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Brief Report

Zinc Deficiency among Lactating Mothers from a Peri-Urban Community of the Ecuadorian Andean Region: An Initial Approach to the Need of Zinc Supplementation

by
Camila Narváez-Caicedo
1,
Gabriela Moreano
1,
Bernardo A. Sandoval
1,2 and
Miguel Á. Jara-Palacios
1,*
1
Escuela de Medicina, Facultad de Ciencias Médicas de la Salud y de la Vida, Universidad Internacional del Ecuador, 170113 Quito, Ecuador
2
Servicio de Cirugía, Hospital Metropolitano, 170521 Quito, Ecuador
*
Author to whom correspondence should be addressed.
Nutrients 2018, 10(7), 869; https://doi.org/10.3390/nu10070869
Submission received: 26 May 2018 / Revised: 1 July 2018 / Accepted: 3 July 2018 / Published: 5 July 2018
(This article belongs to the Special Issue Breastfeeding and Human Lactation)
Versions Notes

Abstract

:
Zinc is an important mineral for biological and physiological processes. Zinc deficiency (ZD) is one of the most common micronutrient deficiencies worldwide and a crucial determinant of pregnancy outcomes and childhood development. Zinc levels and the zinc supplementation rate among lactating women have not been assessed neither in Ecuador nor in the Andean region. We conducted a pilot study including 64 mothers of infants between eight days to seven months old from a primary care center located in Conocoto, a peri-urban community of Quito, Ecuador. The mothers were interviewed and a fasting blood sample was taken to determine plasma zinc levels. The prevalence of ZD was calculated and compared with the prevalence of ZD among Ecuadorian non-pregnant non-lactating women, and the sample was analysed considering zinc supplementation during pregnancy. The prevalence of ZD among the participants was 81.3% (95% CI: 71.7–90.9), higher than the reported among non-pregnant non-lactating women (G2 = 18.2; p < 0.05). Zinc supplementation rate was 31.2%. No significant differences were found comparing the groups considering zinc supplementation. The insights obtained from this study encourage extending studies to document zinc levels and its interactions among breastfeeding women in areas with a high prevalence of ZD in order to determine the need of zinc supplementation.

1. Introduction

Zinc is an ubiquitous mineral within the body that has catalytic, structural, and regulatory biological functions [1]. This mineral is known to be an essential micronutrient for development and normal cell activity [2]. Zinc deficiency (ZD) is one of the most common micronutrient deficiencies worldwide, affecting around 2 billion people, especially among developing countries. ZD has important consequences especially during pregnancy, lactation, and childhood development [3,4].
In spite of the physiological adjustment, which increases the zinc absorption during pregnancy and lactation, women and children are still affected by zinc deficiency due to increased nutrient requirements [5,6]. During pregnancy, ZD can affect multiple systems and could increase the risk of infections, preeclampsia, miscarriages, and adverse fetal outcomes, such as fetal growth restriction, low weight at birth, neurological malformations, and/or neurological impairment [2,4,5,6,7,8,9,10,11]. If ZD in the mothers persists after birth, particularly if their infants are exclusively breastfed, adverse infant development outcomes may occur [2,8].
Approximately 82% of mothers around the world do not have an adequate zinc intake in their diet, but the prevalence of ZD during pregnancy worldwide has not been determined [12]. It has been reported a higher prevalence of zinc deficiency among pregnant, compared to non-pregnant, women in India (65; 41%), Ethiopia (56; 34%), and Pakistan (48; 42%) [13,14,15,16]. In lactating women, the prevalence of ZD varied widely among small cohorts from different countries, such as Indonesia (25%) and Vietnam (55%) [17,18].
In Ecuador, according to the Ecuadorian National Health and Nutrition Survey (ENSANUT-ECU, 2014), 56.1% (95% CI: 54.9–57.1) of women of reproductive age have ZD. Pregnant and lactating women were not sampled in this survey [19]. On the other hand, a study conducted previously by our research group, found a prevalence of ZD of 31.4% (95% CI: 17.1–48.6) in a small cohort of mothers of children with non-syndromic cleft lip with or without cleft palate. It is important to clarify that these women did not exclusively breastfed their babies due to the oral malformation [20].
Micronutrient deficiencies have been observed in Ecuador for at least two decades, particularly in vulnerable segments of the population [21]; in part, it could be affected by globalization through multiple pathways, such as urbanization, economic growth, trade, and investments [21,22]. Processes of urbanization are associated with higher inequality and changes in the food environment, subsequently affecting the nutritional status, especially in poor people who cannot afford food of high nutritional quality [22]. Nowadays, peri-urban areas of Quito are suffering accelerated urbanization, growing in population at a higher index than the urban area [23,24].
The suggested association between maternal zinc depletion and poor outcomes of pregnancy and lactation have raised the possibility of prevention by using supplementary zinc, but results of previous studies have not been conclusive and still need to be assessed, especially focusing on populations with low dietary zinc intake [25].
The objective of the present study was to assess plasma zinc (PZn) levels and zinc supplementation rate during pregnancy, among lactating women attending to a public care center from a peri-urban Andean community of Quito, Ecuador in order to make an initial approach to the zinc status of lactating women in the region.

