Abstract
Background:
Iron depletion results from reduced iron stores, and it is an early stage of disease progression before iron deficiency, which leads to iron deficiency anaemia (IDA). IDA is associated with delayed infant growth and development, diminished cognitive function, poor academic performance, decreased exercise tolerance, and impaired immune function. This study aimed to determine the prevalence of iron depletion and IDA and factors associated with low ferritin levels among children under 5-years-old receiving care at Kilimanjaro Christian Medical Centre (KCMC) in Moshi, Tanzania.
Methods:
Under-5 children presenting at KCMC were successively enrolled and screened for iron depletion and IDA using complete blood count and serum ferritin levels. The generally accepted World Health Organization cut-off levels for normal haemoglobin (Hb) and ferritin level were used. Iron depletion, iron deficiency, and IDA prevalences were estimated in relation to the combination measures of haemoglobin, mean corpuscular volume, and ferritin levels. Dietary and sociodemographic characteristic of the children were recorded after parents or caretakers provided informed consent. Data analysis was conducted using SPSS version 21.0.
Results:
A total of 303 children aged 2 to 59 months were enrolled in the study. Anaemia was detected in169 (55.8%) children. Children aged 2 to 12 months had a higher prevalence of anaemia (n=101, 60.1%). The overall prevalences of iron depletion, iron deficiency with no anaemia, and IDA were 2.6% (n=8), 9.6% (n=29), and 28.1% (n=84), respectively. Low ferritin levels were detected in 124 (40.9%) children. Drinking more than 500 ml of cow's milk per day was associated with an increased risk of anaemia (adjusted odds ratio [AOR] 5.6; 95% confidence interval [CI], 2.6 to 12.1) relative to those not drinking cow's milk. Children whose families had meals that included beef more than 3 times per week were less likely to have low ferritin (AOR 0.6; 95% CI, 0.3 to 1.3), though the difference was not significant.
Conclusion:
The IDA prevalence among children in the Kilimanjaro area was high, with more than 50% of infants being anaemic. Drinking cow's milk was associated with an increased risk of IDA. Future community-based research is recommended to elucidate more details about iron deficiency in the general population.
INTRODUCTION
Iron depletion results from reduced iron stores and is an early asymptomatic stage of micronutrient deficiency. If not corrected, iron depletion has the potential to progress to iron deficiency and iron deficiency anaemia (IDA). The progression is usually considered in 3 phases; iron depletion (normal haemoglobin, normal Mean corpuscular volume (MCV) but low ferritin level), iron deficiency with no anaemia (normal haemoglobin, low MCV level and low ferritin level) and IDA (low haemoglobin, low MCV and low ferritin levels).1 IDA is associated with delayed infant growth and development, diminished cognitive function, poor academic performance, decreased exercise tolerance, and impaired immune function.2-5
IDA among children under 5 years of age has a prevalence of 47.4% worldwide and ranges from 18% to 26% among children under 5 years old in developed countries.6-8 A recent report, which included several African countries, reported a prevalence of anaemia in children below 5 years old, ranging from 10.5% in South Africa to 75% in Cote d'Ivoire, while IDA ranged from 11% in South Africa to 64% in Egypt.9 In Tanzania, the overall prevalence of anaemia was 77.2%, and the prevalence of IDA based on the ferritin level was 22.6%.10 Several risk factors have been associated with IDA and low ferritin levels, which include; poverty, being born prematurely, maternal anaemia, intestinal infestations like worms, infections, haematological disorders and nutritional factors like poor eating behaviours and use of cow's milk in children below the age of twelve months.4,11,12
There are several different methods for measuring anaemia, including complete blood count (CBC), total iron-binding capacity, serum iron, serum transferrin, and serum ferritin levels which are used either singly or in combination to assess iron levels in patients. Serum ferritin is the major form in which iron is stored in the body, and measurement of this can easily detect early changes in body iron storage, thereby making it the preferred single best blood test for the diagnosis of iron deficiency.4,13-15
Despite the high prevalence of IDA (11%-64%) in developing countries,9,10 the challenge is lack of resources for early diagnosis for iron depletion and iron deficiency. Iron depletion is asymptomatic and has unclear risk factors, thereby hampering a clinical diagnosis. Early detection would enable early intervention; therefore, knowing the risk factors and magnitude of the problem in a specific setting will allow primary prevention and hence prevent the harmful effects of IDA which are not reversible.
