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Abstract

Objective:

To perform a systematic review to evaluate iron, vitamin A, zinc, and iodine status and intakes in children and adolescents (0-19 years) in Ethiopia, Kenya, Nigeria, and South Africa.

Method:

Both national and subnational data published from the year 2005 to 2015 were searched via MEDLINE, Scopus, and national public health websites. For each micronutrient and country, status data from relevant studies and surveys were combined into an average prevalence and weighted by sample size (WAVG). Inadequate intakes were estimated from mean (SD) intakes.

Results:

This review included 55 surveys and studies, 17 from Ethiopia, 11 from Kenya, 12 from Nigeria, and 16 from South Africa. The WAVG prevalence of anemia ranged from 25% to 53%, iron deficiency from 12% to 29%, vitamin A deficiency (VAD) from 14% to 42%, zinc deficiency from 32% to 63%, and iodine deficiency from 15% to 86% in children aged 0 to 19 years from 4 countries. Generally, children <5 years had higher prevalence of anemia (32%-63%), VAD (15%-35%), and zinc deficiency (35%-63%) compared to children aged 5 to 19 years. Studies with intake data indicated that inadequate intakes ranged from 51% to 99% for zinc, 13% to 100% for iron, and 1% to 100% for vitamin A. Households failing to consume adequately iodized (>15 ppm) salt ranged from 2% in Kenya to 96% in Ethiopia.

Conclusion:

With large variation within the 4 African countries, our data indicate that anemia and vitamin A, zinc, and iodine deficiencies are problems of public health significance. Effective public health strategies such as dietary diversification and food fortification are needed to improve micronutrient intake in both younger and older children.

Keywords

anemia iron vitamin A zinc iodine deficiency intake Ethiopia Kenya Nigeria South Africa

Introduction

Iron, vitamin A, zinc, and iodine are important micronutrients for growth, development, and survival of children, making them important micronutrients in global public health terms.¹ Both iron deficiency (ID) and ID anemia (IDA) as well as iodine deficiency are known to adversely affect cognitive development in children which may result in lower educational achievements and hence impact economic development negatively.^2,3 Vitamin A deficiency (VAD) affects immune function and leads to an increased risk of morbidity (often from diarrhea and measles).⁴ Zinc deficiency may lead to growth failure and impaired immune function.⁵ Both vitamin A and zinc deficiencies increase the risk of mortality in children.^4,5 Children, especially younger than 5 years from low- and middle-income countries, are particularly vulnerable to micronutrient deficiencies due to relatively high requirements of micronutrients for rapid growth and development,⁶ accompanied with lower energy and micronutrient intakes and higher infection burden.⁵ The 2013 Lancet series on Maternal and Child Undernutrition reported that stunting, wasting, and micronutrient deficiencies were associated with almost 45% of all deaths in young children worldwide, with the vast majority being from sub-Saharan Africa and South Central Asia.⁶

Recent reviews showed that the sub-Saharan Africa region has the highest rates of anemia (46%-71%) and VAD (48%) prevalence in children <5 years,^7,8 while the prevalence of iodine deficiency (42%) and estimated inadequate zinc nutrition (25%) were also high in Africa.^9
–11 Majority of the surveys included in these reviews concern children <5 years only and were published more than 10 years ago, while data for school-age children and adolescents are largely lacking. Besides, most African countries lack nationally representative and up-to-date figures for micronutrient intake in children. Monitoring micronutrient status and intake is important, especially for countries with rapid population growth and urbanization.¹² Therefore, this study aims to perform a comprehensive systematic review to evaluate micronutrient status and dietary intake of iron, vitamin A, zinc, and iodine in children and adolescents aged 0 to 19 years in 4 of the 7 largest and rapidly growing countries in Africa,¹³ including Ethiopia, Kenya, Nigeria, and South Africa, based on data reported in the last 10 years.

Method

Search Strategy

We followed a systematic approach to select all studies with data on iron, vitamin A, zinc, and iodine status and intakes in Ethiopia, Kenya, Nigeria, and South Africa. A literature search was conducted on MEDLINE, Scopus, World Health Organization (WHO), and The United Nations Children’s Fund (Vitamin and Mineral Nutrition Information System) databases from October (2015) to March (2016). A combination of the following terms were used to search abstracts and titles: anemia/iron/zinc/iodine/vitamin A AND deficiency/intake/status/prevalence AND Nigeria/Ethiopia/Kenya/South Africa AND infants/children/adolescents.

Full-text articles were obtained and reviewed to identify those that met the selection criteria given subsequently. The reference lists of all articles of interest were checked for additional studies. Websites of public health organizations were searched, and local experts were contacted to get access to additional studies and surveys.

Inclusion Criteria

After the initial search, all the publications and reports were screened to determine eligibility of data based on the following inclusion criteria.

Reported data on the prevalence of micronutrient deficiencies in apparently healthy children (free of overt diseases) aged 0 to 19 years in Ethiopia, Kenya, Nigeria, and South Africa as assessed by the following biomarkers:

For iron:

Anemia: for 0 to 6 months to 5 years hemoglobin (Hb) <110 g/L; for 5 to 11 years Hb <115 g/L; and for >12 years Hb <120 g/L/130 g/L (boys). Roughly, 50% of anemia is caused by ID¹⁴; therefore, anemia prevalence was also included.

Iron deficiency: Serum ferritin <5 years at <12 µg/L and >5 years at <15 µg/L,¹⁴ regardless of correction for inflammation.

Iron deficiency anemia: Combination of anemia and ID¹⁴

For VAD: serum retinol <0.7 nmol/L (20 µg/dL).¹⁵

For zinc deficiency: serum zinc <65 ug/dL (9.9 umol/L).¹⁶

For iodine deficiency: Urinary iodine excretion (UIE) <100 µg/L.¹⁷ WHO recommends school-based (6-12 years) sampling to be used when measuring UIE, and this can be used as a proxy for the younger age-group¹⁷; thus, data in >6 to 12 years also applies to <5 years and >12 years.

Surveys and studies providing micronutrient intake data measured at individual level

Study types: national surveys, population-based observational (cross-sectional or longitudinal) studies, or baseline or control group data from intervention studies

Surveys and studies published and conducted later than year 2005 till 2015.

Data Extraction

Status data

For micronutrient deficiencies, we extracted the prevalence of anemia, ID, IDA, VAD, zinc, and iodine deficiency as specified in the inclusion criteria.

The prevalence of clinical signs of deficiency for vitamin A (ie, night blindness, bitot spots, corneal xerosis, and xeropthalmia)¹⁵ and iodine (ie, goiter)¹⁸ were also extracted and reported separately. For the biochemical markers of micronutrient status, we extracted the means, and when reported, standard deviations (SD) from each data source and report separately.

Intake data

Information on daily dietary intake of iron, vitamin A, and zinc in children aged 0 to 19 years was included as reported. For iodine, little data were available and therefore, data on household consumption of iodized salt were used.

When data were reported for subgroups (eg, by age range or gender), a weighted mean was calculated by weighing the mean intake of each subgroup by the number of the participants in the subgroup. When SDs were not reported, they were calculated from the standard error of mean or confidence interval. When data were reported as median (and ranges), we converted it to mean (±SD) by taking an average of median and the interquartile ranges (IQR). For converting the ranges to SD, we divided the difference between high and low IQR by 1.35.

Data Analysis

When, within a country, more than 1 study and/or survey was included on the status data of the same micronutrient, the results of these were pooled for each biomarker separately into an average that was weighted for the sample size of the studies (subnational data) and national surveys (national data).

Per country, and per micronutrient, the weighted average (WAVG) was calculated for all children (0-19 years) and specific age groups, including <5 y, >5-10 years, and 10-19 years.

Within these age subgroups, the WAVG from national and subnational data were calculated separately. Studies reporting on age groups combining both <5 years or >5-10 years (eg, 3-8 years) or >10- 19 years were included in the age group where majority of the children belonged (>5 years in this case).