2. Materials and Methods

2.1. Study Setting and Participants

Between October 2015 and July 2016, a case study series was conducted in order to determine the rate of ZD among Ecuadorian mothers who have a breastfeeding infant, lived in Conocoto, and attended to the Primary Health Centre of Conocoto for regular paediatric and/or gynaecological check-ups. This health center belongs to the Ministry of Public Health which offers its services to the general population especially to people who have no private or social insurance [26].
Conocoto is one of the 33 rural parishes of Quito, the capital of Ecuador, located in the Andean region. Today, it is a heterogeneous territory with extensively urbanized areas and a few rural neighbourhoods pressed by growing urbanization. According to the last national census conducted in 2010, in Conocoto there were 82,072 inhabitants of whom 42,381 were women, with a population density of 1594 people/km2 and a birth rate of 16.98 [27]. Of the 33 rural parishes of Quito, eight have been characterised as peri-urbans [23].
We collected pertinent clinical information and a single blood sample to quantify zinc levels from the mothers; after they read and signed an informed consent.
Inclusion criteria were women who lived in Conocoto and had a child who was being fed mainly with breast milk. By mainly, we mean that at the time of the interview at least 90% of the children’s diet was breast milk, but three or fewer times a week some of them received other types of foods, such as “coladas” (a beverage made out of water and any kind of cereal flour), water, or formula.
As exclusion criteria, we considered the following: diagnosis of any chronic disease, any malformation in the index child, use of oral contraceptives, consumption of alcohol, cigarettes or any recreational drug at any time, any respiratory or gastrointestinal infection during the fifteen days prior to sampling and use of pharmacological therapy within this period. Additionally, we excluded pregnant women, non-fasting women, women with any disability that interferes with sample collection, and women who consumed alcohol or performed extreme exercise the night before sampling, factors that were contemplated by ENSANUT-ECU. We followed these guidelines following the methodology of a previous report of our research group [20].
This study was conducted following the Declaration of Helsinki, approved by the Bioethics Committee of the Universidad Internacional del Ecuador and registered it under the number 04-2013.

2.2. Measurements

Maternal variables recorded were age, educational level, number of pregnancy check-ups, and intake of vitamin and mineral supplements. In regards to vitamin and mineral supplements, we asked at what time during pregnancy they started consuming it, doses, frequency, and the form of the supplement ingested. Infant variables registered were age at the time of the interview, sex, weight at birth, length at birth, and gestational age at birth. The weight, length, and gestational age at birth were obtained from hospital records. All other information was based on self-report by the mothers.

2.3. Collection of Blood Samples and Determination of Zinc Levels

A single blood sample was obtained between 8 and 10 a.m. from fasting mothers using tubes coated with lithium heparin and a gel separator (BD Vacutainer® PSTTM, Becton-Dickinson Inc, Franklin Lakes, NJ, USA). The tubes were centrifuged for 10 min and refrigerated at 2–8 °C during 3–6 h. In the laboratory, the plasma was separated into additional tubes and stored at −80 °C. Plasma samples contaminated with lysed red blood cells were discarded. Then, prior to zinc quantification, the refrigerated samples were thawed at room temperature (20–24 °C), and mixed with a vortex. PZn were measured by flame-atomic-absorption spectrophotometry (AAnalyst 400, PerkinElmert, Billerica, MA, USA), the coefficient of variation for the essay was 6.2%. A standard solution of zinc in 1000 ± 4 mg/L of nitric acid (Fluka™ Analytical, Steinheim, Germany) (2% p/p) was used for the calibration curve with dilutions from 25 to 300 ppb. All chemicals were of analytical grade purity (Type I water, nitric acid 69%). Zinc quantification of all the samples was performed at the same time in dust-free fume hoods with minimal contact with air. We followed the same criteria that in our previous report [20].
Previous reports suggest 10.70 µmol/L as the cut-off point for zinc deficiency in fasting females over 10 years-old [6,28], and this value was utilized as the cut-off point by ENSANUT-ECU [19]. Therefore, we adopted this cut-off point in order to determine ZD in the present study and to compare it with the general population of Ecuadorian women of reproductive age.

