Bioavailability of Single-dose Magnesium Salts

NCT ID: NCT04139928

Last Updated: 2024-04-23

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 17 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2018-08-01
• Study Completion Date: 2020-04-28

Brief Summary

Magnesium plays a role in an array of critical body functions, controls normal adenosine triphosphate function, the metabolism of glucose, and cardiac muscle function, as well as the maintenance of cell membrane function. Low magnesium intakes and blood levels have been associated with a number of chronic diseases including hypertension, type 2 diabetes, metabolic syndrome, vascular disease, osteoporosis, and colon cancer. Magnesium deficiency is common. In the U.S. population, nearly 4% of men and 7% of women have hypomagnesemia (typically defined as a serum concentration <0.75 mmol/L, or < 17mg/L), which has been previously shown to be associated with an increased risk of all-cause mortality after 30 years of follow-up. In addition, hypomagnesemia is seen in approximately 11% of hospitalized patients and 52% of patients in coronary care units. Approximately half of the U.S. population does not currently reach the estimated average requirement (EAR) for magnesium from food. Yet magnesium deficiency is often overlooked.

Magnesium is relatively well absorbed by the gut; oral bioavailability varies from 35 to 70% and depends on a variety of factors such as the form of the magnesium salt (organic vs. inorganic), its rate and extent of uptake from the intestine into the blood, and its transfer into tissues because magnesium is primarily an intracellular cation. The absorption rate increases when dietary intake is low. In terms of the effectiveness of oral dietary supplements, bioavailability and tolerability of various formulations are important considerations. Similar bioavailability has been demonstrated between inorganic formulations (magnesium oxide vs. magnesium chloride), however some studies have shown magnesium oxide to be less bioavailable. Diarrhea and abdominal cramping are side effects that are commonly reported from oral oral supplementation. These symptoms are thought to be due to the osmotic activity of unabsorbed salts in the intestine and colon and the stimulation of gastric motility. A new picometer-ionic form of magnesium chloride, was developed to efficiently deliver stabilized magnesium ions that are similar in size to plant magnesium. Picometer magnesium is smaller in diameter than the body's cell mineral ion channels, therefore it has the potential to be completely absorbed and not cause adverse side effects in the gastrointestinal system (e.g., diarrhea). The aim of this research is to assess the bioavailability of this new picometer-ionic form of magnesium chloride by comparing its bioavailability to that of a standard magnesium oxide and magnesium citrate supplement in healthy, adult, normotensive subjects.

Conditions

Bioavailability

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: PREVENTION
• Blinding Strategy: QUADRUPLE

Study Groups

Picometer-ionic form of magnesium chloride

Group Type: EXPERIMENTAL

Picometer-ionic form of magnesium chloride

Intervention Type: DIETARY_SUPPLEMENT

Single-dose (300 mg) of the picometer-ionic form of magnesium chloride

Magnesium citrate or magnesium oxide

Group Type: ACTIVE_COMPARATOR

Magnesium citrate or magnesium oxide

Intervention Type: DIETARY_SUPPLEMENT

Single-dose (300 mg) of magnesium citrate or magnesium oxide

Placebo

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DIETARY_SUPPLEMENT

Placebo

Interventions

Picometer-ionic form of magnesium chloride

Single-dose (300 mg) of the picometer-ionic form of magnesium chloride

Intervention Type: DIETARY_SUPPLEMENT

Magnesium citrate or magnesium oxide

Single-dose (300 mg) of magnesium citrate or magnesium oxide

Intervention Type: DIETARY_SUPPLEMENT

Placebo

Placebo

Intervention Type: DIETARY_SUPPLEMENT

Eligibility Criteria

Inclusion Criteria

1. Age 18- 65 years

2. Body mass index 18 to 35 kg/m2 , body weight ≥ 110 pounds or 50 kg

3. All race/ethnicities and both sexes, are eligible.

4. Normal blood pressure (BP) ≤ 120/80 mm Hg.

Exclusion Criteria

1. Participant has a diagnosis of hypertension, prehypertension, diabetes, cardiovascular or other chronic disease (e.g., cancer).

2. Participant has a diagnosis of hypermagnesemia (defined as a serum concentration of > 22.8 mg/L of Magnesium) (4).

3. Participant is already taking magnesium supplementation prior to the study or taking medications that interfere with magnesium metabolism, we are providing examples in an appendix.

4. Participant has concurrent use of magnesium supplements and/or other nutrient supplements that interfere with magnesium absorption (e.g., calcium supplements) within 2-wk prior the first treatment or during the course of this study.

5. Participant has gastrointestinal disease, hepatitis, anemia, or hepatic enzyme abnormalities.

6. Women subjects are currently pregnant or trying to become pregnant.

7. Participant has a history of hospitalization for acute illness in the previous 1 month.

8. Participants who do not speak English or are unable to read or fail to comprehend the informed consent form.

9. Participants fail to complete the full medical questionnaire reviewed with them during the initial phone call (whether it be because they refuse to answer or because they don't know/understand the questions).

10. Participants who have a body weight less than 110lbs (or 50kg).

11. Participants who have donated blood within the last month, or are currently giving blood for other clinical or research purposes.

12. Participants who smoke and/or use tobacco products.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Indiana University

OTHER

Sponsor Role: collaborator

Think Healthy Group, Inc.

NETWORK

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Taylor C. Wallace, PhD

Role: PRINCIPAL_INVESTIGATOR

Think Healthy Group, LLC

Nana Gletsu-Miller, PhD

Role: PRINCIPAL_INVESTIGATOR

Indiana University

Locations

Indiana University

Bloomington, Indiana, United States

Countries

United States

References

Ansu Baidoo VY, Thiagarajah K, Tekwe CD, Wallace TC, Gletsu-Miller N. Relationship between short-term self-reported dietary magnesium intake and whole blood ionized magnesium (iMg2+) or serum magnesium (s-Mg) concentrations. Ann Med. 2023 Dec;55(1):2195702. doi: 10.1080/07853890.2023.2195702.

Reference Type: BACKGROUND

PMID: 37036758 (View on PubMed)

Zhan J, Wallace TC, Butts SJ, Cao S, Ansu V, Spence LA, Weaver CM, Gletsu-Miller N. Circulating Ionized Magnesium as a Measure of Supplement Bioavailability: Results from a Pilot Study for Randomized Clinical Trial. Nutrients. 2020 Apr 28;12(5):1245. doi: 10.3390/nu12051245.

Reference Type: RESULT

PMID: 32353962 (View on PubMed)

Other Identifiers

THG-IU-MG-1

Identifier Type: -

Identifier Source: org_study_id