An Evaluation of Zinc Status Biomarkers

Sponsor
UCSF Benioff Children's Hospital Oakland (Other)
Overall Status
Completed
CT.gov ID
NCT02861352
Collaborator
(none)
18
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Study Details

Study Description

Brief Summary

The purpose of this study is to determine the effect of a moderate decrease in dietary zinc on DNA strand breaks and other cellular zinc biomarkers.

Condition or Disease Intervention/Treatment Phase
  • Other: Diet zinc
N/A

Detailed Description

Assessing the zinc status of humans has proven to be difficult because of the unique physiological features of zinc homeostasis. Animal and human studies show that a small, vulnerable pool of cellular zinc is sensitive to changes in dietary zinc. The protein, Metallothionein (MT), is made within cells to stabilize this transient zinc pool and to provide a means to 'park' a small zinc reserve. The overall goal is to develop a new method for measuring MT in cells and to assess other cellular responses to changes in small changes in dietary zinc. Culture models of zinc deficiency and excess have been developed and used to test the response of cellular MT levels and mineralization to changes in zinc availability. In Phase II, the changes in the expression of leukocytic zinc transporters and the cellular in vitro uptake of isotopic zinc will be measured. Healthy men will be recruited to participate in a 6-week feeding trial to be followed by a 3-week recovery period. The results of this study will determine if potential new cellular zinc biomarkers respond to changes in zinc status when the men are fed an additional 4 mg zinc/d incorporated into a rice-based meal. These findings will provide essential, new information for designing an efficacy trial of biofortified rice and the zinc status of infants and young children.

Study Design

Study Type:
Interventional
Actual Enrollment :
18 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Testing Novel Biomarkers of Zinc Status for Use in Human Zinc Supplementation Trials
Study Start Date :
Mar 1, 2011
Actual Primary Completion Date :
Feb 1, 2014
Actual Study Completion Date :
Feb 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Experimental: diet zinc

3 dietary zinc levels: 6 mg/d, 10 mg/d and 25 mg supplemental zinc/d

Other: Diet zinc
4 mg zinc, as zinc sulfate, was added to a controlled diet; 25 mg supplemental zinc was given during the final recovery period when an ad lib diet was consumed

Outcome Measures

Primary Outcome Measures

  1. Change in the percent of leukocytic DNA strand breaks [Change in DNA strand breaks measured at baseline, 2, 4, and 3 week intervals with changes in diet zinc]

    Baseline measurements were made upon entry into the study. Subsequent measurements were made after 2 weeks on a low zinc diet (6 mg/d), 4 weeks on a moderate zinc intake (10 mg/d) and after 3 weeks of consuming a 25 mg zinc supplement.

Secondary Outcome Measures

  1. Cellular zinc biomarkers [At baseline and at 3 time points during the 9 week study: after 2, 6, and 9 weeks.]

    Specific measurements included the gene expression of zinc transporters, the in vitro uptake of leukocytic radioactive Zn, and a comprehensive serum metabolomic and proteomic analysis.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 50 Years
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • willing to limit food and beverage intake to that provided by the study

  • willing to discontinue consumption of alcoholic beverages during the study

  • has an operative understanding of English

  • no plans to move from the area during the study period

Exclusion Criteria:
  • chronic or acute metabolic disease (i.e., diabetes or asthma)

  • taking medications for a metabolic disorder

  • evidence of alcohol abuse or use of illicit drugs

Contacts and Locations

Locations

Site City State Country Postal Code
1 Children's Hospital Oakland Research Institute Oakland California United States 94609

Sponsors and Collaborators

  • UCSF Benioff Children's Hospital Oakland

Investigators

  • Principal Investigator: Janet C King, Ph.D., UCSF Benioff Children's Hospital Oakland

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
UCSF Benioff Children's Hospital Oakland
ClinicalTrials.gov Identifier:
NCT02861352
Other Study ID Numbers:
  • CHO14
First Posted:
Aug 10, 2016
Last Update Posted:
Nov 24, 2020
Last Verified:
Nov 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Keywords provided by UCSF Benioff Children's Hospital Oakland
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 24, 2020