2.4. Data Processing

The sample was evaluated as one group and divided in two subgroups based on the mothers’ declaration of zinc consumption during pregnancy. The data were analyzed using the Statistical Package for Social Science (SPSS) Statistics for Windows, version 20.0 (IBM Corp., Armonk, NY, USA). Correlations were assessed by Spearman’s rho, and p < 0.05 was considered as statistical significant. The t-test was used to compare the plasma zinc level means of the supplemented and non-supplemented groups.
In order to compare the prevalence of ZD in our sample with the reported among women of reproductive age by ENSANUT-ECU, we used the likelihood ratio and its corresponding statistic (G2); p < 0.05 was considered as statistical significant.

3. Results

We collected data and blood samples from 64 mothers, 3.2 (1.8) months postpartum. The mothers were between 15 and 39 years old with a mean age of 26.8 (6.4) years old. The majority of their infants were full-term (93.8%), and had adequate weight (76.6%) and length (62.5%) at birth (Table 1).
The percentages of women who consumed folic acid, iron, and zinc during pregnancy were 96.9%, 93.8%, and 31.2%, respectively (Table 1). The participants who reported ingesting zinc during pregnancy affirmed to have consumed zinc as part of a multivitamin supplement, but the majority of them were not able to accurately provide the doses and frequency of the supplements consumed and it was not possible to analyze this data.
The PZn levels were between 3.9 to 13.0 µmol/L, the mean PZn concentration was 9.3 (1.8) µmol/L. The first, second, third, and fourth quartiles were 8.1, 9.2, 10.3, and 13.0 µmol/L, respectively. We found ZD in 52 women with a prevalence of ZD of 81.2% (95% CI: 71.7–90.9), which is statically different to the reported among women of reproductive age by ENSANUT-ECU of 56.1% (95% CI: 54.9–57.1) (G2 = 18.23; p < 0.05) [19]. There was no difference between the means of plasma zinc levels of the supplemented and non-supplemented groups (t = 1.34; p > 0.05).

