You are here

  • Home
  • Archive
  • Volume 8, Issue 2
  • Oral iron supplementation and anaemia in children according to schedule, duration, dose and cosupplementation: a systematic review and meta-analysis of 129 randomised trials

Article Text

Article menu
Original research
Oral iron supplementation and anaemia in children according to schedule, duration, dose and cosupplementation: a systematic review and meta-analysis of 129 randomised trials
  1. Christopher T Andersen1,
  2. Daniel M Marsden2,
  3. Christopher P Duggan3,4,5,
  4. Enju Liu3,6,
  5. Dariush Mozaffarian7,8,
  6. Wafaie W Fawzi4
  1. 1Department of Epidemiology, Harvard University T H Chan School of Public Health, Boston, Massachusetts, USA
  2. 2The George Washington University School of Medicine and Health Sciences, Washington, DC, USA
  3. 3Division of Gastroenterology, Hepatology, and Nutrition, Boston Children's Hospital, Boston, Massachusetts, USA
  4. 4Department of Global Health and Population, Harvard University T H Chan School of Public Health, Boston, Massachusetts, USA
  5. 5Department of Nutrition, Harvard T H Chan School of Public Health, Boston, Massachusetts, USA
  6. 6Institutional Centers of Clinical and Translational Research, Boston Children's Hospital, Boston, Massachusetts, USA
  7. 7Tufts University Friedman School of Nutrition Science and Policy, Boston, Massachusetts, USA
  8. 8Division of Cardiology, Tufts University School of Medicine, Boston, Massachusetts, USA
  1. Correspondence to Dr Christopher T Andersen; chrisandersen{at}mail.harvard.edu

Abstract

Introduction WHO guidelines on iron supplementation among children call for further research to identify the optimal schedule, duration, dose and cosupplementation regimen.

Methods A systematic review and meta-analysis of randomised controlled trials was undertaken. Randomised controlled trials providing ≥30 days of oral iron supplementation versus placebo or control to children and adolescents aged <20 years were eligible. Random-effects meta-analysis was used to summarise the potential benefits and harms of iron supplementation. Meta-regression was used to estimate iron effect heterogeneity.

Results 129 trials with 201 intervention arms randomised 34 564 children. Frequent (3–7/week) and intermittent (1–2/week) iron regimens were similarly effective at decreasing anaemia, iron deficiency and iron deficiency anaemia (p heterogeneity >0.05), although serum ferritin levels and (after adjustment for baseline anaemia) haemoglobin levels increased more with frequent supplementation. Shorter (1–3 months) versus longer (7+ months) durations of supplementation generally showed similar benefits after controlling for baseline anaemia status, except for ferritin which increased more with longer duration of supplementation (p=0.04). Moderate-dose and high-dose supplements were more effective than low-dose supplements at improving haemoglobin (p=0.004), ferritin (p=0.008) and iron deficiency anaemia (p=0.02), but had similar effects to low-dose supplements for overall anaemia. Iron supplementation provided similar benefits when administered alone or in combination with zinc or vitamin A, except for an attenuated effect on overall anaemia when iron was cosupplemented with zinc (p=0.048).

Conclusions Weekly and shorter duration iron supplementation at moderate or high doses might be optimal approaches for children and adolescents at risk of deficiency.

Trial registration number CRD42016039948.

  • Systematic review
  • Anaemia
  • Treatment
  • Nutrition
  • Child health

Data availability statement

Data are available upon reasonable request.

https://creativecommons.org/licenses/by/4.0/

This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/.

https://doi.org/10.1136/bmjgh-2022-010745

Statistics from Altmetric.com

    Request Permissions

    If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.

    WHAT IS ALREADY KNOWN ON THIS TOPIC

    • Prior meta-analyses have established that paediatric oral iron supplementation is safe and effective for reducing anaemia.

    • Consequently, WHO recommends 3 months annually of daily oral iron supplementation for children aged 6 months to 12 years living in regions with a high burden of anaemia.

    • However, the 2016 WHO guidelines call for further research to identify the optimal schedule, duration, dose and cosupplementation regimen.

    WHAT THIS STUDY ADDS

    • Our study adds to previous meta-analyses of paediatric iron supplementation by using meta-regression to compare the effect sizes of randomised controlled trials with different schedules, durations, doses and cosupplementation schemes.

    • As a result, we are able to marshal a much larger body of literature than prior studies which have been restricted to trials specifically designed to answer questions of effect heterogeneity.

    HOW THIS STUDY MIGHT AFFECT RESEARCH, PRACTICE OR POLICY

    • Our results generally support the WHO recommendations regarding the frequency, duration and dose of iron supplementation.

    • However, weekly iron supplementation might be considered as an alternative to the recommended daily regimen in some contexts, given evidence of similar efficacy.

    • Furthermore, vitamin A and zinc can be cosupplemented without reducing the benefits of iron.