Calculating inadequacy of micronutrient intakes

The Estimated Average Requirement (EAR) cutpoint method provides a way to estimate the prevalence of inadequate nutrient intake in a population. The proportion of participants with intakes below the EAR was used to estimate the prevalence of inadequate intake of micronutrients in the population. Per Institute of Medicine guidelines,¹⁹ the conversion factor of 1.4 was used for iron and vitamin A, and 1.2 for zinc was used for calculating EAR from Recommended Daily Allowance set by WHO/Food and Agriculture Organization for each of the micronutrients.²⁰ For iron, the same conversion factor was used for children <9 years and for children >9 years to calculate the EAR. The bioavailability of 10% was used for dietary iron, and the “lowest bioavailability” was used for dietary zinc. For each survey/study, the prevalence of inadequate intake for iron, vitamin A, and zinc were estimated by comparing the reported mean ± SD to the corresponding EAR, assuming a normal distribution of the data.²¹ For iodine, percentage of households consuming inadequately iodized salt (<15 ppm) or noniodized was included as reported.

Results

Data Availability

A total of 147 studies and 8 surveys were identified from the literature search, whereas only 55 data sets met the inclusion criteria. Of the 55 studies and surveys that were included in this review, 17 were from Ethiopia, 11 from Kenya, 12 from Nigeria (1 study reported data from both Kenya and Nigeria²²), and 16 from South Africa (Figure 1). Of the total 55 data sets, 15 surveys and studies included both urban and rural area. Twenty-four studies and surveys included only rural area and were mostly conducted in subsistence farmers or resource-poor settings. Thirteen studies and surveys included only urban areas and were mostly conducted in low socioeconomic settings (Table 1).

Figure 1.

PRISMA Flow diagram²³ of the identification of literature for inclusion in this systematic review.

Table 1.

Characteristics of the Studies and Surveys Included From Ethiopia, Kenya, Nigeria, and South Africa.

Reference	Year of Survey	Study Location	State	Age	N	Study Design	Data Included
Ethiopia
National data
Abuye²⁴	2005	10 regional states	National	6-12 years	9430	Nationwide cross-sectional study	Iodine status and iodized salt usage
Central Statistical Agency and ICF International²⁵	2011	Nationwide	National	6-59 months	9157	Demographic and Health Survey	Iron status
Ethiopia Public Health Institute²⁶	2011	Nationwide	National	6-35 months	8079	National Food consumption survey	Iron, vitamin A, zinc intake
Ethiopian Public Health Institute²⁷	2015	Nationwide	National	6 months-15 years	∼ 3000	National (micronutrient) survey	Iron, vitamin A, zinc status
Demissie²⁸	2005-06	Amhara, Tigray, Oromiya, Beneshengue-Gumuz, SNNPR, Afar, Harrair & two city administrations Addis Ababa, Dire Dawa	7 national states	6-71 months	∼1200	National vitamin A survey, cross-sectional study	Vitamin A status
Subnational data
Amare²⁹	2013^a	Gondar town (urban)	Amhara	10-14 years	100	Cross-sectional study	Zinc status
Aweke³⁰	2010	Burrie and Womberma districts (endemic goiter prevalence)	Amhara	6-12 years	403	Cross-sectional study	Iodine status
Baye³¹	2010	Gobalafto district (rural)	Amhara	12-23 months	76	Cross-sectional study	Iron, vitamin A, zinc intake
Desalegn³²	2013	Jimma (urban)	Oromia	6-12 years	616	Cross-sectional study	Iron status
Gashu³³	2011-12	West Gojjam, East Gojjam, North Gondar, North Wollo, South Wollo and Wagehmera-six districts (rural & resource poor setting)	Amhara	54-60 months	628	Cross-sectional study	Iron status
Girma³⁴	2009	Hawassa town (urban)	Sidamo	7-9 years	116	Cross-sectional study	Iodine status
Girma³⁵	2011-12	Metekel Zone (rural)	Benishangul-Gumuz	6-18 years	200	Cross-sectional study	Iodine status
Habtamu³⁶	2012	Goba town (urban)	Oromia	6-12 years	397	Cross-sectional study	Iodized salt usage
Herrador³⁷	2009	Libo, Kemkem, & Fogera (urban & rural)	Amhara	4-15 years	764	Cross-sectional study	Iron, vitamin A, zinc status
Mesele³⁸	2012	Lay Armachiho district (rural)	Amhara	6-12 years	694	Cross-sectional study	Iodine status & iodized salt usage
Mezgebu³⁹	2011	Shebe Senbo District (rural)	Oromia	6-12 years	389	Cross-sectional study	Iodine status & iodized salt usage
Woldie⁴⁰	2013	Tsitsika Health Center, Wag-Himra Zone (rural, subsistence farming)	Amhara	6-23 months	347	Institution-based cross-sectional study	Iron status
Kenya
National data
KNBS and ICF Macro⁴¹	2008-09	National	National	<5 years	4743	Demographic and Health survey	Iodized salt usage
Subnational data
Cherop⁴²	2005	Eldoret (urban)	Rift valley	0-6 months	384	Cross-sectional study	Iron, vitamin A intake
Frosch⁴³	2007	Kapsisiywa and Kipsamoite (rural, subsistence farming)	Rift Valley	4-59 months	188	Prospective study (baseline data)	Iron status
Foote⁴⁴	2010	Nyando Division, (rural, subsistence farming)	Nyanza	6-35 months	858	Cross-sectional survey	Iron status
Gegios²²	2009	Lake Victoria- (rural) Kenya ; humid-forest zone data from national survey (urban & rural)- Nigeria	Rift valley-Kenya; Southern States-Nigeria	2-5 years	449 Kenyan 793 Nigerian	Cross-sectional study	Iron, vitamin A, zinc intake
KNBS⁴⁵	2011	Siaya, Kisumu, Homa Bay, Migori, Kisii, and Nyamira (urban & rural)	Nyanza Province	<5 years	na	Multiple Indicator Cluster Survey (MICS) (cross-sectional data)	Iodized salt usage
Macharia-Mutie⁴⁶	2010-11	Migwani Division, Mwingi District, (rural, resource poor setting)	Eastern Province	12-59 months	93 (CG)	Intervention study (control group data)	Iron status
M’Kaibi, 2015⁴⁷	2015^a	Meru (rural, resource poor household)	Eastern Province	24-59 months	525	Cross-sectional study	Iron, vitamin A, zinc intake
Suchdev⁴⁸	2007-08	Nyando, (rural, subsistence farming)	Western Province	6-35 months	502 (CG)	Intervention study (control group data)	Iron, vitamin A status
Suchdev⁴⁹	2014^a	Kibera in southern Nairobi, (urban, slums)	Nairobi	6 months-14 years	693	Cross-sectional survey	Iron, vitamin A status
Talsma⁵⁰	2010	Kibwezi and Makindu Districts,	Eastern Province	6-12 years	375	Cross-sectional study	Vitamin A status
Nigeria
Subnational data
Aaron⁵¹	2007	Akanga and Akaleku, (rural, subsistence farming)	Nasarawa	5-13 years	566	Intervention study (baseline data)	Iron, vitamin A status
Abua⁵²	2008^a	Boki LGA, predominantly rural; Ikom LGA, predominantly urban	Cross River State	8-12 years	400	Cross-sectional survey	Iodine status
Ayogu⁵³	2015^a	Ede-Oballa, Nsukka, (rural, multi-stage sampling)	Enugu	6-15 years	90	Cross-sectional survey	Iron status and intake
Ekpo⁵⁴	2006^a	Sixteen local government areas	Akwa Ibom	12-18 years	418	Cross-sectional study	Iron intake
Hassan⁵⁵	2012^a	Kaduna (urban)	Kaduna	7-11 years	394	Cross-sectional study	Iron, vitamin A intake
Ibeanu⁵⁶	2012^a	Ozubulu, (peri-urban)	Anambra State	<5 years	240	Cross-sectional study	Zinc status
Jeremiah⁵⁷	2007^a	Port Harcourt (urban with high malaria epidemic)	Rivers	1-8 years	240	Prospective cross-sectional study	Iron status
Madukwe⁵⁸	2012	Nsukka (urban, multistage sampling)	Enugu	6-12 years	200	Cross-sectional study	Iodine status & iodized salt usage
Nwamarah⁵⁹	2015^a	Nsukka, (rural, subsistence farming)	Enugu	6-12 years	395	Cross-sectional Survey	Iodine status & iodized salt usage
Onabanjo⁶⁰	2014^a	Odeda Local Government Area, (rural, low socioeconomic)	Ogun	10-19 years	127	Cross-sectional study	Iron status, iron, vitamin A and zinc intake
Osazuwa⁶¹	2010	Evbuomore, Isiohor, and Ekosodin (rural)	Edo	1-15 years	316	Cross-sectional study	Iron status
South Africa
National data
NFCS-FB⁶²	2005	Nationwide	National	1-9 years	2469	National Food consumption survey	Iron, vitamin A, zinc, iodine status & iodized salt usage
Shisana⁶³	2012	Nationwide	National	6-59 months	>400†	SANHANES-1, 2012	Iron, vitamin A status
Subnational data
Balogun⁶⁴	2011	Breede Valley (disadvantage communities)	Western Cape	12-36 months	248	Cross-sectional study	Iron, vitamin A, zinc Intake
Faber a⁶⁵	2005^a	Valley of a Thousand Hills, (rural, disadvantage communities)	KwaZulu-Natal	6-12 months	475	Randomized controlled trial (baseline data)	Iron, vitamin A, zinc intake
Faber⁶⁶	2011	Two rural areas, an urban area and an urban metropolitan area	KwaZulu-Natal, Limpopo, Northern Cape, Western Cape	1.5-6 years	743	Cross-sectional study	Vitamin A status and intake
Faber⁶⁷	2007^a	Valley of a Thousand Hills, (rural)	KwaZulu-Natal	6-12 months	505	Cross-sectional survey	Iron, vitamin A, zinc status
Grobbelaar⁶⁸	2013^a	Durban, (urban, residence children home)	KwaZulu-Natal	4-18 years	143	Cross-sectional survey	Iron, vitamin A, zinc intake
Mamabolo⁶⁹	2006	Capricorn, (rural, resource poor setting)	Limpopo	1 and 3 years	127	Prospective cohort study, longitudinal data (at age 3)	Iron status
Motadi⁷⁰	2015^a	Vhembe district, (rural)	Limpopo	3-5 years	349	Cross-sectional survey	Iron and zinc status
Onabanjo⁷¹	2012^a	Jouberton, (disadvantage communities)	North-West	7-10 years	556	Cross-sectional study	Iron status
Samuel⁷²	2010^a	Vaal region, (peri-urban, disadvantage setting)	Gauteng	7-11 years	149	Cross-sectional study	Zinc status and intake
Smuts⁷³	2005^a	Valley of a Thousand Hills, (rural)	KwaZulu-Natal	6-12 months	265	Randomized control trial (baseline data)	Iron, zinc status
Taljaard⁷⁴	2010	Peri-urban settlement, (low socioeconomic school setting)	North West	6-11 years	414	Randomized control trial (baseline data)	Iron status
Troesch⁷⁵	2009	Kimberley, (urban, in a low socioeconomic setting)	Northern Cape	8 years	97 (CG)	Intervention study (control group data)	Iron status
Van der Hoeven⁷⁶	2012	Rural area approximately 50 km from Potchefstroom, (less privilege setting)	North West	6-12 years	81 (CG)	Randomized control trial (control group data)	Iron status
Van Stuijvenberg⁷⁷	2010-11	Calvinia West, Hantam district, (semi-urban, low socio-economic)	Northern Cape	2-5 years	149	Cross-sectional study	Iron, vitamin A, zinc intake

