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. 2022 Jan 27;14(3):543. doi: 10.3390/nu14030543

Comparative Effects between Oral Lactoferrin and Ferrous Sulfate Supplementation on Iron-Deficiency Anemia: A Comprehensive Review and Meta-Analysis of Clinical Trials

Xiya Zhao 1,†, Xu Zhang 1,†, Teng Xu 1, Junjie Luo 1,*, Yongting Luo 1,*, Peng An 1,*
Editor: James H Swain1
PMCID: PMC8838920  PMID: 35276902

Abstract

Ferrous sulfate is a commonly used iron supplement for the correction of iron-deficiency anemia but with frequent gastrointestinal side effects. Milk-derived iron-binding glycoprotein lactoferrin possesses well gastrointestinal tolerance and fewer side effects caused by the intake of high-dose iron. However, the underlying mechanism of the iron-enhancing effect of lactoferrin remains unclear. In addition, the comparative efficacies between lactoferrin and ferrous sulfate are also remained to be determined. We conducted a systematic review and meta-analysis on published intervention studies to investigate how lactoferrin modulate iron metabolism and evaluate the comparative effects between lactoferrin and ferrous sulfate supplementation on iron absorption, iron storage, erythropoiesis and inflammation. Lactoferrin supplementation had better effects on serum iron (WMD: 41.44 ug/dL; p < 0.00001), ferritin (WMD: 13.60 ng/mL; p = 0.003) and hemoglobin concentration (11.80 g/dL; p < 0.00001), but a reducing effect on fractional iron absorption (WMD: −2.08%; p = 0.02) and IL-6 levels (WMD: −45.59 pg/mL; p < 0.00001) compared with ferrous sulfate. In conclusion, this study supports lactoferrin as a superior supplement to ferrous sulfate regarding the improvement in serum iron parameters and hemoglobin levels. Considering the weak influence of lactoferrin on iron absorption, the anti-inflammation effect of lactoferrin may be the potential mechanism to explain its efficacy on iron status and erythropoiesis.

Keywords: lactoferrin, ferrous sulfate, iron

1. Introduction

Iron is a necessary trace element for all mammals and involved in many essential metabolic processes such as oxygen transport, mitochondrial respiration and enzymatic activities [1]. Therefore, the deficiency of iron will lead to the metabolic abnormality in all parts of human bodies. The most common manifestations of iron deficiency are fatigue, headache and paleness [2]. Iron deficiency (ID) impairs cardiac function in the elderly and neurocognitive development in infants [1]. Children suffering from severe iron deficiency are associated with cognitive dysplasia, delayed body development, and low productivity [3,4]. The depletion of iron will also restrict hemoglobin synthesis and result in iron-deficiency anemia (IDA) [5,6]. IDA is the unique preventable and theorical easier treatable of the main and more frequent years lived with disabilities (YLDs) in the whole world [7].

Anemia has already become a global public health concern [8]. One in third people worldwide are affected by anemia; pregnant women and children are the most susceptible populations due to the increasing demand of iron for fetus or body development [9]. About half of pregnant women are diagnosed with anemia in low- and middle-income countries [10], and it is estimated that global anemia prevalence is more than 40% in pre-school children [8,11]. Anemia is also the first and main preventable cause of maternal mortality. An analysis of 312,281 pregnancies in 29 countries shows that the odds of maternal death were twice as high in those women with severe anemia compared with those not [12]. According to World Health Organization, 50% of anemia worldwide is caused by iron deficiency. The lack of iron additionally raises the specific risks for the mother and the fetus during pregnancy, such as intra-uterine growth retardation, prematurity, fetoplacental miss ratio and peripartum blood transfusion [13]. Therefore, the reduction of anemia is one of the World Health Assembly Global Nutrition Targets for 2025 and of the Sustainable Development Goals, with the attention to iron supplement and other nutritional needs of adolescent girls, pregnant women and children. However, the global progress in reducing anemia is not on track for reaching the 2025 target [8,14].

Generally, there are 6 “right treatment” guidelines regarding iron supplementation: at the right moment (not only when anemia is present), at the right dose (ensuring efficacy and tolerance of different populations); the right moment (breakfast is not the best meal to intake oral iron considering gastrointestinal reaction); the right route (oral iron is not always the first option, dietetical supplements, fortified powders, delay clamping umbilical cord or intravenous iron administration have respective advantages [4]); the right pharmacology (not all the oral iron are equal, neither the intravenous iron); and the right management (identifying the causes of IDA and the health problem that may weaken the effect of iron supplementation, including obesity/overweight, inflammation, and infection) [15].