    Background

    Iron deficiency (ID) is the most common micronutrient deficiency globally, with children at particular risk.1 2 Among children aged 6–59 months, approximately half of the 273 million cases of anaemia in 2011 were estimated to be due to ID.3 4 ID is furthermore a key risk factor for cognitive impairment, impaired immune function and decreased capacity for physical activity.5–7

    WHO recommends daily oral iron supplementation for all children in regions with a prevalence of anaemia ≥40%. In malaria-endemic settings, iron supplementation is recommended in conjunction with measures to prevent, diagnose and treat malaria.8 These recommendations are supported by prior meta-analyses establishing the benefits of iron supplementation in the treatment of anaemia along with safety in the presence of malaria control programmes.9–12 However, prior meta-analyses have not investigated the optimal delivery of iron supplementation among children. The 2016 WHO guidelines therefore highlight the need for additional evidence regarding the optimal schedule, duration and dose of iron supplementation, as well as the efficacy of iron supplementation in the presence of cosupplemented micronutrients.8

    We conducted a systematic review and meta-analysis of randomised controlled trials of oral iron supplementation among children and adolescents aged <20 years and compared the impact of interventions by schedule, duration, dose and cointerventions. Haematologic, anthropometric, infectious and developmental outcomes were included to assess both safety and efficacy.

    Methods

    Search strategy and selection criteria

    We adhered to the Cochrane Collaboration’s guidelines for this review.13 The protocol was pre-registered with the International Prospective Register of Systematic Reviews (CRD42016039948). Systematic literature searches were performed using PubMed, Scopus, Web of Science and the Cochrane Central Register of Controlled Trials from inception through November 2020. References of eligible articles and previous systematic reviews were additionally reviewed. No language restrictions were placed on the search strategy, although studies were excluded if a translation could not be obtained for those published in a language not spoken by one of the authors. Search terms are presented in online supplemental appendix 1.

    Supplemental material

    Studies were eligible for inclusion if they met the following criteria:

    • Oral iron supplementation was randomly assigned.

    • Oral iron supplementation was compared with control or placebo. (Studies comparing multiple doses of iron supplementation and which did not include a group randomised to no iron were excluded due to the lack of a common referent for meta-analysis.)

    • Intervention groups differed by iron alone (eg, studies randomising children to iron folate vs placebo were not eligible unless the placebo also included folate, due to potential independent effects of these other components).

    • Oral iron supplementation was administered for a minimum period of ≥1 month (≥30 days).

    • Participants were aged <20 years.

    • Participants did not have any chronic illness (eg, HIV) or belong to a special subpopulation (eg, athletes).

    Data extraction and management

    One reviewer screened the titles and abstracts of records identified by the search, and excluded those that indicated clear ineligibility. Two reviewers independently reviewed the full text of all positively screened studies to establish final eligibility, after which data were extracted from eligible studies in duplicate using standardised forms. Online supplemental appendix 2 provides a list of variables extracted from eligible studies. Discrepancies between reviewers were resolved through discussion or through arbitration with a third reviewer. Factorial trials were extracted as two separate experiments (iron vs control, iron+cointervention vs control+cointervention).

    Assessment of risk of bias

    Two authors independently assessed risk of bias using the Cochrane Risk of Bias Tool, and discrepancies were resolved by discussion.13

    Outcomes

    To assess the relative benefits and risks of oral iron supplementation among children and adolescents, we included the following outcomes: haemoglobin (g/L), anaemia (defined by study authors), serum ferritin (μg/L), ID (defined by study authors), iron deficiency anaemia (IDA, defined by study authors); physical growth (height-for-age, weight-for-height, weight-for-age, stunting, wasting and underweight; primarily using the National Center for Health Statistics reference and WHO growth standards and growth reference14–16); indicators of infection (diarrhoea, respiratory infection, malaria and intestinal helminths); and child development (standardised means of cognitive, motor and socioemotional domain scores). In order to account for repeated use of the same control group in trials comparing multiple iron treatments to a single control (n=18 trials), the variance of the outcome in the control group was adjusted by dividing the control group sample size by the number of comparisons.

    Statistical analysis

    Meta-analysis was conducted for outcomes reported by four or more trials. We used inverse-variance weighted random-effects meta-analysis to account for underlying differences in the trial populations.17 Binary outcomes were summarised using risk ratios, prevalence ratios (PR) or rate ratios with 95% CIs. Continuous measures on the same scale were presented using mean differences, and measures reported on different scales using standardised mean differences (SMD). For ferritin, geometric means or medians were included when arithmetic means were not reported. Heterogeneity of effects was measured using the I2 statistic. We assessed effect modification using univariate meta-regression for prespecified supplementation variables: schedule (1–2 times/week; 3–7 times/week), duration (1–3 months; 4–6 months; ≥7 months), dose (age-adjusted tertiles; see online supplemental appendix 3) and cointerventions (zinc; vitamin A).18 19 In secondary analyses, we explored effect modification by baseline anaemia (all anaemic; all non-anaemic; mixed population of anaemic and non-anaemic; missing baseline anaemia data), child age (0–5 months; 6–23 months; 2–4 years; 5–11 years; 12–19 years), child sex (all female; all male; mixed female and male; missing baseline sex data), WHO region (Africa; Americas; Eastern Mediterranean; Europe; South-East Asia; Western Pacific) and iron formulation (ferrous sulfate; ferrous fumarate; other or unspecified). We conducted multivariate meta-regression to investigate collinearity between potential effect modifiers.20 Small study effects were assessed using funnel plots and Egger’s test for all outcomes reported by ≥10 iron intervention groups. Sensitivity analyses correcting for small study effects were conducted using trim and fill.21

    Role of the funder

    The funder was not involved in the study design, data collection, analysis, interpretation or manuscript writing. The corresponding author had access to all data in the study and assumes full responsibility for the accuracy of the results.