Abbreviation: CG, control group; na, not available.

^aYear of survey not available, hence year of publication was assumed to be the year of survey.

Of the 55 data sources, 8 were national data and 47 were subnational data (37 cross-sectional studies, 7 intervention studies, 3 three prospective cohorts). For national data, 5 surveys were from Ethiopia,^24

–28 1 was from Kenya (iodine data only),⁴¹ and 2 from South Africa.^62,63 No national survey was found for Nigeria. Majority of the data were on iron, and fewer data were found on vitamin A, iodine, and zinc (Figure 1). For 6 studies the sample size was <100, and for the other studies and surveys it ranged from 100 to 9430. All the included studies and surveys represent a total of ∼54 905 children aged 0 to 19 years in the 4 countries.

With regard to age-groups, there were 25 data sets for 0 to 5 years, 7 data sets for 5 to 10 years, and 3 data sets for 10 to 19 years, and 19 data sets had data for ages ranging from >5 to 19 years. Therefore, it was decided to create 2 separate age categories, including 0 to 5 years and >5 to 19 years.

Prevalence of Micronutrient Deficiencies in Children (0-19 Years)

Iron

Anemia prevalence in children (0-19 years) ranged from 25% to 53% (WAVG) in the 4 countries (Figure 2). Prevalence of ID ranged from 12% to 29% and IDA from 11 to 14% in the 4 countries. The prevalence of anemia was higher in children <5 years of age than in children >5 years of age in all countries except Nigeria (Table 2). Mean hemoglobin concentration ranged from 98 to 133 g/L, and mean serum ferritin concentration from 10 to 64 µg/L (see Supplemental Figure S1a).

Figure 2.

Prevalence of micronutrient deficiencies in children (0-19 years) in Ethiopia, Kenya, Nigeria, and South Africa. Abbreviation: na, not available.

Table 2.

Prevalence of Micronutrient Deficiencies (%) in Children (0-19 years) in Ethiopia, Kenya, Nigeria, and South Africa.

	Anemia			Iron Deficiency			Iron Deficiency Anemia			Vitamin A Deficiency			Zinc Deficiency			Iodine deficiency
	Prevalence, % (range)^a	Sample, n	Data, n	Prevalence, % (range)^a	Sample, n	Data, n	Prevalence, % (range)^a	Sample, n	Data, n	Prevalence, % (range)^a	Sample, n	Data, n	Prevalence, % (range)^a	Sample, n	Data, n	Prevalence, % (range)^a	Sample, n	Data, n
Ethiopia
Children <5 years	40 (14-44)	11469	4	18 (9-32)	2312	3	9 (5-18)	2312	3	25 (14-38)	2144	2	35	1143	1	–	–	–
National data	42 (35-44)	10494	2	18	1337	1	9	1337	1	25 (14-38)	2144	2	35	1143	1	–	–	–
Subnational data	19 (14-29)	975	2	17 (9-32)	975	2	10 (5-18)	975	2	–	–	–	–	–	–	–	–	–
Children >5-19 years	31 (31-44)	2957	3	7 (3-9)	2957	2	13 (4-37)	2193	2	12 (11-29)	1655	2	29 (13-47)	2433	3	86 (84-100)	9,986	6
National data	26	1577	1	9	1577	1	4	1577	1	11	1555	1	36	1569	1	86	9,430	1
Subnational data	37 (31-44)	1380	2	3	764	1	37	616	1	29	100	1	17 (13-47)	864	2	88 (84-100)	557	5
Children 0-19 years	39 (14-44)	14,426	6^b	12 (3-32)	5,271	4 ^b	11 (4-37)	4,5051	4 ^b	19 (11-38)	3,7991	3 ^b	32 (13-47)	4,002	3 ^b	86 (84-100)	9,986	6
Kenya
Children <5 years	63 (38-72)	1846	5	35 (20-42)	1846	5	19 (11-27)	486	3	15 (15-17)	1268	2	–	–	–	–	–	–
National data	–	–	–	–	–	–	–	–	–	–	–	–	–	–	–	–	–	–
Subnational data	63 (38-72)	1846	5	35 (20-42)	1846	5	19 (11-27)	486	3	15 (15-17)	1268	2	–	–	–	–	–	–
Children >5-19 years	14	487	1	4	487	1	4	487	1	11 (6-18)	862	2	–	–	–	–	–	–
National data	–	–	–	–	–	–	–	–	–	–	–	–	–	–	–	–	–	–
Subnational data	14	487	1	4	487	1	4	487	1	11 (6-18)	862	2	–	–	–	–	–	–
Children 0-19 years	53 (14-72)	2,333	5^b	29 (4-42)	2,333	4 ^b	12 (4-27)	973	3 ^b	14 (6-18)	2,130	3 ^b	–	–	–	–	–	–
Nigeria
Children <5 years	34	240	1	15	240	1	–	–	–	–	–	–	63	240	1	–	–	–
National data	–	–	–	–	–	–	–	–	–	–	–	–	–	–	–	–	–	–
Subnational data	34	240	1	25	240	1	–	–	–	–	–	–	63	240	1	–	–	–
Children >5-19 years	40 (24-85)	1089	4	12 (10-15)	999	3	17	127	1	16	556	1	–	–	–	59(4-75)	679	3
National data	–	–	–	–	–	–	–	–	–	–	–	–	–	–	–	–	–	–
Subnational data	40 (24-85)	1089	4	12 (10-15)	999	3	17	127	1	16	556	1	–	–	–	59(4-75)	679	3
Children 0-19 years	39 (24-85)	1,329	5	12 (10-25)	1,239	4	17	127	1	16	556	1	63	240	1	59 (4-75)	679	3
South Africa
Children <5 years	32 (11-52)	3131	6	28 (7-67)	3492	6	16 (2-32)	1113	2	35 (16-65)	2920	5	40 (32-48)	1314	4	–	–	–
National data	26 (11-32)	1742	2	15 (8-18)	1742	2	2	511	1	58 (44-65)	1402	2	48	195	1	–	–	–
Subnational data	40 (22-52)	1389	4	37 (7-67)	1389	4	32	505	1	14 (10-20)	1513	3	39 (32-47)	1119	3	–	–	–
Children >5-19 years	17 (7-49)	2184	8	18 (4-31)	2184	8	6 (1-9)	1498	5	62	419	1	37 (36-75)	684	4	–	–	–
National data	19	499	1	4	499	1	–	–	–	62	419	1	36	105	1	15	1332	1
Subnational data	13 (7-49)	1685	7	22 (14-31)	1685	7	6 (1-18)	1498	5	–	–	–	37 (25-75)	579	3	–	–	–
Children 0-19 years	25 (7-49)	5,315	13 ^b	25 (4-56)	5,315	13 ^b	11 (1-18)	2,611	7	42 (10-65)	3,758	5 ^b	39 (25-75)	1,998	7 ^b	15	1332	1