There are several approaches for iron supplementation, including dietary or intravenous iron administration. Considering cost-effectiveness and adherence, oral iron ingestion is the main therapy for pregnant women and children with ID or IDA. Oral iron therapies include different iron supplements such as ferrous sulfate, ferrous gluconate and some other iron abundant substances. However, the absorption of iron across intestine epithelium is restricted by ferrous iron ion channel and influenced by body iron needs. Inorganic, non-heme iron from food is absorbed by duodenal enterocytes through divalent metal transporter 1 (DMT1), exported by ferroportin (FPN) and bound by transferrin within blood circulation [16]. The major delivery target of transferrin-bound iron is erythroid in the bone marrow, which can acquire transferrin through transferrin receptor 1 (TfR1) on the erythroid cell surface. Senescent erythrocytes will be lysed by macrophages and iron can be recycled into circulation. Excess iron is stored in the liver as ferritin. High level of iron storage will trigger hepcidin gene (HAMP) transcription to block iron absorption from intestine and iron recycling from macrophages [17]. Hepcidin can bind to FPN, trigger the internalization and degradation of FPN, reducing circulating iron level [18,19]. In addition, hepcidin plays an important role in innate immunity. The expression of hepcidin can be induced by inflammatory cytokines during infection, such as interleukin-6 (IL-6) [20,21], which is regarded to deprive invading microorganisms of iron. During nutrient scarcity, the microbiota can also compete with their hosts for iron by inhibiting host iron transport and storage [22].

Although the regulatory mechanism of iron absorption, utilization, storage and regulation has been discovered, ferrous sulfate is still a very frequently used oral iron supplement for the correction of ID or IDA, sometimes cooperated with vitamin C as adjuvant therapy. However, ferrous iron supplements frequently lead to serious gastrointestinal side effects such as vomiting, nausea, epigastric discomfort and further results in low patients’ compliance [23]. In recent years, milk-derived iron-binding glycoprotein lactoferrin has been used as iron supplement for the correction of ID/IDA [24,25,26]. Lactoferrin shares structural similarities with transferrin [27]. Lactoferrin displays high iron-binding affinity within a wide range of pH values, and the iron-binding capacity can be maintained after heating [1]. In commercially available lactoferrin, lactoferrin attains 10–20% iron saturation. Due to the iron-binding properties, it proposed that lactoferrin can enhance intestinal iron absorption and improve hemoglobin production [1]. However, the underlying mechanism of the iron-enhancing effect of lactoferrin remains unclear. Lactoferrin is a relatively large protein (~80 kD) that is unlikely to cross blood/gut barrier and directly contribute to iron supplementation [28]. Regarding the comparative efficacy between oral lactoferrin and traditional ferrous sulfate therapy on iron absorption, iron storage, erythropoiesis and inflammation, a high-quality comprehensive assessment is still needed to elucidate the potential mechanism of iron-enhancing effect of lactoferrin. Therefore, we conducted a systematic review and meta-analysis on published intervention studies to determine the comparative effects between lactoferrin and ferrous sulfate supplementation in the treatment of ID and IDA.

2. Materials and Methods

This systematic review was conducted in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement. Following keywords were used to perform a systematic search in PubMed, Web of Science and Cochrane Library: lactoferrin AND (iron OR anemia OR hemoglobin OR ferritin). Only clinical trials written in English were included and searching result was updated monthly until submission for publication. Literature search and evaluation were performed by two reviewers independently according to title, abstract and full text. The third reviewer re-examined searching result. Following criteria were used in literature evaluation: (1) clinical trials conducted in ID/IDA or healthy individuals; (2) study reporting baseline and post-intervention results on iron status (including at least one of the following outcomes: hemoglobin concentration; total serum iron (SI); serum ferritin (SF); and fractional iron absorption (FIA); (3) the intervention substance was lactoferrin or bovine lactoferrin, and ferrous sulfate must be used in control groups. The following exclusion criteria were used: (1) no control group in study; (2) animal research; (3) the mean change and standard deviation (SD) in the outcomes is unreported or cannot be calculated.

2.1. Data Extraction

Two independent reviewers screened and evaluated the full text of eligible research, and evaluation results were re-examined by another 2 reviewers. The primary outcomes included SI, SF concentration and hemoglobin concentration. Secondary outcomes included interleukin-6 (IL-6) and fractional iron absorption. A characteristic table was used to present extracted detail information of eligible studies. Following information were extracted: (1) the last name of the first author; (2) year of publication; (3) the study design (randomization, single- or double-blinded); (5) the population and health status of participants; (6) the duration and type of intervention in comparison and experiment groups; (7) number of participants in the intervention and comparison groups; and (8) outcomes. If outcomes measures were not reported as means and SDs, the following calculation processes were adopted to obtain the means and SDs: outcomes presented as the “median and range” were converted using VassarStats (Richard Lowry, New York, NY, USA) [29]; for studies not reporting the SD of mean difference, the following formula was used to estimate the SD of mean change between baseline and endpoint: SD change = square root [(SDbaseline2 + SDendpoint2)/2].

2.2. Quality Assessment

RoB2 (Cochrane, London, United Kingdom) [30] was used to assess the risk of bias in included articles by two independent researchers. The following 5 domains were considered to assess the quality of clinical trials: (1) possibly bias from unjustified randomized process; (2) bias caused by deviation from intended interventions; (3) bias due to missing data; (4) bias from measurement of the outcome; (5) bias in selection of the reported result. The tool contains algorithms which calculate the risk-of-bias based on response to each question. The possible risk-of-bias judgments were as follows: (1) low risk-of-bias (represented by a green mark); (2) some concerns (represented by a yellow mark); and (3) high risk of bias (represented by a red mark). The assessment results were presented by Review Manager (RevMan, version 5.4; Cochrane, London, United Kingdom).