    Patient and public involvement

    Our prior clinical and research experiences with iron-deficient paediatric patients led us to develop the idea for this study. No patients were involved in the meta-analysis design or conduct, though we aim to present findings of clinical relevance to patients. We anticipate that the results of this study would be of interest to clinicians and health policy makers globally, which could in turn contribute to improved patient care.

    Results

    Literature search

    A total of 12 350 unique publications were retrieved from PubMed, Scopus, Web of Science and Cochrane Central search. An additional 13 records identified from the reference lists of eligible articles or prior meta-analyses were also screened. Of these, 955 records were selected for full text review, of which 79 required discussion between independent reviewers to determine eligibility, and 13 required arbitration from a third coauthor. One hundred and forty-two studies met the final eligibility criteria for inclusion (figure 1). Online supplemental appendix 4 provides references to all included publications.

    Figure 1
    Figure 1

    Flow diagram for selection process of eligible studies.

    Trial characteristics

    The 142 eligible publications represented 129 unique trials with 201 trial arms randomised to iron supplementation and 177 trial arms randomised to control or placebo, and 34 564 total participants analysed (table 1). Children under 5 years of age were most frequently studied, with children aged <6 months (n=45 trial arms, 22%), 6–23 months (n=44, 22%) and 2 to <5 years (n=37, 18%) representing roughly equal proportions of this population. School-age children of 5–11 years (n=50, 25%) and adolescents aged 12–19 years (n=25, 12%) were less frequently studied than children under 5. About half of studies were in anaemic only (n=36, 18%) or mixed anaemic and non-anaemic (n=70, 35%) children, and about 1 in 6 (n=32, 16%) in non-anaemic children; the remainder (n=63, 32%) did not report baseline anaemia status. Most studies (n=163, 81%) provided iron supplementation 3–7 days/week, although many (n=35, 17%) supplemented only 1–2 days/week. About half of studies (n=113, 56%) provided supplementation for 1–3 months; about one-third (n=62, 31%) for 4–6 months; and the remainder (n=26, 13%) for ≥7 months. About one-fifth (n=30, 23%) of eligible studies were factorial trials, among which the most frequent cointerventions were zinc (n=11) and vitamin A (n=6). The characteristics of individual studies are available in online supplemental appendix 5.

    View this table:
    Table 1

    Characteristics of studies included in meta-analysis of randomised iron supplementation trials for child health

    Main effects of iron supplementation on haematologic outcomes

    In aggregate, oral iron supplementation versus placebo or control demonstrated clear benefits for haematologic indices (table 2). Haemoglobin levels rose by 6.3 g/L (95% CI 5.5, 7.1) along with serum ferritin increases of 18.5 ng/mL (16.1, 20.9). Iron supplementation reduced the prevalence of overall anaemia by 39% (33%, 45%), and even larger impacts were observed for ID (reduction of 70% (63%, 76%)) and IDA (reduction of 80% (69%, 87%)). Heterogeneity was observed between studies for these haematologic outcomes (I2 ranging from 80% to 100%), which was further explored using meta-regression (see below).

    View this table:
    Table 2

    Effect of oral iron supplementation versus placebo or control among children and adolescents aged <20 years

    Assessment of heterogeneity for haematologic outcomes

    When comparing trials of frequent (3–7 times/week) versus intermittent (1–2 times/week) supplementation, no significant differences in treatment effects were observed for haemoglobin, anaemia, ID and IDA outcomes (table 3). However, trials of frequent supplementation achieved larger increases in serum ferritin than trials of intermittent supplementation (20.9 ng/mL (18.2, 23.7) vs 6.7 ng/mL (3.7, 9.6); p interaction <0.001). After control for baseline anaemia in the study population, frequent supplementation was associated with a larger increase in both ferritin and haemoglobin levels as compared with intermittent supplementation (online supplemental appendix 6).

    View this table:
    Table 3

    Comparison of iron supplementation effects across schedule, duration and dosing schemes

    Increasing duration of supplementation was generally associated with diminished impacts on haemoglobin, ID and IDA (table 3). However, trials of short duration were more likely to have a higher proportion of patients with anaemia, which could lead to larger effects. After controlling for baseline anaemia, no significant associations were observed between duration of supplementation and haemoglobin, anaemia, ID or IDA outcomes. Trials of longer duration were associated with greater increases in serum ferritin after adjustment for baseline anaemia (online supplemental appendix 6).

    When we evaluated age-adjusted doses of supplementation (see online supplemental appendix 3 for the age-specific dose categories), trials in the lowest dose tertile across all ages used lower amounts than recommended by WHO (10–12.5 mg/day for ages 6–23 months, 30 mg/day for ages 24–59 months and 30–60 mg/day for ages 5–12 years).8 Compared with lower age-adjusted doses of supplementation and adjusting for baseline anaemia, moderate doses were associated with greater improvements in haemoglobin, ferritin and IDA (table 3; online supplemental appendix 6). However, the lower dose still produced benefits; and no linear dose–response was seen: compared with lower dose, the highest doses were not associated with significantly greater effects.

