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Anemia Is a Poor Predictor of Iron Deficiency Among Toddlers in the United States: For Heme the Bell Tolls

Department of Pediatrics, Contra Costa Regional Medical Center and Health Centers, Martinez, California; and Department of Family and Community Medicine, University of California, Davis, California

	ABSTRACT

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Context. Many toddlers in the United States have their hemoglobin (Hb) measured periodically. Is this worthwhile?

Objective. To determine if the presence of anemia correctly diagnoses iron deficiency (ID) and if the absence of anemia correctly rules out ID in young children.

Methodology. An analysis of data from the US National Health and Nutrition Examination Survey III (1988–1994) was performed. Subjects were children 12 to 35 months old for whom complete blood counts and cardinal measures of iron nutrition (ferritin, transferrin saturation, and free erythrocyte protoporphyrin) were reported.

Results. In the US National Health and Nutrition Examination Survey III, the prevalence of ID ranged from 6% to 18% in various subpopulations of toddlers. In the general population, the positive predictive value of Hb concentration ([Hb]) <110 g/L for ID was 29% (95% confidence interval [CI]: 20–38%), and the sensitivity was 30% (95% CI: 20–40%). Changing the diagnostic cutoff point to [Hb] <107 g/L resulted in a positive predictive value of 38% (95% CI: 24–52%) but lowered the sensitivity to 15% (95% CI: 7–22%).

Conclusions. ID remains common in the United States. In agreement with other reports, anemia in toddlers in developed countries is more likely to be due to causes other than ID. Conversely, most children with ID are not anemic. Many false-positive and false-negative results render the measurement of Hb a screening test of relatively little value. The current detection strategy needlessly treats and retests many children without ID and leaves many iron-deficient toddlers unattended.

Key Words: African Americans • anemia • child • preschool • evidence-based medicine • hemoglobin • Mexican Americans • iron deficiency • iron-deficiency anemia • NHANES III • positive predictive value • poverty • sensitivity • toddlers • United States

Abbreviations: Hb, hemoglobin • ID, iron deficiency • WIC, Supplemental Nutrition Program for Women, Infants, and Children • NHANES, National Health and Nutrition Examination Survey • IDA iron-deficiency anemia • PPV, positive predictive value • BRR, balanced repeated replication • EPP, erythrocyte protoporphyrin • MCV, mean corpuscular volume • CI, confidence interval

Many of the 8 million American children between 1 and 3 years old routinely have their hemoglobin (Hb) measured. Economically disadvantaged children are more likely to be screened for iron deficiency (ID) by this method. Many Medicaid programs require universal screening, and the Supplemental Nutrition Program for Women, Infants, and Children (WIC) program requires a Hb determination for children to enroll. Although children in this age group are the most likely to be iron-deficient^1,2 and are least likely to meet their recommended intakes for iron,^3,4 there is scant evidence to support this current practice. The National Health and Nutrition Examination Survey (NHANES) II (1976–1980) showed that the likelihood of an anemic child 1 to 5 years old being iron-deficient was <50%.⁵ The utility of this test has not been considered in 20 years.

The prevalence of ID and iron-deficiency anemia (IDA) in NHANES III was reported previously.¹ That study did not report the prevalence of anemia of all causes, permitting the calculation of the positive predictive value (PPV) of anemia for ID. Was the PPV different from NHANES II? The previous study did not apply demographic stratification. Is the sensitivity of screening with the Hb test higher in children living below the poverty line? How does the usefulness of the test compare in children from different ethnic groups?

This is the first consideration of the prevalence of ID, IDA, and anemia of all causes in young children living in different economic strata and different ethnic groups. The resulting statistics are intended for practitioners.

	MATERIALS AND METHODS

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The NHANES III (1988–1994) was 1 of a series of surveys designed to provide national estimates of the health and nutritional status of the US population 2 months old. The NHANESs are performed continuously across the United States in specially designed medical examination centers. They are excellent sources of data of very high quality.

