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Anaemia prevalence and nutrient intake among women in peri-urban settlements in Accra, Ghana.


Anaemia among women is a major public health concern globally. In developing countries, nutritional anaemia may be due to poor bioavailability of dietary iron, haemoglobinopathies, or intestinal parasites. The study objectives were to determine the prevalence of anaemia and current nutrient intakes essential to erythropoiesis among women of reproductive age (WRA) in peri-urban settlements in the Ga-East Municipality, Accra, Ghana. This cross-sectional study assessed the nutrient intake, sickling and haemoglobin levels of 134 women aged 15-49 years enrolled in a peanut-based field trial at baseline. A pretested semi-quantitative food frequency questionnaire was used to assess energy and nutrient intake using the Food Processor (ESHA) software. Whole blood was used to determine full blood count using the haematology automated analyser. Sickling was determined by blood staining. Anaemia was classified based on recommended cut-offs. Chi-square analysis was used as a test of independence between anaemia and age groups. Linear regression was used to determine predictors of haemoglobin concentration. The mean age of the women was 29 [+ or -] 8 years. The mean total caloric intake was 2315 [+ or -] 915 kcal, whilst protein and fat intakes were 67 [+ or -] 27g and 68[+ or -] 30g, respectively. Almost three-quarters of the women met the recommended dietary allowance (RDA) for iron and vitamin C. However, only a third met the RDA for fat, and about two-thirds met their needs for energy and protein. None of the women met the RDA for folate which is integral for haem formation. Also 17% (23/134) of the women were sickle cell anaemia positive. Mean haemoglobin concentration was 12.1 [+ or -] 1.8 g/dL. Mild, moderate and severe anaemia due to iron deficiency was present in 35.8%, 6.7% and 1.5%, of the women respectively. All categories of anaemia was present in 44% of the women. Anaemia, prevalence increased during the early stages of the reproductive age (15-29 years) and declined towards the end of the reproductive age period (40-49 years). An increase in age of one year was significantly associated with a 0.056 g/dL rise in haemoglobin level (p=0.014). Anaemia due to iron deficiency exists as a public health problem among women in peri-urban settlements in the Ga-East Municipality, Accra, Ghana. Dietary diversity to include green leafy vegetables which are rich in folate and pro-vitamin A may reduce the current level of prevalence.

Key words: Anaemia, Nutrients, Peri-urban, Women, RDA, sickling test, Food Processor software


Globally, anaemia is the most common nutritional deficiency and has received much attention for targeted improvements. Nonetheless, its prevalence remains unacceptably high. About one-third of the global population (over 2 billion) is anaemic [1]. Age-specific anaemia prevalence estimates of 47% in children under 5 years, 30% in non-pregnant non-lactating women and 42% in pregnant women has been reported by McLean et al. [2]. Anaemia prevalence among women of reproductive age (WRA: 15-49 years) in West and Central Africa was 48% as at 2011 [3]. Statistics in Ghana indicate that 4 out of every 10 WRA are anaemic [4].

Anaemia is a condition in which the body does not have enough healthy red blood cells or decreased normal quantity of haemoglobin (Hb) in the blood. Anaemia aetiology can be due to deficiency of one or more essential nutrients needed for erythrocyte formation as well as potential risk factors such as malaria, infectious diseases, parasitic infections and haemoglobin related disorders [5, 6]. For women, other risk factors include recurrent menstrual loss, pregnancy demands, short birth intervals, poor access to antenatal care and inadequate micronutrient supplementation [7]. Deficiencies in haematopoietic nutrients (iron, folic acid and vitamin A, vitamin B12) have been described by the World Health Organization as nutritional anaemia. Increasing intake of foods rich in anti-nutritive factors (phytic acid, trypsin inhibitors, oxalates, tannins, polyphenols, heamagglutinin) as well as low fruit and vegetable intake has brought about a decline in bioavailable haematopoietic nutrients such as iron and its absorption enhancers including vitamin C [8]. Folic acid is required for the synthesis and maturation of the erythrocytes. Vitamin A has also been shown to increase haemoglobin concentration [9]. Nutritional anaemia contributes to high maternal mortality and morbidity [10]. Annually, anaemia is estimated to contribute to more than 115,000 maternal deaths [3].