    When comparing the effect of iron stratified by the baseline prevalence of anaemia, trials conducted among entirely anaemic populations demonstrated approximately twofold increases in haemoglobin (global p interaction <0.001) and reductions in endline anaemia (global p interaction=0.004) relative to non-anaemic populations (online supplemental appendix 7). Heterogeneity was observed for some outcomes by child age and sex, although there was no consistent pattern. Effects of iron on haematologic outcomes were similar across WHO regions, except for the impact on IDA (global p interaction=0.007). Comparing types of supplements, ferrous sulfate was associated with the largest increases in haemoglobin (p=0.02) and serum ferritin (p=0.005) and the largest reduction in IDA (p<0.001) compared with other iron formulations.

    Cosupplementation

    In factorial trials of iron and zinc supplementation, a borderline interaction was seen for iron effects on the prevalence of anaemia, with stronger reductions in anaemia among children not receiving zinc (PR=0.41 (0.33, 0.50)) versus those receiving zinc (PR=0.64 (0.48, 0.84)) (p interaction=0.048) (table 4). No significant differences by zinc cosupplementation were seen for haemoglobin, ferritin, ID or IDA, although effects generally appeared qualitatively stronger without zinc cosupplementation for each of these outcomes. Zinc alone provided no statistically significant benefits for haematologic outcomes (online supplemental appendix 8). There was no statistically significant difference in the effect of iron supplementation when administered with or without vitamin A. Vitamin A alone improved haemoglobin and anaemia outcomes (online supplemental appendix 8).

    View this table:
    Table 4

    Comparison of iron supplementation effects within factorial trials

    Safety outcomes

    No statistically significant changes due to oral iron supplementation were observed for anthropometric or infectious indices (table 2). In meta-regression analyses, no significant differential impacts of iron on these outcomes were seen by schedule, duration or dose, except for an observed increase in the cumulative incidence of respiratory illness associated with iron supplements that were 1–2 per week, low dose or lasting for ≥7 months (online supplemental appendix 9). However, these differential effects were due to a single factorial trial of iron and polyunsaturated fatty acids that differed from the other trials in terms of schedule, dose and duration22; excluding this trial, no significant difference remained. Iron increased height-for-age z score (HAZ) by 0.20 (95% CI 0.01, 0.40) in trial arms composed exclusively of anaemic children (but based on only n=2 trial arms); no effect on HAZ was seen among trial arms of non-anaemic children (−0.02 (−0.18, 0.14); n=3) or mixed anaemic and non-anaemic children (0.00 (−0.03, 0.02); n=25) (p interaction=0.013). Improvements in cognitive development were seen in one trial arm among anaemic children (Bayley Cognitive SMD=1.39 (0.75, 2.04); Bayley Motor SMD=1.46 (0.81, 2.11)) compared with no effect seen in four trial arms among non-anaemic children (Bayley Cognitive SMD=0.29 (−0.12, 0.71); Bayley Motor SMD=0.03 (−0.31, 0.38)) or four trial arms among mixed anaemic and non-anaemic children (Bayley Cognitive SMD=0.07 (−0.10, 0.23); Bayley Motor SMD=0.11 (−0.16, 0.37)) (p interaction=0.020 for cognitive and 0.023 for motor scores).

    Risk of bias

    The risk of bias within each trial is reported in online supplemental appendix 10. Many trials (16%–75%) did not report sufficient information to calculate the risk of bias according to one or more of the five criteria (online supplemental appendix 11). Forty-eight of the 129 trials (37%) were judged to be at high risk of bias for at least one of the criteria, with incomplete outcome data being the most frequent reason for a study to be assessed at high risk of bias (n=24, 19%). In sensitivity analyses excluding these 48 studies, the effects of iron supplementation on haematologic outcomes were similar (online supplemental appendix 12).

    Small study effects

    For haematologic outcomes, studies with larger SEs tended to demonstrate more protective effect sizes (Egger’s test p<0.001) (online supplemental appendix 13). Attenuated but still statistically significant benefits were obtained during trim-and-fill sensitivity analyses for haemoglobin (2.2 g/L (1.2, 3.1)) and ferritin (4.1 ng/mL (1.6, 6.5)).

    Discussion

    This systematic review and meta-analysis of 129 randomised controlled trials, including 201 trial arms of oral iron supplementation in children, demonstrates significant benefits on haematologic outcomes including haemoglobin (+6.3 g/L; 95% CI 5.5, 7.1), ferritin (+18.5 ng/mL; 16.1, 20.9) and prevalence of anaemia (39% reduction; 33%, 45%), ID (70% reduction; 63%, 76%) and IDA (80% reduction; 69%, 87%). Children under age 5 years were most frequently studied (63% of trial arms), including trials throughout this age range, but with meaningful numbers of trials among children aged 5–11 years (25%) and adolescents aged 12–19 years (12%). In sum, these findings provide strong evidence for the benefits of iron supplementation among children.

