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Impact of Lowering Phosphate Additive Intake on Metabolism and Cardiovascular Health in Community-Living Adults

Primary Purpose

Healthy, Chronic Kidney Disease

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Diet
Sponsored by
University of Alabama at Birmingham
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Healthy focused on measuring phosphorus, fibroblast growth factor 23, diet

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • (i.) Inclusion criteria for healthy volunteers: ≥18 years of age, normal kidney function (eGFR > 60 and normal urinalysis).

Exclusion Criteria:

  • Exclusion criteria for healthy volunteers will include:

    • current smoking
    • extreme obesity (BMI ≥ 35 kg/m2)
    • pregnancy or breastfeeding
    • conditions affecting phosphate metabolism (e.g., hyper- or hypothyroidism; irregular menses for menstruating women)
    • current intake of medications that impact phosphate metabolism (high-dose vitamin D, chronic antacid use)
    • current use of blood pressure medications
    • abnormal serum phosphate (≥ 4.6 or < 2.5 mg/dl) or calcium levels (≥ 10.6 or < 8.5 mg/dl)
    • severe anemia (hemoglobin < 8 g/dl for women and < 9 g/dl for men).
    • Inability to receive weekly shipments of food at home.
    • Requirement for any special diet other than a regular diet.
    • Allergies to any foods in the standardized diets (ii.) Inclusion criteria for CKD patients: ≥18 years of age, eGFR 20-50 ml/min

Exclusion criteria for CKD patients will include:

  • clinical need for a low potassium, low sodium or low protein diet
  • new or recent change (<3 months) in dosage of medications known to impact vascular reactivity
  • current smoking
  • poorly controlled hypertension (≥160/100 mmHg)
  • extreme obesity (BMI ≥ 35 kg/m2)
  • pregnancy or breastfeeding
  • conditions affecting phosphate metabolism (e.g., hyper- or hypothyroidism)
  • current intake of medications that impact phosphate metabolism (e.g., high-dose vitamin D)
  • abnormal serum phosphate (≥ 4.6 or < 2.5 mg/dl) or calcium levels (≥ 10.6 or < 8.5 mg/dl)
  • severe anemia (hemoglobin < 8 g/dl for women and < 9 g/dl for men).
  • Inability to receive weekly shipments of food at home.
  • Allergies to any foods in the standardized diets

Sites / Locations

  • University of Alabama

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

single arm study

Arm Description

Outcomes

Primary Outcome Measures

Change in circulating fibroblast growth factor 23 (FGF23) concentrations
Longitudinal change in FGF23 concentrations over 8 weeks
Change in brachial flow-mediated dilatation (FMD)
Longitudinal changes in FMD over 8 weeks
Change in pulse wave velocity (PWV)
longitudinal changes in PWV over 8 weeks

Secondary Outcome Measures

Full Information

First Posted
November 25, 2015
Last Updated
March 10, 2021
Sponsor
University of Alabama at Birmingham
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1. Study Identification

Unique Protocol Identification Number
NCT02620449
Brief Title
Impact of Lowering Phosphate Additive Intake on Metabolism and Cardiovascular Health in Community-Living Adults
Official Title
Impact of Lowering Phosphate Additive Intake on Metabolism and Cardiovascular Health in Community-Living Adults (Phosphate and Fibroblast Growth Factor 23 [FGF23]: Dietary and Molecular Mediators of Health and Disparities in Cardiovascular and Kidney Diseases)
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Completed
Study Start Date
August 28, 2015 (Actual)
Primary Completion Date
March 5, 2020 (Actual)
Study Completion Date
March 30, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Alabama at Birmingham

