Homocystinuria
Conditions
Keywords
cystathionine beta-synthase (CBS)
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 risk for developing blood clots and are at risk for developing eye and bone abnormalities. Current treatments are generally difficult to follow and can fail. Development of additional therapies has been limited by lack of understanding of how the disease works. The purpose of this study is to see if oxidative stress and inflammation are involved in the disease process and if short-term supplementation with taurine is an effective treatment. Funding source: FDA.
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 have a very high risk for developing blood clots that can cause a stroke or other life-threatening problems. In addition, these individuals have bone and joint tissue abnormalities. Current treatment with an extremely strict diet and medication (betaine) is very difficult to follow, and often fails. Development of additional treatment strategies has been limited by a lack of knowledge and understanding of how this disease works. Hence, there is a need to better understand what causes the blood clots and the bone and joint tissue abnormalities. New data suggest that oxidative stress and inflammation play a central role in animals with this disease. Limited data on humans with this disease support this as well. Further, data from animals with this disease suggests that taurine, a natural body substance and food product, which is low in these patients, mitigates this effect. This study is designed to follow-up on these data. The purpose of the study is to increase our understanding of the disease process in this disorder, and to see in a pilot study if short-term supplementation with taurine is an effective intervention. The aims of the study are to: 1. see if substances (markers) associated with oxidative stress and inflammation are increased in individuals with CBSDH 2. see if the levels of these markers relate to the levels of homocysteine 3. see if the levels of these markers decrease with short-term taurine supplementation 4. see how bood vessels and platelets (small substances in the blood that help blood clot) work in individuals with CBSDH, if their ability to work is related to levels of markers of oxidative stress and inflammation, and if taurine supplementation improves how they work 5. see if alterations of bone strength are related to levels of markers of inflammation. The hypotheses to be investigated are as follows: * Biomarkers of oxidative stress and inflammation are increased in individuals with CBSDH * The degree of elevation of the biomarkers of oxidative stress and inflammation is relative to the degree of elevation of homocysteine, the main accumulating substance for this disease. * Treatment with taurine mitigates the elevation of biomarkers of oxidative stress and inflammation. * Endothelial function (blood vessel function) is abnormal in individuals with CBSDH even when receiving standard therapy and is improved with taurine supplementation. * Chronic platelet aggregation, a variable finding in individuals with CBSDH, is mitigated with taurine supplementation. * Decreased bone mineral density relates to the increase in inflammatory markers in CBSDH. In addition, baseline pharmacokinetics (how much taurine is in the blood) of oral pharmacologic doses of taurine will be developed.
Interventions
DRUGtaurine
Take Taurine for 4 1/2 days, two doses per day
Sponsors
University of Colorado, Denver
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
8 Years to 49 Years
Healthy volunteers
No
Inclusion criteria
1. A confirmed biochemical, molecular, or enzymatic diagnosis of classic homocystinuria due to cystathionine beta-synthase deficiency (OMIM 236200) 2. And not fully responsive to therapy (eg, total homocysteine (tHcy) levels above 50 µmol/L on therapy including on B6 therapy) 3. Be over 8 years old and less than 50 years. The first four patients will be adults (age 18-50 years) 4. Be able and willing to provide informed consent
Exclusion criteria
1. 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. 2. Continued antioxidant intake: 1. 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. 2. 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.) 3. 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. 3. 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. 4. Inflammatory status: 1. 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. 2. 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. 5. 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. 6. Hypertriglyceridemia. Individuals with a triglyceride level above 300 mg/dl will be excluded from the study. 7. 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. 8. Study compliance and integrity: Individual who anticipate an inability to comply with study procedures and requirements will be excluded. \-