In 2012, the 65th World Health Assembly approved an action plan with commitment to halve anaemia prevalence in WRA by 2025 from the 2011 levels [3]. This calls for the implementation of proven effective nutrition intervention strategies. For effective management and evaluation of prioritized country-specific nutrition interventions to curtail anaemia, information is needed about haemoglobin status in the population of concern. Also consumption and preparation of iron, folate and vitamin A rich foods varies between urban and rural dwellers. However, there is paucity of data on consumption and nutrient intake among peri-urban dwellers in Ghana. This study therefore, seeks to determine the prevalence of anaemia and the intake of nutrients essential for erythropoiesis among WRA in peri-urban settlements in the Ga-East Municipality in the Greater Accra region of Ghana.


Design and setting

This was a cross-sectional study conducted among women of reproductive age (WRA: 15-49 years) who reside in five peri-urban communities in the north-eastern horn of the Ga-East municipality in the Greater-Accra region of Ghana (Ayimensa, Kweiman, Danfa, Adoteiman and Otinibi). The municipality was created in December 2004 with a land area of 166 square metres and Abokobi as the capital. The population density of the municipality is 1633.34 with an estimated population of 259,668 of which 51% are females [11]. The main occupation of the women in these communities is farming, gari production and petty trading. A tarred road links these communities. A borehole system provides all the communities with a source of drinking water. This is provided through Water and Sanitation Development Boards for piped schemes. A central health centre at Danfa called Danfa Health Centre provides all the communities with medical services. A signed informed consent was obtained from all recruited participants after the study protocol had been explained to them. The study protocol was approved by the institutional review board of Noguchi Memorial Institute for Medical Research, University of Ghana, Legon and permission also obtained from the Ga-East Municipal Chief Executive.

Data collection

Data on background characteristics, dietary and biochemical were collected following standard procedures. A simple population proportion formula assuming underweight prevalence of 10.1% [4], alpha level of 0.05 and 80% power was used to obtain a sample size of 121 and this was

rounded up to 134 using a margin of error of 10% to improve the precision of the estimates [12]. Cluster sampling was used to select houses in each of the communities and any WRA living in the houses was recruited. Non-pregnant, non-lactating healthy WRA who reside in Ayimensa, Kweiman, Danfa, Adoteiman and Otinibi were recruited as study participants from January to February, 2012. For a woman (15-49 years) to be included, she should not have been on vitamin-mineral supplements at least 6 months prior to recruitment.

Information on participants' background characteristics was obtained using a pre-tested questionnaire. The initial questionnaire was pre-tested in another community in Ga-East municipality called Amarhyia, a community with similar characteristics as the study communities. Thirty questionnaires were used for the pre-testing after which questions that were difficult to understand by participants were reworded to ensure that all the questions in the questionnaire were easy to understand. Questions on age, level of education, marital status and occupation were obtained from the respondents through one-on-one interview. A semi-quantitative validated food frequency questionnaire was used to obtain information on participants' usual dietary intake in the previous one month [four weeks] prior to the study. For a particular food item, the frequency of intake in a week was recorded. Household food measures, food models and other eating wares were shown to the participants to improve estimation of portion sizes.

Blood sampling, Haemoglobin and Sickling test

A 2ml sterile syringe was used to draw venous blood from each participant by a trained phlebotomist on the third and fourth weekends in February 2012. The sampled blood was dispensed into a labelled ethylenediaminetetraacetic acid (EDTA) tube and transported on ice to the laboratory. The EDTA tubes containing 2 ml of blood were vortexed to ensure uniform mixing of the cellular components using Coultre mixer (UK). Haemoglobin (Hb) was measured using Olympus sysmex kx--21N haematology fully automated analyser (France) [13]. Haemoglobin (Hb) was determined within two days after sample collection.