^aThe prevalence in percentage (%) are reported as weighted average (WAVG), that is, an average that was weighted for the sample size of the studies (subnational data) and national surveys (national data); data (n) shows number of studies and surveys included; sample (n) shows total number of children included in these studies and surveys.

^bNumbers do not add up since same survey/study reports for 2 age-groups (0-5 and 5-19 years).

Vitamin A

Prevalence of VAD in children (0-19 years) ranged from 14% to 42% (WAVG) in the 4 countries (Figure 2). No data on VAD were found for children aged 0 to 5 years in Nigeria. Mean serum retinol concentration ranged from 0.61 to 1.1 µmol/L (see Supplemental Figure S1b). Prevalence of VAD in <5 years was higher than in >5 to 19 years except for South Africa, where older children had higher (62%) prevalence of VAD. In South Africa, WAVG VAD reported in the 2 national surveys was more than double that of the WAVG of independent studies in children aged <0 to 5 years (Table 2). Mean serum retinol concentration ranged from 0.6 to 1.1 nmol/L (see Supplemental Figure S1b). The prevalence of xeropthalmia was reported in Ethiopia only, with night blindness at 0.8% and Bitot spot at 1.7% (see Supplemental Table S1).

Zinc

No data on zinc deficiency were found in children aged 0 to 19 years in Kenya. The prevalence of zinc deficiency in children (0-19 years) ranged from 32% to 63% in Ethiopia, Nigeria, and South Africa (Figure 2). Rates of zinc deficiency in <5 years were higher in both Ethiopia and South Africa (Table 2). Mean serum zinc concentration ranged from 6.6 to 13.3 µmol/L (see Supplemental Figure S1c).

Iodine

No data on iodine deficiency were found in Kenya. The prevalence of iodine deficiency showed a large variation among the 3 countries and was highest in Ethiopia at 86% (84%-100%), followed by Nigeria at 59%, and South Africa at 15% (Figure 2). Urinary iodine excretion ranged from 24 to 214 µg/L (see Supplemental Figure S1d). Prevalence of goiter was reported at 14% to 59% for Ethiopia (see Supplemental Table S2).

Dietary Intake of Iron, Vitamin A, Zinc, and Household Consumption of Iodized Salt in Children (0 to 19 years)

Iron

Mean dietary iron intake ranged from 4 to 28 mg/d, and the percentage of children with inadequate intake ranged from 13% to 100% (Table 3). In all 4 countries, up to 62% of the children aged <5 years had inadequate intake of iron. Data for children aged 5 to 19 years was available from Nigeria and South Africa, where 51% to 100% had inadequate intake of iron.

Table 3.

Average Iron, Vitamin A, Zinc, and Iodized Salt Intake and Percentage of Children (0-19 years) Population Failing to Meet the Recommended Intake in Ethiopia, Kenya, Nigeria, and South Africa.

Country	Reference	n	Age Group	Dietary Information	Iron		Vitamin A		Zinc		Iodine
Country	Reference	n	Age Group	Dietary Information	mg/d	Inadequate Intake, %	µg RE/d	Inadequate Intake, %	mg/d	Inadequate Intake, %	Households Not Consuming Adequately Iodized Salt, %
0-5 years
Ethiopia	Baye^a,31	62 BF	12-23 months	24-hour recall on nonconsecutive days	15 (11)	33	53 (51)	100	3.3 (2)	96
	Baye^a,31	14NBF	12-23 months	24-hour recall on nonconsecutive days	28 (19)	13	39 (81)	100	6.7 (4.2)	51
	FCS^b,c,26	8079	6-35 months	Single 24-hour dietary recall	11.6 (12)	34	38^e (76)″	100	2 (2.1)	99
Kenya	Cherop, 2010^d ⁴²	244	0-6 months	Single 24-hour dietary recall	4.1		87
	KNBS⁴¹		>5 years	na							2
	Gegios²²	449	2-5 years	Single 24-hour dietary recall	5.9 (3.7)	34	378 (679)	45	2.8 (1.5)	99
	M’Kaibi⁴⁷	525	24-59 months	4 × 24-hour recall (year-round)	5.5		465		3.1
Nigeria	Gegios²²	793	2-5 years	Single 24-hour dietary recall	11.5 (9)	22	221 (228)	61	3.8 (2.9)	91
South Africa	Balogun^b,d, ⁶⁴	128	12-36 months	Validated quantitative FFQ	5.3 (3.5)	62	501 (477)	33	4 (2.1)	90
	Faber^b, ⁶⁶	743	1.5-6 years	Single 24-hour dietary recall			255 (136)″	58
	Faber^{b,c, 65}	475	6-12 months	Single 24-hour dietary recall	3.5 (4)	nc	567 (193)	nc	2.7 (1.3)	nc
	van Stuijvenberg⁷⁷	149	2-5 years	Single 24-hour dietary recall	8.1 (4.6)	44	947 (259)	1	7.2 (3.7)	55
>5-19 years
Ethiopia	Abuye²⁴	10,965	6-12 years	Salt analyzed by rapid test kit							96
	Mesele³⁸	694	6-12 years	Salt analyzed by spot testing kit							70
	Mezgebu³⁹	389	6-12 years	Salt analyzed by iodometric titration							71
	Habtamu³⁶	397	6-12 years	Salt analyzed by test kit							70
Kenya	KNBS⁵³	na	<5 years	Salt tested by a kit							13
Nigeria	Ayogu⁵³	80	6-15 years	Validated questionnaire	16.8 (7)	51
	Abua⁵²	400	8-12 years	Salt analyzed by titrimetric method							26
	Madukwe⁵⁸	200	6-12 years	Salt analyzed by field test kit							36
	Hassan⁵⁵	394	7-11 years	Single 24-hour dietary recall	10.9 (3.3)	97	736 (288)	10
	Nwamarah⁵⁹	395	6-12 years	Salt analyzed by test kit							6
	Ekpo⁵⁴	418	12-18 years (f)	na	10 (5.4)	98
	Onabanjo⁶⁰	127	10-19 years	3 × 24-hour dietary recalls	8.1 (7)	97	729 (16)	30
South Africa	Samuel⁷²	149	7-11 years	Single 24-hour dietary recall					4.6 (2.2)	98
	Grobbelaar⁶⁸	143	4-18 years	7-day cycle menu	9.2 (1.9)	100	581 (142)	7	9.2 (2.9)	87
	NFCS-FB⁶²	1332	5-9 years	Salt analyzed by titration method							23

Abbreviations: BF, breast fed; NBF, non-breast fed.

^aBreast-fed infants report complementary feeding and breast milk intake, non-breast-fed report only complementary feeding.

^bMeans ± SD converted from median and IQ.

^cData on only complementary feeding, % inadequate intake therefore not calculated (nc).

^dMixed feeding, not clear if breast-milk considered; vitamin A reported as retinol activity equivalent (RAE).

^eVitamin A intake varied a lot per region within the same country.

Vitamin A

Mean dietary vitamin A intake ranged from 38 to 947 µg/d, and the percentage of children with inadequate intake ranged from 1% to 100% (Table 3). For 5 to 19 years, data were available in Nigerian and South African children, and 7% to 30% had inadequate intakes.