4. Discussion

The prevalence of ZD worldwide is unknown. Nevertheless, a global inadequate zinc intake rate of 17.3% has been estimated with a high geographical variation. The Andean region, which Ecuador is part of, has an estimated inadequate zinc intake of 17.0% [29]. ZD is widespread especially among developing countries affecting mainly children, and pregnant and lactating women [2,3,5,9], and it is expected to especially affect people living in areas of high urbanization that have been associated with higher levels of inequality and subsequent micronutrient deficiencies [21,22].
Many studies have found that ZD is higher among pregnant than non-pregnant women [13,14,15,16] and that zinc levels between pregnancy and postpartum periods do not differ significantly [30], which raises the need to evaluate zinc status among pregnant and lactating women in Ecuador, where high rates of ZD have been reported [19].
In Ecuador, the prevalence of ZD reported by ENSANUT-ECU among women of reproductive age from the general population is 56.1% and varies across the country, being higher in the urban coast (62.9%) and lower in the rural highlands (46.6%). In Quito, the prevalence of ZD is 55.6% [19].
Our results showed a higher prevalence of ZD among lactating women than in non-pregnant non-lactating women of reproductive age reported by ENSANUT-ECU [19], which agrees with previous reports from India, Ethiopia, and Pakistan. However, it is worth clarifying that the studies performed in Ethiopia and Pakistan evaluated zinc deficiency in both groups which were part of the same cohort [14,15,16]. Additionally, it is important to note that we are comparing two groups with different physiological status because lactating women are in a period of high metabolic demand in order to supply milk for their offspring [5,6].
Another factor that could be related to the high prevalence of ZD in our sample is the fact that nearly all the participants received iron supplements during pregnancy. The competition between iron and zinc absorption is well known, which means that PZn levels will be lower when iron is concurrently supplemented [6,31,32].
Although a mother with ZD most likely would have breast milk with a normal zinc concentration due to a physiological adjustment that tries to supply enough zinc for their offspring, it has been found that children of mothers with profound ZD are at risk of ZD and its consequences [17,31,33]. Therefore, an adequate zinc nutrition is necessary for normal pregnancy outcomes, child growth, adequate immune function and neurocognitive development [2,4,5,7,8,9,10,11]. We could not find any association between maternal zinc levels, zinc supplementation, and the anthropometry of their infants at birth, probably because our sample was small with the majority having ZD; nevertheless, the rates of ZD, premature delivery, and low weight and length at birth are not negligible [11]. Despite this, comparing the groups based on the declaration of zinc ingestion during pregnancy, we observed a slightly lower prevalence of zinc deficiency among the supplemented group than the non-supplemented group which was not statistically significant. The aforementioned statements raise the necessity to extend studies in order to assess the need of zinc supplementation among lactating women in disadvantaged groups with similar conditions.
Zinc supplementation has proven to reduce the rate of premature delivery, and improve linear growth and weight gain, especially in children of short stature, and decrease morbidity, duration, and severity of diarrhea and acute lower respiratory infection [1,8,34]. Supplementing zinc during pregnancy and lactation increases the mothers’ PZn concentration by 3% and 1%, respectively, which could protect the mothers’ nutritional status and, therefore, their children during these periods of life [35].
In spite of the aforementioned health zinc benefits, the World Health Organization (WHO) recommends zinc supplementation for pregnant women only in the context of rigorous research due to the moderate to low certainty evidence related to maternal, fetal, and neonatal outcomes, and no guidelines for zinc supplementation during lactation exist [7,36]. Nevertheless, we found that 31.2% of the participants were supplemented with zinc during pregnancy and suspended after delivery. Maternal zinc supplementation during lactation has yielded inconsistent results regarding the improvement of breast milk zinc concentrations or to demonstrate benefits for mothers and their infants [37,38]; however, considering the high rates of ZD among lactating women, it is worth extending studies to address the need of zinc supplementation identifying a profile of mothers that could benefit from this.
It is important to mention that in a previous report following the same methodology, we evaluated PZn levels in a cohort of 35 women who had a child between 1 and 12-months-old with an oral malformation, reporting a prevalence of ZD of 31.4; these results were probably due to the use of formula to feed the children because the oral malformation causes breastfeeding difficulties [20]. Lactation is a risk factor for zinc deficiency and the recommended dietary allowance is higher among pregnant and lactating women than in non-pregnant non-lactating women [6]. Therefore, the use of formula could have protected the mothers of children with the oral malformation from developing ZD in the postpartum period and could explain its lower ZD prevalence compared with the women of the present study.
Our study had several limitations. First, the sample corresponds to a small group of women from a single peri-urban community of Quito which does not allow extending these results, as the prevalence of zinc deficiency could differ by taking into account differences in socio-economic status or geographical location, however, this could be an example of what is happening among women from communities under pressure of accelerated urbanization where inequality levels are high [21,22].
Second, even though women who were going through any type of clinical infection or disease were excluded from the study, we did not assess any inflammatory marker, such as alpha 1 glycoprotein, C-reactive protein and interleukin-6; that would allow exclusion of women with an inflammatory process that could be related to decreased PZn [39,40]. It is also important to note that postpartum women, in general, have a more active immune system and higher serum levels of proinflammatory cytokines, and it is somewhat more active among breastfeeding than formula-feeding women [41]. Third, we were unable to register the doses, frequency, and forms of zinc ingested as, most of time, it was part of a multivitamin and mineral supplement; this did not allow for a deep analysis regarding zinc supplementation. Finally, we included only healthy women, therefore, this prevalence would likely increase if women with any comorbidity were included.
The results of this study raise the necessity to evaluate zinc supplementation during pregnancy and the extension to the lactation period in breastfeeding women who attend public care centers for their controls after delivery living in communities experiencing accelerated urbanization, such as Conocoto. Furthermore, we recommend extending studies in the Andean region and in areas with a suspected or confirmed high prevalence of ZD to document levels of zinc among breastfeeding women.

Author Contributions

M.Á.J.-P. conceived the study, analyzed and interpreted the results, helped draft the manuscript, and provided overall coordination of the study. C.N.-C. collected data, analyzed the results, and drafted the manuscript. G.M. collected data and helped draft the manuscript. B.A.S. participated in the study design and analyzed the results. All authors read and approved the final manuscript.

