Hostname: page-component-8448b6f56d-c47g7 Total loading time: 0 Render date: 2024-04-16T19:30:43.659Z Has data issue: false hasContentIssue false

Anaemia, lead poisoning and vitamin D deficiency in low-income children: do current screening recommendations match the burden of illness?

Published online by Cambridge University Press:  10 February 2011

Margaret Kersey*
Affiliation:
Department of Pediatrics, University of Minnesota, Hennepin County Medical Center, G7, 701 Park Avenue South, Minneapolis, MN 55415, USA
Ming Chi
Affiliation:
Internal Medicine Residency, Saint Joseph's Hospital, Chicago, IL, USA
Diana B Cutts
Affiliation:
Department of Pediatrics, University of Minnesota, Hennepin County Medical Center, G7, 701 Park Avenue South, Minneapolis, MN 55415, USA
*
*Corresponding author: Email kerse003@umn.edu
Rights & Permissions [Opens in a new window]

Abstract

Objective

Low-income children are routinely screened for anaemia and elevated blood lead levels (EBLL) but not for vitamin D deficiency. We sought to determine the relative prevalence of and the relationship among vitamin D deficiency, anaemia and EBLL among healthy low-income paediatric clinic patients.

Design

Retrospective chart review.

Setting

Paediatric outpatient clinic in an urban safety net hospital in a northern US state.

Subjects

Healthy toddlers and children under 6 years of age (n 127) who were seen for a routine well child check-up (WCC).

Results

The prevalence of vitamin D insufficiency (25-hydroxyvitamin D (25(OH)D) < 30 ng/ml) was 62 %; the prevalence of vitamin D deficiency (25(OH)D < 20 ng/ml) was 29 %. These rates were far higher than those for anaemia (Hb < 11·0 g/dl) at 10 %, EBLL (Pb > 9 μg/dl) at 1 % or even mildly EBLL (Pb 5–9 μg/dl) at 4 % (range: 1–11). There was no relationship among any of the following: vitamin D status, anaemia or EBLL. The vast majority of children with vitamin D deficiency had both normal Hb (86 %) and Pb level (100 %). After controlling for child's age, gender and race/ethnicity, there was no association between Hb (continuous, g/dl) and vitamin D deficiency (adjusted OR (aOR) = 0·97, 95 % CI 0·64, 1·47; P = 0·88). The only significant predictor of vitamin D deficiency was increasing age in years (aOR = 1·39, 95 % CI 1·03, 1·86; P = 0·03). None of these associations changed materially when deficiency was defined as <15 ng/ml.

Conclusions

Vitamin D deficiency was far more common than anaemia or EBLL, and Hb and Pb status were not predictors of vitamin D status.

Type
Research paper
Copyright
Copyright © The Authors 2011

Considerable resources have been devoted to screening for anaemia and elevated blood lead levels (EBLL) among young low-income children. Despite increasing evidence that vitamin D deficiency may have serious adverse health effects and that many children in the USA are at risk of vitamin D deficiency(Reference Kumar, Muntner and Kaskel1Reference Ziegler, Hollis and Nelson4), no universal or even risk-based vitamin D screening recommendations have emerged to date.

We sought to determine the relative prevalence of and the relationship among vitamin D deficiency, anaemia and EBLL among healthy children in a low-income urban paediatric clinic population in a northern US state. Only one published study to date has examined the relationship between vitamin D deficiency and anaemia(Reference Sim, Lac and Liu5), and found a positive association between the two in adults. To our knowledge, this has not yet been studied in children.

Experimental methods

Study participants

A total of 127 children between the ages of 9 months and 5 years meeting study eligibility criteria with 25-hydroxyvitamin D (25(OH)D) levels measured at the Hennepin County Medical Center (HCMC) Pediatric Outpatient Clinic were assessed in the present study. HCMC is a safety net hospital in Minneapolis, MN (latitude 45°N), serving a low-income, urban, mostly non-white, largely immigrant (Latin American and East African) patient population. In all, 94 % of our paediatric clinic patients were either publicly insured (88 %) or uninsured (6 %) in 2009.

Partly because of reports of a high prevalence of vitamin D deficiency among adults at our institution, and other studies documenting a very high prevalence of vitamin D deficiency among darker-skinned immigrants to northern latitude countries(Reference McGillivray, Skull and Davie6Reference Hintzpeter, Scheidt-Nave and Muller8) and also among breast-fed infants in a neighbouring state(Reference Ziegler, Hollis and Nelson4), several paediatric practitioners began measuring 25(OH)D levels in asymptomatic patients. Paediatric patients considered to be at increased risk of vitamin D deficiency because of increased skin pigmentation and/or possible inadequate dietary intake assessed on the basis of diet history were screened by their paediatricians. Thus, the sample represents a subset of our clinic patients thought to be at higher risk.