A thin film of blood from the EDTA containing tube was put on a slide and a drop of sickling fluid (sodium metabisulphite) was added to the blood. The blood-metabisulphite mixture was smeared on the slide and covered with a cover slip and allowed to dry. The prepared slide was observed under the electron microscope (Olympus--Germany) to identify at least a sickle shaped red blood cell in order to declare the participant as being sickling positive. All blood samples that tested positive for sickling were further examined through electrophoresis to determine those who had sickle cell disease or were carriers of the sickle cell trait. This was done with the help of a certified laboratory technologist.

Statistical analysis

The responses obtained on participants' dietary intake from the semi-quantitative food frequency questionnaire were analysed using ESHA FPRO (Athens, Georgia, USA) version 10.0.1. The total weekly dietary intake was calculated and the average of the weekly intake used as the usual daily nutrient intake of the participant. Each participant's nutrient intake was classified. The classification was done as follows: a participant was classified as having a low intake when the recommended dietary allowance (RDA) for a particular nutrient was not met, and at least meeting the RDA when the woman's dietary intake was within or above the RDA. The RDA values were obtained from Whitney and Rolfes [14].

Data were coded, entered into SPSS version 21 (Athens, Georgia, USA) and cleaned before analysis. Haemoglobin (Hb) concentration was classified as severe anaemia (<7.0 g/dL), moderate anaemia (7.0-9.9 g/dL), mild anaemia (10.0-11.9 g/dL), all forms of anaemia (<12.0 g/dL) and non-anaemic ([greater than or equal to]12.0 g/dL) [4]. Descriptive statistics was performed for the socio-demographic characteristics of the women. Independent-sample T-Test was used to test for differences in mean nutrient intakes and haemoglobin levels (anaemia and non-anaemia). Pearson's chi-square was used to examine associations between categorical variables. Pearson's correlation was used to determine relationship between haemoglobin and the different continuous variables. Linear regression was used to determine predictors of haemoglobin concentration. For the regression analysis, dummies were created for all categorical variables and were put in the model together with the continuous variables. The result of the most stable linear regression model has been presented. Minimum 95% confidence intervals and p-value of less than 0.05 were considered significant.


A total of 134 WRA were enrolled in the study with mean age of 29 [+ or -] 8 years. About 50% of the participants were in the 20-29-year age category. Majority had basic education (67.2%), most of them were employed (61.2%) and married (53.7%). Sickle cell trait was identified in 17.2% (23/134) of the participants; 16.4% were sickle cell carriers and one participant had sickle cell Hb C disease (Table 1).

The mean caloric, protein and fat intake were 2315 kcal, 67 g and 68 g, respectively (Table 2). These mean intakes were higher than their corresponding RDA for calories but protein was within the RDA range whilst fat was below the RDA range. The mean iron intake of 24 mg was above the RDA of 15-18 mg whilst folate (119 [micro]g) was far below the RDA (400 [micro]g). From Table 2, it was also evident that the mean vitamin A intake was below the RDA whilst that of vitamin C was above the RDA. A significant number of women (41.8%) did not meet their RDA for calories. The number of women who did not meet their fat intake was twice (65.7%) the number that did not meet their RDA for proteins. Caloric and vitamin A intakes were much higher for non-anaemic women as compared to anaemic women (Table 2). There was no significant difference in iron intake for anaemic and non-anaemic women. In Table 3, all the women did not meet their RDA for folate and a greater majority (74.6%) also ate less vitamin A rich foods. Majority (73.9%) and 75.4% met their iron and vitamin C daily requirements, respectively. Nutrient intake generally increased from 15 to 29 years and then declines from 30 to 49 years. Nonetheless, there was no significant difference between nutrient intake and the age of the respondents as shown in Table 3.

The mean haemoglobin (Hb) concentration was 12.1 [+ or -] 1.8 g/dL. Hb levels increased from 11.7 g/dL to 12.7 g/dL from the 20-29 year group to the 40-49 year group. However, this increase was not different among the various age groups (Table 4). Anaemia prevalence was 44.0% in this study population. Of this percentage, 35.8% were mildly anaemic, 6.7% were moderately anaemic and 1.5% were severely anaemic (Figure 1).