    Importantly, the number and diversity of identified trials allowed us to assess factors that might modify these benefits. Our results suggest that frequent (3–7 times/week) and intermittent (1–2 times/week) iron supplementation may be equally effective at increasing haemoglobin and decreasing anaemia, ID and IDA. While WHO recommends daily oral iron supplementation for all children in regions with an anaemia prevalence of 40% or more, the success of such programmes may be threatened by low adherence from adverse gastrointestinal reactions or high caregiver burden to provide daily supplements.23 Weekly iron supplementation has been promoted as an alternative to reduce these barriers.24 25 Furthermore, since mammalian gastrointestinal epithelial cells turn over every 2–6 days, weekly supplementation may not be at a great disadvantage relative to daily supplementation with respect to the total amount of absorbed iron.26 27 Some evidence points to changes in gastrointestinal epithelial cells following a large bolus of iron that results in reduced transport of iron into portal blood.28 A prior meta-analysis of 21 trials concluded that, compared with daily iron supplements, intermittent supplementation had similar effects on haemoglobin levels but was less effective in reducing anaemia.29 Our findings, based on a much larger number of trials, suggest that frequent and intermittent supplementation are similarly effective in reducing anaemia.

    Studies of longer duration were more likely to have a lower prevalence of baseline anaemia (online supplemental appendix 5). As a result, the apparently diminishing impacts of iron with increased duration were entirely explained on control for baseline anaemia (online supplemental appendix 6). Some prior studies have shown that impacts of iron on haemoglobin persist for several months after the cessation of supplementation,30 31 though the period of durability likely depends on the availability of dietary iron, burden of infection and degree of blood loss experienced by the population. The findings of this study support the current WHO recommendation of a 3-month course of iron supplementation, though a longer duration may be considered in order to maintain haemoglobin levels.

    For all ages, the lowest dose tertile of iron received less than the WHO recommended daily supplement (10–12.5 mg/day for ages 6–23 months, 30 mg/day for ages 24–59 months, 30–60 mg/day for ages 5–12 years). Moderate age-adjusted doses appeared to be more effective than lower doses at increasing haemoglobin, but all doses effectively improved outcomes, even doses below current WHO recommendations. Interestingly, more frequent supplementation, longer durations of supplementation and higher doses each were associated with greater increases in serum ferritin. These novel findings can inform the design of future supplementation programmes, suggesting that flexibility is possible depending on specific aims.

    Importantly, we found that benefits were generally similar across diverse ages from <5 months to >12 years, in males and in females and across world regions. This supports initiation of iron supplementation programmes in a diverse range of young populations. As might be expected, increases in haemoglobin and reductions in anaemia were approximately twice as large in populations in which all children were anaemic at baseline, compared with mixed or non-anaemic populations. Yet, even among children who were non-anaemic at baseline, iron supplementation effectively reduced the future risk of anaemia by 37%, and of ID and IDA by about 80%. These findings indicate that iron supplementation is effective for primary prevention among at-risk children.

    Factorial trials of iron and zinc supplementation (n=11) found that cosupplementation of iron with zinc did not diminish impacts on haemoglobin, serum ferritin, ID or IDA. However, there was some evidence that iron supplementation alone decreases anaemia more than when given along with zinc supplementation. There was also a qualitative trend towards attenuated effects for all outcomes in children who received iron and zinc concurrently. Uptake of both iron and zinc is mediated by divalent metal transporter-1 and ferroportin, which may result in absorptive antagonism.32 33 However, the evidence from this meta-analysis suggests that in contexts where prevalent zinc deficiency is suspected, cosupplementation of iron can still yield population benefits.

    There was no statistically significant difference in the effect of iron comparing children in factorial trials randomised additionally to vitamin A versus those randomised to no vitamin A (n=6 trials). The mechanism of iron and vitamin A interaction remains incompletely understood. Prior research has indicated that vitamin A may increase nonheme iron absorption, which is perhaps achieved through mobilising iron stores or stimulating the synthesis of transferrin.34–36 However, one bioavailability study in non-anaemic adults found that absorption of a single dose of iron (10 mg) was increased when cosupplemented with a dose of vitamin A of 1500 or 3000 IU, but inhibited when cosupplemented with dose of vitamin A of 6000 IU.37 Two trial arms in this meta-analysis gave single vitamin A doses of 200 000 IU at enrolment, two trial arms gave daily doses of 5000 or 10 000 IU and two trial arms gave 15 000 IU weekly. On balance, the evidence from this meta-analysis suggests that vitamin A can be given in combination with iron in order to improve haematologic outcomes.

    In our meta-analysis, iron supplementation had no significant effect on infections, although small effects on diarrhoea or malaria could not be excluded. Iron is an essential nutrient for pathogenic microbes, and several studies have investigated whether iron status or supplementation relates to infection risk.38 One trial of iron-folic acid supplementation in a malaria-endemic region was halted early due to higher mortality among those randomised to iron39; and Cochrane review concluded that iron supplementation in malaria-endemic areas without malaria control programmes may increase the incidence of malaria, although iron may also reduce clinical malaria in regions where malaria control programmes are available.10 Relatively few studies included in this meta-analysis reported data on infections, those which did reported varying outcomes (eg, incidence, prevalence, mean number of episodes, average duration) and several studies excluded children on the basis of an infection, creating a possibility of reporting and selection bias. Our findings add to the body of literature on iron and infection, and the interaction between iron supplementation and infection remains an important area for future study.