A total of 253 children between the ages of 9 months and 5 years had a 25(OH)D level measured between May 2008 and June 2009. Because we were interested in healthy, asymptomatic children for this retrospective chart review, we restricted our analysis to those with a 25(OH)D level measured along with Hb and Pb at well child check-ups (WCC). Our standard practice is to measure both Hb and Pb levels at both 1- and 2-year WCC and at least one time thereafter for new patients with unknown levels up to the age of 5 years as per Medicaid (known in our state as MinnesotaCare) guidelines(9). Hb and Pb levels are occasionally measured at the 9-month rather than the 1-year WCC on the basis of clinical suspicion of increased Pb or nutritional risk.

The sample was further restricted by excluding those with chronic illness likely to interfere with vitamin D intake or metabolism, or any other physical findings consistent with vitamin D deficiency, including growth failure (<5 % weight-for-age), gross motor delay or genu varus. Children with any chronic nutritional or neurological condition likely to interfere with nutritional intake or absorption were excluded, as were any with haemoglobinopathies. A three-physician panel of general paediatricians (M.K., D.B.C. and M.H.) blinded to the potential participant's vitamin D status reviewed all cases in which there was any question about study eligibility. Children were deemed eligible if a majority (two out of three) of clinicians believed that a child's underlying medical condition or diagnosis was unlikely to be related to their vitamin D status.

The Institutional Review Board of the Human Subjects Research Committee at HCMC approved the protocol for this anonymous retrospective chart review since no protected health information, or potentially identifiable patient information, was collected.

Laboratory measurements

25(OH)D (ng/ml), Hb (g/dl) and Pb (μg/dl) levels were measured in our hospital clinical laboratory. 25(OH)D concentration was measured using RIA (DiaSorin, Stillwater, MN, USA). Because our laboratory does not report Pb levels below 2 μg/dl, any measured level below 2 μg/dl was recoded as 2 μg/dl. Thus, our estimates of Pb level overestimate the true values at the very lowest levels.

Definitions

The measurement and definition of vitamin D deficiency and its functional outcomes in children are hotly debated topics(Reference Greer10, Reference Holick11), and no consensus exists. For this analysis, vitamin D deficiency was defined as serum 25(OH)D <20 mg/ml(Reference Holick12Reference Cole, Grant and Tangpricha15); vitamin D insufficiency was defined as serum 25(OH)D <30 ng/ml(Reference Holick11, Reference Cole, Grant and Tangpricha15, 16). The more restrictive definition of deficiency as 25(OH)D <15 ng/ml as has been used by others(Reference Kumar, Muntner and Kaskel1) was also utilized.

Anaemia was defined using WHO criteria as Hb < 11·0 g/dl for ages 0·5–4·99 years and <11·5 g/dl for ages 5–11·99 years(Reference McLean, Cogswell and Egli17).

EBLL was defined using the definition of the Centers for Disease Control and Prevention (CDC) ≥10 μg/dl Pb. However, on the basis of evidence of Pb neurotoxicity even at levels <10 μg/dl(Reference Jusko, Henderson and Lanphear18, Reference Canfield, Henderson and Cory-Slechta19), we created a category that we called ‘mildly EBLL’, defined as Pb level ≥5 μg/dl but <10 μg/dl, based on the threshold reported by Jusko et al.(Reference Jusko, Henderson and Lanphear18) as a more sensitive measure of elevated risk.

Clinical and anthropometric data

Clinical data, including the patient's problem list and past medical history, diagnosis at current visit, height, weight and BMI percentile (BMI%ile) data, were extracted by chart review of the well child notes from our electronic health record (EHR). Race/ethnicity data were extracted from the demographics section of the EHR, which is originally determined by parental report, although we were unable to determine country of birth. We were also unable to extract usable data on vitamin D intake from the WCC notes since providers generally documented the type of milk (breast, formula, soya or cow's milk) consumed but not the volume, which prevented abstractors from determining whether the dietary intake was adequate. Similarly, although many infants and children had been prescribed a multivitamin, providers were inconsistent about documenting adherence unless there was a significant concern.

Statistical analysis

Analyses were conducted with the STATA statistical software package version 8·0 (StataCorp, College Station, TX, USA). Bivariate statistics were determined using χ 2 tests for categorical data, t tests for continuous variables with normal distributions and Pearson's product–moment correlations for pairwise correlations.