A CD-ROM of public-use data files from NHANES III was obtained from the National Technical Information Service (www.ntis.gov/fcpc). The Statistical Program for the Social Sciences (SPSS) version 11.0⁶ and Wesvar 4.2⁷ were used to analyze the data.

The US NHANES⁸ is a multistage, stratified population survey (rather than a random sample), which is a common sampling design. Populations of particular interest are oversampled to assure their representation. For example, black children comprised 29% of children tested in NHANES III, although they represented 17% of the population in this age range in 1988-1994. Children living below the poverty line comprised 40% of the children surveyed but represented 27% of the toddlers in the United States in those years. The methodology of NHANES acknowledges these biases and assigns sampling weights, numerical factors that are inversely proportional to the likelihood of a subject being selected. Other weights are assigned to correct for nonresponse and adjustments in estimates of the census.

A full sample weight and 52 partial sampling weights are calculated for each study subject. Balanced repeated replication (BRR)⁹ is a statistical method recommended to calculate estimates for the NHANES.⁸ The Fay method, with K = 0.3, was used.

Subjects were 12 to 35 months (inclusive) old at the time of examination. The poverty index ratio was used to stratify the subjects according to their families' incomes. NHANES assigned the poverty index ratio based on a family's self-reported income and size, using tables published each year by the Bureau of the Census. The race/ethnicity classification of the subjects was based on self-report.

All subjects had complete blood counts and cardinal measures of iron nutrition (ferritin, transferrin saturation, and free erythrocyte protoporphyrin [EPP]). Concentrations of lead in serum were also considered when available. According to the documentation accompanying the NHANES, blood was collected by venipuncture and samples were processed at the Division of Environmental Health Laboratory Sciences, National Center for Environmental Health, Centers for Disease Control and Prevention. Analyses were performed according to detailed plans.¹⁰

In this study, ID was diagnosed if 2 of the following pertained: ferritin <10 µg/L, transferrin saturation <10%, and EPP >1.42 µmol/L red blood cells. Anemia was diagnosed if Hb concentration ([Hb]) was <110 g/L. IDA was diagnosed if anemia accompanied ID. The National Center for Health Statistics of the US Centers for Disease Control and Prevention^1,2 and other authorities¹¹ use this criterion standard; it was developed by the Expert Scientific Working Group.¹²

	RESULTS

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Table 1 is a description of laboratory and demographic characteristics of children from the general population of US toddlers without ID (n = 1149) and with ID (n = 140). The estimates followed BRR. Children with ID had statistically lower concentrations of Hb (on the average lower by 5% of the mean value), were more likely to be from households with incomes below the poverty line, and were more likely to have parents who described themselves as Mexican American. Children from non-Hispanic white households had a smaller chance of being iron-deficient.

Figure 1 depicts the relative distributions of the 1289 subjects from NHANES III who had complete values for [Hb], [ferritin], % transferrin saturation, and [EPP]. Of these subjects, 140 could be classified as ID (Fig 1, bottom half), 48 had IDA (Fig 1, lower-left quadrant), and 106 had anemia without ID (Fig 1, upper-left quadrant). The histogram compares the distributions before the consideration of sampling weights and qualitatively displays the overlap of iron-sufficient and iron-deficient populations.

View larger version (22K): [in this window] [in a new window]   Fig 1. Comparisons of distributions of [Hb] of toddlers in US NHANES III. Grey bars indicate ID–; black bars, ID+. Observations are not corrected for sampling weights. The vertical line indicates the usual [Hb] defining anemia.

View larger version (14K): [in this window] [in a new window]   Fig 2. PPV versus [Hb] threshold: estimates and 95% CIs.

View larger version (13K): [in this window] [in a new window]   Fig 3. Sensitivity versus [Hb] threshold: estimates and 95% CIs.

View larger version (28K): [in this window] [in a new window]   Fig 4. Venn diagram illustrating overlap of groups with ID and anemia.

