A Long-Term Study of Cholesterol Supplements for Smith-Lemli-Opitz Syndrome
| Status: | Recruiting |
|---|---|
| Healthy: | No |
| Age Range: | Any |
| Updated: | 11/30/2013 |
| Start Date: | June 2011 |
| Contact: | Sandra K Conley, C.R.N.P. |
| Email: | sconley@mail.nih.gov |
| Phone: | (301) 594-2005 |
Smith-Lemli-Opitz Syndrome: A Longitudinal Clinical Study of Patients Receiving Cholesterol Supplementation
Background:
- Smith-Lemli-Opitz syndrome (SLOS) is a genetic disorder that prevents the body from making
enough cholesterol. People who have SLOS often need to take extra cholesterol, either in
food or in supplements, for their bodies to work properly. Cholesterol is very important for
the brain and nervous system. Therefore SLOS is highly related to autism, mental
retardation, and other brain and nervous system disorders. Not much is known about how
people with SLOS handle cholesterol and how taking extra cholesterol helps them. A long-term
study of people with SLOS will help answer these and other questions.
Objectives:
- To study the effects of a high-cholesterol diet on people with Smith-Lemli-Opitz syndrome.
Eligibility:
- Individuals of any age who have Smith-Lemli-Opitz syndrome.
Design:
- Participants will have study visits up to two times in the first year and once a year
every year after that. Each visit will last between 3 and 5 days.
- Participants will be screened with a physical exam, medical history, and blood and
urine tests.
- Participants will provide regular blood, urine, stool, saliva, and skin cell samples
for testing.
- Participants will keep track of the foods they eat at home. During the study, they will
eat a high-cholesterol diet at all times, except for the second study visit (3 to 6
months after the screening visit). That visit will involve a cholesterol-free diet for
4 weeks.
- Participants will have special cholesterol tests with blood samples at different times
during the study.
- At different study visits, participants will have tests of mental and physical skills
(including tests for autism). They will answer questions about their diet and food
habits. They will also have hearing and eye tests, body and bone measurements, and
imaging studies. Not all of the tests will be done at every study.
- Participants will be allowed to leave the study at any time.
The purpose of this study is to learn as much as possible about Smith-Lemli-Opitz Syndrome
(SLOS) by following a large group of individuals with SLOS over a period of time. We plan to
measure cholesterol and other sterol levels, perform clinical observations, whole body
testing and imaging studies (brain MRIs), to learn more about disease mechanisms and
progression, variations in the clinical features among individuals with SLOS, and evaluate
the effect of cholesterol supplementation in this condition.
Smith-Lemli-Opitz syndrome (SLOS) is a disorder of cholesterol synthesis, or production. It
is caused by mutations in the DHCR7 gene which encodes for 7-dehydrocholesterol-reductase,
an enzyme necessary for the production of cholesterol in the body. Affected individuals
exhibit multiple malformations and mental retardation. The features of SLOS are thought to
be primarily related to cholesterol deficiency and accumulation of cholesterol precursors.
However, the clinical phenotype is not well characterized, the biochemical pathogenesis is
incompletely understood, and there is no proven therapy for this devastating condition. Thus
our primary objective is to better define the clinical and biochemical phenotypes of the
disease using a natural history study design. The study will contribute to creating a
comprehensive SLOS patient registry, identify biomarkers that can be used for diagnostic
testing, screening and outcome measures in future therapeutic trials. All patients with SLOS
receive dietary cholesterol supplementation with the hope that cholesterol supplementation
will improve the clinical manifestation of the disease. However, there is no evidence
supporting a clinical benefit of cholesterol supplementation. Thus a secondary objective of
the study is to determine if cholesterol intake correlates with changes in whole body
cholesterol homeostasis and clinical end-points.
- INCLUSION CRITERIA:
Inclusion of children:
The population being studied is subjects with SLOS. Children will not be excluded, in
fact, the majority of subjects being studied will be infants and children. Relatively few
adults with SLOS are known. We will continue to recruit subjects of all ages from newborn
to adult of both genders.
Inclusion of women:
Women and girls will certainly be included in the study. Women should be equally
represented in this study. SLOS is an autosomal recessively inherited condition that
affects males and females equally. However, since these disorders are uncommon
autosomal-recessively inherited inborn errors of metabolism, STAIR investigators will have
limited control over the gender mix of the study population.
Inclusion of Minorities:
As mentioned for gender, STAIR investigators will have limited control over the race and
ethnicity mix of the study population. In order to increase the enrollment of minority
subjects, with permission, we will inform the national disease support group of our
studies so that subjects in other regions of the US with ethnically and racially more
diverse populations may be recruited. SLOS seems to be most common in Caucasians. In the
current SLOS study at OHSU, only one of the 34 SLOS subjects is Hispanic. There is only 1
report of carriers in Blacks (Nowaczyk, 2001) and only 31 cases reported in a Japanese
survey. In Oregon at least, we will advertise the study at local community health clinics
where large numbers of Hispanics are seen.
EXCLUSION CRITERIA:
None.
We found this trial at
1
site
9000 Rockville Pike
Bethesda, Maryland 20892
Bethesda, Maryland 20892
301-496-4000
National Institutes of Health Clinical Center The National Institutes of Health (NIH) Clinical Center in...
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