    Forty-three trials reported data on height-for-age, and no significant effects were seen on child growth. This finding is consistent with results of prior meta-analyses based on fewer studies.9 11 12 Furthermore, no effect modification was seen for growth-related outcomes for any of the eight potential modifiers that were investigated. Combined with the findings of prior research, this meta-analysis suggests that iron supplementation does not promote linear growth in children. With respect to cognitive function, a diverse set of measures and reporting scales was used; using the most frequently reported measure, the Bayley Index, we found some evidence of benefits of iron supplementation on mental performance (p=0.05).

    Potential limitations of this research should be considered. Many studies had insufficient information that could be used to determine risk of bias, thereby impeding the exploration of iron effects according to study quality. Furthermore, when data were available on adherence to iron supplements, it was reported in numerous ways, similarly preventing a quantitative summary. As with all meta-analyses, publication bias cannot be ruled out; trim-and-fill methods suggested that effects were attenuated but still statistically significant when accounting for potentially missing studies. A large number of tests for effect heterogeneity were conducted (total of 25 tests across tables 3 and 4, and 110 in online supplemental appendices 7 and 8) without adjustment for multiple comparisons, and the positive findings from these tests should be interpreted accordingly with caution. Lastly, results for effect heterogeneity can be confounded due to collinear effect modifiers. Although we conduct sensitivity analyses controlling for baseline anaemia, the lack of individual-level data reduces the degree to which this and other factors can be precisely controlled.

    The 2016 WHO guidelines on iron supplementation in infants and children were informed by systematic reviews of randomised controlled iron supplementation trials that found clear benefits of iron supplementation on haematologic outcomes.9–12 In this large systematic review of iron supplementation trials, our work extends these prior meta-analyses by exploring effect heterogeneity according to schedule, duration, dose and cosupplementation regimen. We find that the evidence supports the currently recommended dose and duration of iron supplementation, although weekly supplementation might be reasonable in certain contexts, especially at moderate or high doses. We also identified no evidence for harms of iron supplementation on anthropometrics or risk of infection, and possibly improved mental development. Furthermore, evidence from this meta-analysis suggests that cosupplementation of iron with zinc or vitamin A generally results in similar impacts on haematologic outcomes, although there is some evidence for these effects being attenuated for zinc. Our findings could be considered in clinical decision-making and the development of further guidelines on oral iron supplementation among children and adolescents.

    Data availability statement

    Data are available upon reasonable request.