	DISCUSSION

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This Gaussian definition of abnormality does not permit the calculation of the diagnostic probability that a patient has ID. That essential measure is the PPV, where PPV = true-positives/(true-positives + false-positives). One needs to know the prevalence of anemia of all causes (the denominator of this equation). Surprisingly, the prevalence of anemia of all causes was omitted in most previous reports about NHANES.^1,2 An exception was a report¹³ of 9.6% prevalence for anemia of all causes in children 1 to 5 years old from the general population sampled in NHANES III. This finding compares closely with the 9% (7–12%) presented in the first row, third column of Table 2.

The results of the present study indicate that Hb is not a clinically useful test for assessment of iron adequacy among toddlers in the United States. The PPV reflects how accurately [Hb] diagnoses ID. Among the general population, an anemic toddler has 1 chance in 3 of being iron-deficient. The sensitivity of this test is of similar magnitude: a [Hb] of <110 g/L is only seen in ID one third of the time. Lowering the [Hb] used as a cutoff does increase the PPV slightly but at the cost of a lower test sensitivity. At best, the Hb test is a screening procedure of relatively little value.

Dividing the subjects into subsets does not reveal any striking difference in the utility of the test for any economic or ethnic group. The overall trend was PPV and sensitivities of 30%. Some of the estimates are possibly unreliable, because smaller sample sizes (n < 30) may not allow normal approximations. For example, among Mexican American children depicted in Table 2 (indicated by ), 23 had IDA and 47 had anemia of all types. The resulting estimate of the PPV after BRR was 53% (35-72%), an estimate with a wide, unsatisfactory CI. Even large and well-conducted surveys such as NHANES III cannot provide enough statistical power to assess the utility of the Hb test with precision.

The methodology of NHANES specified collection of venous blood and analysis by carefully calibrated Coulter counters.¹⁰ In clinical practice, capillary blood is often collected and analyzed with bench-top hemoglobinometers or by centrifuging microhematocrit tubes. Specimens obtained by these methods cannot be compared with those reported here.

The cause of the majority of anemia among the children with adequate stores of iron in NHANES III cannot be explained completely from the available data. Serum folate, B₁₂, Hb electrophoresis, and reticulocyte counts were not performed in subjects in the 12- to 35-month-old age group. and ß thalassemia traits, hemoglobinopathies (such as S, C, and E traits), cytostructural abnormalities, and enzyme defects (glucose-6-phosphate dehydrogenase deficiency) are hypothetical contributors. Exact estimates of these conditions in the US population are not available. Anemia associated with acute and chronic infections¹⁴ possibly explains many cases.

Other Populations
Limited recent data from NHANES were available at the time of writing (July 2004). The NHANES 1999–2000 data release contains complete hematologic and nutritional observations of only 319 young children, and the NHANES 2001–2002 release contains none. According to the release schedule for NHANES,¹⁵ we will have to wait until at least 2006 to extend these studies among toddlers in the US.

Soh et al¹⁶ performed a community-based cross-sectional survey of randomly selected, 6- to 24-month-old children in New Zealand. Their criterion for ID was the ferritin, EPP, and MCV model. Children with a C-reactive protein level of >10 mg/L (who might have suffered recent infections) were excluded from consideration. Among 169 toddlers 12 to 24 months old, 22% had [Hb] of <110 g/L, 2.5% had IDA, and 5.0% had ID without anemia. In that study, the PPV of [Hb] for ID can be calculated as 2.5%/22% = 11% (95% CI: 9–13%) and the sensitivity can be calculated as 2.5%/7.5% = 33% (95% CI: 26–40%).

