Abstract
Background
Zinc deficiency has been associated with increased incidence, severity and duration of childhood diarrhoea.
Objective
The objective of the study was to determine the prevalence of zinc deficiency among under-five children with acute diarrhoea.
Methods
The study was a comparative cross-sectional study in which serum zinc levels were determined using atomic absorption spectrometry in under-five children with acute diarrhoea and in apparently healthy contols. Two hundred and fifty children with acute diarrhoea and 250 controls were studied at the Wesley Guild Hospital, Ilesa, Nigeria.
Results
The diarrhoea patients had a mean ± SD serum zinc level of 78.8 ± 35.6 µg/dl, while the controls had a mean of 107.3 ± 46.8 µg/dl. The mean serum zinc level was significantly lower in the patients than the controls (t = -7.66; p < 0.001). Furthermore, the prevalence of zinc deficiency was significantly higher among the patients (30.4% versus 12.4% in the controls; OR = 3.09; 95% CI = 1.94 – 4.90; χ2 = 24.08; p < 0.001). Low social class was associated with a significantly higher prevalence of zinc deficiency among the patients (p = 0.013).
Conclusion
Zinc deficiency is significantly associated with diarrhoea among under-five children in the study community. Hence, routine zinc supplementation should be encouraged for the treatment of diarrhoea, and availability should be ensured.
Keywords: Zinc deficiency, diarrhoea, children, Nigeria
Introduction
Diarrhoeal disease represents a major public health problem, accounting for almost 10 percent of under-five deaths, with an estimated 0.6 million deaths per year globally.1 In Nigeria, diarrhoea accounts for about 16 percent of under-five mortality, with an estimated 150,000 deaths annually.2 Zinc is an essential micronutrient that is important for growth and development as well as immune function.3 Zinc deficiency contributes substantially to the morbidity and mortality of young children throughout the world.4 It is particularly common in developing countries because the commonly consumed staple foods have low zinc contents and are rich in phytates. Phytates bind zinc and inhibit its absorption, resulting in lower bioavailability of zinc from such food items.4,5 A national survey in Nigeria showed that 20% of under-five children were zinc deficient.6
Zinc deficiency is associated with increased occurrence, severity and prolongation of diarrhoeal illnesses in children, resulting in increased morbidity and mortality.7 A vicious cycle operates between diarrhoea and zinc deficiency such that diarrhoea reduces net absorption of zinc and other nutrients due to rapid intestinal transit and deterioration of the absorptive mucosa. On the other hand, zinc deficiency impairs absorption of water and electrolytes as well as clearance of aetiologic pathogens, thus delaying the termination of normally self-limiting diarrhoea episodes.8
Zinc supplementation has been recommended for the treatment of diarrhoea by the World Health Organization (WHO) and United Nations Children's Fund (UNICEF) since year 2004,9 yet access to this essential treatment remains limited in many countries.10 Low rates of prescription of zinc for childhood diarrhoea by healthcare workers have previously been reported in Nigeria.11 Hence, children who are zinc-deficient may sometimes be deprived of this vital treatment, despite visiting health care facilities for the treatment of diarrhoea.
There have been very few studies geared towards investigating the relationship between zinc deficiency and diarrhoea among Nigerian children, and such studies are not generalizable to other parts of the country because staple foods and their zinc contents vary among different communities.5 Children suffering from diarrhoeal diseases are frequently from low socioeconomic class,12 and may therefore be at a disadvantage for consuming zinc-rich food items, which are usually expensive.5 Furthermore, zinc supplements were not readily available in most of the pharmacy shops in the study community prior to commencement of the present study. The study was therefore carried out to assess the burden of zinc deficiency in our community, especially in relation to diarrhoeal diseases, with the ultimate aim of reducing the morbidity and mortality associated with diarrhoea.
Methods
The study was a comparative cross-sectional study involving under-five children with acute diarrhoea. Acute diarrhoea was defined as the passage of unusually loose or watery stools, at least three times in a 24 hour period, with duration less than 14 days. The subjects were children between the ages of six to 59 months who had presented with acute diarrhoea. They were recruited consecutively at the under-five welfare clinic and the children's emergency ward of the Wesley Guild Hospital (WGH), Ilesa, Osun State, Nigeria. The WGH is one of the units of the Obafemi Awolowo University Teaching Hospitals' complex (OAUTHC), Ile-Ife, Osun state, Nigeria.