Funding

This research was funded by Universidad Internacional del Ecuador.

Acknowledgments

The authors wish to thank Angélica C. Cornejo for the critical review and Andrés A. Galvis for his help with the statistical analysis. We also thank David Acosta and the staff of the Public Medical Center of Conocoto who helped us planning the sampling, and to the mothers who participated in the study; contributing considerably.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Brown, K.H.; Wuehler, S.E.; Peerson, J.M. The importance of zinc in human nutrition and estimation of the global prevalence of zinc deficiency. Food Nutr. Bull. 2001, 22, 113–125. [Google Scholar] [CrossRef]
  2. Colombo, J.; Zavaleta, N.; Kannass, K.; Lazarte, F.; Albornoz, C.; Kapa, L.; Caulfield, L. Zinc supplementation sustained normative neurodevelopment in a randomized, controlled trial of peruvian infants aged 6–18 months. J. Nutr. 2014, 144, 1298–1305. [Google Scholar] [CrossRef] [PubMed]
  3. Bailey, R.L.; West, K.P.; Black, R.E. The epidemiology of global micronutrient deficiencies. Ann. Nutr. Metab. 2015, 66, 22–33. [Google Scholar] [CrossRef] [PubMed]
  4. Institute of Medicine (US) Committee on Micronutrient Deficiencies; Howson, C.P.; Kennedy, E.T.; Horwitz, A. Prevention of Micronutrient Deficiencies: Tools for Policymakers and Public Health Workers; National Academies Press (US): Washington, DC, USA, 1998. Available online: https://www.ncbi.nlm.nih.gov/books/NBK230107/ (accessed on 3 July 2018).
  5. Ejezie, F.E.; Nwagha, U.I. Zinc Concentration During pregnancy and Lactation in Enugu, South-East Nigeria. Ann. Med. Health Sci. Res. 2011, 1, 69–76. [Google Scholar] [PubMed]
  6. King, J.C.; Brown, K.H.; Gibson, R.S.; Krebs, N.F.; Lowe, N.M.; Siekmann, J.H.; Raiten, D.J. Biomarkers of Nutrition for Development (BOND)—Zinc Review. J. Nutr. 2016, 146, 858S. [Google Scholar] [CrossRef] [PubMed]
  7. Ota, E.; Mori, R.; Middleton, P.; Tobe-Gai, R.; Mahomed, K.; Bhutta, Z. Zinc supplementation for improving pregnancy and infant outcome. Cochrane Database Syst. Rev. 2012, 1–97. [Google Scholar] [CrossRef] [PubMed]
  8. Black, M. Zinc deficiency and child development. Am. J. Clin. Nutr. 1998, 68, 464S–469S. [Google Scholar] [CrossRef] [PubMed]
  9. Liu, J.; Hanlon, A.; Ma, C.; Zhao, S.R.; Cao, S.; Compher, C. Low blood zinc, iron, and other sociodemographic factors associated with behavior problems in preschoolers. Nutrients 2014, 6, 530–545. [Google Scholar] [CrossRef] [PubMed]
  10. Tamura, T.; Goldenberg, R.L.; Ramey, S.L.; Nelson, K.G.; Chapman, V.R. Effect of zinc supplementation of pregnant women on the mental and psychomotor development of their children at 5 years of age. Am. J. Clin. Nutr. 2003, 77, 1512–1516. [Google Scholar] [CrossRef] [PubMed]
  11. Wang, H.; Hu, Y.-F.; Hao, J.-H.; Chen, Y.-H.; Su, P.-Y.; Wang, Y.; Yu, Z.; Fu, L.; Xu, Y.-Y.; Zhang, C.; et al. Maternal zinc deficiency during pregnancy elevates the risks of fetal growth restriction: A population-based birth cohort study. Sci. Rep. 2015, 5, 11262. [Google Scholar] [CrossRef] [PubMed]
  12. Caulfield, L.E.; Zavaleta, N.; Shankar, A.H.; Merialdi, M. Potential contribution of maternal zinc supplementation during pregnancy to maternal and child survival 1–3. Am. J. Clin. Nutr. 1998, 68, 499S–508S. [Google Scholar] [CrossRef] [PubMed]
  13. Pathak, P.; Kapil, U.; Dwivedi, S.N.; Singh, R. Serum zinc levels amongst pregnant women in a rural block of Haryana state, India. Asia Pac. J. Clin. Nutr. 2008, 17, 276–279. [Google Scholar] [PubMed]
  14. Harika, R.; Faber, M.; Samuel, F.; Kimiywe, J.; Mulugeta, A.; Eilander, A. Micronutrient status and dietary intake of iron, Vitamin A, iodine, folate and zinc in women of reproductive age and pregnant women in Ethiopia, Kenya, Nigeria and South Africa: A systematic review of data from 2005 to 2015. Nutrients 2017, 9, 1096. [Google Scholar] [CrossRef] [PubMed]
  15. Akhtar, S. Zinc status in South Asian populations—An update. J. Health Popul. Nutr. 2013, 31, 139–149. [Google Scholar] [CrossRef] [PubMed]
  16. Bhutta, Z. Pakistan National Nutrition Survey 2011. Natl. Nutr. Surv. 2012, 1–84. Available online: http://www.mhinnovation.net/sites/default/files/downloads/innovation/research/Pakistan%20National%20Nutrition%20Survey%202011.pdf (accessed on 3 July 2018).