The most common causes of iron deficiency in children include insufficient intake together with rapid growth, low birth weight and gastrointestinal losses related to excessive intake of cow's milk,16 and parasites infestation such as helminth.17 Therefore, the main management of IDA should include identification and treatment of the underlying cause for IDA, iron replacement, nutritional counselling and advice as well as educational to the parent and family as well as helminthic control through deworming.16,17
This study aimed to determine the prevalence of iron depletion and IDA and factors associated with low ferritin levels among under-5 children receiving care at Kilimanjaro Christian Medical Centre (KCMC) paediatric department to inform planning for interventions to prevent IDA in children.
METHODS
Study Design and Study Site
This was a cross-sectional, hospital-based study carried out at the paediatric outpatient clinic (POPD), Reproductive and Child Health service (RCHS), Human Immunodeficiency Virus (HIV) exposed clinic and within the paediatric ward from August 2014 to July 2015 at KCMC in Moshi, Tanzania. KCMC is a faith-based organisation located in Kilimanjaro region in the northern part of Tanzania serving a population of approximately 15 million. KCMC has the official bed capacity of 638 beds with 130 beds, specifically being for paediatric care. The hospital receives referrals from the northern zone of Tanzania, and several outpatient clinics are attended daily. Daily, more than 1,000 patients are seen as outpatients, with about 20% being children. Paediatric outpatient clinics include HIV/AIDS clinic known as Child Centred family care clinic (CCFCC), general paediatric known as POPD clinic, neuropaediatric outpatient clinic (NPOC) for children with neurological disorders, paediatric outpatient neonatal follow-up clinic (POPNF) as well as the reproductive and child health services (RCHS) for wellbeing under 5 for vaccination and development. For this study, we included children attending POPD, CCFCC and RCHS.
In the Kilimanjaro region, the main activities remain agricultural production with the main being coffee, banana, maize and beans plantation. The region is divided into 4 different zones which favour the agro-economic activities in the region: (1) the Coffee Zone (coffee, bananas, maize, beans, and dairy production), (2) the Wheat Zone (wheat, beans, maize and dairy production), (3) the Lower Zone (maize, cotton, beans, paddy, and suitable for ranching), and (4) the Forestry Zone, which accounts for 388,500 ha of forest and national park.18
Study Population, Inclusion and Exclusion Criteria
The study population included children aged 2-59 months who attended POPD, CCFCC and RCHS clinics as outpatients or inpatients, whose mothers agreed to sign informed consent. Children who had a history of blood transfusion within 3 months before recruitment, regular iron supplementation for more than 2 months with a known haematological disorder, tuberculosis, HIV/AIDS, history of prematurity, or active haemorrhage were excluded. Information on age, sex, birth weight, residential address, breastfeeding history, use of cow's milk (including amount used), child's intake of meat (including amount).
This study used CBC and serum ferritin level to assess the level of iron storage in the study population using the World Health Organization (WHO) general accepted cut-off levels as; Hb >11mg/dl, MCV >80fl and serum ferritin (SF) level 12 ng/ml, Mild moderate and severe anaemia was considered when Hb level is = 10.0-10.9 mg/dl (Mild), 7.0-9.9 mg/dl (moderate) Less than 7 mg/dl (severe).19,20 Iron depletion was defined as a state when Hb >11mg/dl, normal MCV (80fl) and serum ferritin (SF) level is below 12 ng/ml, while iron deficiency is when the Hb is >11mg/dl with low MCV (<80fl) and low SF (<12ng/ml) while IDA is when Hb is <11mg/dl, and MCV <80fl with low SF (<12ng/ml).6,13,21
Sample Size Estimation
The minimum sample size was estimated using a formula by the Survey System Creative Research and Joint WHO (1988) expressed as sample size = Z2(p)(1-p)/ε2, where, Z = value (1.96 for 95 % confidence level). A prevalence (P) of 24 % for IDA reported from the Tanzania demographic and health 201022 and ε = minimal tolerable error at the 95% confidence level, expressed as a decimal (0.05). The minimum estimated sample size was 303 participants. The study used a convenience sampling technique where all children seen at the outpatient and inpatient who fulfilled the inclusion criteria during the study period were enrolled.