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Difference in Thiobarbituric Acid Reactive Substances (TBARS) in Individuals With Cystathionine Beta Synthase Deficient Homocystinuria (CBSDH) Pre and Post Taurine Treatment. | Baseline and after 4 days of therapy. | TBARS were measured in plasma via colorimetric absorbance. TBARS are a marker of oxidative stress. They are formed as a by-product of lipid (fat) oxidation. TBARS predominantly reflect the level of malondialdehyde (MDA) a substance that is formed from the breakdown of polyunsaturated fatty acids. |
| Difference in Tumor Necrosis Factor Alpha (TNF-alpha) in Individuals With CBSDH Pre and Post Taurine Treatment. | Baseline and after 4 days of treatment. | TNF-alpha was measured in plasma via Luminex high sensitivity assay. TNF-alpha is a signaling protein, or cytokine that promotes an inflammatory response. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Difference in Endothelial Function (Blood Vessel Function) in Individuals With CBSDH Pre and Post Taurine Treatment | Baseline and after 4.5 days of taurine treatment | Endothelial function was measured by doppler brachial artery flow-mediated dilation (FMD) studies. |
| Difference in Endothelial Function (Blood Vessel Function) in Individuals With CBSDH and Homocysteine Levels Greater Than 125 Micromole/L Pre and Post Taurine Treatment. | Baseline and after 4.5 days of therapy. | Endothelial function was measured by doppler brachial artery flow-mediated dilation (FMD) studies. |
| Difference in Endothelial Function (Blood Vessel Function) in Individuals With CBSDH and Pre Taurine Exposure FMD Values Less Than 10 mm Pre and Post Taurine Treatment. | Baseline and after 4.5 days of therapy. | Endothelial function was measured by doppler brachial artery flow-mediated dilation (FMD) studies. |
| Percent of Individuals With Decreased Bone Mineral Density. | Baseline | Bone mineral density was assessed via whole body dual energy X-ray absorptiometry (DEXA) with bone density corrected for age. The absolute DEXA value was not used for analysis, rather values below 2 standard deviations of normal were taken as evidence of osteoporosis. |
Other
| Measure | Time frame | Description |
|---|---|---|
| Thiobarbituric Acid Reactive Substances (TBARS) in Individuals With CBSDH Compare to Homocysteine Level. | Baseline | TBARS were measured in plasma via colorimetric absorbance. Homocysteine was measured in serum by gas chromatography/mass spectrometry (GC/MS) in a Clinical Laboratory Improvements Amendments (CLIA) approved clinical laboratory. TBARS are a marker of oxidative stress. TBARS are formed as a by-product of lipid (fat) oxidation. TBARS predominantly reflect the level of malondialdehyde (MDA) a substance that is formed from the breakdown of polyunsaturated fatty acids. |
| Determination of Baseline Taurine Level, Peak Taurine Level on Day One, Trough Level on Day One and Trough Level on Day Four of Taurine Treatment. | Taurine levels were obtained prior to taurine adminstration and at , t=0.5, t=1, t=2, t=3, t=4, t=6, t=8, t=12 and 96 hours. | Taurine was measured in plasma via liquid chromatogram(LC)-MS/MS. |
| Difference in Triglycerides in Individuals With CBSDH Receiving Both Low Dose and Target Dose Taurine Pre and Post Taurine Treatment (Safety Assessment) | Baseline and after 4 days of treatment. | Triglycerides were measured in a CLIA approved clinical laboratory.Triglycerides are a natural occurring fat. High levels over a long period of time can increase the chances for heart disease. Levels greater that 1000 mg/dl over a short period of time can increase chances of pancreatitis. |
| Difference in Triglycerides in Individuals With CBSDH Receiving Target Dose Taurine Pre and Post Taurine Treatment (Safety Assessment) | Baseline and after 4 days of treatment. | Triglycerides were measured in a CLIA approved clinical laboratory. Triglycerides are a natural occurring fat, High levels over a long period of time can increase the chances for heart disease. Levels greater that 1000 mg/dl over a short period of time can increase chances of pancreatitis. |
| Difference in Systolic Blood Pressure in Individuals With CBSDH Receiving Both Low Dose and Target Dose Taurine Pre and Post Taurine Treatment (Safety Assessment). | Baseline and after 4 days of treatment. | — |
| Difference in Diastolic Blood Pressure in Individuals With CBSDH Receiving Both Low Dose and Target Dose Taurine Pre and Post Taurine Treatment (Safety Assessment). | Baseline and after 4 days of treatment. | — |
Countries
United States
Participant flow
Recruitment details
Subjects were screened and recruited from three sites in the United States.
