Status:

COMPLETED

Oxidative Stress Markers In Inherited Homocystinuria And The Impact Of Taurine

Lead Sponsor:

University of Colorado, Denver

Conditions:

Homocystinuria

Eligibility:

All Genders

8-49 years

Phase:

PHASE1

PHASE2

Brief Summary

Cystathionine beta-synthase deficiency is an inherited disease that results in elevation of a substance called homocysteine (Hcy) in blood and urine. Individuals with this disorder have a very high ri...

Detailed Description

Cystathionine beta-synthase deficient homocystinuria(CBSDH) is an inherited disease that results in elevation of a substance called homocysteine(Hcy)in blood and urine. Individuals with this disorder ...

Eligibility Criteria

Inclusion

  • A confirmed biochemical, molecular, or enzymatic diagnosis of classic homocystinuria due to cystathionine beta-synthase deficiency (OMIM 236200)
  • And not fully responsive to therapy (eg, total homocysteine (tHcy) levels above 50 µmol/L on therapy including on B6 therapy)
  • Be over 8 years old and less than 50 years. The first four patients will be adults (age 18-50 years)
  • Be able and willing to provide informed consent

Exclusion

  • Pregnancy: Females who are pregnant or lactating will be excluded from the study as the influence of pregnancy on the markers is not known nor is the safety of taurine supplementation in pregnancy.
  • Continued antioxidant intake:
  • Individuals currently taking taurine, over the counter energy drinks containing taurine or other high dose antioxidants and unwilling to discontinue this for the study period (including a 2 week wash out period) will be excluded as such intake will likely impact laboratory results.
  • Individuals taking Vitamin C as a prescribed treatment for their homocystinuria will be excluded as the antioxidant therapy may impact antioxidant and inflammation markers. (As Vitamin C is not standard of care for this disease we anticipate this to have minimal impact on recruitment.)
  • Individuals currently taking platelet aggregation inhibitors such as salicylate on a self prescribed basis and unwilling to discontinue this for the study period (including a washout period of at least two weeks prior to the study) will be excluded as salicylate intake will impact platelet study results. Individuals taking salicylate (or other platelet aggregation inhibitors) prescribed as a therapy for their homocystinuria or other health issues will not be asked to stop the medication. They will participate in the study, but will be excluded only from the platelet studies.
  • Medication interactions: Individuals unable or unwilling to abstain from use of cyclic guanosine monophosphate (cGMP) phosphodiesterase 5 inhibitors (such as Viagra) during the study period will be excluded from the nitroglycerin-induced flow-mediated dilatation studies in accordance with known labeling contraindications.
  • Inflammatory status:
  • Individuals who have a significant chronic illness that has a marked inflammatory component will be excluded from the study as the illness will impact inflammatory markers.
  • Patients with an acute illness, which may impact inflammatory biomarkers, will be postponed for study entry until the acute illness is resolved. Entry into the study at a later day will be offered.
  • Recent cardiovascular event. Cardiovascular events (stroke, myocardial infarct, deep vein thrombosis, pulmonary embolus, thrombosis, or uncontrolled hypertension) may interfere with platelet function studies and with various mediators during the first months after the event. Patients who had such an event within the last 6 months will be excluded.
  • Hypertriglyceridemia. Individuals with a triglyceride level above 300 mg/dl will be excluded from the study.
  • Informed consent: Individuals who are unwilling or unable to consent, or in the case of minors who are unwilling or unable to assent will be excluded due to lack of ability to ensure informed consent.
  • Study compliance and integrity: Individual who anticipate an inability to comply with study procedures and requirements will be excluded.
  • \-

Key Trial Info

Start Date :

January 1 2010

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

December 1 2017

Estimated Enrollment :

15 Patients enrolled

Trial Details

Trial ID

NCT01192828

Start Date

January 1 2010

End Date

December 1 2017

Last Update

July 9 2018

Active Locations (4)

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Page 1 of 1 (4 locations)

1

Childrens Hospital Colorado

Aurora, Colorado, United States, 80045

2

University of Colorado

Aurora, Colorado, United States, 80045

3

Duke University

Durham, North Carolina, United States, 27708

4

Childrens Hospital of Philadelphia

Philadelphia, Pennsylvania, United States, 19104

Oxidative Stress Markers In Inherited Homocystinuria And The Impact Of Taurine | DecenTrialz