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Home > "U" Clinical Trials Conditions > Urinary Vitamin C Loss in Diabetic Subjects  Urinary Vitamin C Loss in Diabetic Subjects
Urinary Vitamin C Loss in Diabetic Subjects
For Condition: Diabetes Mellitus
Status: Recruiting
Sponsor(s): National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) ,
Synopsis: The human body absorbs vitamin C from the intestine. Many different tissues store the vitamin but it is also lost in the urine. This study will examine whether patients with diabetes have low plasma vitamin C concentrations and lose more vitamin C in their urine than healthy people do. To find if this is the case, vitamin C concentrations in blood and urine will be measured. Certain proteins allow the body to absorb and store the vitamin. Variations in these proteins can be found by testing for genetic parameters called single nucleotide polymorphisms (SNPs), which are markers of genetic variation among people. We will test blood samples for specific SNPs related to vitamin C metabolism. This will show whether participants have genetic differences in the proteins that allow them to absorb and store vitamin C. Patients 18 to 65 years of age who are either healthy or have diabetes, have no major illnesses other than diabetes, have no serious complications of the disease and whose blood pressure is well controlled may be eligible for this study. Participants will choose to be studied either as outpatients or inpatients. They will undergo the following tests and procedures: -Medical history -Physical examination. -Blood and urine tests for complete blood count, vitamin C, various chemistries, hepatitis B, hepatitis C, HIV, cotinine and other tests. Participants will be asked to stop taking all vitamin preparations for 2 weeks before the study. Outpatients will provide a blood and urine sample after an overnight fast. The procedure will take a little over 1 hour. Inpatients will also provide a blood and urine sample, and afterward they will be hospitalized for 24 hours and placed on a diet free of vitamin C. They will be asked to eat and drink only food and beverages given to them during those 24 hours. A 24-hour urine sample will be collected for measurement of protein, creatinine, and vitamin C. Another blood sample will be collected on the morning of the second day, along with a sample of urine for vitamin C measurement.
Details: Several studies have reported that diabetic subjects have lower plasma vitamin C concentrations than non-diabetic subjects. Although urinary vitamin C loss in diabetic subjects was reported to be increased in two studies, these are difficult to interpret due to lack of controlled vitamin C intake, inadequate sampling, lack of control subjects, or methodology uncertainties in vitamin C assay and sample processing. Consequently, it is unclear whether diabetic subjects truly have both low plasma and high urine vitamin C concentrations. We propose that low plasma vitamin C concentrations in diabetic subjects are due in part to inappropriate renal loss of vitamin C in these subjects but not in healthy controls. We will study vitamin C concentrations in patients with type 1 and type 2 diabetes and in matched healthy research subjects. Vitamin C concentrations in plasma, neutrophils (as a proxy for tissue concentrations) and in urine will be measured in outpatients. In those willing to be admitted to the Clinical Center, we will measure 24-hour urinary excretion of vitamin C while on a vitamin C free diet, and creatinine clearance, a measure of glomerular filtration rate. Single nucleotide polymorphisms (SNPs) will be determined in genomic DNA responsible for the two proteins mediating sodium-dependent vitamin C transport, SVCT1 and SVCT2. If low plasma and high urine vitamin C concentrations are found in diabetic subjects, further studies will be needed to explore mechanisms and to determine recommended dietary allowances for this patient population.
Eligibility:
Study Type: Observational, Screening
Minimum Age/Maximum Age: /
Genders: Both
Protocol Entry Criteria: INCLUSION CRITERIA: We propose to study 150 male and female subjects between the ages of 18 and 65. This will include 50 healthy subjects and 100 subjects with type 1 or type 2 diabetes. To be included in the study, study subjects should: -be non smokers and be in good general health. -have no significant illnesses other than the complications of diabetes mellitus but should not have neuropathy affecting the functioning of internal organs such as the stomach and urinary bladder. -have serum creatinine less than 2. -be normotensive at the time of the study, with a blood pressure less than or equal to 140/90. Acceptable medications include insulin and ACE inhibitors or ARBs for type 1 diabetes and oral hypoglycemic agents and ACE inhibitors or ARBs in the case of type 2 diabetes. Type 1 and type 2 diabetic subjects on aspirin are also eligible provided they are not taking it for known ischemic heart disease or cerebrovascular disease. The aim of this study is to determine whether diabetic subjects lose vitamin C in the urine in their normal clinical condition (i.e while on treatment) and not in the native untreated state of uncontrolled hyperglycemia. Therefore the patients will not discontinue medication. EXCLUSION CRITERIA: Exclusion criteria will include the following: -significant organ malfunction including liver disease, pulmonary disease, ischemic heart disease, heart failure, stroke, peripheral vascular disease, and anemia. -other serious or chronic illness; history of serious or chronic illness; coronary artery disease, or peripheral vascular disease. -pregnancy or acromegaly. -alcohol abuse, drug addiction or the use of illegal drugs. -use of vitamin supplements within 2 weeks prior to sample procurement. -positive HIV or hepatitis (B or C) screening tests (subjects will be notified of these test results). -presence of other concomitant conditions which in the judgment of the investigators can influence vitamin C metabolism or vitamin C renal handling. For inpatient subjects, an additional exclusion criterion is consumption during the hospitalization of any foods or beverages other than those in the vitamin C free diet.
Total Enrollment: 150
Location and Contact Information:
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) *Recruiting*
Bethesda, Maryland, 20892
United States
Recruiting Patient and Public Liaison Office 1-800-411-1222
Additional Information:
Study ID Numbers: 040021; 04-DK-0021
Study Start Date: October 24, 2003
Record last reviewed: October 21, 2003
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00071526
Other Diabetes Mellitus Studies:
1. Genetics of the Metabolic Syndrome in Japanese Americans
2. Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (ALLHAT)
3. Cohort Study of Heart Rate Variability
4. Effect of AC2993 with or without Immunosuppression on Beta Cell Function in Patients with Type I Diabetes
5. Finding Diabetes Mellitus Among Veterans
Related Studies:
Other Diabetes Mellitus Clinical Trials
Other Maryland Clinical Trials
Other Bethesda Clinical Trials
Urinary Vitamin C Loss in Diabetic Subjects
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