Pre-assignment details
After enrollment a washout period for medications was required. At first study visit, assignment to arm occurred. One individual, while consented, did not participate at first study visit due to acute illness, was never rescheduled, and was removed. Number of subjects who started arm and completed study was thus 14.
Participants by arm
| Arm | Count |
|---|---|
| Taurine Intervention Treatment with taurine for 4 1/2 days, two doses per day | 14 |
| Total | 14 |
Baseline characteristics
| Characteristic | Taurine Intervention |
|---|---|
| Age, Customized Age Distribution by Meaningful Groups Older Adults (30-50 years) | 2 Participants |
| Age, Customized Age Distribution by Meaningful Groups Prepubertal (8-12 years) | 4 Participants |
| Age, Customized Age Distribution by Meaningful Groups Teenagers (12-<20 years) | 4 Participants |
| Age, Customized Age Distribution by Meaningful Groups Young Adults (20-<30 years) | 4 Participants |
| Race/Ethnicity, Customized Categories Asian | 0 Participants |
| Race/Ethnicity, Customized Categories Black | 2 Participants |
| Race/Ethnicity, Customized Categories Hispanic | 3 Participants |
| Race/Ethnicity, Customized Categories Native American | 0 Participants |
| Race/Ethnicity, Customized Categories Other | 0 Participants |
| Race/Ethnicity, Customized Categories White | 9 Participants |
| Sex: Female, Male Female | 6 Participants |
| Sex: Female, Male Male | 8 Participants |
Adverse events
| Event type | EG000 affected / at risk |
|---|---|
| deaths Total, all-cause mortality | 0 / 14 |
| other Total, other adverse events | 5 / 14 |
| serious Total, serious adverse events | 0 / 14 |
Outcome results
Primary
Difference in Thiobarbituric Acid Reactive Substances (TBARS) in Individuals With Cystathionine Beta Synthase Deficient Homocystinuria (CBSDH) Pre and Post Taurine Treatment.
TBARS were measured in plasma via colorimetric absorbance. TBARS are a marker of oxidative stress. They are formed as a by-product of lipid (fat) oxidation. TBARS predominantly reflect the level of malondialdehyde (MDA) a substance that is formed from the breakdown of polyunsaturated fatty acids.
Time frame: Baseline and after 4 days of therapy.
Population: Analyzable data from all individuals with CBSDH who received the target dose of taurine were used for the calculations. The two individuals treated with low dose taurine were excluded from he analysis.
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Taurine Intervention Group | Difference in Thiobarbituric Acid Reactive Substances (TBARS) in Individuals With Cystathionine Beta Synthase Deficient Homocystinuria (CBSDH) Pre and Post Taurine Treatment. | Pre Treatment | 3.47 nmol/ml | Standard Error 0.18 |
| Taurine Intervention Group | Difference in Thiobarbituric Acid Reactive Substances (TBARS) in Individuals With Cystathionine Beta Synthase Deficient Homocystinuria (CBSDH) Pre and Post Taurine Treatment. | Post treatment | 3.16 nmol/ml | Standard Error 0.27 |
Comparison: Null hypothesis applied.p-value: 0.235t-test, 2 sided
Primary
Difference in Tumor Necrosis Factor Alpha (TNF-alpha) in Individuals With CBSDH Pre and Post Taurine Treatment.
TNF-alpha was measured in plasma via Luminex high sensitivity assay. TNF-alpha is a signaling protein, or cytokine that promotes an inflammatory response.
Time frame: Baseline and after 4 days of treatment.
Population: Analyzable data from all individuals with CBSDH who received the target dose of taurine were used for the calculations. The two individuals treated with low dose taurine were excluded from the analysis.