2.3. Statistical Analysis

Effect sizes were expressed as the weighted mean difference (WMD) and 95% confidence interval (CI) using random-effects model. Changes in the means and SDs of iron status parameters were considered as the representation of overall effects of iron supplement in intervention groups. The heterogeneity among the studies was assessed using the I2 statistic. Funnel’s plot and Egger test were used for the evaluation of publication bias. Sensitive analysis was used to judge the influence of individual study in pooled effect size by omitting one study. Forest plot was generated using RevMan (version: 5.4); funnel’s plot and sensitive analysis were performed in Stata/MP 16.0 (StataCorp, College Station, TX, USA).

3. Results

3.1. Study Characteristic

The literature search was conducted with key words mentioned in the method to identify studies comparing the effects of lactoferrin and ferrous sulfate on iron status or erythropoiesis. We initially identified 237 clinical trials articles, 60 from PubMed, 56 from Web of Science, and 121 from Cochrane Library. Seventy articles were reserved after removing duplication. Based on abstracts, 22 articles were reserved for full-text examination. Trials on pregnant and non-pregnant women reported in the same articles were regarded as separate studies. For trials with different intervention durations or doses in the same article, study with the longest intervention duration or the maximum dose were adopted. Finally, 9 randomized trials and 2 non-randomized trials from 8 articles were included for further analysis. Literature searching and selection process are presented in Figure 1. Of the 11 eligible studies, 8 studies were conducted on individuals with ID or IDA [31,32,33,34,35,36]; 6 studies were performed in pregnant women [31,32,33,34,35,36] and 4 studies in non-pregnant women [34,36,37]. There are 8 studies reporting iron status outcomes, including ferritin [33,34,35], serum iron [32,33,34,35,36] and hemoglobin concentration [31,32,33,34,35,36]; 3 studies measured the iron absorption [37,38]. A total of 680 participants were assigned to lactoferrin group and 582 participants were assigned to ferrous sulfate group. The characteristics of the included studies are presented in Table S1.

Figure 1.

Figure 1

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Study identification and selection flow diagram.

3.2. Effect of Lactoferrin and Ferrous Sulfate Supplementation on SI

SI was used to assess the iron supplementation effect of lactoferrin and ferrous sulfate on circulating iron concentrations. Means and SD data were extracted from 8 studies. Random-effects model was used to evaluate the WMD of SI after lactoferrin and ferrous sulfate supplementation. Lactoferrin had a superior effect on SI compared with ferrous sulfate (WMD: 41.44 ug/dL; 95% CI: 26.29, 56.59; I2 = 98%; Figure 2). Although heterogeneity was observed across studies, no publication bias was found by funnel plot (Figure S1) and Egger’s test (p = 0.990; Table S2). Sensitive analysis also indicated that there was no single study affecting the total effect size (Figure S2).

Figure 2.

Figure 2

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Effect of lactoferrin and ferrous sulfate on serum iron (SI). 1, converted from median and minimum-maximum range. 2. Mean and SD were estimated from histogram. Risk of bias legend: A = random sequence generation (selection bias); B = allocation concealment (selection bias); C = blinding of participants and personnel (performance bias); D = blinding of outcome assessment (detection bias); E = incomplete outcome data (attrition bias); F = selective reporting (reporting bias); G = other bias. Data expressed as weighted mean difference (95% CI). IV, inverse variance.

3.3. Effect of Lactoferrin and Ferrous Sulfate Supplementation on SF

We examined iron supplementation effect on iron storage level by analyzing serum ferritin from 6 studies. Lactoferrin still had a better effect on SF than ferrous sulfate (WMD: 13.6 ng/mL; 95% CI: 4.53, 22.66; I2 = 99%; Figure 3). Significant heterogeneity was observed across studies. Funnel plot (Figure S1) and Egger’s test (p = 0.036; Table S2) indicated that a small study effect may exist in the effect size. However, sensitivity analysis suggested that the effect size was robust (Figure S2).

Figure 3.

Figure 3

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Effect of lactoferrin and ferrous sulfate on serum ferritin (SF) concentrations. 1. converted from median and minimum-maximum range. 2. Mean and SD were estimated from histogram. Risk of bias legend: A = random sequence generation (selection bias); B = allocation concealment (selection bias); C = blinding of participants and personnel (performance bias); D = blinding of outcome assessment (detection bias); E = incomplete outcome data (attrition bias); F = selective reporting (reporting bias); G = other bias. Data expressed as weighted mean difference (95% CI). IV, inverse variance.

3.4. Effect of Lactoferrin and Ferrous Sulfate Supplementation on Hemoglobin Concentration

Most participants included in this study are pregnant women who are at high risk for IDA. Hemoglobin is the major blood determinant in the clinical diagnosis of IDA. We extracted and analyzed hemoglobin concentration data from 9 studies. Analysis results using random-effects model favored oral lactoferrin intervention over ferrous sulfate with a WMD of 11.80 g/L (95% CI: 8.19, 15.41; I2 = 96%; Figure 4), which indicates the better erythropoiesis improving effect of oral lactoferrin. There was no publication bias of hemoglobin concentration in the included studies, based on funnel plot (Figure S1) and Egger’s test (p = 0.376; Table S2). Sensitivity analysis indicated that no single study affected the total effect size of hemoglobin concentration (Figure S2).

