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Completed

NCT Number: NCT00474396

Dietary Interventions Evaluating Transport of Uric Acid Across the Tubules

The purpose of the study is to determine whether low fat dairy diet reduces serum uric acid levels.

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Key information

Conditions

Age range

18 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

Uric acid plays a role not only in the pathogenesis of gout but is also a predictor of cardiovascular disease, hypertension and renal disease in man. We have identified the human urate ion channel transporter (hUAT), located in the proximal convoluted tubule of the kidney that is involved in both the secretion and reabsorption of urate across the tubule. This channel has a unique lectin binding site that in in-vitro studies, has been found to be modulated by glucose, galactose and lactose. We have also identified a mutation (G/A polymorphism) in our laboratory, that in in-vitro studies has demonstrated diminished hUAT channel activity. Cross-sectional studies have earlier shown that uric acid levels vary with serum glucose levels. Studies have also reported that a low-fat dairy diet reduces the incidence of gout, while others have shown that this diet reduces blood pressure significantly when compared with a non-dairy diet. We hypothesize that the effect of blood glucose levels in lowering uric acid levels is through the regulation of hUAT channel activity. We also hypothesize that a low-fat dairy diet reduces serum uric acid levels through hUAT regulation leading to a decrease in the incidence of gout and a reduction in blood pressure levels. In our proposed randomized, controlled, cross-over trial in healthy adult volunteers, we aim to study the effect of a low-fat dairy diet and a non-dairy diet on serum uric acid levels, the renal fractional excretion of uric acid and blood pressure. We will also study the effect of an acute intravenous infusion of glucose on these parameters. DNA analysis for hUAT mutations of study subjects will be done to assess if there is a blunted response of hUAT activity in subjects with the polymorphism as compared to normal individuals.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • • Healthy adult volunteers
  • Coronary artery disease
  • Glucose intolerance or Diabetes(a fasting blood sugar of less than 100 mg/dl as per the American Diabetes Association guidelines)
  • CHF
  • Gout
  • Lactose intolerance
  • Milk allergy
  • Women who are pregnant or lactating
  • Subjects who are on any medications except birth control pills
  • Subjects who drink more than 3 servings of beer or liquor per week.
  • Normal blood pressure ( less than 120 mmHg systolic and 80 mmHg diastolic)
  • Normal serum UA levels
  • Normal renal funcion (calculated GFR >90ml/min)

Exclusion criteria

  • • Coronary artery disease
  • Glucose intolerance or Diabetes(a fasting blood sugar of less than 100 mg/dl as per the American Diabetes Association guidelines)
  • CHF
  • Gout
  • Lactose intolerance
  • Milk allergy
  • Women who are pregnant or lactating
  • Subjects who are on any medications except birth control pills
  • Subjects who drink more than 3 servings of beer or liquor per week

Treatment and study plan

Low fat dairy diet

Behavioral

Primary outcomes

  1. Lowering of serum uric acid levels

Secondary outcomes

  1. Lowering of the fractional excretion of uric acid and blood pressure

Sponsors and collaborators

Lead sponsor

Icahn School of Medicine at Mount Sinai

Other

Registry information

Acronym: dietUAT

Important dates

Study start
2005
Study completion
2006
First posted
May 16, 2007
Registry last updated
May 16, 2007

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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