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Taurine Intervention Group | Difference in Tumor Necrosis Factor Alpha (TNF-alpha) in Individuals With CBSDH Pre and Post Taurine Treatment. | Pre treatment | 5.95 pg/ml | Standard Error 0.39 |
| Taurine Intervention Group | Difference in Tumor Necrosis Factor Alpha (TNF-alpha) in Individuals With CBSDH Pre and Post Taurine Treatment. | Post treatment | 6.07 pg/ml | Standard Error 0.49 |
Comparison: Null hypothesis assumed.p-value: 0.701t-test, 2 sided
Secondary
Difference in Endothelial Function (Blood Vessel Function) in Individuals With CBSDH and Homocysteine Levels Greater Than 125 Micromole/L Pre and Post Taurine Treatment.
Endothelial function was measured by doppler brachial artery flow-mediated dilation (FMD) studies.
Time frame: Baseline and after 4.5 days of therapy.
Population: Analyzable data from all individuals with CBSDH having baseline homocysteine levels greater than 125 micromole/L who received the target dose of taurine were used for the calculations. The two individuals treated with low dose taurine were excluded from the analysis.
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Taurine Intervention Group | Difference in Endothelial Function (Blood Vessel Function) in Individuals With CBSDH and Homocysteine Levels Greater Than 125 Micromole/L Pre and Post Taurine Treatment. | Pre treatment | 7.25 mm | Standard Error 1.23 |
| Taurine Intervention Group | Difference in Endothelial Function (Blood Vessel Function) in Individuals With CBSDH and Homocysteine Levels Greater Than 125 Micromole/L Pre and Post Taurine Treatment. | Post treatment | 11.10 mm | Standard Error 1.48 |
Comparison: Null hypothesis applied.p-value: 0.052t-test, 2 sided
Secondary
Difference in Endothelial Function (Blood Vessel Function) in Individuals With CBSDH and Pre Taurine Exposure FMD Values Less Than 10 mm Pre and Post Taurine Treatment.
Endothelial function was measured by doppler brachial artery flow-mediated dilation (FMD) studies.
Time frame: Baseline and after 4.5 days of therapy.
Population: Analyzable data from all individuals with CBSDH studied with baseline flow mediated dilation values of less than 10 mm and who received the target dose of taurine were used for the calculations. The two individuals treated with low dose taurine were excluded from the analysis.
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Taurine Intervention Group | Difference in Endothelial Function (Blood Vessel Function) in Individuals With CBSDH and Pre Taurine Exposure FMD Values Less Than 10 mm Pre and Post Taurine Treatment. | Pre Treatment | 5.98 mm | Standard Error 0.51 |
| Taurine Intervention Group | Difference in Endothelial Function (Blood Vessel Function) in Individuals With CBSDH and Pre Taurine Exposure FMD Values Less Than 10 mm Pre and Post Taurine Treatment. | Post Treatment | 9.86 mm | Standard Error 1.28 |
Comparison: Null hypothesis assumed.p-value: 0.014t-test, 2 sided
Secondary
Difference in Endothelial Function (Blood Vessel Function) in Individuals With CBSDH Pre and Post Taurine Treatment
Endothelial function was measured by doppler brachial artery flow-mediated dilation (FMD) studies.
Time frame: Baseline and after 4.5 days of taurine treatment
Population: Analyzable data from all individuals with CBSDH who received the target dose of taurine were used for the calculations. The two individuals treated with low dose taurine were excluded from the analysis.
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Taurine Intervention Group | Difference in Endothelial Function (Blood Vessel Function) in Individuals With CBSDH Pre and Post Taurine Treatment | Pre treatment | 9.80 mm | Standard Error 1.76 |
| Taurine Intervention Group | Difference in Endothelial Function (Blood Vessel Function) in Individuals With CBSDH Pre and Post Taurine Treatment | Post treatment | 11.57 mm | Standard Error 1.21 |
Comparison: Null hypothesis applied.p-value: 0.19t-test, 2 sided
Secondary
Percent of Individuals With Decreased Bone Mineral Density.