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of the study is to learn more about how common food additives can affect phosphorus metabolism in people with normal kidney function and people with chronic kidney disease.
Detailed Description
Disturbances in phosphate homeostasis are strongly associated with cardiovascular morbidity and mortality. High dietary phosphate intake plays a central role in the development of disturbed phosphate metabolism and is common in persons consuming typical American diets rich in processed and fast foods. An important reason for the high phosphate content of these foods is the widespread use of phosphate-based food additives in the food supply. Phosphate additives are heavily utilized by the food manufacturing industry to enhance the appearance, taste and shelf-life of processed foods, accounting for as much as 50% of total phosphate intake per day. Prior work from our group suggest that high phosphate additive intake has serious cardiovascular consequences. We showed that phosphate excess induces heart disease and inflammation in experimental studies, and associates with heart disease and death independently of classic risk factors in epidemiology studies. Further, we showed that high phosphate additive intake stimulates the secretion of fibroblast growth factor 23 (FGF23), a phosphate-regulatory hormone directly implicated in the pathogenesis of cardiovascular disease. Together, these data strongly suggest that high phosphate additive intake promotes cardiovascular disease, with important potential implications for efforts to reduce disparities in cardiovascular disease. This is because individuals with low socioeconomic status have limited means to purchase healthy foods, resulting in excessive consumption of processed foods rich in phosphate additives. Moreover, low income neighborhoods have a disproportionately high prevalence of individuals with chronic kidney disease and black individuals, both groups that have impaired ability to excrete excess phosphate. Together, these data support our overriding hypothesis that high phosphate additive intake is a novel target for reducing socioeconomic and racial disparities in cardiovascular. We will test this hypothesis in detailed feeding studies of 80 individuals fed standardized meals with low phosphate additive content for 6 weeks. We will investigate the impact of reducing phosphate additive intake on changes in FGF23 levels, inflammatory markers and vascular function, and test for effect modification by race and chronic kidney disease (CKD). The results of these studies will help determine whether high phosphate additive intake is a modifiable risk factor for disparities in cardiovascular disease.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Healthy, Chronic Kidney Disease
Keywords
phosphorus, fibroblast growth factor 23, diet

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Arm Title
single arm study
Arm Type
Experimental
Intervention Type
Other
Intervention Name(s)
Diet
Intervention Description
Participants will be fed a low-additive diet as the primary intervention
Primary Outcome Measure Information:
Title
Change in circulating fibroblast growth factor 23 (FGF23) concentrations
Description
Longitudinal change in FGF23 concentrations over 8 weeks
Time Frame
8 weeks
Title
Change in brachial flow-mediated dilatation (FMD)
Description
Longitudinal changes in FMD over 8 weeks
Time Frame
8 weeks
Title
Change in pulse wave velocity (PWV)
Description
longitudinal changes in PWV over 8 weeks
Time Frame
8 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: (i.) Inclusion criteria for healthy volunteers: ≥18 years of age, normal kidney function (eGFR > 60 and normal urinalysis). Exclusion Criteria: Exclusion criteria for healthy volunteers will include: current smoking extreme obesity (BMI ≥ 35 kg/m2) pregnancy or breastfeeding conditions affecting phosphate metabolism (e.g., hyper- or hypothyroidism; irregular menses for menstruating women) current intake of medications that impact phosphate metabolism (high-dose vitamin D, chronic antacid use) current use of blood pressure medications abnormal serum phosphate (≥ 4.6 or < 2.5 mg/dl) or calcium levels (≥ 10.6 or < 8.5 mg/dl) severe anemia (hemoglobin < 8 g/dl for women and < 9 g/dl for men). Inability to receive weekly shipments of food at home. Requirement for any special diet other than a regular diet. Allergies to any foods in the standardized diets (ii.) Inclusion criteria for CKD patients: ≥18 years of age, eGFR 20-50 ml/min Exclusion criteria for CKD patients will include: clinical need for a low potassium, low sodium or low protein diet new or recent change (<3 months) in dosage of medications known to impact vascular reactivity current smoking poorly controlled hypertension (≥160/100 mmHg) extreme obesity (BMI ≥ 35 kg/m2) pregnancy or breastfeeding conditions affecting phosphate metabolism (e.g., hyper- or hypothyroidism) current intake of medications that impact phosphate metabolism (e.g., high-dose vitamin D) abnormal serum phosphate (≥ 4.6 or < 2.5 mg/dl) or calcium levels (≥ 10.6 or < 8.5 mg/dl) severe anemia (hemoglobin < 8 g/dl for women and < 9 g/dl for men). Inability to receive weekly shipments of food at home. Allergies to any foods in the standardized diets
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Orlando Gutierrez, MD
Organizational Affiliation
University of Alabama at Birmingham
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Alabama
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35294
Country
United States

12. IPD Sharing Statement

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Impact of Lowering Phosphate Additive Intake on Metabolism and Cardiovascular Health in Community-Living Adults

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