  17. Dijkhuizen, M.A.; Wieringa, F.T.; West, C.E.; Muherdiyantiningsih; Muhilal. Concurrent micronutrient deficiencies in lactating mothers and their infants in Indonesia. Am. J. Clin. Nutr. 2001, 73, 786–791. [Google Scholar] [PubMed]
  18. Nakamori, M.; Ninh, N.X.; Isomura, H.; Yoshiike, N.; Hien, V.T.T.; Nhug, B.T.; Nhien, N.V.; Nakano, T.; Khan, N.C.; Yamamoto, S. Nutritional status of lactating mothers and their breast milk concentration of iron, zinc and copper in rural Vietnam. J. Nutr. Sci. Vitaminol. 2009, 55, 338–345. [Google Scholar] [CrossRef] [PubMed]
  19. Freire, W.B.; Ramírez-Luzuriaga, M.J.; Belmont, P.; Mendieta, M.J.; Silva-Jaramillo, K.; Romero, N.; Sáenz, K.; Piñeiros, P.; Gómez, L.F.; Monge, R. Tomo I: Encuesta Nacional de Salud y Nutrición de la población ecuatoriana de cero a 59 años; ENSANUT-ECU 2012; Ministerio de Salud Pública/Instituto Nacional de Estadísticas y Censos: Quito, Ecuador, 2014. Available online: http://www.ecuadorencifras.gob.ec/documentos/web-inec/Estadisticas_Sociales/ENSANUT/MSP_ENSANUT-ECU_06-10-2014.pdf (accessed on 3 July 2018).
  20. Jara-Palacios, M.A.; Cornejo, A.C.; Narváez-Caicedo, C.; Moreano, G.; Vásquez, K.P.; Moreno-Izquierdo, C.; Romero-Sandoval, N. Plasma zinc levels in Ecuadorian mothers of infants with nonsyndromic cleft lip with or without cleft palate: A case series. Birth Defects Res. 2018, 495–501. [Google Scholar] [CrossRef] [PubMed]
  21. Freire, W.; Silva-jaramillo, K.; Ramírez-Luzuriaga, M.; Belmont, P.; Waters, W. The double burden of undernutrition and excess body weight in Ecuador. Am. J. Clin. Nutr. 2014, 100, 1636–1643. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  22. Schram, A.; Labonté, R.; Sanders, D. Urbanization and international trade and investment policies as determinants of noncommunicable diseases in sub-saharan Africa. Prog. Cardiovasc. Dis. 2013, 56, 281–301. [Google Scholar] [CrossRef] [PubMed]
  23. Pinto-Valencia, P. Las parroquias rurales de Quito y sus interrelaciones con el espacio urbano. Revista del Instituto de la Ciudad 2013, 2, 71–119. Available online: http://repositorio.flacsoandes.edu.ec/bitstream/10469/6454/1/REXTN-QUR5-03-Pinto.pdf (accessed on 3 July 2018).
  24. Diagnóstico del Territorio del Distrito Metropolitano de Quito. Unidad del Plan de Desarrollo y Ordenamiento Territorial del DMQ. Municipio del Distrito Metropolitano de Quito: Diagnóstico Estratégico-Eje Territorial. 2014. Available online: http://gobiernoabierto.quito.gob.ec/wp-content/uploads/documentos/pdf/diagnosticoterritorio.pdf (accessed on 3 July 2018).
  25. Mahomed, K.; James, D.K.; Golding, J.; McCabe, R. Zinc supplementation during pregnancy: A double blind randomised controlled trial. Br. Med. J. 1989, 299, 826–830. [Google Scholar] [CrossRef]
  26. Lucio, R.; Villacrés, N.; Henríquez, R. Sistema de salud de Ecuador. Salud Pub. Mex. 2011, 53, 177–187. [Google Scholar] [CrossRef]
  27. Gobierno Autónomo Descentralizado Parroquial de Conocoto. Plan De Desarrollo y Ordenamiento Territorial de Conocoto 2012–2025; Dirección de Gestión de Desarrollo Comunitario e Inclusión Social/Dirección de Gestión de Planificación: Quito, Ecuador, 2012. Available online: http://181.112.151.230:8081/attachments/download/558/PDOT%20CONOCOTO%202012.pdf (accessed on 3 July 2018).
  28. Hotz, C.; Peerson, J.M.; Brown, K.H. Suggested lower cutoffs of serum zinc concentrations for assessing zinc status: Reanalysis of the second National Health and Nutrition Examination Survey data (1976–1980). Am. J. Clin. Nutr. 2003, 78, 756–764. [Google Scholar] [CrossRef] [PubMed]
  29. Wessells, K.R.; Brown, K.H. 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, e50568. [Google Scholar] [CrossRef] [PubMed]
  30. Severi, C.; Hambidge, M.; Krebs, N.; Alonso, R.; Atalah, E. Zinc in plasma and breast milk in adolescents and adults in pregnancy and pospartum: A cohort study in Uruguay. Nutr. Hosp. 2013, 28, 223–228. [Google Scholar] [CrossRef] [PubMed]
  31. Donangelo, C.M.; King, J.C. Maternal zinc intakes and homeostatic adjustments during pregnancy and lactation. Nutrients 2012, 4, 782–798. [Google Scholar] [CrossRef] [PubMed]