Multivariate logistic regression models were constructed with vitamin D status (‘deficient’ v. ‘not deficient’) as the outcome variable, Hb as the independent variable and relevant patient demographics and health status variables included as covariates. Both Hb and several of the demographic covariates were modelled in several different ways (i.e. Hb as both a continuous and categorical variable; age as continuous, multiple categorical and dummy variables). We were unable to include Pb as a predictor variable because of the narrow range of values found for serum Pb. Potentially confounding variables were assessed by serially adding and removing each variable to assess its effect on the point estimates and statistical significance of the remaining variables in the model. The final model was chosen on the basis of its parsimony and ease of interpretation (e.g. with Hb modelled as a continuous variable); its results did not differ materially from those of alternative models. 25(OH)D was also modelled as a continuous outcome for multivariate linear regression. For all analyses, P < 0·05 was considered statistically significant.

Results

The final sample consisted of 127 children (Table 1). The prevalence of vitamin D insufficiency (25(OH)D < 30 ng/ml) was 62 %; the prevalence of vitamin D deficiency (25(OH)D < 20 ng/ml) was 29 %. These rates were far higher than those for anaemia (Hb < 11·0 g/dl) at 10 %, EBLL (Pb > 9 μg/dl) at 1 % (one child, with a level of 11 μg/dl) or even mildly EBLL (level 5–9 μg/dl) at 4 %.

Table 1 Characteristics of the study population: low-income children under 6 years of age (n 127), Minnesota, USA

25(OH)D, 25-hydroxyvitamin D; EBLL, elevated blood lead levels.

*Data are mean, sd and range.

†Lead reported as median rather than mean because of right skew; values <2 are collapsed and thus reported as 2 for analysis.

We were unable to measure the effect of season of the year since our practitioners did not begin measuring vitamin D 25(OH)D levels in earnest until the winter of 2009, and the chart review was completed on 1 June 2009. Thus, 93 % of sampling occurred during the winter and spring months. In addition, although others have documented a higher risk of vitamin D deficiency among overweight patients, we did not measure the effect of weight status on vitamin D status, since age- and sex-specific BMI%ile data were available only for children aged ≥3 years, who comprised <50 % of our sample (forty-six out of 127).

There was no statistically significant relationship among any of the following outcomes: vitamin D status, anaemia or EBLL (Figs 1 and 2). Bivariate associations are shown in Table 2. Furthermore, the vast majority of children with vitamin D deficiency had both a normal Hb level (32/37 or 86 %) and a normal Pb level (37/37 or 100 %). Although elevated blood Pb can suppress Hb production and is thus an important risk factor for anaemia, this possible interaction was not tested in our sample since, according to CDC, blood Pb does not begin to suppress Hb until it reaches 25–40 μg/dl(16), which is far higher than even the highest blood Pb levels seen in our sample.

Fig. 1 Two-way scatterplot of vitamin D status and Hb level (n 127; r = 0·12; P = 0·18) among low-income children under 6 years of age (n 127), Minnesota, USA

Fig. 2 Two-way scatterplot of vitamin D status and lead level (n 127; r = 0·03; P = 0·71) among low-income children under 6 years of age (n 127), Minnesota, USA

Table 2 Associations of vitamin D deficiency and insufficiency among low-income children under 6 years of age (n 127), Minnesota, USA

25(OH)D, 25-hydroxyvitamin D; EBLL, elevated blood lead levels.

*P values for equal prevalence in all categories determined by the χ 2 statistic.

After controlling for child's age, gender and race/ethnicity, there was no association between Hb (continuous, g/dl) and vitamin D deficiency (adjusted OR (aOR) = 0·97; 95 % CI 0·64, 1·47; P = 0·88; Table 3). The only significant predictor of vitamin D deficiency was increasing age in years (aOR = 1·39; 95 % CI 1·03, 1·86; P = 0·03). None of these associations changed materially when deficiency was defined more restrictively at <15 ng/ml.

Table 3 Multivariate logistic regression model for vitamin D deficiency (25(OH)D < 20 ng/ml) among low-income children under 6 years of age (n 127), Minnesota, USA

25(OH)D, 25-hydroxyvitamin D; aOR, adjusted OR; ref., reference category.

25(OH)D was also modelled as a continuous outcome in multivariate linear regression. Age in years remained inversely associated with 25(OH)D level, with a −1·92 ng/dl change in 25(OH)D level for each increasing year of age (95 % CI −3·34, −0·48, P < 0·01). All other predictor variables (Hb, race/ethnicity and gender) remained non-significant (P > 0·10).