Figure 1: Anaemia prevalence among study participants

Anaemia prevalence increased during the early stages of the reproductive age (15-29 years). This was followed by a decline in anaemia rates towards the end of the reproductive age period (40-49 years). There was a significant difference in anaemia and non-anaemic rates within an age group (Figure 2).

There was a weak but positive relationship between Hb and age (r=0.175, p<0.05) (Table 5). With the exception of vitamin A, there was no significant association between Hb and the other haematopioetic nutrients. A weak inverse relationship was observed between Vitamin A intake and Hb. An increase in age of one year was significantly associated with a 0.056 g/dL rise in Hb level (Table 6). Also a unit increase in calorie intake was significantly associated with a 0.002 g/dL rise in Hb levels. Nonetheless, a unit rise in fat intake was associated with a 0.020 g/dL fold decrease in Hb level. Women who did not have sickle cell as compared to those with sickle cell were more likely to have an increase in their haemoglobin level by 0.580 g/dL fold.


Prevalence of iron deficiency anaemia (IDA) defined as low haemoglobin (Hb) concentration exceeded the threshold of 30.2% stated for non-pregnant and non-lactating women globally [8]. Anaemia prevalence in this study was 44.0%. The global anaemia prevalence of 48% estimated for non-pregnant non-lactating women of reproductive age in Central and West Africa [3] compares well with the 44% anaemia prevalence reported in this study. Nonetheless, the 2014 Ghana Demographic and Health Survey (GDHS) reported that 42% of women aged 15-49 years have some form of anaemia [4]. Anaemia prevalence reported in this study is similar to that reported by the GDHS in 2014 [4]. Anaemia is higher in the urban areas than the rural areas in Ghana [4]. The observed prevalence suggests that in the peri-urban areas anaemia prevalence is high just as in the urban areas. Most of the women are mildly anaemic and this may not contribute to mortality and morbidity but may negatively affect reproduction and productivity. This prevalence may be chronic considering that over 17% suffer from sickle cell disease [15]. In sickle cell, the circulating red blood cells (RBC) are fewer and have a lifespan of 10-20 days as compared to a normal RBC with a life span of 120 days. The presence of the sickle cell trait in some participants (17.2%) and a form of sickle cell disease (sickle cell haemoglobin C disease) in one participant could also contribute to anaemia rates in the study population. Both haemoglobinopathies can lead to haemolytic anaemia and because it is benign, its aetiology is different from nutrition related anaemia.

The cause of anaemia is multifactorial, the commonest being iron, folate, B12 and Vitamin A and C deficiencies, worm infestation and malaria as well as other infections and inflammations [6]. The high prevalence of anaemia in this study population could be attributed to the fact that Africa and for that matter Ghana is prone to malaria. Malaria contributes to anaemia by causing intravascular haemolysis with subsequent blood loss [6]. Also, malaria causes an immune response that suppresses erythropoietin and erythropoiesis [16].

The mean iron intake was 24 [+ or -] 12 mg, a value higher than the daily requirements, but iron bioavailability greatly depends on the dietary composition. Besides, in the absence of severe malnutrition or co-morbidity, the diet in itself infrequently causes IDA [6]. This is because increased intake of dietary factors such as polyphenols (examples: tea, coffee and so on), phytates (whole grains and cereals) and calcium (dairy products) reduce the bioavailability of non-heme iron [17, 18]. Probably heme iron intake of the women was low as reported in Nepal [19]. This is probably due to their low level of education and financial difficulties since most are engaged in low income generating activities (personal observation). In times of financial difficulty, carbohydrate intake may be maintained through alternative food sources that may be cheaper whilst affordability of micronutrient food sources may have been reduced [20]. More importantly, the absorption of nutrients that promote haemopoiesis can be affected by physiological and pathological factors. For example, helicobacter pylori is associated with reduced iron stores. It has also been documented that infections and inflammations inhibit iron absorption even if it is readily available in the diet [21].