Bone mineral density was assessed via whole body dual energy X-ray absorptiometry (DEXA) with bone density corrected for age. The absolute DEXA value was not used for analysis, rather values below 2 standard deviations of normal were taken as evidence of osteoporosis.
Time frame: Baseline
Population: Analysis was on all analyzable data from subjects with CBSDH who participated in the active study and data from control population as provided by DEXA report.
| Arm | Measure | Group | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|---|
| Taurine Intervention Group | Percent of Individuals With Decreased Bone Mineral Density. | Normal bone mineral denisty | 14 Participants |
| Taurine Intervention Group | Percent of Individuals With Decreased Bone Mineral Density. | Abnormal bone mineral density | 0 Participants |
Other Pre-specified
Determination of Baseline Taurine Level, Peak Taurine Level on Day One, Trough Level on Day One and Trough Level on Day Four of Taurine Treatment.
Taurine was measured in plasma via liquid chromatogram(LC)-MS/MS.
Time frame: Taurine levels were obtained prior to taurine adminstration and at , t=0.5, t=1, t=2, t=3, t=4, t=6, t=8, t=12 and 96 hours.
Population: Analyzable data from all individuals with CBSDH who received the target dose of taurine were used for the calculations. The two individuals treated with low dose taurine were excluded from the analysis.
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Taurine Intervention Group | Determination of Baseline Taurine Level, Peak Taurine Level on Day One, Trough Level on Day One and Trough Level on Day Four of Taurine Treatment. | Baseline value | 40.5 microM | Standard Deviation 11.9 |
| Taurine Intervention Group | Determination of Baseline Taurine Level, Peak Taurine Level on Day One, Trough Level on Day One and Trough Level on Day Four of Taurine Treatment. | Peak Value Day One | 753.0 microM | Standard Deviation 240 |
| Taurine Intervention Group | Determination of Baseline Taurine Level, Peak Taurine Level on Day One, Trough Level on Day One and Trough Level on Day Four of Taurine Treatment. | Trough Value Day One 12h | 50.0 microM | Standard Deviation 14 |
| Taurine Intervention Group | Determination of Baseline Taurine Level, Peak Taurine Level on Day One, Trough Level on Day One and Trough Level on Day Four of Taurine Treatment. | Trough Value Day Four | 82.0 microM | Standard Deviation 36.2 |
Other Pre-specified
Difference in Diastolic Blood Pressure in Individuals With CBSDH Receiving Both Low Dose and Target Dose Taurine Pre and Post Taurine Treatment (Safety Assessment).
Time frame: Baseline and after 4 days of treatment.
Population: Analyzable data from all individuals with CBSDH who were treated with taurine, this being both low dose and targeted dose of medication.
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Taurine Intervention Group | Difference in Diastolic Blood Pressure in Individuals With CBSDH Receiving Both Low Dose and Target Dose Taurine Pre and Post Taurine Treatment (Safety Assessment). | Pre Taurine | 70 mmHg | Standard Deviation 10 |
| Taurine Intervention Group | Difference in Diastolic Blood Pressure in Individuals With CBSDH Receiving Both Low Dose and Target Dose Taurine Pre and Post Taurine Treatment (Safety Assessment). | Post Taurine | 68 mmHg | Standard Deviation 8 |
p-value: 0.1t-test, 2 sided
Other Pre-specified
Difference in Systolic Blood Pressure in Individuals With CBSDH Receiving Both Low Dose and Target Dose Taurine Pre and Post Taurine Treatment (Safety Assessment).
Time frame: Baseline and after 4 days of treatment.
Population: Analyzable data from all individuals with CBSDH who were treated with taurine, this being both low dose and targeted dose of medication.
