Nutritional correction of iron metabolism in women of reproductive age: results of an open-label, prospective, postregistration study with active parallel-group control

BACKGROUND: Iron deficiency anemia is one of the most common conditions worldwide and ranks first in prevalence among women of reproductive age. Conventional iron formulations are frequently associated with a high incidence of adverse effects. Therefore, there is a need to identify novel iron compounds that offer improved tolerability without compromising efficacy. AIM: To compare the outcomes of dietary correction in nonpregnant women receiving iron bisglycinate vs those receiving iron sulfate. MATERIALS AND METHODS: The study included 120 women of reproductive age (18–49 years) with mild iron deficiency anemia who met the inclusion criteria. Patients were randomized into 2 groups. The main group received the investigational product containing 30 mg of elemental iron in chelated bisglycinate form combined with vitamins C, B6, B12, and L-methylfolate (the dietary supplement VitaFerr), administered as 1 capsule once a day with food. The control group received a preparation containing 100 mg of elemental iron as sulfate combined with 60 mg of vitamin C, taken as 2 tablets per day. The total duration of therapy was 60 days. RESULTS: After adjustment for baseline hemoglobin levels, the proportion of female patients who achieved the target hemoglobin level was 88.9% in the main group and 94.3% in the control group (p=0.240). No statistically significant between-group differences were observed in hemoglobin, ferritin, or serum iron levels after 60 days (p 0.05), indicating comparable efficacy of the treatment regimens. The study showed that a daily dose of 30 mg of iron bisglycinate significantly increased serum ferritin levels — from 24.1 to 32.3 ng/mL by day 15, with a mean ferritin concentration of 39.1 ng/mL on day 60 (p 0.001). A statistically significant difference in the frequency of adverse events was observed between groups: 16 (26.7%) in the main group and 37 (61.7%) in the control group (p 0.001). CONCLUSION: The dietary supplement VitaFerr may be considered an effective and safe option for the prevention and treatment of iron deficiency and anemia.

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Journal
Cardiosomatics
Published
2025-04-15
DOI
https://doi.org/10.17816/cs677071
Citations
3
Primary Topic
Iron Metabolism and Disorders
Type
article
Field-Weighted Citation Impact
5.31
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article

Nutritional correction of iron metabolism in women of reproductive age: results of an open-label, prospective, postregistration study with active parallel-group control

Ildar Nagaev, Б. А. Бакиров, Sergey V. Donskov
3 citations
Cardiosomatics
Iron Metabolism and Disorders
5.31
article

Nutritional correction of iron metabolism in women of reproductive age: results of an open-label, prospective, postregistration study with active parallel-group control

Ildar Nagaev, Б. А. Бакиров, Sergey V. Donskov
article en
3 citations

Abstract

BACKGROUND: Iron deficiency anemia is one of the most common conditions worldwide and ranks first in prevalence among women of reproductive age. Conventional iron formulations are frequently associated with a high incidence of adverse effects. Therefore, there is a need to identify novel iron compounds that offer improved tolerability without compromising efficacy. AIM: To compare the outcomes of dietary correction in nonpregnant women receiving iron bisglycinate vs those receiving iron sulfate. MATERIALS AND METHODS: The study included 120 women of reproductive age (18–49 years) with mild iron deficiency anemia who met the inclusion criteria. Patients were randomized into 2 groups. The main group received the investigational product containing 30 mg of elemental iron in chelated bisglycinate form combined with vitamins C, B6, B12, and L-methylfolate (the dietary supplement VitaFerr), administered as 1 capsule once a day with food. The control group received a preparation containing 100 mg of elemental iron as sulfate combined with 60 mg of vitamin C, taken as 2 tablets per day. The total duration of therapy was 60 days. RESULTS: After adjustment for baseline hemoglobin levels, the proportion of female patients who achieved the target hemoglobin level was 88.9% in the main group and 94.3% in the control group (p=0.240). No statistically significant between-group differences were observed in hemoglobin, ferritin, or serum iron levels after 60 days (p 0.05), indicating comparable efficacy of the treatment regimens. The study showed that a daily dose of 30 mg of iron bisglycinate significantly increased serum ferritin levels — from 24.1 to 32.3 ng/mL by day 15, with a mean ferritin concentration of 39.1 ng/mL on day 60 (p 0.001). A statistically significant difference in the frequency of adverse events was observed between groups: 16 (26.7%) in the main group and 37 (61.7%) in the control group (p 0.001). CONCLUSION: The dietary supplement VitaFerr may be considered an effective and safe option for the prevention and treatment of iron deficiency and anemia.

CardiosomaticsVol. 16(1)
Bashkir State Medical University (RU)
Openalex Percentile: Top 5%
Iron Metabolism and Disorders
5.31
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