    Ethics statements

    Patient consent for publication

    References

    1. ↵
      1. Bailey RL,
      2. West KP,
      3. Black RE
      . The epidemiology of global micronutrient deficiencies. Ann Nutr Metab 2015;66 Suppl 2:22–33. doi:10.1159/000371618
      OpenUrlPubMed
    2. ↵
      1. Pasricha S-R,
      2. Drakesmith H,
      3. Black J, et al
      . Control of iron deficiency anemia in low- and middle-income countries. Blood 2013;121:2607–17. doi:10.1182/blood-2012-09-453522
      OpenUrlAbstract/FREE Full Text
    3. ↵
      1. Kassebaum NJ,
      2. Jasrasaria R,
      3. Naghavi M, et al
      . A systematic analysis of global anemia burden from 1990 to 2010. Blood 2014;123:615–24. doi:10.1182/blood-2013-06-508325
      OpenUrlAbstract/FREE Full Text
    4. ↵
      1. Stevens GA,
      2. Finucane MM,
      3. De-Regil LM, et al
      . 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:e16–25. doi:10.1016/S2214-109X(13)70001-9
      OpenUrl
    5. ↵
      1. Cherayil BJ
      . Iron and immunity: immunological consequences of iron deficiency and overload. Arch Immunol Ther Exp (Warsz) 2010;58:407–15. doi:10.1007/s00005-010-0095-9
      OpenUrlCrossRefPubMed
    6. ↵
      1. Haas JD,
      2. Brownlie T
      . Iron deficiency and reduced work capacity: a critical review of the research to determine a causal relationship. J Nutr 2001;131:676S–688S; doi:10.1093/jn/131.2.676S
      OpenUrlAbstract/FREE Full Text
    7. ↵
      1. Walker SP,
      2. Wachs TD,
      3. Gardner JM, et al
      . Child development: risk factors for adverse outcomes in developing countries. Lancet 2007;369:145–57. doi:10.1016/S0140-6736(07)60076-2
      OpenUrlCrossRefPubMedWeb of Science
    8. ↵
      1. World Health Organization
      . Guideline: daily iron supplementation in infants and children. Geneva, 2016.
    9. ↵
      1. Low M,
      2. Farrell A,
      3. Biggs B-A, et al
      . Effects of daily iron supplementation in primary-school-aged children: systematic review and meta-analysis of randomized controlled trials. CMAJ 2013;185:E791–802. doi:10.1503/cmaj.130628
      OpenUrlAbstract/FREE Full Text
    10. ↵
      1. Neuberger A,
      2. Okebe J,
      3. Yahav D, et al
      . Oral iron supplements for children in malaria-endemic areas. Cochrane Database Syst Rev 2016;2:CD006589. doi:10.1002/14651858.CD006589.pub4
    11. ↵
      1. Pasricha S-R,
      2. Hayes E,
      3. Kalumba K, et al
      . Effect of daily iron supplementation on health in children aged 4-23 months: a systematic review and meta-analysis of randomised controlled trials. Lancet Glob Health 2013;1:e77–86. doi:10.1016/S2214-109X(13)70046-9
      OpenUrl
    12. ↵
      1. Thompson J,
      2. Biggs BA,
      3. Pasricha SR
      . Effects of daily iron supplementation in 2- to 5-year-old children: systematic review and meta-analysis. Pediatrics 2013;131:739–53. doi:10.1542/peds.2012-2256
      OpenUrlCrossRefPubMedWeb of Science
    13. ↵
      1. Higgins J,
      2. Thomas J,
      3. Chandler J, et al
      . Cochrane handbook for systematic reviews of interventions. version 5. Oxford: Cochrane Collaboration, 2011.
    14. ↵
      1. Hamill PV,
      2. Drizd TA,
      3. Johnson CL, et al
      . NCHS growth curves for children birth-18 years. united states. Vital Health Stat 11 1977;165:1–74.
      OpenUrlPubMed
    15. ↵
      1. WHO Multicentre Growth Reference Study Group
      . Who child growth standards based on length/height, weight and age. Acta Paediatr Suppl 2006;450:76–85. doi:10.1111/j.1651-2227.2006.tb02378.x
      OpenUrlCrossRefPubMed
    16. ↵
      1. de Onis M,
      2. Onyango AW,
      3. Borghi E, et al
      . Development of a who growth reference for school-aged children and adolescents. Bull World Health Organ 2007;85:660–7. doi:10.2471/blt.07.043497
      OpenUrlCrossRefPubMedWeb of Science
    17. ↵
      1. DerSimonian R,
      2. Laird N
      . Meta-Analysis in clinical trials. Control Clin Trials 1986;7:177–88. doi:10.1016/0197-2456(86)90046-2
      OpenUrlCrossRefPubMedWeb of Science
    18. ↵
      1. Greenland S,
      2. Longnecker MP
      . Methods for trend estimation from summarized dose-response data, with applications to meta-analysis. Am J Epidemiol 1992;135:1301–9. doi:10.1093/oxfordjournals.aje.a116237
      OpenUrlCrossRefPubMedWeb of Science
    19. ↵
      1. Orsini N,
      2. Li R,
      3. Wolk A, et al
      . Meta-Analysis for linear and nonlinear dose-response relations: examples, an evaluation of approximations, and software. Am J Epidemiol 2012;175:66–73. doi:10.1093/aje/kwr265
      OpenUrlCrossRefPubMedWeb of Science
    20. ↵
      1. Sharp S
      . Sbe23: meta-analysis regression. Stata Technical Bulletin 1998;42:16–22.
      OpenUrl
    21. ↵
      1. Duval S,
      2. Tweedie R
      . A nonparametric “ TRIM and fill ” method of accounting for publication bias in meta-analysis. Journal of the American Statistical Association 2000;95:89–98. doi:10.1080/01621459.2000.10473905
      OpenUrlCrossRefWeb of Science
    22. ↵
      1. Malan L,
      2. Baumgartner J,
      3. Calder PC, et al
      . N-3 long-chain PUFAs reduce respiratory morbidity caused by iron supplementation in iron-deficient South African schoolchildren: a randomized, double-blind, placebo-controlled intervention. Am J Clin Nutr 2015;101:668–79. doi:10.3945/ajcn.113.081208
      OpenUrlAbstract/FREE Full Text
    23. ↵
      1. Tolkien Z,
      2. Stecher L,
      3. Mander AP, et al
      . Ferrous sulfate supplementation causes significant gastrointestinal side-effects in adults: a systematic review and meta-analysis. PLoS One 2015;10:e0117383. doi:10.1371/journal.pone.0117383
    24. ↵
      1. Angeles-Agdeppa I,
      2. Schultink W,
      3. Sastroamidjojo S, et al
      . Weekly micronutrient supplementation to build iron stores in female Indonesian adolescents. Am J Clin Nutr 1997;66:177–83. doi:10.1093/ajcn/66.1.177
      OpenUrlAbstract/FREE Full Text
    25. ↵
      1. Viteri FE,
      2. Ali F,
      3. Tujague J
      . Long-Term Weekly iron supplementation improves and sustains nonpregnant women’s iron status as well or better than currently recommended short-term daily supplementation. J Nutr 1999;129:2013–20. doi:10.1093/jn/129.11.2013
      OpenUrlAbstract/FREE Full Text
    26. ↵
      1. Galy B,
      2. Ferring-Appel D,
      3. Becker C, et al
      . Iron regulatory proteins control a mucosal block to intestinal iron absorption. Cell Rep 2013;3:844–57. doi:10.1016/j.celrep.2013.02.026
      OpenUrlCrossRefPubMedWeb of Science
    27. ↵
      1. Williams JM,
      2. Duckworth CA,
      3. Burkitt MD, et al
      . Epithelial cell shedding and barrier function: a matter of life and death at the small intestinal villus tip. Vet Pathol 2015;52:445–55. doi:10.1177/0300985814559404
      OpenUrlCrossRefPubMed
    28. ↵
      1. Shinoda S,
      2. Arita A
      . Regulatory mechanisms of intestinal iron absorption: iron-deficient mucosal cells respond immediately to dietary iron concentration. JPFSM 2014;3:399–407. doi:10.7600/jpfsm.3.399
      OpenUrl
    29. ↵
      1. De-Regil LM,
      2. Jefferds MED,
      3. Sylvetsky AC, et al
      . Intermittent iron supplementation for improving nutrition and development in children under 12 years of age. Cochrane Database Syst Rev 2011;2011:CD009085. doi:10.1002/14651858.CD009085.pub2
    30. ↵
      1. Desai MR,
      2. Mei JV,
      3. Kariuki SK, et al
      . Randomized, controlled trial of daily iron supplementation and intermittent sulfadoxine-pyrimethamine for the treatment of mild childhood anemia in Western Kenya. J Infect Dis 2003;187:658–66. doi:10.1086/367986
      OpenUrlCrossRefPubMedWeb of Science
    31. ↵
      1. Dossa RA,
      2. Ategbo EA,
      3. de Koning FL, et al
      . Impact of iron supplementation and deworming on growth performance in preschool beninese children. Eur J Clin Nutr 2001;55:223–8. doi:10.1038/sj.ejcn.1601126
      OpenUrlCrossRefPubMedWeb of Science
    32. ↵
      1. Kordas K,
      2. Stoltzfus RJ
      . New evidence of iron and zinc interplay at the enterocyte and neural tissues. J Nutr 2004;134:1295–8. doi:10.1093/jn/134.6.1295
      OpenUrlAbstract/FREE Full Text
    33. ↵
      1. Sandström B
      . Micronutrient interactions: effects on absorption and bioavailability. Br J Nutr 2001;85:S181. doi:10.1079/BJN2000312
    34. ↵
      1. Davidsson L,
      2. Adou P,
      3. Zeder C, et al
      . The effect of retinyl palmitate added to iron-fortified maize porridge on erythrocyte incorporation of iron in African children with vitamin A deficiency. Br J Nutr 2003;90:337–43. doi:10.1079/bjn2003914
      OpenUrlCrossRefPubMed
    35. ↵
      1. García-Casal MN,
      2. Layrisse M,
      3. Solano L, et al
      . Vitamin A and beta-carotene can improve nonheme iron absorption from rice, wheat and corn by humans. J Nutr 1998;128:646–50. doi:10.1093/jn/128.3.646
      OpenUrlAbstract/FREE Full Text
    36. ↵
      1. Staab DB,
      2. Hodges RE,
      3. Metcalf WK, et al
      . Relationship between vitamin A and iron in the liver. J Nutr 1984;114:840–4. doi:10.1093/jn/114.5.840
      OpenUrlAbstract/FREE Full Text
    37. ↵
      1. Gabriel F,
      2. Suen W,
      3. Marchini JS, et al
      . High doses of vitamin A impair iron absorption. NDS 2012;61. doi:10.2147/NDS.S23608
    38. ↵
      1. Cassat JE,
      2. Skaar EP
      . Iron in infection and immunity. Cell Host Microbe 2013;13:509–19. doi:10.1016/j.chom.2013.04.010
      OpenUrlCrossRefPubMed
    39. ↵
      1. Sazawal S,
      2. Black RE,
      3. Ramsan M, et al
      . Effects of routine prophylactic supplementation with iron and folic acid on admission to hospital and mortality in preschool children in a high malaria transmission setting: community-based, randomised, placebo-controlled trial. Lancet 2006;367:133–43. doi:10.1016/S0140-6736(06)67962-2
      OpenUrlCrossRefPubMedWeb of Science

