Salivary Cystatin SN Binds to Phytic Acid and is a Predictor of Non-heme Iron Bioavailability With Phytic Acid Supplementation
| Registry | NCT03030703 |
|---|---|
| Status | Completed |
| Phase | Not applicable |
| Study type | Interventional; na, single group, masking: none, prevention |
| Enrollment | 7 (Actual) |
| Sponsor | Kansas State University (Other); collaborators: United States Department of Agriculture Foreign Agricultural Service, American Academy of Nurse Practitioners |
| Conditions | Iron-deficiency, Iron Deficiency Anemia |
| Interventions | phytic acid (Dietary supplement) |
| Dates | start 2016-11-11, primary completion 2016-12-10, completion 2016-12-10, first posted 2017-01-25, last updated 2017-01-25 |
| Locations | 1 site in United States |
Related Papers Related Patents Related Grants Related Experts
All trials for Iron-deficiency All trials for Iron Deficiency Anemia All trials of phytic acid
Phytic acid is a known inhibitor of iron bioavailability, although long term studies have suggested possibly exaggerated findings compared to single meal studies, pointing to phytic acid adaptation over time. Salivary proline-rich proteins have been found to reduce tannin-iron chelation, but studies have not explored changes in salivary proteins that may result in phytic acid adaptation. The primary objectives of this study are: 1) To determine whether phytic acid impacts iron bioavailability or status when consumed over time 2) to test whether salivary protein production may impact iron bioavailability with phytic acid supplementation, and 3) to explore in vitro phytic acid salivary binding. Secondary objectives included assessment of the reliability of astringency as a measure of salivary protein production and iron absorption.
The study was conducted in an iron absorption study of 7 women, aged 18-35 years old, to determine iron bioavailability with supplementation of 350 mg phytic acid before and after regular, three times daily supplementation for four weeks. Direct iron absorption was measured using area under the curve. Iron status was measured by changes in hemoglobin and ferritin, and was adjusted by participant c-reactive protein levels. Salivary samples were collected before and after supplement consumption during meal challenges, and analyzed on HPLC and by ELISA. Astringency testing was conducted at the end of each meal challenge. In vitro saliva-phytic acid modeling was explored on HPLC, MALDI-TOF, and ELISA. Iron absorption and status markers were analyzed by ANOVA, and mixed-modeling followed by pairwise comparison by least significant differences. Pearson's correlations were used to correlated salivary proteins and astringency with iron bioavailability.
The present study will provide important information regarding the approximate influence of phytic acid consumption on iron bioavailability and storage over time in regards to salivary proteins. It will also give context to the role of salivary proteins with phytic acid consumption over time. Data will also help to delineate possible physiological mechanisms underlying phytic acid adaptation and possible ways to detect individuals who better adapt than others.
| Arm | Type | Interventions | Description |
|---|---|---|---|
| 350 mg phytic acid | Experimental | Dietary Supplement: phytic acid | 350 mg phytic acid (inositol hexaphosphate) at week 0 (before supplementation) and at week 4 (after supplementation) |
Sex: Female, ages: 18 Years to 35 Years, accepts healthy volunteers
Inclusion Criteria: * Female, 18-35 years' old * Non-obese BMI (18-29.9) * Signed informed consent Exclusion Criteria: * Oral disease * Gastrointestinal disease * Tobacco user * Heavy alcohol user * Pregnancy (assessed by pregnancy test) * Lactation * Medications affecting iron bioavailability * Vitamin or mineral supplementation (other than vitamin B12)
| Facility | City | Country | Status |
|---|---|---|---|
| Physical Activity and Nutrition Research Consortium | Manhattan, Kansas | United States |