Sample size was estimated using the formula for estimating proportions,13 with prevalence of zinc deficiency taken as 20%,6 sampling error as 5% and confidence interval as 95%. Children with severe undernutrition (z-score below -3 on a WHO growth chart, or presence of oedema), sepsis, sickle cell anaemia and HIV infection were excluded from the study, as these conditions have been associated with zinc deficiency.14–17 Retroviral screening was done for all the children, while relevant investigations were done to exclude sepsis or sickle cell anaemia, only in children who had suggestive history or examination findings. Apparently healthy children without diarrhoea were recruited as controls and were matched for age and sex with the subjects. The controls were recruited from the under-five welfare clinic of the WGH. They included children who presented for immunization or routine blood tests such as haemoglobin genotype.
Ethical clearance was obtained for the study from the Ethics and research committee of the Obafemi Awolowo University Teaching Hospitals' complex (OAUTHC). A written informed consent was obtained from the parent (s) or the accompanying guardian of each of the study participants. History about the nature and duration of diarrhoea as well as socio-economic background were obtained and all the patients were examined. The children were classified into those from high and low social class based on the occupation and highest level of education of their parents.18 Anthropometric measurements including weight and height/length were obtained for the assessment of nutritional status and the WHO child growth standards in form of z-scores19 were used to classify the nutritional status of the children. Children who had z-score < -2, but ≥ -3, were considered to be underweight, stunted or wasted, using the appropriate WHO growth chart. Signs of dehydration were documented when present. The degree of dehydration was subsequently classified as mild, moderate or severe according to ‘the guide to clinical assessment of dehydration’.20 Blood samples were collected for zinc assay at presentation, and the serum was separated by centrifugation at 3000 revolutions per minute using a clinical macro-centrifuge. Laboratory quality control was ensured by applying standard clotting times before separation of blood in order to prevent haemolysis, and also by adequate centrifugation procedures to ensure removal of all blood cells, as well as proper storage/refrigeration of serum samples before analysis. Serum zinc levels were determined using atomic absorption spectrophotometry (AAS) at the Central Science Laboratory of the Obafemi Awolowo University, Ile-Ife, Nigeria. The AAS machine used was AAnalyst 400 model by PerkinElmer. Values of serum zinc less than 65 µg/dl were considered low as recommended by the IZiNCG (International zinc nutrition consultative group),21 and such were classified as zinc deficiency.
Data analysis was done using the statistical programme for social sciences (SPSS) version 16.0. Means and standard deviations (SD) were computed for continuous variables while proportions were calculated for discrete variables. Means were compared using the independent samples t-test (t), while proportions were compared using the Pearson's chi-square test (χ2). Probability values (p) <0.05 were accepted as statistically significant.
Results
Of the 250 diarrhoea patients, 147 (58.8%) were males and 103 (41.2%) were females. Their ages ranged from six to 56 months with mean and standard deviation (SD) of 16.6 ± 9.4 months. The controls had a mean age ± SD of 16.6 ± 9.3 months. Table I shows a comparison of the socio-economic and nutritional status of the patients and controls. A significantly higher proportion of the patients were from low social class, compared with the controls (p <0.001). Underweight, stunting and wasting were also more prevalent among the patients (p = 0.002, 0.009 and 0.006, respectively).
Table I.
Socio- economic/ Nutritional status |
Subjects n (%) |
Controls n (%) |
Total n (%) |
Statistical comparison |
Social class | ||||
Low | 204 (81.6) | 167 (66.8) | 371 (74.2) | χ2 = 14.30, |
High | 46 (18.4) | 83 (33.2) | 129 (25.8) | p <0.001 |
Total | 250 (100.0) | 250 (100.0) | 500 (100.0) | |
Underweight | ||||
Underweight | 45 (18.0) | 21 (8.4) | 66 (13.2) | χ2 = 10.05, |
Normal | 205 (82.0) | 229 (91.6) | 434 (86.8) | p = 0.002 |
Total | 250 (100.0) | 250 (100.0) | 500 (100.0) | |
Stunting | ||||
Yes | 36 (14.4) | 18 (7.2) | 54 (10.8) | χ2 = 6.73, |
No | 214 (85.6) | 232 (92.8) | 446 (89.2) | p = 0.009 |
Total | 250 (100.0) | 250 (100.0) | 500 (100.0) | |
Wasting | ||||
Yes | 44 (17.6) | 23 (9.2) | 67 (13.4) | χ2 = 7.60, |
No | 206 (82.4) | 227 (90.8) | 433 (86.6) | p = 0.006 |
Total | 250 (100.0) | 250 (100.0) | 500 (100.0) |
The mean ± SD duration of diarrhoea at presentation was 3.4 ± 2.5 days with the duration ranging from one to 13 days. The number of episodes of watery stool per day ranged from three to 12 episodes with a mean ± SD of 4.9 ± 2.2. A history of fever was present in 182 (72.8%) of the patients, while 151 (60.4%) had one or more episodes of vomiting. Reduction in urinary output was reported in 17 (6.8%) of them. One hundred and eighty-two (72.8%) of them had no evidence of dehydration while 36 (14.4%) had mild dehydration, 20 (8.0%) moderate dehydration, and 12 (4.8%) severe dehydration. Table II shows the mean and classification of serum zinc levels in the patients and controls. The mean ± SD serum zinc level in the diarrhoea patients was significantly lower than that of the controls (t = -7.66; p <0.001). Furthermore, the prevalence of zinc deficiency was significantly higher among the patients than the controls (χ2 = 24.08; p <0.001; OR = 3.09; 95% CI = 1.94 – 4.90).