Figure 4.

Figure 4

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Effect of lactoferrin and ferrous sulfate on hemoglobin concentrations. 1, converted from median and minimum-maximum range. 2. Mean and SD were estimated from histogram. Risk of bias legend: A = random sequence generation (selection bias); B = allocation concealment (selection bias); C = blinding of participants and personnel (performance bias); D = blinding of outcome assessment (detection bias); E = incomplete outcome data (attrition bias); F = selective reporting (reporting bias); G = other bias. Data expressed as weighted mean difference (95% CI). IV, inverse variance.

3.5. Effect of Lactoferrin and Ferrous Sulfate Supplementation on FIA

We next compared the effects of lactoferrin and iron ferrous on iron absorption. FIA can better reflect iron absorption from intestine. FIA is calculated from iron-isotopic ratios, iron circulating in the body, and the total amounts of isotope-labeled iron administrated in the participant [37,38]. Although lactoferrin displayed a superior effect on circulating iron, iron storage level (Figure 2, Figure 3 and Figure 4), lactoferrin had an unexpectedly inferior effect on FIA when compared with ferrous sulfate (WMD: −2.08%; 95% CI: −3.85, 0.31; I2 = 0%; Figure 5). There is low heterogeneity in included studies and no publication bias was found in FIA (Figures S1 and S2; Table S2).

Figure 5.

Figure 5

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Effect of lactoferrin and ferrous sulfate on fractional iron absorption (FIA). Risk of bias legend: A = random sequence generation (selection bias); B = allocation concealment (selection bias); C = blinding of participants and personnel (performance bias); D = blinding of outcome assessment (detection bias); E = incomplete outcome data (attrition bias); F = selective reporting (reporting bias); G = other bias. Data expressed as weighted mean difference (95% CI). IV, inverse variance.

3.6. Effect of Lactoferrin and Ferrous Sulfate Supplementation on Inflammatory Cytokine IL-6

Lactoferrin has immunomodulatory activity [39]. Inflammatory cytokines IL-6 levels were extracted from 4 studies to evaluate inflammatory status after lactoferrin or ferrous sulfate intervention. Lactoferrin supplementation group had a lower IL-6 levels (WMD: −45.59 pg/mL; 95% CI: −50.82, −40.36; I2 = 85%; Figure 6) compared with ferrous sulfate (Figure 6). Funnel plot (Figure S1) and Egger’s test (p = 0.345; Table S2) were performed to evaluate publication bias and no bias was observed. Sensitive analysis also indicated a reliable effect of lactoferrin on IL-6 (Figure S2).

Figure 6.

Figure 6

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Effect of lactoferrin and ferrous sulfate on serum IL-6 levels. 1. Mean and SD were estimated from histogram. Risk of bias legend: A = random sequence generation (selection bias); B = allocation concealment (selection bias); C = blinding of participants and personnel (performance bias); D = blinding of outcome assessment (detection bias); E = incomplete outcome data (attrition bias); F = selective reporting (reporting bias); G = other bias. Data expressed as weighted mean difference (95% CI). IV, inverse variance.

3.7. Subgroup Analyses of Ferrous Sulfate Supplementation on Iron Status

We further identified studies according to 2 factors which might affect outcomes, including participants’ populations (pregnant women or non-pregnant women) and health status (the presence of ID/IDA or hereditary thrombophilia). No significant difference was observed in the WMDs of SI, ferritin, hemoglobin and IL-6 levels among subgroups. WMD, heterogeneity within groups and meta-regression results were presented in Table S3.

4. Discussion

Lactoferrin is a multifunctional iron-binding protein possessing anti-inflammatory and anti-microbial effects. The major advantages of lactoferrin compared with traditional iron supplement ferrous sulfate are well gastrointestinal tolerance and fewer side effects caused by the intake of high-dose iron. In this meta-analysis, we compared the iron- and erythropoiesis-improving effects between lactoferrin and ferrous sulfate based on 11 intervention studies. Lactoferrin supplementation displayed better improvement for blood iron parameters including serum iron (Figure 3) and ferritin (Figure 2) when compared with ferrous sulfate. Moreover, a superior erythropoiesis-improving effect was observed in individuals receiving lactoferrin (Figure 4). Participants receiving lactoferrin had reduced IL-6 levels compared with those receiving ferrous sulfate, indicating lactoferrin mitigated inflammation.

Contradictorily, lactoferrin has less FIA than ferrous sulfate based on 3 studies (Figure 5) [37,38], suggesting that the iron-improving effect of lactoferrin is not completely brought by the iron within lactoferrin. The lower FIA of lactoferrin is probably due to its iron-binding activity, which sequesters iron rather than promotes iron absorption in the intestine [38]. This hypothesis can be supported by the phenotypes of lactoferrin knockout mice, in which increased serum transferrin saturation and liver iron stores were observed [40]. However, there is an inconsistent explanation about the effect of iron-binding capacity of lactoferrin on iron absorption. It regarded that lactoferrin may sequester dietary iron from binding to iron-chelating compounds in foods (such as polyphenols and phytic acid), which promotes extra iron absorption in foods. This hypothesis can be supported by the results from isotope-labeled iron absorption trial using apo-lactoferrin [38]. Higher FIA was observed in individuals receiving apo-lactoferrin than those who received holo-lactoferrin.

