DNA Damage, Immune System Disorder
Conditions
Brief summary
This is a study to assess the effect of dietary zinc supplementation to mitigate biomarkers of metal toxicity in exposed tribal populations.
Detailed description
Communities living in proximity to abandoned uranium mines have documented exposures to metals in drinking water, soil and dust. Exposure to these metals, principally uranium and arsenic, and metal mixtures is associated with dysregulation of immune function and other health effects. The objective of this study is to conduct an intervention trial to assess the effect of dietary zinc supplementation to mitigate the toxicity of metal exposures. The current project is part of a larger research effort funded by the NIH Superfund Program to study environmental metals exposures in tribal communities in New Mexico.
Interventions
DRUGZinc Picolinate 15 Mg
zinc picolinate, 15 mg/day for 6 months
Sponsors
University of New Mexico
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE
Intervention model description
This is a one-armed cohort intervention of zinc supplementation. Data will be collected for each participant before and after zinc supplementation.
Eligibility
Sex/Gender
ALL
Age
21 Years to 64 Years
Healthy volunteers
Yes
Inclusion criteria
* Men or women between the ages of 21 and 64 years of age * Lives in or near the participating communities of Blue Gap-Tachee Arizona or Red Water Pond Road Community New Mexico * Willing to provide blood and urine samples * Willing to attend study visits on scheduled dates * Willing to take a daily zinc supplement
Exclusion criteria
* Women who are pregnant or nursing or women who plan to become pregnant during the course of the study. * Individuals who have self-reported diabetes, report that they are undergoing treatment for diabetes, or are currently taking medication for diabetes. * Known or suspected allergy to zinc. * Individuals previously diagnosed with syndromes of copper homeostasis (Menkes disease or Wilsons disease). * Individuals consuming zinc supplements or multivitamins and are unwilling to stop for the duration of the study.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Metal biomonitoring to compare change from baseline versus zinc supplement | Visit 1 (0 months-baseline 1), Visit 2 (3 months-baseline 2), Visit 3 (6 months-zinc 1), Visit 4 (9 months-zinc 2) | urinary and serum metal levels to be measured by inductively coupled plasma mass spectrometry |
| Lymphocyte phenotyping to compare change from baseline versus zinc supplement | Visit 1 (0 months-baseline 1), Visit 2 (3 months-baseline 2), Visit 3 (6 months-zinc 1), Visit 4 (9 months-zinc 2) | Lymphocyte phenotypes will be measured in blood samples |
| Cytokine level measurement to compare change from baseline versus zinc supplement | Visit 1 (0 months-baseline 1), Visit 2 (3 months-baseline 2), Visit 3 (6 months-zinc 1), Visit 4 (9 months-zinc 2) | A cytokine panel will be used to measure levels of multiple cytokines in blood samples |
| Autoantibody measurement to compare change from baseline versus zinc supplement | Visit 1 (0 months-baseline 1), Visit 2 (3 months-baseline 2), Visit 3 (6 months-zinc 1), Visit 4 (9 months-zinc 2) | Autoantibody panel titers will be measured in blood samples |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| DNA damage assays to compare change from baseline versus zinc supplement | Visit 1 (0 months-baseline 1), Visit 2 (3 months-baseline 2), Visit 3 (6 months-zinc 1), Visit 4 (9 months-zinc 2) | DNA damage measurements in cells retrieved from blood samples |
| PARP activity assays to compare change from baseline versus zinc supplement | Visit 1 (0 months-baseline 1), Visit 2 (3 months-baseline 2), Visit 3 (6 months-zinc 1), Visit 4 (9 months-zinc 2) | Activity measurement of the DNA repair enzyme poly (ADP ribose) polymerase (PARP) |
Countries
United States
Contacts
CONTACTLaurie G Hudson, PhD
CONTACTDebra MacKenzie, PhD
Outcome results
None listed