Laboratory Sample Analysis
Venous blood (4 to 5 ml) was drawn where, 2 ml of blood was placed in the EDTA tube for analysis of Complete blood count with Mindray 3200 haematology analyser (Shenzhen Mindray Bio-Medical Electronics Co., Ltd) at the KCMC Clinical laboratory. The remaining 3 ml of blood was placed in a serum separation tube (SST) then transported to Kilimanjaro Christian Research Institute (KCRI) – Biotechnology laboratory, situated within KCMC campus. The KCRI-Biotechnology Laboratory is located on the campus of KCMC, about 500 meters from the Hospital buildings. It supports both clinical trials and basic science research.
Centrifugation was done at 1,000 to 1,300 rpm for 10 minutes. Serum was collected in cryotubes and stored in a refrigerator at −20°C. Samples batched and tested for serum ferritin by ELISA using a commercial kit (Pishlaz Teb Diagnostics Zaman; catalogue no PT –Ferr -96, Germany). Laboratory data sheets were used to record all laboratory results. All children identified with iron depletion, iron deficiency, or IDA were started on iron supplementation and follow up given at the regular paediatric outpatient clinic every 3 months until 6 months after MCV and MCH have normalised.
Data Analysis
Data analysis was done using SPSS version 21.0 (IBM Corp., Armonk, NY, USA). Descriptive statistics were estimated where frequency count, and percentages were reported. Logistic regression was used to determine factors associated with iron depletion, iron deficiency, and IDA. Chi-square tests were used to test for significance in each of characteristics of the population at P≤.05.
Ethical Considerations
The ethical clearance was obtained from Kilimanjaro Christian Medical University College (KCMUCo) ethical review committee with a certificate No. 711. Informed consent was obtained from the parents/guardian of the study participants before enrollment. To ensure confidentiality, no names were used, and to minimise pain, the smallest needle was used to collect the minimum amount of blood required. Each participant's parent/guardian was informed of the results of haemoglobin level and the implications. Iron supplementation was prescribed when necessary. Children whose parents or guardians refused to consent received the same service provision and care as children who participated in the study.
RESULTS
We enrolled 314 children aged below 60 months, of which 6 did not show up for sample collection, and the samples from another 4 were insufficient for complete blood count and serum ferritin and 1 sample clotted. Therefore, 303 children samples were obtained and analysed, of which 153 (50.5%) were male and 150 (49.5 %) female. Median (IQR) age in months was 10 (6-18). The majority, (n=169, 55.8%) were in the age group 2-12 months. Two hundred fifty-eight (85.1%) had a normal birth weight between 2.5 and 4.0 kg with a median weight (IQR) at birth of 3.2 kg (2.9-3.5) and 74 (24.4%) of children being exclusively breastfed at the time of the study (Table 1).
TABLE 1.
Characteristics | n | % |
---|---|---|
Sex | ||
Male | 153 | 50.5 |
Female | 150 | 49.5 |
Age, months | ||
2-12 | 169 | 55.8 |
13-23 | 78 | 25.7 |
24-59 | 56 | 18.5 |
Median | 10 (IQR: 6-18) | |
Religion | ||
Christian | 263 | 86.8 |
Muslim | 40 | 13.2 |
Region of residence | ||
Kilimanjaro | 283 | 93.4 |
Manyara | 5 | 1.7 |
Arusha | 13 | 4.3 |
Other | 2 | 0.7 |
Birth weight, kg (aN=299) | ||
<2.5 | 30 | 9.9 |
2.5-4.0 | 258 | 85.1 |
>4 | 11 | 3.6 |
Median | 3.2 (IQR: 2.9-3.5) |
Missing data for 4 participants
Abbreviation: IQR, interquartile range
Prevalence of Iron Depletion, Iron Deficiency, and IDA
Of the 303 participants, 168 (55.5%) had anaemia, of these 79/168 (47.1%) had mild anaemia (Hb 10.0 - 10.9mg/dl) 87/168 (51.7%) had moderate anaemia (Hb 7.0 - 9.9mg/dl) and 2/168 (1.2%) had severe anaemia (Hb Less than 7mg/dl). In total, 84 (28.1%) children had IDA, 29 (9.6%) had iron deficiency with no anaemia, and 8 (2.6%) had iron depletion. A total of 124 (40.9%) children in the study had low ferritin level. Among children with anaemia, the majority (n=101, 60.1%) were aged 2 to 12 months (Table 2).
TABLE 2.