Discussion

This sample of low-income, at-risk urban young children had much higher rates of vitamin D deficiency than of either anaemia or EBLL, although study generalizability may be limited because of the far northern latitude of our state, the fact that the majority of blood sampling occurred in winter and spring and because of small sample size.

Our sample was likely too small in size and had too high a proportion of darkly pigmented children for variation to be examined by ethnicity. On the basis of the unpublished findings of our adult medicine colleagues, who documented a 94 % prevalence of vitamin D insufficiency in Somali Americans at our institution (D Pryce, personal communication), the prevalence of vitamin D deficiency among Somali-American toddlers in our clinic was much lower than we initially expected. However, we believe that this can be explained largely by our Somali mothers’ very low rates of exclusive breast-feeding, as a systematic chart review at our institution found that only 4 % (one of the twenty-six) of Somali mothers were exclusively breast-feeding at postpartum hospital discharge (A Mueller, personal communication). Therefore, most Somali infants in our practice receive at least some vitamin D in formula. This finding would explain the low rate of deficiency (13 %) but high rate of insufficiency (60 %) among this patient population.

The prevalence of vitamin D deficiency was far higher than for anaemia or Pb poisoning. It may seem surprising that our rates of vitamin D deficiency and insufficiency were not much higher than national estimates such as those found by Kumar et al.(Reference Kumar, Muntner and Kaskel1), given our far northern latitude, dark-skinned urban patient population and season of the bulk of blood sampling (winter and spring). However, the prevalence of vitamin D deficiency is strongly associated with increasing age in childhood(Reference Kumar, Muntner and Kaskel1, Reference Yetley20), and our sample was much younger than Kumar's, with a mean age of only 2·6 years compared with a National Health and Nutrition Examination Survey sample uniformly distributed between the ages of 1 and 21 years. Our prevalence was higher than that found in a sample of children of roughly similar age, ethnic background and northern latitude(Reference Gordon, Feldman and Sinclair13).

Two recent articles have been published that document low (<50 %) rates of vitamin D supplementation among breast-fed infants, even among parents who admit to receiving information from their child's paediatrician about the importance of supplementation(Reference de Nooijer, Onnink and Van Assema21, Reference Taylor, Geyer and Feldman22). Thus, although we agree that screening has significant costs (both direct and indirect), a policy of ‘universal’ supplementation also has significant limitations, as the available evidence suggests that it is likely to result in supplementation far below recommended levels(Reference de Nooijer, Onnink and Van Assema21, Reference Taylor, Geyer and Feldman22). We eagerly await evidence-based guidelines on this much debated topic.

Conclusion

There was no correlation among vitamin D, anaemia and Pb status in our low-income paediatric population. Further studies that examine the geographical variability and clinical significance of vitamin D deficiency are anticipated. In the interim, our data suggest that new recommendations for vitamin D screening, or universal supplementation, are sorely needed for at-risk children.

Acknowledgements

The present study did not receive any external funding. The authors have no conflict of interest to declare. M.K. conceived of the study, performed a portion of the data analysis and wrote the paper; M.C. performed a portion of the data analysis and edited the manuscript; D.B.C. collaborated on study conception, data analysis and edited the manuscript.

