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CompletedNCT02620449Updated Mar 11, 2021

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

An interventional study of Diet in Healthy and Chronic Kidney Disease, sponsored by University of Alabama at Birmingham. Completed at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2021-03-11.

Sponsored by University of Alabama at Birmingham · Not applicable, Interventional, and Other

Phase
Not applicable
Study type
Interventional
Enrollment
50
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study 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.

Read the 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.

02

Conditions studied

  • Healthy
  • Chronic Kidney Disease

Keywords

  • phosphorus
  • fibroblast growth factor 23
  • diet
03

In context

Kidney Diseases

3,840 studies on the registry are indexed under Kidney Diseases; 500 are open to participants now.

This study's enrollment of 50 is below the median of 70 across 2,640 interventional studies indexed under Kidney Diseases.

Browse Kidney Diseases studies →

Lead sponsor

University of Alabama at Birmingham is the lead sponsor of 1,396 studies on the registry; 284 are open to participants now.

Of its 156 completed or terminated interventional studies of FDA-regulated products, 124 (79%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

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
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
50 participants (actual)

Study arms

  • Experimental
    single arm study

    Other: Diet

Interventions

  • OtherDiet

    Participants will be fed a low-additive diet as the primary intervention

06

What researchers measure

Primary outcomes

  1. Change in circulating fibroblast growth factor 23 (FGF23) concentrations

    Longitudinal change in FGF23 concentrations over 8 weeks

    Time frame: 8 weeks

  2. Change in brachial flow-mediated dilatation (FMD)

    Longitudinal changes in FMD over 8 weeks

    Time frame: 8 weeks

  3. Change in pulse wave velocity (PWV)

    longitudinal changes in PWV over 8 weeks

    Time frame: 8 weeks

07

Study locations

1 site
  • University of Alabama
    Birmingham, Alabama 35294, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 11, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02620449
Lead sponsor
University of Alabama at Birmingham
Responsible party
Orlando M. Gutierrez, MD, MMSc (Principal Investigator, University of Alabama at Birmingham) — Principal investigator
First posted
Dec 3, 2015
Start date
Aug 28, 2015
Primary completion
Mar 5, 2020
Completion
Mar 30, 2020
Last update
Mar 11, 2021

Study contacts

Orlando Gutierrez, MD
principal investigator · University of Alabama at Birmingham

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2021. You cannot join it, but the record below documents what was studied.

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