The Effects of Dietary Phosphate Intake on Calciotropic Hormones and FGF23.

NCT ID: NCT00305279

Last Updated: 2013-10-10

Basic Information

• Recruitment Status: WITHDRAWN
• Clinical Phase: NA
• Study Classification: INTERVENTIONAL
• Study Start Date: 2006-02-28
• Study Completion Date: 2009-12-31

Brief Summary

The purpose of this study is to determine the effects of different amounts of phosphorus in the diet on hormones that control phosphorus and bone health both in people who are healthy and in ones who have moderate kidney disease.

Detailed Description

Chronic kidney disease affects 11% of the US population; over half of those affected have skeletal manifestations of their renal disease. Renal osteodystrophy is a complex disease, in which multiple mineral systems and related hormones play a role, including phosphate homeostasis. Phosphate regulation primarily depends on renal handling of phosphate, which is partly controlled by parathyroid hormone and vitamin D. However, other mediators in this system clearly exist. Recently, evidence has been accruing that one such factor may be FGF23, a protein produced by osteogenic cells. States of excess FGF23 are associated with marked phosphate wasting, hypophosphatemia, osteomalacia, and inappropriately low calcitriol. FGF23 levels are measurable in healthy humans and markedly elevated in patients who require hemodialysis, although its physiologic role in either state is unknown. Some retrospective evidence suggests that FGF23 is affected by phosphate intake. We are performing a study to gather data describing the response of FGF23 to changes in dietary phosphorus intake in healthy men and women and in men and women with moderate renal insufficiency. The specific aims of this pilot study are: 1) To examine the physiologic effects of alterations in dietary phosphorus on FGF23 in healthy subjects; 2) To examine the physiologic response of FGF23 to dietary phosphorus alterations in patients with moderate renal failure; and 3) To assess whether serum levels of 1,25-dihydroxyvitamin D vary inversely with those of FGF23 when dietary phosphate is changed. The proposed research plan is a dietary intervention trial in which we will study the response of serum FGF23 levels to diets with varying phosphorus contents in healthy adults and adults with moderate renal insufficiency.

Conditions

Healthy; Kidney Failure, Chronic

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Blinding Strategy: SINGLE

Study Groups

1

Group Type: ACTIVE_COMPARATOR

Dietary

Intervention Type: OTHER

Dietary

2

Group Type: ACTIVE_COMPARATOR

Dietary

Intervention Type: OTHER

Dietary

3

Group Type: ACTIVE_COMPARATOR

Dietary

Intervention Type: OTHER

Dietary

Interventions

Dietary

Dietary

Intervention Type: OTHER

Dietary

Dietary

Intervention Type: OTHER

Dietary

Dietary

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

HEALTHY SUBJECTS:

• Men 21-65 years of age;
• Premenopausal women over 21 years of age taking oral contraceptives;
• Postmenopausal women less than 65 years of age;

CHRONIC KIDNEY DISEASE SUBJECTS:

• Men 21-65 years of age;
• Premenopausal women over 21 years of age taking oral contraceptives;
• Postmenopausal women less than 65 years of age;
• Creatinine clearance between 30 and 59 ml/min/1.73 m2 as calculated using the equation derived from the Modification of Diet in Renal Disease (MDRD) study.

Exclusion Criteria

• Medications affecting bone metabolism;
• Abnormal liver or GI function;
• Extreme electrolyte abnormalities;
• BMI >30 kg/m2.

• Minimum Eligible Age: 21 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

National Institutes of Health (NIH)

NIH

Sponsor Role: collaborator

University of California, San Francisco

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Diana M Antoniucci, MD

Role: PRINCIPAL_INVESTIGATOR

University of California, San Francisco

Locations

University of California

San Francisco, California, United States

Countries

United States

Other Identifiers

1K23RR020343

Identifier Type: NIH

Identifier Source: secondary_id

View Link

H40550-27771

Identifier Type: -

Identifier Source: org_study_id