  32. Swanson, C.A.; King, J.C. Zinc utilization in pregnant and nonpregnant women fed controlled diets providing the zinc RDA. J. Nutr. 1982, 112, 697–707. [Google Scholar] [CrossRef] [PubMed]
  33. Donangelo, C.M.; Vargas-Zapata, C.L.; Woodhouse, L.R.; Shames, D.M.; Mukherjea, R.; King, J.C. Zinc absorption and kinetics during pregnancy and lactation in Brazilian women. Am. J. Clin. Nutr. 2005, 82, 118–124. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  34. Bhutta, Z.A.; Black, R.E.; Brown, K.H.; Meeks-Gardner, J.; Gore, S.; Hidayat, A.; Khatun, F.; Martorell, R.; Ninh, N.X.; Penny, M.E.; et al. Prevention of diarrhea and pneumonia by zinc supplementation in children in developing countries: Pooled analysis of randomized controlled trials. J. Pediatr. 1999, 135, 689–697. [Google Scholar] [CrossRef]
  35. Moran, V.H.; Skinner, A.L.; Medina, M.W.; Patel, S.; Dykes, F.; Souverein, O.W.; Dullemeijer, C.; Lowe, N.M. The relationship between zinc intake and serum/plasma zinc concentration in pregnant and lactating women: A systematic review with dose-response meta-analyses. J. Trace Elem. Med. Biol. 2012, 26, 74–79. [Google Scholar] [CrossRef] [PubMed]
  36. World Health Organization (WHO). WHO Recommendation on Antenatal Care for a Positive Pregnancy Experience; WHO: Geneva, Switzerland, 2016. [Google Scholar]
  37. Krebs, N. Zinc supplementation during lactation. Am. J. Clin. Nutr. 1998, 510S–512S. [Google Scholar] [CrossRef] [PubMed]
  38. Sazawal, S.; Black, R.E.; Dhingra, P.; Jalla, S.; Krebs, N.; Malik, P.; Dhingra, U.; Bhan, M.K. Zinc Supplementation does not Affect the Breast Milk Zinc Concentration of Lactating Women Belonging to Low Socioeconomic Population. J. Hum. Nutr. Food Sci. 2013, 1, 1–6. [Google Scholar]
  39. Karakochuk, C.D.; Barr, S.I.; Boy, E.; Bahizire, E.; Tugirimana, P.L.; Akilimali, P.Z.; Houghton, L.A.; Green, T.J. The effect of inflammation on serum zinc concentrations and the prevalence estimates of population-level zinc status among Congolese children aged 6–59 months. Eur. J. Clin. Nutr. 2017, 71, 1467–1470. [Google Scholar] [CrossRef] [PubMed]
  40. MacDonell, S.O.; Miller, J.C.; Harper, M.J.; Reid, M.R.; Haszard, J.J.; Gibson, R.S.; Houghton, L.A. A comparison of methods for adjusting biomarkers of iron, zinc, and selenium status for the effect of inflammation in an older population: A case for interleukin 6. Am. J. Clin. Nutr. 2018, 932–940. [Google Scholar] [CrossRef] [PubMed]
  41. Groer, M.W.; Davis, M.W.; Smith, K.; Casey, K.; Kramer, V.; Bulovsky, E. Immunity, inflammation and infection in post-partum breast and formula feeders. Am. J. Reprod. Immunol. 2005, 54, 222–231. [Google Scholar] [CrossRef] [PubMed]
Table
Table 1. Plasma zinc levels, maternal and infant characteristics of zinc supplemented and non-supplemented women during their pregnancies (n = 64).
Table 1. Plasma zinc levels, maternal and infant characteristics of zinc supplemented and non-supplemented women during their pregnancies (n = 64).
Recorded VariablesAll the Sample
n = 64		Women Who Did Not Received Zinc Supplements
n = 44		Women Who Received Zinc Supplements
n = 20		ρ (Rho) de Spearmanp−Value
Maternal variables
Age (years, mean ± SD) *26.8 ± 6.526.1 ± 6.828.4 ± 5.70.170.17
Level of education (%)
 Elementary school only21.922.720.00.030.81
 High school or any superior level78.177.380.0
Number of prenatal check−ups (%)
 <56.26.85.00.040.79
 ≥593.893.295.0
Consumption of iron during pregnancy (%)
 Yes93.890.91000.170.17
 No6.29.10
Consumption of folic acid during pregnancy (%)
 Yes96.995.51000.120.34
 No3.14.50
PZn (µmol/L, mean ± SD) *9.3 ± 1.89.07 ± 1.79.72 ± 2.0
Zinc deficiency n (%)52 (81.2)37 (84.1)15 (75)−0.110.40
Infant variables
Infants’ age (months, mean ± SD) *3.2 ± 1.83.3 ± 1.83.0 ± 1.7
Sex (Male/Female)32/3222/2210/10
Gestational age at birth (%)
 37 weeks or more92.290.995.00.070.58
 Less than 37 weeks7.89.15.0
Weight at birth
 2500 g or more78.179.575.0−0.050.69
 Less than 2500 g21.920.525.0
Length at birth (%)
 48 cm or more62.561.465.00.040.79
 Less than 48 cm37.538.635.0
* t was calculated with non-statistical significant results. SD: Standard deviation.