References

1.Kumar, J, Muntner, P, Kaskel, FJ et al. (2009) Prevalence and associations of 25-hydroxyvitamin D deficiency in US children: NHANES 2001–2004. Pediatrics 124, e1e9.CrossRefGoogle ScholarPubMed
2.Gordon, CM, Williams, AL, Feldman, HA et al. (2008) Treatment of hypovitaminosis D in infants and toddlers. J Clin Endocrinol Metab 93, 27162721.CrossRefGoogle ScholarPubMed
3.Mansbach, JM, Ginde, AA & Camargo, CA (2009) Serum 25-hydroxyvitamin D levels among US children aged 1 to 11 years: do children need more vitamin D? Pediatrics 124, 14041410.CrossRefGoogle ScholarPubMed
4.Ziegler, EE, Hollis, BW, Nelson, SE et al. (2006) Vitamin D deficiency in breastfed infants in Iowa. Pediatrics 118, 603610.CrossRefGoogle ScholarPubMed
5.Sim, JJ, Lac, PT, Liu, IL et al. (2009) Vitamin D deficiency and anemia: a cross-sectional study. Ann Hematol 89, 447452.CrossRefGoogle ScholarPubMed
6.McGillivray, G, Skull, SA, Davie, G et al. (2007) High prevalence of asymptomatic vitamin D and iron deficiency in East African immigrant children and adolescents living in a temperate climate. Arch Dis Child 92, 10881093.CrossRefGoogle Scholar
7.Madar, AA, Stene, LC & Meyer, HE (2009) Vitamin D status among immigrant mothers from Pakistan, Turkey and Somalia and their infants attending child health clinics in Norway. Br J Nutr 101, 10521058.CrossRefGoogle ScholarPubMed
8.Hintzpeter, B, Scheidt-Nave, C, Muller, MJ et al. (2008) Higher prevalence of vitamin D deficiency is associated with immigrant background among children and adolescents in Germany. J Nutr 138, 14821490.CrossRefGoogle ScholarPubMed
9.Minnesota Department of Human Services and Health (2006) Child and Teen Checkups (C&TC) Screening Components Standards and Guidelines. St Paul, MN: Minnesota Department of Human Services and Health.Google Scholar
10.Greer, FR (2009) Defining vitamin D deficiency in children: beyond 25-OH vitamin D serum concentrations. Pediatrics 124, 14711473.CrossRefGoogle ScholarPubMed
11.Holick, MF (2009) Vitamin D status: measurement, interpretation, and clinical application. Ann Epidemiol 19, 7378.CrossRefGoogle ScholarPubMed
12.Holick, MF (2006) High prevalence of vitamin D inadequacy and implications for health. Mayo Clin Proc 81, 353373.CrossRefGoogle ScholarPubMed
13.Gordon, CM, Feldman, HA, Sinclair, L et al. (2008) Prevalence of vitamin D deficiency among healthy infants and toddlers. Arch Pediatr Adolesc Med 162, 505512.CrossRefGoogle ScholarPubMed
14.Lee, JM, Smith, JR, Philipp, BL et al. (2007) Vitamin D deficiency in a healthy group of mothers and newborn infants. Clin Pediatr (Phila) 46, 4244.CrossRefGoogle Scholar
15.Cole, CR, Grant, FK, Tangpricha, V et al. (2010) 25-Hydroxy vitamin D status of healthy, low-income, minority children in Atlanta, Georgia. Pediatrics 125, 633639.CrossRefGoogle Scholar
16.Agency for Toxic Substances and Disease Registry, Centers for Disease Control and Prevention (2007) Lead toxicity: what are the physiologic effects of lead exposure? http://www.atsdr.cdc.gov/csem/lead/pbphysiologic_effects2.html (accessed April 2010).Google Scholar
17.McLean, E, Cogswell, M, Egli, I et al. (2009) Worldwide prevalence of anaemia, WHO Vitamin and Mineral Nutrition Information System, 1993–2005. Public Health Nutr 12, 444454.CrossRefGoogle ScholarPubMed
18.Jusko, TA, Henderson, CR, Lanphear, BP et al. (2008) Blood lead concentrations <10 μg/dl and child intelligence at 6 years of age. Environ Health Perspect 116, 243248.CrossRefGoogle Scholar
19.Canfield, RL, Henderson, CR Jr, Cory-Slechta, DA et al. (2003) Intellectual impairment in children with blood lead concentrations below 10 μg per deciliter. N Engl J Med 348, 15171526.CrossRefGoogle Scholar
20.Yetley, EA (2008) Assessing the vitamin D status of the US population. Am J Clin Nutr 88, 558S564S.CrossRefGoogle ScholarPubMed
21.de Nooijer, J, Onnink, M & Van Assema, P (2010) Vitamin D supplementation in young children: associations with Theory of Planned Behavior variables, descriptive norms, moral norms, and habits. Public Health Nutr 13, 12791285.CrossRefGoogle ScholarPubMed
22.Taylor, JA, Geyer, LJ & Feldman, KW (2010) Use of supplemental vitamin D among infants breastfed for prolonged periods. Pediatrics 125, 105111.CrossRefGoogle ScholarPubMed
Figure 0

Table 1 Characteristics of the study population: low-income children under 6 years of age (n 127), Minnesota, USA

Figure 1

Fig. 1 Two-way scatterplot of vitamin D status and Hb level (n 127; r = 0·12; P = 0·18) among low-income children under 6 years of age (n 127), Minnesota, USA

Figure 2

Fig. 2 Two-way scatterplot of vitamin D status and lead level (n 127; r = 0·03; P = 0·71) among low-income children under 6 years of age (n 127), Minnesota, USA

Figure 3

Table 2 Associations of vitamin D deficiency and insufficiency among low-income children under 6 years of age (n 127), Minnesota, USA

Figure 4

Table 3 Multivariate logistic regression model for vitamin D deficiency (25(OH)D < 20 ng/ml) among low-income children under 6 years of age (n 127), Minnesota, USA