Table II.
Serum zinc | Patients (n = 250) |
Controls (n = 250) |
Statistical comparison |
Mean ± SD (µg/dl) | 78.8 ± 35.6 | 107.3 ± 46.8 | t = − 7.66; p <0.001 |
Low | 76 (30.4%) | 31 (12.4%) | |
Normal | 174 (69.6%) | 219 (87.6%) | χ2 = 24.08; p <0.001 |
There was no significant correlation between serum zinc levels and duration of diarrhoea (r = -0.01, p = 0.943) or stool frequency (r = 0.01, p = 0.845). Table III shows the relationships between zinc deficiency and other variables among the diarrhoea patients. Fever and low social class were associated with a significantly higher prevalence of zinc deficiency among the patients (p = 0.018 and 0.013, respectively). There was no significant difference in the prevalence of zinc deficiency between patients that were underweight and those who were not (p = 0.637). Similarly, there was no statistically significant difference in the prevalence of zinc deficiency in relation to stunting (p =0.983), wasting (p = 0.558), vomiting (p = 0.097) or the presence of dehydration (p = 0.409) among the patients (Table III). Nevertheless, the prevalence of zinc deficiency was significantly higher among the severely dehydrated patients, compared with those who had mild or moderate dehydration (p = 0.044).
Table III.
Parameter | Zinc status | Statistical comparison | ||
Zinc- deficient n (%) |
Normal n (%) |
Total n (%) |
||
Socio-economic status | ||||
Low social class | 69 (33.8) | 135 (66.2) | 204 (100.0) | χ2 = 6.14, p = 0.013 |
High social class | 7 (15.2) | 39 (84.8) | 46 (100.0) | |
Fever | ||||
Yes | 119 (65.4) | 63 (34.6) | 182 (100.0) | χ2 = 5.62, p = 0.018 |
No | 55 (80.9) | 13 (19.1) | 68 (100.0) | |
Vomiting | ||||
Yes | 111 (73.5) | 40 (26.5) | 151 (100.0) | χ2 = 2.76, p = 0.097 |
No | 63 (63.6) | 36 (36.4) | 99 (100.0) | |
Underweight | ||||
Underweight | 15 (33.3) | 30 (66.7) | 45 (100.0) | χ2 = 0.22, p = 0.637 |
Normal | 61 (29.8) | 144 (70.2) | 205 (100.0) | |
Stunting | ||||
Yes | 11 (30.6) | 25 (69.4) | 36 (100.0) | χ2 = 0.00, p = 0.983 |
No | 65 (30.4) | 149 (69.6) | 214 (100.0) | |
Wasting | ||||
Yes | 15 (34.1) | 29 (65.9) | 44 (100.0) | χ2 = 0.34, p = 0.558 |
No | 61 (29.6) | 145 (70.4) | 206 (100.0) | |
Dehydration status | ||||
Dehydrated | 18 (26.5) | 50 (73.5) | 68 (100.0) | χ2 = 0.68, p = 0.409 |
No signs of dehydration |
58 (31.9) | 124 (68.1) | 182 (100.0) | |
Severity of dehydration | ||||
Mild | 10 (27.8) | 26 (72.7) | 36 (100.0) | χ2 = 6.23, p = 0.044 |
Moderate | 2 (10.0) | 18 (90.0) | 20 (100.0) | |
Severe | 6 (50.0) | 6 (50.0) | 12 (100.0) |
Among the controls, underweight status (33.3% underweight versus 10.5% non-underweight were zinc-deficient, χ2 = 9.25, p = 0.002) and wasting (34.8% versus 10.1%, χ2 = 11.68, p = 0.001) were significantly associated with a higher prevalence of zinc deficiency, whereas, stunting (p = 0.189) and low social class (p = 0.486) were not.