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Narváez-Caicedo, C.; Moreano, G.; Sandoval, B.A.; Jara-Palacios, M.Á. Zinc Deficiency among Lactating Mothers from a Peri-Urban Community of the Ecuadorian Andean Region: An Initial Approach to the Need of Zinc Supplementation. Nutrients 2018, 10, 869. https://doi.org/10.3390/nu10070869

AMA Style

Narváez-Caicedo C, Moreano G, Sandoval BA, Jara-Palacios MÁ. Zinc Deficiency among Lactating Mothers from a Peri-Urban Community of the Ecuadorian Andean Region: An Initial Approach to the Need of Zinc Supplementation. Nutrients. 2018; 10(7):869. https://doi.org/10.3390/nu10070869

Chicago/Turabian Style

Narváez-Caicedo, Camila, Gabriela Moreano, Bernardo A. Sandoval, and Miguel Á. Jara-Palacios. 2018. "Zinc Deficiency among Lactating Mothers from a Peri-Urban Community of the Ecuadorian Andean Region: An Initial Approach to the Need of Zinc Supplementation" Nutrients 10, no. 7: 869. https://doi.org/10.3390/nu10070869

APA Style

Narváez-Caicedo, C., Moreano, G., Sandoval, B. A., & Jara-Palacios, M. Á. (2018). Zinc Deficiency among Lactating Mothers from a Peri-Urban Community of the Ecuadorian Andean Region: An Initial Approach to the Need of Zinc Supplementation. Nutrients, 10(7), 869. https://doi.org/10.3390/nu10070869

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