Zinc

Mean dietary zinc intake ranged from 2 to 9 mg/d, and the percentage of children with inadequate intake ranged from 51% to 99% (Table 3). For 5 to 19 years, data were only available in South African children, and 87% to 98% of them had inadequate intakes.

Iodine

The percentage of households not consuming adequately iodized salt (>15 ppm) ranged from 2% to 96% (Table 3). Ethiopian households reported the highest (70%-96%) intake of inadequately iodized salt followed by South Africa (23%), Nigeria (6%-36%), and Kenya (2%-13%).

Discussion

This systematic review, based on both national and subnational data published in the last 10 years, shows that with large variation within and among the 4 African countries, prevalence of anemia, vitamin A, zinc, and iodine deficiencies are of public health significance. The prevalence of anemia is higher (25%-53%) than VAD (14%-42%) in all countries except South Africa while zinc deficiency (>30%) is also high in Ethiopia, Nigeria, and South Africa. The prevalence of iodine deficiency is high in Ethiopia (86%) and Nigeria (59%). Generally, children <5 years had a higher prevalence of anemia, VAD, and zinc deficiency compared to children aged 5 to 19 years. Data on inadequate intake of iron, vitamin A, and zinc and household consumption of iodized salt largely correspond to the prevalence figures for micronutrient deficiencies.

This systematic review is the first to provide an overview of both status and dietary intakes of iron, vitamin A, zinc, and iodine in children aged 0 to 19 years in 4 sub-Saharan African countries. Another strength of this review is the use of most recent data from 2005 to 2015 including both national and subnational data to determine the prevalence of deficiencies and inadequate intakes. Therefore, this review may help guide public health practitioners and policy makers in advocacy for public health strategies to prevent micronutrient deficiencies in children of different age-groups, especially where nationally representative data are lacking.

However, there are a few limitations to this systematic review. First, our figures of WAVG on the prevalence of micronutrient deficiencies for each country were based on both national and subnational data (which primarily were conducted in specific regions and rural areas) and need to be interpreted with caution. In our review, the prevalence of micronutrient deficiencies in rural areas was often higher than that of urban areas (data not shown) and may have therefore overestimated the problem of micronutrient deficiencies at a national level. Similarly, the subnational data (studies) were mostly conducted in children from low socioeconomic backgrounds, which may have led to an overestimation of the prevalence of micronutrient deficiencies and inadequate intakes. This is especially the case for Kenya and Nigeria and for children aged 5 to 19 years, where subnational data provided substantial weight to the overall figures on micronutrient deficiencies as national data were generally missing.

Second, dietary intake data from both national and subnational studies were based mostly on a single 24-hour dietary recall, which may have resulted in an under- or overestimation of micronutrient inadequacy because of day-to-day (within-person) variability in dietary intake. Within-person variability can be adjusted for if at least 2 nonconsecutive recalls (either on the full sample or on a subsample) are available.⁷⁸ Collecting repeated 24-hour recalls in large community-based surveys may however be challenging. Micronutrient intakes reported in the studies may also have been affected by the food composition tables used to calculate micronutrient intake. Nutrient content of certain foods, for example, fortified foods, biofortified foods, and indigenous foods, are often very country specific. If the food composition database did not reflect the country-specific nutrient content of these foods at the time of the survey, the nutrient values reported may have been an underestimation of actual intake and therefore leading to an overestimation of inadequacy.

Finally, for calculations of inadequate intake, it was assumed that the nutrient intake data were normally distributed, which may not have been the case, particularly for the nutrients under investigation. In addition, for 3^42, ^64,65 of 5 studies in children younger than 2 years, information on breast-milk consumption was not provided explicitly which may have led to an underestimation of micronutrient intake. Therefore, figures for inadequate intake of iron, vitamin A, and zinc are crude approximations and should be interpreted as such.

Despite these limitations, the available data provide useful insights into the current ranges of the prevalence of deficiency and inadequate intake of iron, vitamin A, zinc, and iodine in children and adolescents in the 4 African countries as published during the past 10 years.

With a WAVG prevalence of >20% in all 4 countries, anemia is a moderate to severe public health problem as per WHO criteria.¹⁴ The prevalence of anemia in children aged <5 years (32%-63%) was higher than in older children (14%-40%) in Ethiopia, Kenya, and South Africa. For Nigeria, it is not possible to make this comparison because only a small study (n = 240) was available for children <5 years. Drorbaugh and Neumann⁷⁹ reviewed the micronutrient status in 7 food aid beneficiary countries in Africa, including Niger, Ethiopia, Kenya, Uganda, Rwanda, Zambia, and Zimbabwe. Similar to our review, they reported that >40% of children <5 years had anemia. Furthermore, 2 recent global reviews covering population-representative data from 1995 to 2011, from up to 187 countries, reported that children <5 years living in African countries were among the populations with the highest prevalence of anemia (70%) next to South Asia.⁸⁰ More importantly, this was the only age-group in which anemia prevalence increased from 1990 to 2010.⁸⁰ This is of concern, as younger children are most vulnerable to detrimental long-term effects of anemia.⁸¹ World Health Organization estimates that ID is the major cause of anemia responsible for almost half of anemia cases¹⁴; however, most surveys only report figures for anemia, while data on iron status (ID and IDA) are limited. For the few studies that did report iron status, the prevalence of ID was 12% to 29% and IDA 11% to 14%. However, it should be noted that there is uncertainty for most of these studies whether serum ferritin levels were corrected for inflammation, and therefore the prevalence of ID in our review may be underestimated.⁸² In line with high prevalence of anemia, inadequate intakes of iron were also reported in children <5 years (13%-62%) in all 4 countries. The prevalence of inadequate iron intake was particularly high (51%-100%) in children >5 years (data from Nigeria and South Africa only), which may be due to higher daily requirements for adolescents.⁸³

The prevalence of VAD indicates varying degrees of severity in the 4 countries (severe in South Africa and moderate for the other 3 countries) and is considered a significant public health problem as per WHO criteria.⁸⁴ Similar to anemia, VAD prevalence is higher (14%-35%) in <5 years children except for South Africa. This difference in South Africa may be explained by the difference in time frame, since the data in >5- to 19-year-old children (VAD 62%) is predominantly based on an older national survey from 2005,²³ whereas that of children <5 years (VAD 35%) also included a more recent national survey (2012) and studies. This decrease in VAD could be attributed to national vitamin A supplementation (VAS) program (since 2002) and mandatory fortification of 2 staple foods (maize meal and wheat flour that is used for making bread; since 2003).⁶³

The prevalence for VAD in children aged <5 years in the 4 countries are lower than the 48% (95% CI 25%-75%) prevalence estimated by the WHO from studies published 1991 to 2013 in sub-Saharan African <5 years children.⁷ The higher estimates from WHO could be due to inclusion of African countries with a higher prevalence of VAD. It could also be that prevalence of VAD may have decreased over time due to VAS and fortification programs as shown for South Africa. Similar to status data, the intake data on vitamin A showed large variation within and among the 4 countries. The large variation in intake of vitamin A could be due to seasonal differences in consumption of vitamin A-rich fruits and vegetables or consumption of high liver products⁷⁷ or due to lack of clarity in some of the studies regarding the conversion factors used to calculate retinol equivalents from carotenoid intake, particularly in populations where plant foods are the major source of dietary vitamin A.

Our review showed that data on zinc status are limited which may be due to high costs, logistical challenges, and the limited number of valid biomarkers.⁸⁵ National and subnational data from Ethiopia and South Africa have reported the prevalence of zinc deficiency, which ranged from 32% to 39% in children aged 0 to 19 years, whereas only 1 subnational data reported zinc deficiency in Nigeria at 63% (<5 years). The prevalence of high zinc deficiency is in line with the large percentage (51%-98%) of children with inadequate zinc intakes in these countries. Wessells and Brown predicted that 25.6% of the sub-Saharan African population had inadequate intake based on estimated absorbable zinc supply from food balance sheets⁸⁶ which is lower than that found in our review. This difference may be explained by the fact that food balance sheet data may be more reflective of adult dietary intakes than intakes of children, since the type of foods consumed and the adequacy of food intakes by young children may differ substantially from those of adults in the same population.⁸⁵ The difference between estimated zinc intake based on calculations using food balance sheets and that reported by subnational studies may also reflect unequal access to foods within a country. Moreover, to compare the zinc intake to EAR, we used the lowest bioavailability for zinc, as diets in this region are high in phytic acids,⁸⁷ thus making the gap between current and recommended intake large.