The three patients who died in the course of the study all had a combination of zinc deficiency, severe dehydration and multiple electrolyte derangements.
Discussion
The mean serum zinc levels of the diarrhoea patients (78.8 ± 35.6 µg/dl) was significantly lower than that of the controls (107.3 ± 46.8 µg/dl) in the present study. The prevalence of zinc deficiency was also higher in the patients (30.4% versus 12.4% in the controls). This finding is in keeping with those of the studies by Okolo et al22 and Rani et al23 who also reported lower serum zinc levels in children with diarrhoea. The prevalence of zinc deficiency among the patients in the present study suggests that zinc deficiency is quite common among children with diarrhoea in the study community. In addition, the fact that more than one-tenth of apparently healthy children in the study had zinc deficiency, which could put them at risk of diarrhoea and other problems associated with zinc deficiency, should be of concern. It would therefore be imperative to put in place programmes that will help to make zinc-rich foods more available and affordable to children in the study community so as to reduce the burden of zinc deficiency.
It is not surprising that a significantly higher proportion of the patients belonged to low social class, compared with the controls. This is probably related to the higher prevalence of factors such as poor hygiene, water shortage, poor weaning practices and undernutrition, which predispose to diarrhoea, among people from low social class.12 The higher prevalence of zinc deficiency among the ‘low social class’ group may be related to their restricted access to zinc-rich food items, such as red meat, which are usually expensive.5 Such families may be unable to afford these food items, thereby relying more on the cheaper food items such as cereals and legumes, which have low zinc bio-availability as a result of their high phytate content.5
The absence of a correlation between serum zinc levels and duration of diarrhoea, as well as frequency of passage of stools, may be due to variations in the premorbid body content of zinc in the patients. Diarrhoeal losses may not be immediately reflected in children who previously had relatively higher levels. On the other hand, haemoconcentration in dehydrated persons can result in apparently higher zinc levels.24 This might have contributed to the absence of a significant relationship between dehydration status and zinc deficiency in the present study. However, the higher prevalence of zinc deficiency among the severely dehydrated patients may be a reflection of the propensity of zinc deficiency for causing greater severity of diarrhoea.7 Malnutrition was not found to be a significant risk factor for zinc deficiency among children with diarrhoea. A possible reason for this finding is that diarrhoea itself, through zinc losses in the stools, could have been the precipitating factor for low zinc levels in non-malnourished patients.8
Although the prevalence of zinc deficiency among the controls is seemingly much lower than that reported from other parts of Nigeria,6,25,26 the differences may be more apparent than real because of differences in the definition of zinc deficiency. Using a cut-off value of 80 µg/dl, a national prevalence of 20% was reported from the Nigerian Nutrition survey in 2004,6 whereas using a cutoff value of 70 µg/dl, a prevalence of 21% was reported among 5–13 year old children in Lagos, Nigeria in 2011.25 However, using the same cut-off value of 65 µg/dl as in the present study, a prevalence of 41.5% (35% in urban areas and 48% in rural areas) was reported from under-five children in Imo State, Nigeria in 2011.26 The prevalence reported in Imo was even higher than that observed in children with diarrhoea in the present study (30.4%). The disparity could be related to differences in methods of analysis, as well as the health, socio-economic and nutritional status of the study participants, which were not specified in the Imo study. Differences in the zinc content of soils as well as staple foods across regions may also be contributory.5 The disparities in prevalence across these studies underscore the importance of the use of similar definitions or cut-off values in studies of the prevalence of trace element deficiencies. The IZiNCG recommends the adoption of a cut-off value of 65 µg/dl in the definition of zinc deficiency in children.21
Conclusion
The study showed that zinc deficiency is significantly associated with diarrhoea in under-five children in the study community. Thus, zinc supplementation should be encouraged in addition to oral rehydration therapy for the routine treatment of childhood diarrhoea, and availability should be ensured. The burden of childhood diarrhoeal diseases will thereby be reduced.
Limitations of the study
1. Patients and controls were not matched for socio-economic status.
2. Dietary zinc intake was not assessed in this study.
Conflict of interest
None declared.
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