Based on the results of this study, we proposed that the anti-inflammatory effect of lactoferrin can partially explain why it had a better iron-improving effect even with lower FIA than ferrous sulfate. First, higher inflammatory cytokines will prevent dietary iron absorption and iron mobilization from reticuloendothelial system to meet the need of erythropoiesis because of increased hepcidin synthesis [41,42]. Second, amelioration of inflammation can improve erythropoiesis. Inflammatory cytokines such as IL-6 is a repressive factor for erythropoiesis [43] (Figure 7). Notably, the iron-binding capacity also confers lactoferrin the property of limiting the growth of gut pathogens, which requires iron to proliferate. Simultaneously, lactoferrin can also enhance the growth of gut-beneficial microorganisms such as Bifidobacterium and Lactobacillus [44]. These probiotics have been proven to reduce the adverse effects associated with iron supplementation [45,46].

Figure 7.

Figure 7

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Proposed model describing the iron- and erythropoiesis-improving effects of lactoferrin. Part of the elements in this figure are using resources from Freepik [47] and Servier Medical Art [48] under a Creative Commons Attribution license.

This meta-analysis has several limitations. First, only 8 articles and 1262 participants were included into analysis, which may affect the reliability of the results. For example, the results of IL-6 and FIA were based on data extracted from 3 and 2 articles [33,34,36,37,38]. Moreover, the participants number in these studies is relatively small. Therefore, the comparative effects of lactoferrin on IL-6 and FIA should be cautiously interpreted. Second, 3 included studies did not have randomization [33,36] or blinding [31,32,33,34,36,37]. These risks of bias may downgrade the evidence level of corresponding outcomes.

Whether lactoferrin promotes iron status by mitigating inflammation still needs validating in future studies. Inflammatory cytokines such as IL-6, CRP and TNF-α should be detected in further trials. With respect to the lower fractional iron absorption of lactoferrin compared with ferrous sulfate (Figure 5), more iron absorption investigations on lactoferrin are required. A critical serum parameter needs detection in future trials is hepcidin, especially considering the essential function of hepcidin in iron metabolism [49]. Currently, the effect of lactoferrin on hepcidin remains unclear, and the measurement of serum hepcidin will help to explain the modulatory mechanism of lactoferrin on iron absorption. Moreover, the absorption efficiency difference between apo-lactoferrin and holo-lactoferrin may be another aspect for the further exploration of how lactoferrin modulates iron absorption. Iron absorption efficiency can be detected in animals or human volunteers receiving lactoferrin with different iron saturation levels. It may help to understand the interaction between apo-lactoferrin and dietary free iron in the gut, as well as their effects on intestinal iron absorption.

In conclusion, this study provides evidence to support lactoferrin as a superior supplement to ferrous sulfate to improve serum iron, ferritin and hemoglobin levels. Lactoferrin-bound iron is not an iron supplement per se, but immune modulator affecting iron homeostasis via lactoferrin-dependent signal transduction mechanism [9]. The anti-inflammation effect of lactoferrin may be the potential mechanism to explain its efficacy on iron status and erythropoiesis. Further intervention and mechanistic studies are warranted to explore the functions of lactoferrin in the regulation of iron absorption.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/nu14030543/s1, Table S1: Characteristics of the publications included in the meta-analysis; Table S2: Egger’s linear regression tests of the publications included in the meta-analysis; Table S3: Subgroup analyses of iron parameters and IL-6; Figure S1: Funnel plots for analyzing publication bias; Figure S2: Sensitivity analysis for the included studies.

Click here for additional data file. (328.4KB, zip)

Author Contributions

P.A., Y.L. and J.L. conceived the study; X.Z. (Xiya Zhao), X.Z. (Xu Zhang) and P.A. conducted the systematic search.; X.Z. (Xiya Zhao), X.Z. (Xu Zhang) and T.X. evaluated all articles; X.Z. (Xiya Zhao), X.Z. (Xu Zhang) and T.X. extracted detailed information and outcome data; X.Z. (Xiya Zhao) and Y.L. evaluated the risk of bias; X.Z. (Xiya Zhao), P.A. and J.L. analyzed the data; X.Z. (Xiya Zhao), X.Z. (Xu Zhang) and P.A. drafted the manuscript; Y.L. and J.L. revised the manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by the Beijing Advanced Innovation Center for Food Nutrition and Human Health, the National Natural Science Foundation of China (31970717, 82170429), the Chinese Universities Scientific Fund (2020TC015), the Beijing Municipal Natural Science Foundation (7222111), and the China Postdoctoral Science Foundation (2021M703520).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