Among the 4 countries included in our review, Ethiopia reported the highest iodine deficiency (86%) and high goiter prevalence (14% to 59%; see Supplemental Table S2). Similarly, in a 7 African country survey, Ethiopia (and Zambia) reported the highest prevalence of iodine deficiency.⁷⁹ Compared to Ethiopia, iodine deficiency was lower in South Africa (15%). However, our data show regional differences in the prevalence of iodine deficiency in these countries, with some regions having optimal iodine nutrition, while other regions within the same country reported mild to moderate iodine deficiency. Because of the difficulties in quantifying iodine intake in dietary surveys, and as iodized salt is the main source of dietary iodine intake in many countries,⁸⁸ percentage households consuming inadequately iodized salt was used as proxy measure for iodine intake. Salt iodization data do however not take all dietary iodine sources into account, particularly the contribution of (iodized) salt in processed foods and dairy products that are important sources of iodine in many countries as well as iodine-rich ground water found in some regions. Nevertheless, the high prevalence of iodine deficiency in Ethiopia corresponds with the high number of (70%) of the households consuming inadequately iodized (<15 ppm) salt. Despite mandatory salt iodization in these 4 countries, household coverage rates of adequately iodized salt remain low especially in Ethiopia.²⁶

Fortification programs are implemented in African countries, and most countries are increasingly fortifying wheat and maize flour with iron, zinc, and folic acid, cooking oils and sugar with vitamin A, and salt with iodine. Nevertheless, the progress is made at different pace across countries, where for more than a decade Nigeria and South Africa has mandatory fortification of flour and oil (Nigeria only), Kenya has recently mandated fortifying the staples, and Ethiopia is in the planning phase.⁸⁹ With legislation on mandatory food fortification, the quality of fortified foods is not automatically guaranteed and compliance to legislation may be low.⁹⁰ Therefore, there is a need for strengthening and expanding these programs. Next to staples, fortification of commonly consumed foods such as cooking aids (bouillon cubes, condiments, and seasonings) and nutrition education to promote dietary diversification should be considered together with other programs such as micronutrient supplementation of vitamin A and iron; promotion of breast-feeding, safe water, sanitation, and hygiene interventions; and poverty alleviation.^91
–93 In addition, micronutrient nutrition of older children and adolescent girls, in particular, would need further investigation to identify effective programs to improve their micronutrient intake.

Nationally representative data on micronutrient status and intake are essential to guide the development of public health programs to improve micronutrient intake and to monitor the impact of national programs. Given the observed differences within countries (eg, VAD in South Africa), subnational data may strengthen national data. It is recommended, that in the future surveys should be conducted on a regular basis and include all age-groups, as our review indicates that both young and older children are vulnerable to micronutrient deficiencies.

Conclusion

In conclusion, the available data indicate that the prevalence of anemia, vitamin A, zinc, and iodine deficiencies are of public health significance in children living in Ethiopia, Kenya, Nigeria, and South Africa. Underlying these deficiencies are inadequate dietary intakes. These deficiencies and inadequate intakes may vary largely among different regions within the countries, which may not necessarily be revealed by national surveys only. National representative surveys, covering all age-groups, are needed to monitor micronutrient status and intake in African children and adolescents on a regular basis are however important. Micronutrient deficiencies seem to be more prevalent in children <5 years, but older children and adolescents also have inadequate micronutrient nutrition. Therefore, effective public health strategies are imperative to prevent micronutrient deficiencies to improve growth and development of children. These public health initiatives should focus on improving micronutrient intake of both children aged <5 years and older children (>5-19 years) through fortification of daily consumed and affordable food products as well as by stimulating dietary diversity.

Footnotes

Authors’ Note

R.H. and A.E. initiated the research design and did the data analysis and interpretation. All the authors contributed to data collection and to the writing of the manuscript.

Declaration of Conflicting Interests

The author(s) declared the following potential conflicts of interest with respect to the research, authorship, and/or publication of this article: R.H. and A.E. are employees of Unilever. Unilever sells food products globally including in African countries.

Funding

The author(s) received no financial support for the research, authorship, and/or publication of this article.

Supplemental Material

Supplementary material is available for this article online.

References

World Health Organization. The World Health Report 2002—Reducing Risks, Promoting Healthy Life. World Health Report. Geneva, Switzerland: World Health Organization; 2002.

Stoltzfus

Mullany

Black

. Iron deficiency anaemia. In: Ezzati

M LA

Rodgers

Murray

CLJ

, eds. Comparative Quantification of Health Risks: Global and Regional Burden of Disease Attrib to Selected Major Risk Factors. Geneva, Switzerland: World Health Organization; 2004:163–209.

Bleichrodt

. A meta analysis of research on iodine and its relationship to cognitive development. In: Stanbury

, ed. The Damaged Brain of Iodine Deficiency. New York, NY: Cognizant Communication; 1994:195–200.

Rice

West

Black

. Vitamin A deficiency. In: Ezzati

M LA

Rodgers

Murray

CLJ

, eds. Comparative Quantification of Health Risks: Global and Regional Burden of Disease Attributable to Selected Major Risk Factors. Geneva, Switzerland: World Health Organization; 2004:211–256.

Ploysangam

Falciglia

Brehm

. Effect of marginal zinc deficiency on human growth and development. J Trop Pediatr, 1997;43(4):192–198.

Black

Victora

Walker

. Maternal and child undernutrition and overweight in low-income and middle-income countries. Lancet. 2013;382(9890):427–451.

Stevens

Bennett

Hennocq

. Trends and mortality effects of vitamin A deficiency in children in 138 low-income and middle-income countries between 1991 and 2013: a pooled analysis of population-based surveys. Lancet Glob Health. 2015;3(9):e528–e536.

Stevens

Finucane

De-Regil

. 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(1):e16–e25.

Andersson

Takkouche

Egli

Allen

. Current global iodine status and progress over the last decade towards the elimination of iodine deficiency. Bull World Health Organ. 2005;83(7):518–525.

10.

Wuehler

Peerson

Brown

. Use of national food balance data to estimate the adequacy of zinc in national food supplies: methodology and regional estimates. Public Health Nutr. 2005;8(7):812–819.

11.

Muthayya

Rah

Sugimoto

Roos

Kraemer

Black

. The global hidden hunger indices and maps: an advocacy tool for action. PLoS One. 2013;8(6):e67860.

12.

Frayne

Crush

McLachlan

. Urbanization, nutrition and development in Southern African cities. Food Secur. 2014;6(1):101–112.

13.

United Nations DoEaSA. List of African countries by Population. 2005. http://statisticstimes.com/population/african-countries-by-population.php2015. Updated March 25, 2015. Accessed April 20, 2016.

14.

World Health Organization, The United Nations Children’s Fund, United Nations. Iron Deficiency Anaemia Assessment, Prevention, and Control. A guide for programme managers. Geneva, Switzerland: World Health Organization; 2001.

15.

World Health Organization. Indicators for assessing Vitamin A deficiency and thier application in monitoring and evaluating intervention programmes. Geneva, Switzerland: World Health Organization; 1996.

16.

de BB, Darnton-Hill

Davidsson

Fontaine

Hotz

. Conclusions of the Joint WHO/UNICEF/IAEA/IZiNCG Interagency Meeting on Zinc Status Indicators. Food Nutr Bull. 2007;28(suppl 3):S480–S484.

17.

Urinary iodine concentrations for determining iodine status deficiency in populations. Vitamin and Mineral Nutrition Information System. World Health Organization; 2013. http://www.who.int/nutrition/vmnis/indicators/urinaryiodine. Accessed January 07, 2016.

18.

Goitre as a determinant of the prevalence and severity of iodine deficiency disorders in populations. Vitamin and Mineral Nutrition Information System. 2014. http://apps.who.int/iris/bitstream/10665/133706/1/WHO_NMH_NHD_EPG_14.5_eng.pdf. Accessed March, 2016.

19.

Institute of Medicine. Dietary Reference Intakes: Applications in Dietary Planning. Washington DC: National Academies Press; 2003.

20.

Food and Agriculture Organization/World Health Organization. Human Vitamin and Mineral Requirements. Rome, Italy: Food and Agriculture Organization; 2001. ftp://ftp.fao.org/docrep/fao/004/y2809e/y2809e00.pdf.