The other nutritional causes of anaemia in this population are probably due to the low intake of folate and vitamin A rich foods. All the women did not meet their RDA for folate whilst only 25% met their RDA for vitamin A. Hodges et al. [22] demonstrated that, adult subjects maintained on vitamin A deficient diets developed anaemia despite adequate iron intakes. This observation confirms the results of this study since majority (74%) met their daily iron requirement as compared to the 25% who met their daily requirement for vitamin A. Folate deficiency will account for macrocytic anaemia whilst vitamin A deficiency will decrease Hb concentration. Vitamin A mechanism in anaemia is by the enhancement of growth and differentiation of erythrocyte progenitor cells and mobilization of iron stores from tissues [23]. Thus, the low protein status among some participants (35.8%) could also contribute to anaemia.

A weak correlation was observed between iron intake and Hb. This suggests that the aetiology of the anaemia is not due to iron alone but other causes such as folate and vitamin A. A similar weak positive correlation between Hb and iron intake was reported in another study [24]. In children, dietary iron intake from 9-11 months was associated with Hb concentration at 12 months but iron intake from 12-18 months was not associated with Hb concentration at 18 months [25].

In this study, there was a positive correlation between Hb and age (r=0.175, p=0.04; Table 5). It was realized that a year's increase in age was associated with a 0.056 g/dL increase in Hb concentration. This may be attributed to increased bone marrow haematopoiesis during the reproductive period. According to Kushang, Hb increases with age in WRA but a modest decline occurs after the reproductive age [26]. For the women in this study, Hb generally increased across their reproductive age group, which is in agreement with a study in rural India [27].

The negative correlation between vitamin A intake and Hb is at variance with what Zimmermann and his colleagues reported in 2006 [28]. This difference may be due to the amount of vitamin A consumed by the respondents in each of the studies. Whilst Zimmermann and his colleagues gave their study participants vitamin A supplements, the vitamin A intake reported in this study was from food, which had a lower concentration than the supplement.

Also a possible under-estimation could have resulted in the low vitamin A intake whilst over- estimation could have resulted in the high intake of carbohydrate and iron among the participants. This finding is in consonance with a similar study conducted by Schaefer et al. [29] using a food frequency questionnaire as is the case in this present study. Another study commented on the huge disparity between results of dietary assessment using food frequency questionnaire and those using the gold standards in a research they conducted [30]. Nonetheless, the challenge of underestimation or overestimation of food intake, which is associated with dietary assessment methods, is not different from the food frequency questionnaire used in this study. Underestimation and overestimation was minimised by using food models to help participants to estimate portion sizes. Another limitation of this study was that it was not possible to screen for malaria parasites and worm infections. Also, haemolytic anaemia and anaemia due to hormones and thalassemia were beyond the scope of this study. However, screening for sickle cell is one of the strengths of this study as most studies assessing Hb levels do not screen for it despite its strong effect on Hb values.


Anaemia due to iron deficiency exists as a public health problem among women in periurban settlements in the Ga-East Municipality, Accra, Ghana. Dietary diversity is important and needs to include green leafy vegetables which are rich in folate and provitamin A.


We thank the women for participating in the study. Firibu Kwesi Saalia, Matilda Steiner-Asiedu, Jinru Chen and Robert Dixon Philips designed the research; Isaac Agbemafle and Jacob Setorglo conducted the research; Firibu Kwesi Saalia, Matilda Steiner-Asiedu, Jinru Chen and Robert Dixon Philips provided essential reagents; Isaac Agbemafle, Firibu Kwesi Saalia, and Robert Dixon Philips performed the statistical analysis; Isaac Agbemafle wrote the paper. Isaac Agbemafle, Firibu Kwesi Saalia and Matilda Steiner-Asiedu had primary responsibility for the final content. All authors read and approved the final manuscript. We acknowledge funding from the Department of Food Science, University of Georgia, Griffin, USA.


[1.] IFAD/FAO/WFP The State of Food Insecurity in the World 2011. Rome, FAO (2011).