Categories | Total | 2-12 months | 13-23 months | 24-59 months |
---|---|---|---|---|
n (%) | n (%) | n (%) | ||
Low Serum ferritin | 124 | 60 (48.4) | 49 (39.5) | 15 (12.1) |
Anaemia | 168 | 101 (60.1) | 52 (31.0) | 15 (8.9) |
Mild | 79 | 49 (62.0) | 23 (29.1) | 7 (8.9) |
Moderate | 87 | 52 (59.8) | 28 (32.2) | 8 (8.0) |
Severe | 2 | 0(0) | 1 (50.0) | 1 (50.0) |
Iron depletion | 8 | 4 (50.0) | 1 (12.5) | 3 (37.5) |
Iron deficiency | 29 | 11 (37.9) | 14 (48.3) | 4 (13.8) |
Iron deficiency anaemia | 84 | 43 (50.6) | 34 (40.0) | 8 (9.4) |
Factors Associated With Low Ferritin Levels
The factors found to be independently associated with low ferritin levels after adjustment were sex, whereby males had nearly twice the odds of having a low ferritin level (adjusted odds ratio [AOR] 2.0; 95% confidence interval [CI], 1.2 to 3.4), compared to female counterparts. Infants and toddlers had higher odds of having low ferritin levels as compared to pre-school children (AOR 2.7; 95%CI, 1.2 to 6.1 and AOR 5.0; 95% CI, 2.0 to 11.2, respectively) (Table 3). Drinking more than 500 ml of cow's milk per day was associated with increased risk of anaemia (AOR 5.6; 95%CI, 2.6 to 12.1) as compared to children who had not used cow's milk. Children whose family who ate beef 3 or more times per week were less likely to have low ferritin (AOR 0.6; 95% CI, 0.3 to 1.1) as compared to those who had not used meat; however, this was not significant.
TABLE 3.
Variable | Ferritin | Unadjusted OR (95% CI) | Adjusted ORa 95% CI) | |
---|---|---|---|---|
Normal n (%) | Low n (%) | |||
Sex | ||||
Male | 79 (51.6) | 74 (48.4) | 1.9 (1.2–3.0) | 2.0 (1.2–3.4) |
Female | 100 (66.7) | 50 (33.3) | Ref | Ref |
Age, months | ||||
2-12 (Infants) | 95 (57.2) | 71 (42.8) | 1.2 (0.7–2.3) | 2.7 (1.2–6.1) |
13-23 (Toddlers) | 47 (60.3) | 31 (39.7) | 1.1 (0.6–2.2) | 5.0 (2.2–11.2) |
24-59 (Pre-school) | 37 (62.7) | 22 (37.3) | Ref | Ref |
Use of cow's milk | ||||
No | 60 (81.1) | 14 (18.9) | Ref | Ref |
Yes | 119 (52.0) | 110(48.0) | 4.0 (2.1–7.5) | - |
Amount of cow's milk | ||||
≥500 | 69 (45.1) | 84 (54.9) | 5.2 (2.7–10.1) | 5.6 (2.6–12.1) |
<500 | 50 (65.8) | 26 (34.2) | 2.2 (1.1–4.7) | 2.2 (1.0–5.0) |
No cow's milk | 60 (81.1) | 14 (18.9) | Ref | Ref |
Inclusion of red meat | ||||
≥3 | 38 (65.5) | 20 (34.5) | 0.9 (0.5–1.7) | 0.6 (0.3–1.3) |
<3 | 36 (46.2) | 42 (53.8) | 2.0 (1.2–3.4) | 1.6 (0.7–3.1) |
No red meat | 105 (62.9) | 62 (37.1) | Ref | Ref |
Adjusted for time of weaning, age started cow's milk, birth weight, time of breast feeding and past 2 months medical history
Abbreviations: OR, odds ratio; Ref, reference category
DISCUSSION
In this study, we aimed to determine the prevalence of iron depletion, IDA, and factors associated with low ferritin level in children aged 2-59 months. The overall prevalence of anaemia in this population was 55.8% with more than 60% of anaemia being amongst aged 2-12 months. The prevalence of iron depletion was 2.6%, iron deficiency with no anaemia 9.6%, and IDA 28.1%. Low ferritin level was observed in 40.9% of the children. Various factors were observed to independently affect low ferritin levels the outcome, including young age, male sex, and drinking cow's milk. This suggests a need for nutritional improvement and educational to the parents.