A study of 488 infants from 11 European countries¹⁷ also indicated poor utility of the Hb test. Hb, serum ferritin, MCV, transferrin saturation, and serum transferrin receptor concentrations were measured at 12 months. The prevalence of ID was 7.2%, of ID anemia 2.3%, and of anemia of all causes 9.4%. More than 40% of anemia was associated with normal iron status (all indicators of iron nutrition normal) and associated with an increased frequency of recent infections. Another 35% of anemic patients had only 1 abnormal iron indicator. Thus, at 1 year of age, the PPV of anemia for ID was 2.3%/9.4% = 24% (95% CI: 20–28%) and the sensitivity was 2.3%/7.2% = 32% (95% CI: 28–36%).

The National Diet and Nutrition Survey¹⁸ took place in Mainland Britain in 1992–1993. It was a cross-sectional study considered to be representative of preschool children in the general population. Serum EPP was not measured in this study, so it is not possible to calculate the percentage of children who were iron-deficient by the Centers for Disease Control and Prevention definition. Blood was obtained from 1003 subjects 1.5 to 4.5 years old. Eight percent of the children had a [Hb] of <110 g/L, but only 3.4% had a low Hb with a ferritin level of <10 µg/L. Thus, the PPV of anemia for iron depletion was 3.4%/8% = 42%. Because ID is a less common condition than iron depletion (low [ferritin]), the PPV of anemia for ID in British children in that survey can be estimated at <42%.

Kazal¹⁹ found that the hematocrit failed to detect iron depletion (low [ferritin]) in infants and toddlers in the United States. Hematocrit and ferritin concentrations were measured from capillary blood from 321 children 9 to 18 months old. All were from low-income households. Children with acute illnesses and those receiving medicinal iron were excluded from the study. Six (1.9%) of the children were anemic, but none had low [ferritin]. Fifty-one infants (15.9%) had [ferritin] <10 µg/dL, but none were anemic.

Implications
ID is as important a problem as it ever was, but 2 aspects must be recognized. First, most anemic toddlers in the United States do not have ID. Second, the majority of toddlers with ID in the United States are not anemic. Screening children in this age group for anemia misdirects our attention from these findings. Assuming that [Hb] is an accurate proxy for iron status is misleading. It gives us false assurance that children without anemia are iron-sufficient, although they may be at significant risk. No candidate test for ID (transferrin receptors,²⁰ reticulocyte Hb concentration,²¹ or free erythrocyte protoporphyrin alone¹³) is likely to allow screening for ID in a more selective fashion than [Hb].

Iron is present in 200 to 300 enzymes and is important for health. We work to prevent ID because ID severe enough to cause IDA is associated with developmental disabilities.^22,23 It is unclear if these problems are reversible if iron stores are repleted.^24–27 Because the threshold effects of ID on development have not been established, it is prudent to assure that there are adequate stores during periods of growth and development. How can we assure good nutrition when, currently, secondary prevention is unlikely to be successful?

Much of the decline in the prevalence of IDA in recent years has been a result of primary preventative strategies, especially the fortification of formula and cereals with iron. One author has argued that daily supplementation should be continued through the second year of life.²⁸ Numerous studies worldwide have demonstrated the effectiveness of weekly preventative supplementation.^29–32 Given that most ID is not associated with anemia, these seem the most practical directions for future efforts. Screening toddlers for ID by Hb testing is inefficient. Prophylactic supplementation is likely to be more effective than attempting to identify and treat US children who are iron-deficient.

	ACKNOWLEDGMENTS

 
This study was supported by an educational stipend from the Contra Costa County Health Services Department. I have no financial interests in any organization that may have an interest in any part of this study.

I thank Mitch Watnick, PhD (Senior Statistician, Statistics Laboratory, University of California, Davis, CA), for statistical consultation. Leora Benioff, PhD, Guenter Hofstadler, MD, MPH, and John Lee, MD, provided reviews of this study; Sally Bly provided secretarial assistance; and Sally Chu (Degnan Medical Library, Contra Costa Regional Medical Center, Martinez, CA) provided reference materials.

	FOOTNOTES

 
Accepted Jul 21, 2004.