[2.] McLean E, Cogswell M, Egli I, Wojdyla D and B de Benoist Worldwide prevalence of anaemia, WHO Vitamin and Mineral Nutrition Information System, 1993-2005. Public Health Nutr. 2009; 12: 444-454.

[3.] Stevens GA, Finucane MM, De-Regil LM, Pacjorek CJ, Flaxman SR, Branca F, Pena-Rosas JP, Bhutta ZA and M Ezzati Global, regional, and national trends in haemoglobin concentration and prevalence of total and severe anaemia in children and pregnant and non-pregnant women for 1995-2011: a systematic analysis of population-representative data. Lancet Glob Health. 2013; 1: e16-25.

[4.] Ghana Statistical Service [GSS], Ghana Health Service [GHS], ICF Macro. Ghana Demographic and Health Survey 2014. Accra, 2008.

[5.] Rodriguez GA, Pozo E, Fernandez GR, Amo FJ and GT Nozal Hookworm as cause of iron deficiency anemia in the prison population. Rev Esp Sanid Penit. 2013; 15 (2): 63-65.

[6.] Miller JL Iron deficiency anemia: a common and curable disease. Cold Spring Harb Perspect Med. 2013; 3 (7): a011866.

[7.] Kalaivani K Prevalence and consequences of anaemia in pregnancy. Indian J Med Res. 2009; 130: 627-633.

[8.] WHO. Worldwide prevalence of anaemia 1993-2005: WHO Global Database on Anaemia. Geneva, 2008.

[9.] Fishman SM, Christian P and KP West The role of vitamins in the prevention and control of anaemia. Public Health Nutr. 2000; 3: 125-150.

[10.] Balarajan Y, Ramakrishnan U, Ozaltin E, Shankar AH and SV Subramanian Anaemia in low-income and middle-income countries. Lancet 2011; 378: 2123-2135.

[11.] Ghana Statistical Service. 2010 Population and Housing Census: Summary report of final results. Accra, 2012.

[12.] Daniels WW Biostatistics: A foundation for analysis in the health sciences. [7th edn], John Wiley and sons, New York, 1999.

[13.] Ike SO, Nubila T, Ukaejiofo EO, Nubila IN, Shu EN and I Ezema Comparison of haematological parameters determined by the Sysmex KX - 2IN automated haematology analyzer and the manual counts. BMC Clinical Pathology. 2010; 10 (1): 3-8.

[14.] Whitney E and SR Rolfes Understanding Nutrition. (12th edn). Wadsworth, Spain, 2011.

[15.] Langlois S, Ford J and D Chitayat Carrier screening for thalassemia and haemoglobinopathies in Canada. J Obstet Gynaecol Can. 2008; 30 (10): 950-959.

[16.] Skorokhod OA, Caione L, Marrocco T, Migliardi G, Barrera V, Arese P, Piacibello W and E Schwarzer Inhibition of erythropoiesis in malaria anaemia: Role of hemozoin and hemozoin-generated 4-hydroxynonenal. Blood 2010; 116: 4328-4337.

[17.] Zimmermann MB and RF Hurrell Nutritional iron deficiency. Lancet 2007; 370: 511-520.

[18.] Hurrell RF, Reddy M and JD Cook Inhibition of non-haem iron absorption in man by polyphenolic-containing beverages. Br J Nutr. 1999; 81: 289-295.

[19.] Gittelsohn J, Thapa M and LT Landman Cultural factors, caloric intake and micronutrient sufficiency in rural Nepali households. Soc. Sci. Med. 1997; 44: 1739-1749.

[20.] Skoufias E Income and micronutrient consumption in rural Mexico. World Bank, USA, 2006.

[21.] Vitale G, Barbaro F, Ianiro G, Cesario V, Gasbarrini G, Franceschi F and A Gasbarrini Nutritional aspects of Helicobacter pylori infection. Minerva Gastroenterol Dietol. 2011; 57: 369-377.