The anaemia prevalence among children below 5 years of age was high (55.8%). Similar prevalence rates were reported in Brazil (56.6%)23 and Nigeria (57.1%).24 The prevalence in our study was lower than those reported in Mwanza, Tanzania (72.2%).10 The study in Nigeria is the only study which had a similar age range as our study (2 to 59 months) whereas; other studies used the age group from 6-59 months. The differences noted in children from different settings are most likely due to ingestion of food with low iron contents, a higher burden of worm infestations in other settings and less ingestion of micronutrients with higher use of cow's milk. Despite the high prevalence, in our study, only 2 children were reported to have severe anaemia. This low number is similar to what others have reported, suggesting the condition is often picked up before getting to a severe state.
The observed prevalence of iron depletion in our study was low (2.6%), which differed from other studies from Iran (19.7%),7 United Arab Emirates (26.4%),8 and New Zealand (18.6%).6 The prevalence of iron deficiency with no anaemia was 9.6% which is lower than a previous study conducted in Mwanza, Tanzania, where the prevalence was 33.3%.10 This difference could be due to regional differences in the type of porridge traditionally used for weaning. In Kilimanjaro mothers typically use finger millet porridge with milk being used for weaning while in Mwanza, maize porridge is more commonly used. Finger millet is a better source of iron and folate when compared to maize. The findings from our study are lower than those in developed countries, (for example 5.6% in New Zealand6 and 7% in the USA.8 The use of fortified food/milk and the avoidance of cow's milk before the age of 1 year may be the reason for this low prevalence in the developed countries.
The prevalence of IDA in our study (28.1%) was almost similar to the 24%, which was reported previously in the 2010 Tanzania demographic and health survey.22 However, the prevalence of IDA was higher when compared to what has been reported in previous studies in other developing countries such as Nigeria 14.9% and United Arab Emirates 9.9%,8,25 and developed countries such as USA(8%), New Zealand (4.3%) and Turkey (3.29%).5,6 Cow's milk before the age of 1 year is known to be a risk for anaemia.6,9,26 In our study, we also observed that children who drink more than 500 ml of cow's milk a day had lower ferritin compared to children who drink less than 500 ml per day. Similar findings were also previously reported in New Zealand.6 The lower observed prevalence of IDA compared to a study in Mwanza (37.5%),10 this might be as explained by differences in cultural and socioeconomic status, which may impact the type of food eaten as well as milk consumption. Interestingly, the time of weaning was not an independent predictor for iron deficiency or IDA, and the majority of the children less than 12 months in this study were not supplemented with iron. A study by Kadivar et al. in Iran found that iron supplementation in the first year of life appears to be protective to anaemia and iron deficiency.7
Low ferritin level was observed in 40.9% of children in this study, which is similar to the 32.6% reported in Mexico.27 In this study, female children were less likely to have low ferritin level when compared to males; this was not the case in a study in New Zealand where females were at increased risk of developing anaemia.6 Children who had a lower levels of red meat consumption (less than 3 days per week) had a slightly increased risk of having low ferritin levels. This was consistent with the findings from Nigeria, where dietary intake of vegetables and animal products less than 3 times a week was significantly associated with a lower IDA prevalence.25 Red meat has a high iron content and is a good source of absorbable haeme iron.
In general, cow's milk has several properties that lower iron uptake, including low iron availability and excessive protein and calcium which inhibit the absorption of iron as reported in a review by Olivera et al,28 therefore, iron supplementation should definitively be recommended when using cow's milk to feed infants as not all cow's milk formulae used are fortified with iron.
Limitations
This was a hospital-based study; therefore, the prevalence of IDA may not truly reflect the general population. It is likely that the prevalence in this study overrepresents that of the general population. A community-based study might give us a better estimation of the actual situation within the community.
CONCLUSION AND RECOMMENDATIONS
The prevalence of IDA in children in the Kilimanjaro area was high, with more than 50% of infants in this study having IDA. Nutritional counselling on iron-rich food and the increased risk of IDA if cow's milk is used under 12 months of age may help to prevent IDA to under-5 children. Future community-based study is recommended to get the actual situation on iron deficieny in the general population.
Acknowledgements:
We thank data collection team members, paediatric department Kilimanjaro Christian Medical Centre (KCMC), as well as the children and parents who participated in this study. We appreciate all MEPI team members for facilitation and support the smooth running of this project.
