who show mild to moderate progression of their disease prior to transplantation continue to exhibit disease progression to severe impairment. However, specific degrees of clinical impairment in neurodevelopmental function have not been monitored to determine what level of cognitive and motor impairment can be present and still allow the patient to confer benefits from treatment. Patients with late infantile MLD appear to benefit the least from the transplantation process based on preliminary unpublished data. Several case report studies for patients with late infantile MLD indicate delayed, but continued progression of the disease despite BMT, while others suggest initial deterioration followed by stabilization. Transplantation with allogenic hematopoietic stem cells has been shown to positively influence the disease progression of other lysosomal storage diseases such as Hurler Syndrome and Krabbe Disease and testing for enzyme replacement for MLD is already underway. For future researchers to be able compare the benefits of children with MLD who receive treatment to those who remained untreated, a better understanding of the natural progression of late infantile MLD is necessary. The current literature contains studies of individual or small groups of MLD patients that tracked intelligence quotients and neurophysiologic function, but did not correlate this with patients' neurodevelopment. A longitudinal study of a larger population of patients with late infantile MLD has yet to be performed. This protocol is a longitudinal observational study to capture natural history data in patients with late infantile MLD. This data will provide baseline neurobehavioral, neuroimaging, and neurophysiological information that can in the future be used to evaluate treatment effects.

Other known NCT identifiers

• NCT03333200

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 10
• Est. completion date: January 2030
• Est. primary completion date: January 2030
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A to 6 Years

Eligibility

Inclusion Criteria:

1. The patient must have a confirmed diagnosis of MLD as defined by:

ASA activity < 10 nmol/h/mg in leukocytes Presence of elevated sulfatide in urine

2. The patient must have voluntary function (as judged by the investigator), including cognitive and motor function that is no more than 3 standard deviations below normal at the time of enrollment.

3. The patient must have an age at the time of screening birth to < 6 years

4. The patient must have had onset of symptoms before the age of 4 years

5. The subject and his/her guardian(s) must have the ability to comply with the clinical protocol

Exclusion Criteria:

1. Known multiple sulfatase deficiency

2. Presence of major congenital abnormality

3. Presence of known chromosomal abnormality and other neurological conditions unrelated to MLD that can affect psychomotor development

4. History of hematopoietic stem cell transplantation

5. Presence of known clinically significant cardiovascular, hepatic, pulmonary or renal disease or other medical condition

6. Any other medical condition or serious intercurrent illness, or extenuating circumstance that, in the opinion of the principal investigator, would preclude participation in the trial

7. Use of any investigational product within 30 days prior to study enrollment or currently enrolled in another study which involves clinical investigations.

8. The patient's parent(s) and/or legal guardian is unable to understand the nature, scope, and possible consequences of the study.

9. Patient is unable to comply with the protocol, i.e. inability to return for follow-up evaluations or otherwise unlikely to complete the study as determined by the principal investigator.

Related Conditions & MeSH terms

• Leukodystrophy, Metachromatic
• Metachromatic Leukodystrophy

Locations

Country	Name	City	State
United States	University of Pittsburgh, Children's Hospital of Pittsburgh-UPMC	Pittsburgh	Pennsylvania

Sponsors (1)

Lead Sponsor	Collaborator
University of Pittsburgh

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Results of cognitive and motor testing	Patients receive standardized neurodevelopmental testing Cognitive Motor Language	baseline, 6 months, 12 months and then yearly
Secondary	Audiology	Audiologic examination	baseline, 6, 12, then yearly
Secondary	MRI	Magnetic Resonance Imaging of the Brain	yearly

External Links

•   Information on the Program for the Study of Neurodevelopment in Rare Disorders