Footnotes

Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

  • 1.Donker A.E., van der Staaij H. The critical roles of iron during the journey from fetus to adolescent: Developmental aspects of iron homeostasis. Blood Rev. 2021;50:100866. doi: 10.1016/j.blre.2021.100866. [DOI] [PubMed] [Google Scholar]
  • 2.Lopez A., Cacoub P. Iron deficiency anaemia. Lancet. 2016;387:907–916. doi: 10.1016/S0140-6736(15)60865-0. [DOI] [PubMed] [Google Scholar]
  • 3.Dev S., Babitt J.L. Overview of iron metabolism in health and disease. Hemodial. Int. 2017;21((Suppl. 1)):S6–S20. doi: 10.1111/hdi.12542. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Sundararajan S., Rabe H. Prevention of iron deficiency anemia in infants and toddlers. Pediatr. Res. 2021;89:63–73. doi: 10.1038/s41390-020-0907-5. [DOI] [PubMed] [Google Scholar]
  • 5.Camaschella C. Iron deficiency. Blood. 2019;133:30–39. doi: 10.1182/blood-2018-05-815944. [DOI] [PubMed] [Google Scholar]
  • 6.Pasricha S.-R., Tye-Din J., Muckenthaler M.U., Swinkels D.W. Iron deficiency. Lancet. 2021;397:233–248. doi: 10.1016/S0140-6736(20)32594-0. [DOI] [PubMed] [Google Scholar]
  • 7.Vos T., Abajobir A.A., Abate K.H., Abbafati C., Abbas K.M., Abd-Allah F., Abdulkader R.S., Abdulle A.M., Abebo T.A., Abera S.F., et al. Global, regional, and national incidence, prevalence, and years lived with disability for 328 diseases and injuries for 195 countries, 1990–2016: A systematic analysis for the Global Burden of Disease Study 2016. Lancet. 2017;390:1211–1259. doi: 10.1016/S0140-6736(17)32154-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.World Health Organization . Global Anaemia Reduction Efforts among Women of Reproductive Age: Impact, Achievement of Targets and the Way forward for Optimizing Efforts. World Health Organization; Geneva, Switzerland: 2020. [Google Scholar]
  • 9.Kassebaum N.J., Jasrasaria R., Naghavi M., Wulf S.K., Johns N., Lozano R., Regan M., Weatherall D., Chou D.P., Eisele T.P., et al. A systematic analysis of global anemia burden from 1990 to 2010. Blood. 2014;123:615–624. doi: 10.1182/blood-2013-06-508325. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Stevens G.A., Finucane M.M., De-Regil L.M., Paciorek C.J., Flaxman S.R., Branca F., Peña-Rosas J.P., Bhutta Z.A., Ezzati M., on behalf of Nutrition Impact Model Study Group (Anaemia) Global, regional, and national trends in haemoglobin concentration and prevalence of total and severe anaemia in children and pregnant and non-pregnant women for 1995–2011: A systematic analysis of population-representative data. Lancet Glob. Health. 2013;1:e16–e25. doi: 10.1016/S2214-109X(13)70001-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.World Health Organization . The Global Prevalence of Anaemia in 2011. World Health Organization; Geneva, Switzerland: 2015. [Google Scholar]
  • 12.Daru J., Zamora J., Fernández-Félix B.M., Vogel J., Oladapo O.T., Morisaki N., Tunçalp Ö., Torloni M.R., Mittal S., Jayaratne K., et al. Risk of maternal mortality in women with severe anaemia during pregnancy and post partum: A multilevel analysis. Lancet Glob. Health. 2018;6:e548–e554. doi: 10.1016/S2214-109X(18)30078-0. [DOI] [PubMed] [Google Scholar]
  • 13.Breymann C. Iron Deficiency Anemia in Pregnancy. Semin Hematol. 2015;52:339–347. doi: 10.1053/j.seminhematol.2015.07.003. [DOI] [PubMed] [Google Scholar]
  • 14.Global Nutrition Targets 2025: Anaemia Policy Brief. World Health Organization; Geneva, Switzerland: 2019. [Google Scholar]
  • 15.Azzopardi P.S., Hearps S.J., Francis K.L., Kennedy E.C., Mokdad A.H., Kassebaum N.J., Lim S., Irvine C.M.S., Vos T., Brown A.D., et al. Progress in adolescent health and wellbeing: Tracking 12 headline indicators for 195 countries and territories, 1990–2016. Lancet. 2019;393:1101–1118. doi: 10.1016/S0140-6736(18)32427-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Donovan A., Brownlie A., Zhou Y., Shepard J., Pratt S.J., Moynihan J., Paw B.H., Drejer A., Barut B., Zapata A., et al. Positional cloning of zebrafish ferroportin1 identifies a conserved vertebrate iron exporter. Nature. 2000;403:776–781. doi: 10.1038/35001596. [DOI] [PubMed] [Google Scholar]
  • 17.Pigeon C., Ilyin G., Courselaud B., Leroyer P., Turlin B., Brissot P., Loréal O. A new mouse liver-specific gene, encoding a protein homologous to human antimicrobial peptide hepcidin, is overexpressed during iron overload. J. Biol. Chem. 2001;276:7811–7819. doi: 10.1074/jbc.M008923200. [DOI] [PubMed] [Google Scholar]