[22.] Hodges RE, Sauberlich HE and JE Canham Hematopoietic studies in vitamin A deficiency. Am J Clin Nutr. 1978; 31: 876-85.

[23.] Loukopoulos DL Haemoglobinopathies. Encyclopaedia of life sciences Macmillan Publishers Ltd, Nature Publishing Group, New York, 2002.

[24.] Shimakawa T, Warram JH, Herrera-Acena M and SA Krolewski Usual dietary intake and haemoglobin A1 levels in patients with insulin-dependent diabetes. J. Am Diab. Ass. 1993; 3 (12): 1409-1415.

[25.] Lind T, Hernell O, Lonnerdal B, Stenlund H, Domello M and LA Persson Dietary Iron intake is positively associated with haemoglobin concentration during infancy but not during the second year of life. J. Nutr. 2004; 134: 1064-1070.

[26.] Kushang PV Variability and heritability of haemoglobin concentration: an opportunity to improve understanding of anaemia in older adults. Haematologica 2008; 93(9):1281-1283.

[27.] Mishra P, Ahluwalia SK, Garg PK, Kar R and GK Panda The Prevalence of Anaemia among Reproductive Age Group (15-45 Yrs) Women in A PHC of Rural Field Practice Area of MM Medical College, Ambala, India. J. Women's Health Care 2012; 1 (3): 1000113. doi:10.4172/2167- 0420.1000113-1000115.

[28.] Zimmermann MB, Biebinger R, Rohner F, Dib A, Zeder C, Hurrell RF and N Chaouki Vitamin A supplementation in children with poor vitamin A and iron status increases erythropoietin and hemoglobin concentrations without changing total body iron. Am J Clin Nutr. 2006; 84: 580-586.

[29.] Schaefer EJ, Augustin JL, Schaefer MM, Rasmussen H, Ordovas JM, Dallal GE and JT Dwyer Lack of efficacy of a food-frequency questionnaire in assessing dietary macronutrient intakes in subjects consuming diets of known composition. Am J Clin Nutr. 2000; 71: 746-751.

[30.] Kristal AR, Peters U and JD Potter Editorial: Is it time to abandon the food frequency questionnaire? Cancer Epidemiol Biomarkers Prev. 2005; 14: 2826-2828.

DOI: 10.18697/ajfand.76.15685

Agbemafle I. (1*), Steiner-Asiedu M. (2), Saalia F.K. (2), Setorglo J. (3), Chen J. (4) and R.D. Philips (4)

Isaac Agbemafle

(*) Corresponding author email:

(1) School of Public Health, University of Health and Allied Sciences, Ho, Ghana

(2) Department of Nutrition and Food Science, University of Ghana, Legon, Ghana

(3) School of Medical Sciences, University of Cape Coast, Cape Coast, Ghana

(4) Department of Food Science, University of Georgia, Griffin, USA

Degrees of anaemia

SeA (<7.0g/dL)     1.5%
MoA (7-9.9g/dL)    6.7%
MiA (10-11.9g/dL)  35.8%
AFA (<12.0g/dL)    44.0%
NonA (=12.0g/dL)   56.0%

Key: SeA=Severe anaemix; MoA=Moderate anaemix, MiA=Mid anaemix;
AFA=All forms of anaemix; NonA=Non-anaemix

Figure 1: Anaemia prevalence among study participants

Note: Table made from bar graph.

Age groups (years)  Anaemia  Non-anaemic

15-19                45.0%     54.5%
20-29                54.0%     45.5%
30-39                32.3%     67.7%
40-49                23.5%     76.5%

Figure 2: Anaemia prevalence by age groups

Note: Table made from bar graph.