    Supplementary materials

    • Supplementary Data

      This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.

    Footnotes

    • Handling editor Soumyadeep Bhaumik

    • Contributors DM obtained funding. CTA, DM, CPD and WWF conceived the study idea and designed the search strategy. CTA, DMM and EL reviewed studies for eligibility, extracted data and assessed bias. CTA performed data analysis, wrote the first draft of the manuscript and is the guarantor. CTA, DMM, CPD, EL, DM and WWF interpreted the data analysis and critically revised the manuscript.

    • Funding This research received support from the Bill & Melinda Gates Foundation grant (OPP1099505) and from two National Research Service Awards (T32AI007535-16A1, F31HD093514-01A1). CPD was supported in part by NIH grants K24 DK104676 and P30 DK040561.

    • Competing interests CPD receives chapter royalties from UpToDate and PMPH, USA. DM reports research funding from the National Institutes of Health, the Gates Foundation, The Rockefeller Foundation, Vail Innovative Global Research and Kaiser Permanente Fund at East Bay Community Foundation; reports personal fees from Acasti Pharma and Barilla; is on the scientific advisory boards of Beren Therapeutics, Brightseed, Calibrate, Elysium Health, Filtricine, HumanCo, Instacart, January, Perfect Day, Tiny Organics and (ended) Day Two, Discern Dx and Season Health; has stock ownership in Calibrate and HumanCo; and reports chapter royalties from UpToDate (all outside of the submitted work).

    • Patient and public involvement Patients and/or the public were involved in the design, or conduct, or reporting, or dissemination plans of this research. Refer to the Methods section for further details.

    • Provenance and peer review Not commissioned; externally peer reviewed.

    • Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.