  • 18.Nemeth E., Tuttle M.S., Powelson J., Vaughn M.B., Donovan A., Ward D.M.V., Ganz T., Kaplan J. Hepcidin regulates cellular iron efflux by binding to ferroportin and inducing its internalization. Science. 2004;306:2090–2093. doi: 10.1126/science.1104742. [DOI] [PubMed] [Google Scholar]
  • 19.Muñoz M., García-Erce J.A., Remacha Á.F. Disorders of iron metabolism. Part 1: Molecular basis of iron homoeostasis. J. Clin. Pathol. 2011;64:281–286. doi: 10.1136/jcp.2010.079046. [DOI] [PubMed] [Google Scholar]
  • 20.Lee P., Peng H., Gelbart T., Wang L., Beutler E. Regulation of hepcidin transcription by interleukin-1 and interleukin-6. Proc. Natl. Acad. Sci. USA. 2005;102:1906–1910. doi: 10.1073/pnas.0409808102. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Wrighting D.M., Andrews N.C. Interleukin-6 induces hepcidin expression through STAT3. Blood. 2006;108:3204–3209. doi: 10.1182/blood-2006-06-027631. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Das N.K., Schwartz A.J., Barthel G., Inohara N., Liu Q., Sankar A., Hill D.R., Ma X., Lamberg O., Schnizlein M.K., et al. Microbial Metabolite Signaling Is Required for Systemic Iron Homeostasis. Cell Metab. 2020;31:115–130.e116. doi: 10.1016/j.cmet.2019.10.005. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Griffin I.J. The Effects of Different Forms of Lactoferrin on Iron Absorption. J. Nutr. 2020;150:3053–3054. doi: 10.1093/jn/nxaa314. [DOI] [PubMed] [Google Scholar]
  • 24.Ke C., Lan Z., Hua L., Ying Z., Humina X., Jia S., Weizheng T., Ping Y., Lingying C., Meng M. Iron metabolism in infants: Influence of bovine lactoferrin from iron-fortified formula. Nutrition. 2015;31:304–309. doi: 10.1016/j.nut.2014.07.006. [DOI] [PubMed] [Google Scholar]
  • 25.Macciò A., Madeddu C. Efficacy and Safety of Oral Lactoferrin Supplementation in Combination with rHuEPO-β for the Treatment of Anemia in Advanced Cancer Patients Undergoing Chemotherapy: Open-Label, Randomized Controlled Study. Oncologist. 2010;15:894–902. doi: 10.1634/theoncologist.2010-0020. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Rosa L., Lepanto M.S., Cutone A., Siciliano R.A., Paesano R., Costi R., Musci G., Valenti P. Influence of oral administration mode on the efficacy of commercial bovine Lactoferrin against iron and inflammatory homeostasis disorders. Biometals. 2020;33:159–168. doi: 10.1007/s10534-020-00236-2. [DOI] [PubMed] [Google Scholar]
  • 27.Lambert L.A., Perri H., Meehan T. Evolution of duplications in the transferrin family of proteins. Comp. Biochem. Physiol. Part B Biochem. Mol. Biol. 2005;140:11–25. doi: 10.1016/j.cbpc.2004.09.012. [DOI] [PubMed] [Google Scholar]
  • 28.Kruzel M.L., Olszewska P., Pazdrak B., Krupinska A.M., Actor J.K. New insights into the systemic effects of oral lactoferrin: Transcriptome profiling. Biochem. Cell Biol. 2021;99:47–53. doi: 10.1139/bcb-2020-0069. [DOI] [PubMed] [Google Scholar]
  • 29. [(accessed on 30 September 2021)]. Available online: http://vassarstats.net/
  • 30. [(accessed on 10 October 2021)]. Available online: https://methods.cochrane.org/bias/news/rob-2-tool/
  • 31.Rezk M., Dawood R., Abo-Elnasr M., Al Halaby A., Marawan H. Lactoferrin versus ferrous sulphate for the treatment of iron deficiency anemia during pregnancy: A randomized clinical trial. J. Matern.-Fetal Neonatal Med. 2016;29:1387–1390. doi: 10.3109/14767058.2015.1049149. [DOI] [PubMed] [Google Scholar]
  • 32.Paesano R., Torcia F., Berlutti F., Pacifici E., Ebano V., Moscarini M., Valenti P. Oral administration of lactoferrin increases hemoglobin and total serum iron in pregnant women. Biochem. Cell Biol. 2006;84:377–380. doi: 10.1139/o06-040. [DOI] [PubMed] [Google Scholar]
  • 33.Paesano R., Pacifici E., Benedetti S., Berlutti F., Frioni A., Polimeni A., Valenti P. Safety and efficacy of lactoferrin versus ferrous sulphate in curing iron deficiency and iron deficiency anaemia in hereditary thrombophilia pregnant women: An interventional study. Biometals. 2014;27:999–1006. doi: 10.1007/s10534-014-9723-x. [DOI] [PubMed] [Google Scholar]
  • 34.Paesano R., Berlutti F., Pietropaoli M., Goolsbee W., Pacifici E., Valenti P. Lactoferrin efficacy versus ferrous sulfate in curing iron disorders in pregnant and non-pregnant women. Int. J. Immunopathol. Pharmacol. 2010;23:577–587. doi: 10.1177/039463201002300220. [DOI] [PubMed] [Google Scholar]