Address correspondence to Keith C. White, MD, Contra Costa Regional Medical Center, 2500 Alhambra Ave, Martinez, CA 94553. E-mail: kcwhite{at}ucdavis.edu

No conflict of interest declared.

	REFERENCES

TOP ABSTRACT MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 

1. Looker AC, Dallman PR, Carroll MD, Gunter EW, Johnson CL. Prevalence of iron deficiency the United States. JAMA. 1997;277 :973 –976[Abstract]
2. Looker AC, Cogswell ME, Gunter EW. Iron deficiency—United States, 1999–2000. MMWR Morb Mortal Wkly Rep. 2002;51 :898 –899
3. Fomon S. Infant feeding in the 20th century: formula and beikost. J Nutr. 2001;131 :409S –420S[Abstract/Free Full Text]
4. Food Survey Research Group. US Department of Agriculture Continuing Survey of Food Intake by Individuals, 1994–96, table set 10. Available at: www.barc.usda.gov/bhnrc/foodsurvey/home.htm. Accessed July 6, 2004
5. Federation of American Societies for Experimental Biology. Assessment of the Iron Nutritional Status of the US Population Based on Data Collected in the Second National Health and Nutrition Examination Survey, 1976–1980. Bethesda, MD: Federation of American Societies for Experimental Biology, Life Sciences Research Office; 1984
6. Statistical Program for the Social Sciences (SPSS) [computer program]. Version 11.0. Chicago, IL: SPSS Inc; 2004
7. Wesvar [computer program]. Version 4.2. Rockville, MD: Westat; 2002
8. National Center for Health Statistics. Analytic and Reporting Guidelines: The Third National Health and Nutrition Examination Survey, NHANES III (1988–94) 1996. Hyattsville, MD: Data Dissemination Branch, National Center for Health Statistics, Centers for Disease Control and Prevention; 1996
9. Brick JM, Morganstein M, Valliant DR. Analysis of complex sample data using replication. 2000. Available at: www.westat.com/wesvar/techpapers/index.html. Accessed July 29, 2000
10. Plan and operation of the Third National Health and Nutrition Examination Survey, 1988–94. Series 1: programs and collection procedures. Vital Health Stat 1. 1994;(32) :1 –407
11. Yip R. Iron. In: Bowman B, Russell R, eds. Present Knowledge in Nutrition. Washington, DC: International Life Sciences Institute; 2001:311–328
12. Expert Scientific Working Group. Summary of a report on assessment of the iron nutritional status of the United States. Am J Clin Nutr. 1985;42 :1318 –1330[Abstract/Free Full Text]
13. Mei Z, Parvanta I, Cogswell ME, Gunter EW, Grummer-Strawn LM. Erythrocyte protoporphyrin or hemoglobin: which is a better screening test for iron deficiency in children and women? Am J Clin Nutr. 2003;77 :1229 –1233[Abstract/Free Full Text]
14. Abshire TC. The anemia of inflammation. A common cause of childhood anemia. Pediatr Clin North Am. 1996;43 :623 –637[CrossRef][ISI][Medline]
15. National Health and Nutrition Examination Survey. Available at: www.cdc.gov/nchs/nhanes.htm. Accessed July 6, 2004
16. Soh PF, Ferguson EF, McKenzie JE, Homs MY, Gibson RS. Iron deficiency and risk factors for lower iron stores in 6–24-month-old New Zealanders. Eur J Clin Nutr. 2004;58 :71 –79[CrossRef][ISI][Medline]
17. Male C, Persson LA, Freeman V, Guerra A, van't Hof MA, Haschke F. Prevalence of iron deficiency in 12-mo-old infants from 11 European areas and influence of dietary factors on iron status (Euro-Growth study). Acta Paediatr. 2001;90 :492 –498[ISI][Medline]
18. Thane CW, Walmsley CM, Bates CJ, Prentice AF, Cole TJ. Risk factors for poor iron status in British toddlers: further analysis of data from the National Diet and Nutrition Survey of children aged 1.5–4.5 years. Public Health Nutr. 2000;3 :433 –440[Medline]
