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Cholesterol and Antioxidant Treatment in Patients With Smith-Lemli-Opitz Syndrome (SLOS)

Cholesterol and Antioxidant Treatment in Patients With Smith-Lemli-Opitz Syndrome (SLOS)

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01773278
Enrollment
100
Registered
2013-01-23
Start date
2008-12-31
Completion date
2025-12-31
Last updated
2024-05-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cone-Rod Dystrophy, Hearing Loss, Smith-Lemli-Opitz Syndrome

Keywords

Antioxidant treatment, Oxysterols, Cholesterol deficiency, Accumulation of 7-dehydrocholesterol, electroretinogram (ERG), Auditory Brainstem Response (ABR)

Brief summary

Patients with biochemically confirmed SLOS are being treated with cholesterol supplementation and antioxidant medication. They are carefully monitored with visits to clinic, laboratory testing including cholesterol and 7-dehydrocholesterol levels, vitamin levels, blood counts and liver and kidney function. On a serial basis, no more often than once a year, the patients undergo a series of tests under anesthesia, including electroretinogram (ERG), brainstem audiometry (ABR), and ophthalmologic exam under anesthesia to follow pigmentary retinopathy.

Detailed description

Smith-Lemli-Opitz Syndrome (SLOS) is an autosomal recessive disorder caused by a metabolic error in the final step of cholesterol biosynthesis, leading to cholesterol deficiency and accumulation of the cholesterol precursor, 7-dehydrocholesterol.Patients with SLOS display complex medical problems including growth failure, intellectual disability, behavioral disorders, progressive retinal dystrophy, hearing loss and photosensitivity. Dr Elias was one of the original geneticists who discovered the cause of this disorder in 1994, and ever since has been treating SLOS patients with cholesterol supplementation. In 2008, a second medication called AquADEKS, a mixture of vitamins and other compounds with antioxidant properties was added to the treatment regimen. AquADEKS has since been replaced with a comparable medication named DEKAS plus.The purpose of the DEKAS plus is to allow treatment with antioxidant medications in an effort to prevent retinal degeneration, hearing and skin problems associated with SLOS. This protocol has been approved by the Colorado Multiple Institutional Review Board and supported by the Clinical Translational Research Center (CTRC) since 2001. The following updated information is available about the protocol: 1\. Research has revealed that oxysterols are toxic compounds made from the cholesterol precursor, 7-dehydrocholesterol. These oxysterol compounds are severely neurotoxic and toxic to the retina, and treatment with antioxidants may help lower their levels, resulting in slowing of retinal deterioration. Testing of oxysterol levels in patients with SLOS is now ongoing, in collaboration with a laboratory at University of Washington in Seattle (Dr Libin Xu). It is hoped that testing of oxysterol levels in blood may help provide more updated info to help guide treatment.

Interventions

DRUGAntioxidants

Patients will be prescribed the drug DEKAS plus at a dose based on age and weight. The effects of the treatment will be monitored by serial ERG, ABR, oxysterol levels and clinical findings. Blood levels of 25-Oh vitamin D will be monitored to prevent toxicity.

DRUGCholesterol

Patients with SLOS typically have cholesterol deficiency. They will be treated with cholesterol supplementation to keep cholesterol levels \> 100 mg/dl if possible

Sponsors

University of Colorado, Denver
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
No minimum to 65 Years
Healthy volunteers
No

Inclusion criteria

* Clinical diagnosis of Smith-Lemli-Opitz Syndrome * Elevated levels of 7-dehydrocholesterol and 8-dehydrocholesterol * Must be able to travel to Children's Hospital Colorado annually * Must have insurance coverage for ERG/ABR studies

Exclusion criteria

* absence of detectable 7-dehydrocholesterol/8-dehydrocholesterol * allergy to Antioxidant medication

Design outcomes

Primary

MeasureTime frameDescription
Change in Electroretinogram (ERG) results over time1-2 yearERG testing will be performed on an serial basis while the patient is being treated with antioxidants (AquADEKS), to follow the amplitude and latency time on ERG. Improvement would be determined by an increased amplitude and decreased latency time.

Secondary

MeasureTime frameDescription
Change in ABR (Auditory Brainstem response) testing over time1-2 yearsPatients will be followed serial with ABR to determine the latency time in Wave I, when treated with antioxidant medication

Other

MeasureTime frameDescription
Change in Blood Oxysterol measurements over time12-24 monthsOxysterols can be measured in blood specimens from SLOS patients.

Countries

United States

Contacts

Primary ContactEllen R Elias, MD
ellen.elias@childrenscolorado.org720 777-5401

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026