  • 35.Nappi C., Tommaselli G.A., Morra I., Massaro M., Formisano C., Di Carlo C. Efficacy and tolerability of oral bovine lactoferrin compared to ferrous sulfate in pregnant women with iron deficiency anemia: A prospective controlled randomized study. Acta Obstet. Gynecol. Scand. 2009;88:1031–1035. doi: 10.1080/00016340903117994. [DOI] [PubMed] [Google Scholar]
  • 36.Lepanto M.S., Rosa L., Cutone A., Conte M.P., Paesano R., Valenti P. Efficacy of Lactoferrin Oral Administration in the Treatment of Anemia and Anemia of Inflammation in Pregnant and Non-pregnant Women: An Interventional Study. Front. Immunol. 2018;9:2123. doi: 10.3389/fimmu.2018.02123. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Lönnerdal B., Bryant A. Absorption of iron from recombinant human lactoferrin in young US women. Am. J. Clin. Nutr. 2006;83:305–309. doi: 10.1093/ajcn/83.2.305. [DOI] [PubMed] [Google Scholar]
  • 38.Mikulic N., Uyoga M.A., Mwasi E., Stoffel N.U., Zeder C., Karanja S., Zimmermann M.B. Iron Absorption is Greater from Apo-Lactoferrin and is Similar Between Holo-Lactoferrin and Ferrous Sulfate: Stable Iron Isotope Studies in Kenyan Infants. J. Nutr. 2020;150:3200–3207. doi: 10.1093/jn/nxaa226. [DOI] [PubMed] [Google Scholar]
  • 39.Sienkiewicz M., Jaśkiewicz A., Tarasiuk A., Fichna J. Lactoferrin: An overview of its main functions, immunomodulatory and antimicrobial role, and clinical significance. Crit. Rev. Food Sci. Nutr. 2021:1–18. doi: 10.1080/10408398.2021.1895063. [DOI] [PubMed] [Google Scholar]
  • 40.Ward P.P., Mendoza-Meneses M., Cunningham G.A., Conneely O.M. Iron status in mice carrying a targeted disruption of lactoferrin. Mol. Cell Biol. 2003;23:178–185. doi: 10.1128/MCB.23.1.178-185.2003. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Roy C.N., Mak H.H., Akpan I., Losyev G., Zurakowski D., Andrews N.C. Hepcidin antimicrobial peptide transgenic mice exhibit features of the anemia of inflammation. Blood. 2007;109:4038–4044. doi: 10.1182/blood-2006-10-051755. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.Nicolas G., Bennoun M., Porteu A., Mativet S., Beaumont C., Grandchamp B., Sirito M., Sawadogo M., Kahn A., Vaulont S. Severe iron deficiency anemia in transgenic mice expressing liver hepcidin. Proc. Natl. Acad. Sci. USA. 2002;99:4596–4601. doi: 10.1073/pnas.072632499. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Jeong J.Y., Silver M., Parnes A., Nikiforow S., Berliner N., Vanasse G.J. Resveratrol ameliorates TNFα-mediated suppression of erythropoiesis in human CD34+ cells via modulation of NF-κB signalling. Br. J. Haematol. 2011;155:93–101. doi: 10.1111/j.1365-2141.2011.08800.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Vega-Bautista A., de la Garza M., Carrero J.C., Campos-Rodríguez R., Godínez-Victoria M., Drago-Serrano M.E. The Impact of Lactoferrin on the Growth of Intestinal Inhabitant Bacteria. Int. J. Mol. Sci. 2019;20:4707. doi: 10.3390/ijms20194707. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45.Paganini D., Uyoga M.A., Kortman G.A.M., Cercamondi C.I., Moretti D., Barth-Jaeggi T., Schwab C., Boekhorst J., Timmerman H.M., Lacroix C., et al. Prebiotic galacto-oligosaccharides mitigate the adverse effects of iron fortification on the gut microbiome: A randomised controlled study in Kenyan infants. Gut. 2017;66:1956–1967. doi: 10.1136/gutjnl-2017-314418. [DOI] [PubMed] [Google Scholar]
  • 46.Paganini D., Uyoga M.A., Cercamondi C.I., Moretti D., Mwasi E., Schwab C., Bechtler S., Mutuku F.M., Galetti V., Lacroix C., et al. Consumption of galacto-oligosaccharides increases iron absorption from a micronutrient powder containing ferrous fumarate and sodium iron EDTA: A stable-isotope study in Kenyan infants. Am. J. Clin. Nutr. 2017;106:1020–1031. doi: 10.3945/ajcn.116.145060. [DOI] [PubMed] [Google Scholar]
  • 47.Main Elements of Proposed Model. [(accessed on 20 January 2022)]. Available online: https://www.freepik.com/
  • 48.Main Elements of Proposed Model. [(accessed on 20 January 2022)]. Available online: http://smart.servier.com/
  • 49.Muñoz M., García-Erce J.A., Remacha F. Disorders of iron metabolism. Part II: Iron deficiency and iron overload. J. Clin. Pathol. 2011;64:287–296. doi: 10.1136/jcp.2010.086991. [DOI] [PubMed] [Google Scholar]

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