The Optimization of Bioavailability From Iron Supplements: Examinations of Different Supplementation Regimens Including Hepcidin Profiles
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 20
- 试验地点
- 1
- 主要终点
- Iron bio-availability (%) from oral iron supplementation (3x 120 mg)
研究概览
简要总结
Iron deficiency (ID) with or without anaemia (IDA) is a major public health problem worldwide, especially in women of reproductive age and young children. Iron supplementation is an effective strategy to prevent and treat ID and IDA. There is a lack of data on iron bioavailability from different supplementation regimens and how to optimize bioavailability in a cost-effective and patient-friendly way. The daily supplementation with 1-4 mg Fe/kg body weight for 3 months is reported to be the most effective method to rapidly increase iron stores in subjects with ID and IDA. In IDA patients, medical practitioners often prescribe supplementation regimens with 120 mg iron per day split into 2 doses with 60 mg iron, arguing that the splitting would increase iron bioavailability compared with one single high dose. However, there is no scientific evidence for this assumption; to the contrary, results from a recent study suggest that iron bioavailability from a second supplementation dose of iron after a first supplementation dose of iron is impaired due to increased hepcidin levels. To address this bioavailability issue, the present study will determine iron absorption from 120 mg iron administered for 3 consecutive days and compare it with that from 2 doses of 60 mg iron per day administered for 3 consecutive days. The investigators hypothesize that the iron bioavailability from the single daily dose will be lower than that from the 2 doses. By measuring also hepcidin, this study will provide important insights on the iron bioavailability from a single dose of iron and on the same amount iron split into two doses (b.i.d. administration).
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 主要目的
- Prevention
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 45 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •Female, 18 to 45 years old,
- •Serum Ferritin levels <20 µg/L,
- •Normal body Mass Index (18.5-25 kg/m2),
- •Body weight <65 kg,
- •Signed informed consent
排除标准
- •Anaemia (Hb < 11.7 g/dL),
- •Elevated c-reactive protein or alpha1 glycoprotein concentrations >5.0 mg/L, >1.0 g/L, respectively,
- •Any metabolic, gastrointestinal kidney or chronic disease such as diabetes, renal failure, hepatic dysfunction, hepatitis, hypertension, cancer or cardiovascular diseases (according to the participants own statement),
- •Continuous/long-term use of medication during the whole studies (except for contraceptives),
- •Consumption of mineral and vitamin supplements within 2 weeks prior to 1st supplement administration,
- •Blood transfusion, blood donation or significant blood loss (accident, surgery) over the past 4 months,
- •Earlier participation in a study using stable iron isotopes,
- •Known hypersensitivity or allergy to iron supplements,
- •Women who are pregnant or breast feeding,
- •Intention to become pregnant during the course of the studies,
- •Lack of safe contraception, defined as: Female participants of childbearing potential, not using and not willing to continue using a medically reliable method of contraception for the entire study duration, such as oral, injectable, or implantable contraceptives, or intrauterine contraceptive devices, or who are not using any other method considered sufficiently reliable by the investigator in individual cases.
- •Known or suspected non-compliance, drug or alcohol abuse,
- •Inability to follow the procedures of the studies, e.g. due to language problems, psychological disorders, dementia, etc. of the participant,
- •Participation in another study with investigational drug within the 30 days preceding and during the present studies,
- •Enrolment of the investigator, his/her family members, employees and other dependent persons
研究组 & 干预措施
Single oral iron supplement per day (120 mg)
Single oral iron dose of 120 mg per day for 3 consecutive days
干预措施: Single oral iron dose of 120 mg per day for 3 consecutive days (Dietary Supplement)
B.i.d. oral iron supplement (2x 60 mg)
Two oral iron doses of 60 mg per day (morning + afternoon) for 3 consecutive days
干预措施: Two oral iron doses of 60 mg per day (morning + afternoon) for 3 consecutive days (Dietary Supplement)
结局指标
主要结局
Iron bio-availability (%) from oral iron supplementation (3x 120 mg)
时间窗: 3 days
Iron bioavailability will be assessed with stable isotopic labels. The shift in the isotopic ratio in human whole blood will be measured with Inductively coupled plasma mass spectrometry (ICP-MS).
Serum hepcidin concentrations on the 1st day of iron supplementation
时间窗: 1 day
Iron bio-availability (%) from oral iron supplementation (6x 60 mg)
时间窗: 6 days
Iron bioavailability will be assessed with stable isotopic labels. The shift in the isotopic ratio in human whole blood will be measured with Inductively coupled plasma mass spectrometry (ICP-MS).
Serum hepcidin concentrations on the 2nd day of iron supplementation
时间窗: 2 days
Serum hepcidin concentrations on the 3rd day of iron supplementation
时间窗: 3 days
Serum hepcidin concentrations on the 4th day of iron supplementation
时间窗: 4 days
Serum hepcidin concentrations on the 5th day of iron supplementation
时间窗: 5 days
Serum hepcidin concentrations on the 6th day of iron supplementation
时间窗: 6 days
次要结局
未报告次要终点