21.

Hartung

JEB

Klosener

. Statistik Lehr-und Handbuch Der Angewandten Statistik. 6. Auflage. Konstanz, BW: Deutschland; 1987.

22.

Gegios

Amthor

Maziya-Dixon

. Children consuming cassava as a staple food are at risk for inadequate zinc, iron, and vitamin A intake. Plant Foods Hum Nutr. 2010;65(1):64–70.

23.

Moher

Liberati

Tetzlaff

Altman

. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Int J Surg. 2010;8(5):336–341.

24.

Abuye

Berhane

Akalu

Getahun

Ersumo

. Prevalence of goiter in children 6 to 12 years of age in Ethiopia. Food Nutr Bull. 2007;28(4):391–398.

25.

Central Statistical Agency [Ethiopia] and ICF International. Ethiopia Demographic and Health Survey 2011. Addis Ababa, Ethiopia and Calverton, MD: Central Statistical Agency and ICF International. 2012.

26.

Institute EPH. Ethiopia National Food Consumption Survey. Addis Ababa, Ethiopia: Ethiopian Public Health Institute (EPHI); 2013.

27.

Institute EPH. Ethiopian National Micronutrient Survey 2014/2015: Preliminary Report. 2016.

28.

Demissie

Ali

Mekonen

Haider

Umeta

. Magnitude and distribution of vitamin A deficiency in Ethiopia. Food Nutr Bull. 2010;31(2):234–241.

29.

Amare

Moges

Fantahun

. Micronutrient levels and nutritional status of school children living in Northwest Ethiopia. Nutr J. 2012;11:108.

30.

Aweke

Adamu

Girmay

Yohannes

Alemnesh

Abuye

. Iodine Deficiency Disorders (IDD) in Burie and Womberma districts, West Gojjam, Ethiopia. Afr J Food Agric Nutr Dev. 2014;14(4):9167–9180.

31.

Baye

Guyot

Icard-Verniere

Mouquet-Rivier

. Nutrient intakes from complementary foods consumed by young children (aged 12-23 months) from North Wollo, Northern Ethiopia: the need for agro-ecologically adapted interventions. Public Health Nutr. 2013;16(10):1741–1750.

32.

Desalegn

Mossie

Gedefaw

. Nutritional iron deficiency anemia: magnitude and its predictors among school age children, southwest Ethiopia: a community based cross-sectional study. PLoS One. 2014;9(12):e114059.

33.

Gashu

Stoecker

Adish

Haki

Bougma

Marquis

. Ethiopian pre-school children consuming a predominantly unrefined plant-based diet have low prevalence of iron-deficiency anaemia. Public Health Nutr. 2016;19(10):1834–1841.

34.

Girma

Loha

Bogale

Teyikie

Abuye

Stoecker

. Iodine deficiency in primary school children and knowledge of iodine deficiency and iodized salt among caretakers in Hawassa Town: Southern Ethiopia. Ethiop J Health Dev. 2012;26(1):30–35.

35.

Girma

Nibret

Gedefaw

. The status of iodine nutrition and iodine deficiency disorders among school children in Metekel Zone, northwest Ethiopia. Ethiop J Health Sci. 2014;24(2):109–116.

36.

Hebtamu

Ketema

Addisu

. Prevalence of Goiter and Associated Factors Among Primary School Children Aged 6-12 Years Old in Goba Town, South East, Ethiopia. Inter J Nut Food Sci. 2015;4(3):381–387.

37.

Herrador

Sordo

Gadisa

. Micronutrient deficiencies and related factors in school-aged children in Ethiopia: a cross-sectional study in Libo Kemkem and Fogera districts, Amhara Regional State. PLoS One. 2014;9(12):e112858.

38.

Mesele

Degu

Gebrehiwot

. Prevalence and associated factors of goiter among rural children aged 6-12 years old in Northwest Ethiopia, cross-sectional study. BMC Public Health. 2014;14:130.

39.

Mezgebu

Mossie

Rajesh

Beyene

. Prevalence and severity of iodine deficiency disorder among children 6-12 years of age in shebe senbo district, jimma zone, southwest ethiopia. Ethiop J Health Sci. 2012;22(3):196–204.

40.

Woldie

Kebede

Tariku

. Factors Associated with Anemia among Children Aged 6-23 Months Attending Growth Monitoring at Tsitsika Health Center, Wag-Himra Zone, Northeast Ethiopia. J Nutr Metab. 2015:1–9.

41.

KNBC & ICF Macro. Kenya Demographic and Health Survey 2008-09. Calverton, NY; 2010.

42.

Cherop

Ettyang

Mbagaya

. Mixed feeding among infants aged 0-6 months in an urban setting of Eldoret, Kenya. J Food Agric Environ. 2010;8(1):59–62.

43.

Frosch

AEP

Ondigo

Ayodo

Vulule

John

Cusick

. Decline in childhood iron deficiency after interruption of malaria transmission in highland Kenya. Am J Clin Nutr. 2014;100(3):968–973.

44.

Foote

Sullivan

Ruth

. Determinants of anemia among preschool children in rural, western Kenya. Am J Trop Med Hyg. 2013;88(4):757–764.

45.

KNBS. Kenya National Bureau of Statistics. Nyanza Province Multiple Indicator Cluster Survey 2011. Nairobi, Kenya: Kenya National Bureau of Statistics; 2013.

46.

Macharia-Mutie

Moretti

Van den Briel

. Maize porridge enriched with a micronutrient powder containing low-dose iron as NaFeEDTA but not amaranth grain flour reduces anemia and iron deficiency in Kenyan preschool children. J Nutr. 2012;142(9):1756–1763.

47.

M’Kaibi

Steyn

Ochola

. Effects of agricultural biodiversity and seasonal rain on dietary adequacy and household food security in rural areas of Kenya. BMC Public Health. 2015;15:422.

48.

Suchdev

Ruth

Woodruff

. Selling Sprinkles micronutrient powder reduces anemia, iron deficiency, and vitamin A deficiency in young children in Western Kenya: a cluster-randomized controlled trial. Am J Clin Nutr. 2012;95(5):1223–1230.

49.

Suchdev

Davis

Bartoces

. Soil-transmitted helminth infection and nutritional status among urban slum children in Kenya. Am J Trop Med Hyg. 2014;90(2):299–305.

50.

Talsma

Verhoef

Brouwer

Mburu-de Wagt

Hulshof

Melse-Boonstra

. Proxy markers of serum retinol concentration, used alone and in combination, to assess population vitamin A status in Kenyan children: a cross-sectional study. BMC Med. 2015;13:30.

51.

Aaron

Kariger

Aliyu

: A multi-micronutrient beverage enhances the vitamin A and zinc status of Nigerian primary schoolchildren. J Nutr. 2011;141(8):1565–1572.

52.

Abua

Ajayi

Sanusi

. Adequacy of dietary iodine in two local government areas of Cross River State in Nigeria. Pak J Nutr. 2008;7(1):40–43.

53.

Ayogu

RNB

Okafor

Ene-Obong

. Iron status of schoolchildren (6-15 years) and associated factors in rural Nigeria. Food Nutri Res. 2015;59:26223.

54.

Ekpo

Jimmy

. Dietary and haematological evaluation of adolescent females in Nigeria. Pak J Nutr. 2006;5(3):278–281.

55.

Hassan

Onabanjo

Oguntona

CRB

. Nutritional assessment of school-age children attending conventional primary and integrated Qur’anic Schools in Kaduna. Res J Med Sci. 2012;6(4):187–192.

56.

Ibeanu

Okeke

Onyechi

Ejiofor

. Assessment of anthropometric indices, iron and zinc status of preschoolers in a peri-urban community in south east Nigeria. Int J Basic Appl Sci. 2012;12(5):31.

57.

Jeremiah

Uko

Buseri

Adias

. Baseline iron status of apparently healthy children in Port Harcourt, Nigeria. Eur J Gen Med. 2007;4(4):161–164.

58.

Madukwe

Ani

Maduabuchi

. Iodine content of household salt and urinary iodine of primary school pupils in commercial towns in Nsukka senatorial zone, Enugu state, Nigeria. Pak J Nutr. 2013;12(6):587–593.

59.

Nwamarah

Otitoju Olawale

OGTO

Emewulu

CUD

. Iodine and nutritional status of primary school children in a Nigerian community Okpuje, in Nsukka LGA, Enugu State, Nigeria. Der Pharm Lett. 2015;7(7):271–280.