19. Kazal LA Jr. Failure of hematocrit to detect iron deficiency in infants. J Fam Pract. 1996;42 :237 –240[ISI][Medline]
20. Olivares M, Walter T, Cook JD, Hertrampf E, Pizarro F. Usefulness of serum transferrin receptor and serum ferritin in diagnosis of iron deficiency in infancy. Am J Clin Nutr. 2000;72 :1191 –1195[Abstract/Free Full Text]
21. Mast AE, Blinder MA, Lu Q, Flax S, Dietzen DJ. Clinical utility of the reticulocyte hemoglobin content in the diagnosis of iron deficiency. Blood. 2002;99 :1489 –1491[Abstract/Free Full Text]
22. Grantham-McGregor S, Ani C. A review of studies on the effect of iron deficiency on cognitive development in children. J Nutr. 2001;131 :649S –666S[Abstract/Free Full Text]
23. Pollitt E. The developmental and probabilistic nature of the functional consequences of iron-deficiency anemia in children. J Nutr. 2001;131(2S–2) :669S –675S
24. Lozoff B, Jimenez E, Hagen J, Mollen E, Wolf AW. Poorer behavioral and developmental outcome more than 10 years after treatment for iron deficiency in infancy. Pediatrics. 2000;105(4) . Available at: www.pediatrics.org/cgi/content/full/105/4/e51
25. Hurtado EK, Claussen AH, Scott KG. Early childhood anemia and mild or moderate mental retardation. Am J Clin Nutr. 1999;69 :115 –119[Abstract/Free Full Text]
26. Logan S, Martins S, Gilbert R. Iron therapy for improving psychomotor development and cognitive function in children under the age of three with iron deficiency anaemia. Cochrane Database Syst Rev. 2001(2) :CD001444
27. Algarin C, Peirano P, Garrido M, Pizarro F, Lozoff B. Iron deficiency anemia in infancy: long-lasting effects on auditory and visual system functioning. Pediatr Res. 2003;53 :217 –223[CrossRef][ISI][Medline]
28. Eden AE. Preventing iron deficiency in toddlers: a major public health problem. Contemp Pediatr. 2003;20 :57 –67
29. Young MW. The effectiveness of weekly iron and vitamin supplementation of Malawian preschool children. S Afr Med J. 2001;91 :49 –50[Medline]
30. Schultink W, Gross R, Gliwitzki M, Karyadi D, Matulessi P. Effect of daily vs twice weekly iron supplementation in Indonesian preschool children with low iron status. Am J Clin Nutr. 1995;61 :111 –115[Abstract/Free Full Text]
31. Thu BD, Schultink W, Dillon D, Gross R, Leswara ND, Khoi HH. Effect of daily and weekly micronutrient supplementation on micronutrient deficiencies and growth in young Vietnamese children. Am J Clin Nutr. 1999;69 :80 –86[Abstract/Free Full Text]
32. Liu XN, Kang J, Zhao L, Viteri FE. Intermittent iron supplementation is efficient and safe in controlling iron deficiency and anemia in preschool children. Food Nutr Bull. 1995;16 :139 –146

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This Article Abstract Full Text (PDF) P3Rs: Submit a response Alert me when this article is cited Alert me when P3Rs are posted Alert me if a correction is posted Citation Map Services E-mail this article to a friend Similar articles in this journal Similar articles in ISI Web of Science Similar articles in PubMed Alert me to new issues of the journal Add to My File Cabinet Download to citation manager Citing Articles Citing Articles via HighWire Citing Articles via CrossRef Citing Articles via ISI Web of Science (19) Citing Articles via Google Scholar Google Scholar Articles by White, K. C. Search for Related Content PubMed PubMed Citation Articles by White, K. C. Related Collections Blood

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