Table 1: Background characteristics of study participants (N=134)

Characteristics                      n (%)
Age (years)
  15-19                              20 (14.9)
  20-29                              66 (49.3)
  30-39                              31 (23.1)
  40-49                              17 (12.7)
Marital status
 Single                              62 (46.3)
 Married                             72 (53.7)
Level of education
 Senior High School                  21 (15.6)
 Junior High School/basic education  90 (67.2)
 None                                23 (17.2)
 Employed                            82 (61.2)
 Unemployed                          52 (38.8)
Sickling status
 Positive                            23 (17.2)
  Carrier                            22 (16.4)
  Sickle                             1 (0.7)
  Negative                           111 (82.8)

Table 2: Nutrient intake of study participants in comparison
to RDA (N=134)

Nutrient intake       RDA      Mean [+ or -] SD      Haemoglobin

Calories (kcal)    2000-2200  2315 [+ or -] 915  2257 [+ or -] 860
Protein (g)         50-82.5     67 [+ or -] 27     65 [+ or -] 24
Fats (g)            75-165      68 [+ or -] 30     70 [+ or -] 29
Iron (mg)            15-18      24 [+ or -] 12     23 [+ or -] 12
Folate ([micro]g)     400      119 [+ or -] 85    122 [+ or -] 71
Vit. A (IU)           500      218 [+ or -] 37    160 [+ or -] 36
Vit. C (mg)          40-45      92 [+ or -] 71     91 [+ or -] 61

Nutrient intake    Haemoglobin classification
                      Non-Anaemic      p-value

Calories (kcal)    2361 [+ or -] 960    0.52
Protein (g)          68 [+ or -] 29     0.46
Fats (g)             67 [+ or -] 30     0.53
Iron (mg)            24 [+ or -] 12     0.65
Folate ([micro]g)   116 [+ or -] 95     0.71
Vit. A (IU)         292 [+ or -] 65     0.06
Vit. C (mg)          92 [+ or -] 79     0.98

RDA- recommended dietary allowance (Whitney and Rolfes [14])

Table 4: Mean haemoglobin concentration of the women by age groups

Age groups (years)  Haemoglobin (g/dL)

      15-19         12.1 [+ or -] 1.1
      20-29         11.7 [+ or -] 2.0
      30-39         12.3 [+ or -] 1.9
      40-49         12.7 [+ or -] 1.2
      Total         12.1 [+ or -] 1.8
     p-value               0.13

Table 5: Correlation between haemoglobin, age and nutrient intake

Variables          Haemoglobin (g/dL) r   p-value

Age (years)                0.18            0.043 (*)
Calories (kcal)            0.09            0.33
Proteins (g)               0.08            0.34
Fats (g)                  -0.04            0.62
Iron (mg)                  0.09            0.28
Folate ([micro]g)         -0.02            0.79
Vit. A (IU)               -0.24            0.006 (*)
Vit. C (mg)               -0.02            0.80

(*) Significant at p<0.05

Table 6: Linear regression showing the association between
haemoglobin and nutrient intake and age of respondents

Variable                       Regression       95% Confidence
                          Coefficient ([beta])      Lower

Age (years)                       0.06               0.01
Caloric intake                    0.00               0.00
Protein intake (g)               -0.01              -0.04
Fat intake (g)                   -0.02              -0.04
Iron intake (mg)                 -0.05              -0.12
Folate intake ([micro]g)         -0.00              -0.01
Vit. A intake (IU)               -0.00              -0.00
Vit. C intake (mg)                0.00              -0.01
Sickle cell
Positive                          1.00            Reference
Negative                          0.58              -0.22

Variable                  Interval  p-value

Age (years)                 0.08    0.014 (*)
Caloric intake              0.00    0.012 (*)
Protein intake (g)          0.02    0.52
Fat intake (g)              0.00    0.045 (*)
Iron intake (mg)            0.01    0.08
Folate intake ([micro]g)    0.00    0.49
Vit. A intake (IU)          0.00    0.002 (*)
Vit. C intake (mg)          0.00    0.75
Sickle cell
Negative                    1.37    0.15

Adjusted [R.sup.2]=0.11; (*) Significant at p<0.05
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Author:I., Agbemafle; M., Steiner-Asiedu; F.K., Saalia; J., Setorglo; J., Chen; Philips, R.D.
Publication:African Journal of Food, Agriculture, Nutrition and Development
Article Type:Report
Geographic Code:6GHAN
Date:Nov 1, 2016
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