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Taurine Intervention Group | Difference in Systolic Blood Pressure in Individuals With CBSDH Receiving Both Low Dose and Target Dose Taurine Pre and Post Taurine Treatment (Safety Assessment). | Pre Taurine | 116 mmHg | Standard Deviation 12 |
| Taurine Intervention Group | Difference in Systolic Blood Pressure in Individuals With CBSDH Receiving Both Low Dose and Target Dose Taurine Pre and Post Taurine Treatment (Safety Assessment). | Post Taurine | 112 mmHg | Standard Deviation 12 |
Comparison: Null hypothesis applied.p-value: 0.16t-test, 2 sided
Other Pre-specified
Difference in Triglycerides in Individuals With CBSDH Receiving Both Low Dose and Target Dose Taurine Pre and Post Taurine Treatment (Safety Assessment)
Triglycerides were measured in a CLIA approved clinical laboratory.Triglycerides are a natural occurring fat. High levels over a long period of time can increase the chances for heart disease. Levels greater that 1000 mg/dl over a short period of time can increase chances of pancreatitis.
Time frame: Baseline and after 4 days of treatment.
Population: Analyzable data from all individuals with CBSDH who were treated with taurine, this being both low dose and targeted dose of medication.
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Taurine Intervention Group | Difference in Triglycerides in Individuals With CBSDH Receiving Both Low Dose and Target Dose Taurine Pre and Post Taurine Treatment (Safety Assessment) | Pre Taurine | 77.5 mg/dL | Standard Error 19 |
| Taurine Intervention Group | Difference in Triglycerides in Individuals With CBSDH Receiving Both Low Dose and Target Dose Taurine Pre and Post Taurine Treatment (Safety Assessment) | Post Taurine | 116.7 mg/dL | Standard Error 33.4 |
Comparison: Null hypothesis assumedp-value: 0.014t-test, 2 sided
Other Pre-specified
Difference in Triglycerides in Individuals With CBSDH Receiving Target Dose Taurine Pre and Post Taurine Treatment (Safety Assessment)
Triglycerides were measured in a CLIA approved clinical laboratory. Triglycerides are a natural occurring fat, High levels over a long period of time can increase the chances for heart disease. Levels greater that 1000 mg/dl over a short period of time can increase chances of pancreatitis.
Time frame: Baseline and after 4 days of treatment.
Population: Analyzable data from all individuals with CBSDH who received the target dose of taurine were used for the calculations. The two individuals treated with low dose taurine were excluded from the analysis.
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Taurine Intervention Group | Difference in Triglycerides in Individuals With CBSDH Receiving Target Dose Taurine Pre and Post Taurine Treatment (Safety Assessment) | Pre Treatment | 61.6 mg/dL | Standard Error 12.7 |
| Taurine Intervention Group | Difference in Triglycerides in Individuals With CBSDH Receiving Target Dose Taurine Pre and Post Taurine Treatment (Safety Assessment) | Post Treatment | 98.7 mg/dL | Standard Error 29.7 |
Comparison: Null hypothesis assumedp-value: 0.012t-test, 2 sided
Other Pre-specified
Thiobarbituric Acid Reactive Substances (TBARS) in Individuals With CBSDH Compare to Homocysteine Level.
TBARS were measured in plasma via colorimetric absorbance. Homocysteine was measured in serum by gas chromatography/mass spectrometry (GC/MS) in a Clinical Laboratory Improvements Amendments (CLIA) approved clinical laboratory. TBARS are a marker of oxidative stress. TBARS are formed as a by-product of lipid (fat) oxidation. TBARS predominantly reflect the level of malondialdehyde (MDA) a substance that is formed from the breakdown of polyunsaturated fatty acids.
Time frame: Baseline
Population: Analyzable data from all subjects with CBSDH who completed day one of active study and normal homocysteine values provided by assaying laboratory were used for the calculations.
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Taurine Intervention Group | Thiobarbituric Acid Reactive Substances (TBARS) in Individuals With CBSDH Compare to Homocysteine Level. | TBARS | 0.00365 micromol/l | Standard Error 0.00087 |
| Taurine Intervention Group | Thiobarbituric Acid Reactive Substances (TBARS) in Individuals With CBSDH Compare to Homocysteine Level. | Homocysteine | 161 micromol/l | Standard Error 67.2 |
Comparison: Null hypothesis assumedp-value: 0.541Spearman's rank correlation