60.

Onabanjo

Balogun

. Anthropometric and Iron Status of Adolescents From Selected Secondary Schools in Ogun State, Nigeria. Infant Child Adolesc Nutr. 2014;6(2):109–118.

61.

Osazuwa

Ayo

Imade

. A significant association between intestinal helminth infection and anaemia burden in children in rural communities of Edo state, Nigeria. North Am J Med Sci. 2011;3(1):30–34.

62.

Labadarios

, ed. NFCS: National Food Consumption Survey-Fortification Baseline (NFCS-FB): South Africa, 2005. Tygerberg, South Africa: University of Stellenbosch and Tygerberg Academic Hospital; 2007.

63.

Shisana

Labadarios

Rehle

. South African National Health and Nutrition Examination Survey (SANHANES-1). Cape Town, South Africa: HSRC Press; 2014.

64.

Balogun

Lombard

McLachlan

. The nutrient intake of children aged 12-36 months living in two communities in the Breede Valley, Western Cape province, South Africa. S Afr Fam Pract. 2015;57(1):1–7.

65.

Faber

. Complementary foods consumed by 6-12-month-old rural infants in South Africa are inadequate in micronutrients. Public Health Nutr. 2005;8(4):373–381.

66.

Faber

van Jaarsveld

Kunneke

Kruger

Schoeman

van Stuijvenberg

. Vitamin A and anthropometric status of South African preschool children from four areas with known distinct eating patterns. Nutrition. 2015;31(1):64–71.

67.

Faber

Benada

AJS

. Breastfeeding, complementary feeding and nutritional status of 6 - 12-month-old infants in rural KwaZulu-Natal. S Afr J Clin Nutr. 2007;20(1):16–24.

68.

Grobbelaar

Napier

Oldewage-Theron

. Nutritional status and food intake data on children and adolescents in residential care facilities in Durban. S Afr J Clin Nutr. 2013;26(1):29–36.

69.

Mamabolo

Alberts

. Prevalence of anaemia and its associated factors in African children at one and three years residing in the Capricorn District of Limpopo Province, South Africa. Curationis. 2014;37(1):1–9.

70.

Motadi

Mbhenyane

Mbhatsani

Mabapa

Mamabolo

. Prevalence of iron and zinc deficiencies among preschool children ages 3 to 5 y in Vhembe district, Limpopo province, South Africa. Nutrition. 2015;31(3):452–458.

71.

Onabanjo

Jerling

Covic

Van

Taljaard

Mamabolo

. Association between iron status and white blood cell counts in African schoolchildren of the North-West Province, South Africa. J Epidemiol Glob Healt. 2012;2(3):103–110.

72.

Samuel

Egal

Oldewage-Theron

Napier

Venter

. Prevalence of zinc deficiency among primary school children in a poor peri-urban informal settlement in South Africa. Health SA Gesondheid (Online). 2010;15(1):1–6.

73.

Smuts

Lombard

Benade

. Efficacy of a foodlet-based multiple micronutrient supplement for preventing growth faltering, anemia, and micronutrient deficiency of infants: the four country IRIS trial pooled data analysis. J Nutr. 2005;135(3):631S–638S.

74.

Taljaard

Covic

van Graan

Kruger

Jerling

. Studies since 2005 on South African primary schoolchildren suggest lower anaemia prevalence in some regions. S Afr J Clin Nutr. 2013;26(4):168–175.

75.

Troesch

van Stuijvenberg

Smuts

. A micronutrient powder with low doses of highly absorbable iron and zinc reduces iron and zinc deficiency and improves weight-for-age Z-scores in South African children. J Nutr. 2011;141(2):237–242.

76.

van der Hoeven

Faber

Osei

Kruger

Smuts

. Effect of African leafy vegetables on the micronutrient status of mildly deficient farm-school children in South Africa: a randomized controlled study. Public Health Nutr. 2016;19(5):935–945.

77.

van Stuijvenberg

Nel

Schoeman

Lombard

du Plessis

Dhansay

. Low intake of calcium and vitamin D, but not zinc, iron or vitamin A, is associated with stunting in 2- to 5-year-old children. Nutrition. 2015;31(6):841–846.

78.

Institute of Medicine. Dietary Reference Intakes: Applications in Dietary Assessment. Washington, DC: National Academy Press; 2000.

79.

Drorbaugh

Neuman

. Micronutrient deficiencies in food aid beneficiaries: a review of seven African countries. Afr J Food Agric Nutr Dev. 2009;9(4):990–1018.

80.

Kassebaum

Jasrasaria

Naghavi

. A systematic analysis of global anemia burden from 1990 to 2010. Blood. 2014;123(5):615–624.

81.

Lozoff

Jimenez

Wolf

. Long-term developmental outcome of infants with iron deficiency. N Engl J Med. 1991;325(10):687–694.

82.

Thurnham

McCabe

Haldar

Wieringa

Northrop-Clewes

McCabe

. Adjusting plasma ferritin concentrations to remove the effects of subclinical inflammation in the assessment of iron deficiency: a meta-analysis. Am J Clin Nutr. 2010;92(3):546–555.

83.

Beard

. Iron requirements in adolescent females. J Nutr. 2000;130(suppl 2S):440S–442S.

84.

World Health Organization. Global Prevalence of Vitamin A Deficiency in Populations at Risk 1995–2005. Geneva, Switzerland: WHO Global Database on Vitamin A Deficiency; 2009.

85.

Brown

Rivera

Bhutta

. International Zinc Nutrition Consultative Group (IZiNCG) technical document #1. Assessment of the risk of zinc deficiency in populations and options for its control. Food Nutr Bull. 2004;25(1 suppl 2):S99–S203.

86.

Wessells

Brown

. Estimating the global prevalence of zinc deficiency: results based on zinc availability in national food supplies and the prevalence of stunting. PLoS One. 2012;7(11):e505–e568.

87.

Umeta

West

Fufa

. Content of zinc, iron, calcium and their absorption inhibitors in foods commonly consumed in Ethiopia. J Food Compos Anal. 2005;18:803–817.

88.

World Health Organization. Assessment of Iodine Deficiency Disorders and Monitoring their Elimination. A Guide for Programme Managers. ISBN 978 92 4 159582 7. 2007. Geneva, Switzerland: World Health Organization. http://apps.who.int/iris/bitstream/10665/43781/1/9789241595827_eng.pdf

89.

Food Fortification Initiative. http://ffinetwork.org/regional_activity/africa.php. Accessed, March 2017.

90.

Ogunmoyela

Adekoyeni

Aminu

Umunna

. A critical evaluation of survey results of vitamin A and Fe levels in the mandatory fortified food vehicles and some selected processed foods in Nigeria. Nigerian Food J. 2013;31(2):52–62.

91.

Hess

Brown

Sablah

Engle-Stone

Aaron

Baker

. Results of Fortification Rapid Assessment Tool (FRAT) surveys in sub-Saharan Africa and suggestions for future modifications of the survey instrument. Food Nutr Bull. 2013;34(1):21–38.

92.

Bhutta

Das

Rizvi

; Lancet Nutrition Interventions Review Group; Maternal and Child Nutrition Study Group. Evidence-based interventions for improvement of maternal and child nutrition: what can be done and at what cost? Lancet. 2013;382(9890):452–477.

93.

Ruel

Alderman

, Maternal; Child Nutrition Study G. Nutrition-sensitive interventions and programmes: how can they help to accelerate progress in improving maternal and child nutrition? Lancet. 2013;382(9891):536–551.

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Are Low Intakes and Deficiencies in Iron,Vitamin A,Zinc,and Iodine of Public Health Concern in Ethiopian,Kenyan,Nigerian,and South African Children and Adolescents?

Abstract

Objective:

Method:

Results:

Conclusion:

Keywords

Introduction

Method

Search Strategy

Inclusion Criteria

Data Extraction

Status data

Intake data

Data Analysis

Calculating inadequacy of micronutrient intakes

Results

Data Availability

Prevalence of Micronutrient Deficiencies in Children (0-19 Years)

Iron

Vitamin A

Zinc

Iodine

Dietary Intake of Iron, Vitamin A, Zinc, and Household Consumption of Iodized Salt in Children (0 to 19 years)

Iron

Vitamin A

Zinc

Iodine

Discussion

Conclusion

Footnotes

Authors’ Note

Declaration of Conflicting Interests

Funding

Supplemental Material

References

Supplementary Material