Funding support for this research was obtained from the Medical Education Partnership Initiative (MEPI) award No.T84HA21123-04-02 Grant No.T84HA21123.
Footnotes
Peer Reviewed
Competing Interests: None declared.
REFERENCES
- 1.Tympa-Psirropoulou E, Vagenas C, Psirropoulos D, Dafni O, Matala A, Skopouli F.. Nutritional risk factors for iron-deficiency anaemia in children 12-24 months old in the area of Thessalia in Greece. Int J Food Sci Nutr. 2005;56(1):1-12. 10.1080/09637480500081183. Medline [DOI] [PubMed] [Google Scholar]
- 2.Domello M, Hernell O.. Iron deficiency anaemia during the first two years of life. Scand J Nut. 2002;46(1):20-30. 10.1080/110264802753704091 [DOI] [Google Scholar]
- 3.Clark SF. Iron deficiency anemia. Nutr Clin Pract. 2008;23(2):128-141. 10.1177/0884533608314536. Medline [DOI] [PubMed] [Google Scholar]
- 4.McLean E, Cogswell M, Egli I, Wojdyla D, de Benoist B.. Worldwide prevalence of anaemia, WHO Vitamin and Mineral Nutrition Information System, 1993-2005. Public Health Nutr. 2009;12(4):444-454. 10.1017/S1368980008002401. Medline [DOI] [PubMed] [Google Scholar]
- 5.Akin F, Solak ES, Kilicaslan C, Boke SB, Arslan S.. Iron deficiency anemia among hospitalized children in Konya, Turkey. Anemia. 2013;2013:514801. 10.1155/2013/514801 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Soh P, Ferguson EL, McKenzie JE, Homs MY V, Gibson RS.. Iron deficiency and risk factors for lower iron stores in 6-24-month-old New Zealanders. Eur J Clin Nutr. 2004;58(1):71-79. 10.1038/sj.ejcn.1601751. Medline [DOI] [PubMed] [Google Scholar]
- 7.Kadivar MR, Yarmohammadi H, Mirahmadizadeh AR, Vakili M, Karimi M.. Prevalence of iron deficiency anemia in 6 months to 5 years old children in Fars, Southern Iran. Med Sci Monit. 2003;9(2):CR100-4. Medline [PubMed] [Google Scholar]
- 8.Miller CJ, Dunn EV, Abdouni SF, Shaheen HM, Ullah MS.. Factors associated with iron depletion and iron deficiency anemia among Arabic preschool children of the United Arab Emirates. Saudi Med J. 2004;25(7):843-847. Medline [PubMed] [Google Scholar]
- 9.Mwangi MN, Phiri KS, Abkari A, et al. Iron for Africa-report of an expert workshop. Nutrients. 2017;9(6):E576. 10.3390/nu9060576. Medline [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Simbauranga RH, Kamugisha E, Hokororo A, Kidenya BR, Makani J.. Prevalence and factors associated with severe anaemia amongst under-five children hospitalized at Bugando Medical Centre, Mwanza, Tanzania. BMC Hematol. 2015;15(1):1-9. 10.1186/s12878-015-0033-5. Medline [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Nguyen ND, Allen JR, Peat JK, Beal P, Webster BH, Gaskin KJ.. Iron status of young Vietnamese children in Australia. J Paediatr Child Health. 2004;40(8):424-429. 10.1111/j.1440-1754.2004.00423.x [DOI] [PubMed] [Google Scholar]
- 12.Brotanek JM, Gosz J, Weitzman M, Flores G.. Iron deficiency in early childhood in the United States: risk factors and racial/ethnic disparities. Pediatrics. 2007;120(3):568-575. 10.1542/peds.2007-0572. Medline [DOI] [PubMed] [Google Scholar]
- 13.Choi CW, Cho WR, Park KH, et al. The cutoff value of serum ferritin for the diagnosis of iron deficiency in community-residing older persons. Ann Hematol. 2005;84(6):358-361. 10.1007/s00277-005-1033-5. Medline [DOI] [PubMed] [Google Scholar]
- 14.Ong KH, Tan HL, Lai HC, Kuperan P.. Accuracy of various iron parameters in the prediction of iron deficiency in an acute care hospital. Ann Acad Med Singapore. 2005;34(7):437-440. Medline [PubMed] [Google Scholar]
- 15.Jeremiah ZA, Buseri FI, Uko EK.. Iron deficiency anaemia and evaluation of the utility of iron deficiency indicators among healthy Nigerian children. Hematology. 2007;12(3):249-253. 10.1080/110245330601111821 [DOI] [PubMed] [Google Scholar]
- 16.Özdemir N. Çocuklarda tanıdan tedaviye demir eksikliği anemisi. [Iron deficiency anemia from diagnosis to treatment in children]. Turk Pediatr Ars. 2015;50(1):11-19. Turkish. 10.5152/tpa.2015.2337 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.Stoltzfus R, Dreyfuss M.. Guidelines for the use of iron supplements to prevent and treat iron deficiency anemia. Partners and Food in Emergency and Development Aid (Partenaires et Aliments de l'Aide d'Urgence et du Développement) Website; 1998. http://www.univ-lille1.fr/pfeda/Ngonut/1998/9808e.htm. Accessed 6 August 2019.
