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Potential Harms of Untargeted Iron Supplementation in Cambodia Where Iron Deficiency is Not the Cause of Anemia

Is Iron Supplementation Harmful in Populations Where Iron Deficiency is Not the Cause of Anemia? A 12 Week Randomized Controlled Trial in Cambodia

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04017598
Enrollment
480
Registered
2019-07-12
Start date
2019-12-10
Completion date
2023-12-01
Last updated
2024-05-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anemia, Iron Deficiency, Anemia, Intestinal Inflammation, Inflammation, Intestine; Complaints

Keywords

anemia, gut inflammation, iron deficiency, iron, iron supplementation

Brief summary

In 2016, the World Health Organization (WHO) set a global policy recommending daily oral iron supplementation (60 mg iron) for 12 weeks for all women living in countries where anemia prevalence is \>40%, such as in Cambodia. However, recent studies have shown the prevalence of iron deficiency to be low in Cambodian women and that supplementation would likely only benefit \ 10% of women. Iron supplementation may be harmful in women with genetic blood disorders (e.g. thalassemia), which are common in Cambodia, as these individuals are already at an increased risk of iron overload. The risks are made greater by the fact that iron absorption from most common form of supplementation, ferrous sulfate, is low. Typically less than 20% is absorbed in the gut; the remaining 80% passes unabsorbed into the colon where it can increase the risk of pathogen growth and gut inflammation. Alternatively, ferrous bisglycinate is a newer supplemental form of iron. This amino acid chelate has 2-4x higher bioavailability than ferrous sulfate and is associated with fewer GI side-effects. In view of WHO policy and risks of supplementation, there is a need to determine the potential for harm, and if novel forms of iron supplements are safer.

Detailed description

The World Health Organization (WHO) set a Global Nutrition Target to reduce anemia in women of reproductive age by 50% by 2025. In 2016, the WHO implemented a global policy recommending oral iron supplementation (60 mg daily for 12 weeks) for all women where anemia prevalence is more than 40%, such as in Cambodia. However, recent studies have shown the prevalence of iron deficiency to be low in Cambodian women. If iron deficiency is not the cause of anemia, then iron supplementation will not be effective at treating it. Further, iron supplementation may be harmful in some individuals, especially those with anemia caused by genetic blood disorders (which are common in Cambodia), as these individuals are already at an increased risk of iron overload. The risks are made greater by the fact that the type of iron that is commonly used in supplements (ferrous sulfate) is poorly absorbed. Typically, less than 20% is absorbed in the gut; the remaining 80% is unabsorbed in the colon where it can increase the risk of pathogen growth and gut inflammation. To investigate the safety of untargeted iron supplementation, we will undertake a new study in Cambodia, where we will evaluate a newer type of iron supplement that may be absorbed better, and thus, safer than the conventional type. We will recruit non-pregnant women (18-45 years) and ask them to take one of the two forms of iron (ferrous sulfate or ferrous bisglycinate) or a placebo for 12 weeks (in line with the WHO global policy). We will measure hemoglobin and ferritin levels, which are markers of anemia and iron status, and markers of gut inflammation and gut pathogen abundance, before and after the intervention. This study will contribute to the evidence for safe and effective iron supplementation for women worldwide.

Interventions

DIETARY_SUPPLEMENTFerrous sulfate

60 mg elemental iron as ferrous sulfate

DIETARY_SUPPLEMENTFerrous Bisglycinate

18 mg elemental iron as ferrous bisglycinate

DIETARY_SUPPLEMENTPlacebo of microcrystalline cellulose

placebo

Sponsors

Helen Keller International
CollaboratorOTHER
NCHADS - Ministry of Health of Cambodia
CollaboratorOTHER
BC Children's Hospital Research Institute
CollaboratorOTHER
The National Institute of Public Health Laboratory, Phnom Penh
CollaboratorUNKNOWN
University of British Columbia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Masking description

The manufacturers of the tablets (Dr. Simon Wood, Natural Factors) will be responsible for allocation concealment of the three tablet formulations at time of packaging. All tablets will be non-distinguishable in size, colour, and packaging. Trial investigators, research staff, and participants will all be blinded to the assigned interventions

Intervention model description

12-week double-blind, three-arm, placebo-controlled randomized controlled trial

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* apparently healthy * consent to participate in the study and provide blood, flocked rectal swab and stool samples * expected to reside in the study location for the study period.

Exclusion criteria

* any known illness or disease * pregnant * taking antibiotics, non-steroidal anti-inflammatory drugs, dietary supplements, or vitamin and mineral supplements in the previous 12 weeks.

Design outcomes

Primary

MeasureTime frameDescription
Serum Ferritin12 weeksSerum ferritin concentration (µg/l) at 12 weeks
Fecal calprotectin12 weeksFecal calprotectin concentration (mg/kg stool) at 12 weeks as a measure of gut inflammation.

Secondary

MeasureTime frameDescription
Gut parasite abundance12 weeksReal-time PCR nucleic acid amplification assay with an enteric parasite panel.
DNA damage12 weeksDNA damage will be assessed by measuring DNA single-strand breaks, indicated by olive tail movement with use of alkali single-cell gel electrophoresis (Comet assay).
Alpha-1 acid glycoprotein (AGP, g/l)12 weeks
Gut pathogen abundance12 weeksReal-time PCR nucleic acid amplification assay with an enteric bacterial panel.
Hemoglobin (g/L)12 weeks
Folate (ng/ml)12 weeks
Vitamin B12 (pmol/l)12 weeks
C-reactive protein (CRP, mg/l)12 weeks

Other

MeasureTime frameDescription
Reported side effectsContinuous over 12 weeks(e.g., gastrointestinal pain) as a quality of life measure.
Gut Pathogen abundance12 weeksWhole metagenome shotgun 16S ribosomal RNA sequencing will be conducted on fecal samples, in order to validate the method against the established BD MAX panel in a subset of 150 women from our trial (50 from each study arm).
Genetic hemoglobinopathiesBaselineGenotyping to detect the presence of the most common hemoglobinopathies

Countries

Cambodia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 17, 2026