- 18.The President's Office Regional Administration and Local Government Kiliminjaro Region (PORALGKR) [Tanzania]. Kilimanjaro Region Investment Guide. Moshi, Tanzania: PORALGKR, United Nations Development Programme, and Economic and Social Research Foundation; 2017. https://www.agroberichtenbuitenland.nl/binaries/agroberichtenbuitenland/documenten/rapporten/2018/01/10/regional-investment-guide-kilimanjaro/Kilimanjaro_Region_Investement_Guide.pdf. Accessed 6 August 2019. [Google Scholar]
- 19.World Health Organization (WHO). Haemoglobin Concentrations for the Diagnosis of Anaemia and Assessment of Severity. Geneva: WHO; 2011. https://www.who.int/vmnis/indicators/haemoglobin/en/. Accessed 6 August 2019. [Google Scholar]
- 20.World Health Organization (WHO). Serum ferritin concentrations for the assessment of iron status and iron deficient in populations. In: Vitamin and Mineral Nutrition Information System. Geneva: WHO; 2011. https://www.who.int/vmnis/indicators/serum_ferritin.pdf. Accessed 6 August 2019. [Google Scholar]
- 21.Chifman J, Laubenbacher R, Torti SV.. A systems biology approach to iron metabolism. Adv Exp Med Biol. 2014;844:201-25. 10.1007/978-1-4939-2095-2_10. Medline [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.National Bureau of Statistics (NBS) [Tanzania], ICF Macro. Micronutrients: Results of the 2010 Tanzania Demographic and Health Survey. DHS Nutritional Reports No. 5. Calverton, Maryland, USA: ICF Macro; 2011. https://dhspro-gram.com/publications/publication-nut5-other-nutrition-reports.cfm. Accessed 6 August 2019. [Google Scholar]
- 23.Dos Santos RF, Gonzalez ESC, de Albuquerque EC, et al. Prevalence of anemia in under five-year-old children in a children's hospital in Recife, Brazil. Rev Bras Hematol Hemoter. 2011;33(2):100-104. 10.5581/1516-8484.20110028. Medline [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Ekwochi U, Odetunde O, Maduka I, Azubuike J, Obi IE.. Iron deficiency among non-anemic under-five children in Enugu, South-East, Nigeria. Ann Med Health Sci Res. 2013;3(3):402-406. 10.4103/2141-9248.117943. Medline [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Fajolu IB, Grange OA, Renner JK, et al. Prevalence of iron deficiency in children 6-24 months in Lagos. Nig Q J Hosp Med. 2007;17(3):97-100. 10.4314/nqjhm.v17i3.12553. Medline [DOI] [PubMed] [Google Scholar]
- 26.Eden AN, Sandoval C.. Iron deficiency in infants and toddlers in the United States. Pediatr Hematol Oncol. 2012;29(8):704-709. 10.3109/08880018.2012.725199. Medline [DOI] [PubMed] [Google Scholar]
- 27.Duque X, Martinez H, Vilchis-Gil J, et al. Effect of supplementation with ferrous sulfate or iron bis-glycinate chelate on ferritin concentration in Mexican school-children: A randomized controlled trial. Nutr J. 2014;13:71. 10.1186/1475-2891-13-71. Medline [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Oliveira MA, Osório MM. [Cow's milk consumption and iron deficiency anemia in children]. J Pediatr (Rio J). 2005;81(5):361-367. Portuguese. 10.2223/JPED.1386. Medline [DOI] [PubMed] [Google Scholar]