1. Infant nutrient needs Basis/Approach Public health vs individual
recommendations, guidelines, education
Specific nutrients
water
energy
protein
fatty acids
vitamin K
Vitamin D
Iron
Fluoride

2. Basis of recommendations
Growth and development
Physiology GI
Renal
Programming
Public health vs individual
Optimize growth and development
Prevent deficiencies
Safety
Prevention of chronic illness and optimize health through life cycle

3. Approaches to Estimating Nutrient Requirements
Direct experimental evidence (ie protein and amino acids)
Extrapolation from experimental evidence relating to human subjects of other age groups or animal models
ie thiamin--related to energy intake mg/1000 kcal
Breast milk as gold standard (average [] X usual intake)
Metabolic balance studies (ie protein, minerals)
Clinical Observation (eg: manufacturing errors B6, Cl)
Factorial approach
Population studies

4. Challenges Strength of Evidence Individual vs population
Public health approach
Individual genetics
Maternal-infant dyad
In utero endowment
Beliefs, values, choices
Relationship/nurture
Environmental factors

5. Public health vs individual
Prevalence of nutrient deficiencies
Balance incidence, burden, and treatment
Eg: Vitamin K and hemorrhagic disease of newborn
Prevalence and evidence of chronic conditions associated with dietary practices
Etiology of nutrient deficiencies and/or chronic conditions
Eg: allergy, obesity, anemia, dental caries,…

6. Individual Requirements
Genetics
Adaptation
Environment
Behavior/activity
Choices, access, resources
other

7. 1940’s Rickets (D) Pellagra (Niacin) Scurvy (C) Beriberi (Thiamin)
Xeropthalmia (A)
Goiter (Iodine)

8. United Nations 5th report on World Nutrition: March 2004
Prevalence (%)
1990
2005
underweight
35.2
26.5
Iodine deficiency

9. United Nations 5th report on World Nutrition: March 2004
Vitamin A deficiency
140 million preschoolers
7 million pregnant women
Iron Deficiency
One of most prevalent
4-5 billion affected

10. Reports in US of PEM, Rickets, Zinc deficiencies

11. Causes
Nutrition - Disease Access Food Health Care Environment Economics Education

12. Programming by Early Diet
Nutrient composition in early diet may have long term effects on GI function metabolism and health
Animal models show that glucose and amino acid transport activities are programmed by composition of early diet
Animals weaned onto high CHO diet have higher rates of glucose absorption as adults compared to those weaned on high protein diet
Barker Hypothesis:
Association between BMI and chronic disease: HTN and cardiovascular, SGA/IUGR
Other examples: early diet associations with allergy, obesity, diabetes

13. Allergies: Prevention by Avoidance (Zeigler, Pediatr Allergy Immunol
High risk infants from atopic families, intervention group n=103, control n=185
Restricted diet in pregnancy, lactation, Nutramagen when weaned, delayed solids for 6 months, avoided highly allergenic foods
Results: reduced age of onset of allergies

14. Allergies: Prevention by Avoidance (Zeigler, Pediatr Allergy Immunol

15. Allergies: Early Introduction of Foods (Fergussson et al, Pediatrics, 1990)
10 year prospective study of 1265 children in NZ
Outcome = chronic eczema
Controlled for: family hx, HM, SES, ethnicity, birth order
Rate of eczema with exposure to early solids was 10% Vs 5% without exposure
Early exposure to antigens may lead to inappropriate antibody formation in susceptible children.

16. Early Introduction of Foods (Fergussson et al, Pediatrics, 1990)

17. Allergies: Prevention by Avoidance (Marini, 1996)
359 infants with high atopic risk
279 in intervention group
Intervention: breastfeeding strongly encouraged, no cow’s milk before one year, no solids before 5/6 months, highly allergenic foods avoided in infant and lactating mother

18. Allergies: Prevention by Avoidance (Marini, 1996)

19. Cochrane Review
Osborn et al: Formulas containing hydrolysed protein for prevention of allergy and food intolerance in infants 2006;18
Concluded that use of hydrolysed formula in non breastfed infants at risk for allergy (atopic dermatitis) for at least 4 months reduces the incidence of allergy.

20. DRI
Nutrition Recommendations from the Institute of Medicine (IOM) of the U.S> National Academy of Sciences for general public and health professionals.
Hx: WWII, to investigate issues that might “affect national defense”
Population/institutional guidelines
Application to individuals.

21. DRI
Estimated Average Requirement (EAR): expected to satisfy the needs of 50% of the people in that age group based on review of scientific literature.
Recommended Dietary Allowance (RDA): Daily dietary intake level considered sufficient by the FNB to meet the requirement of nearly all (97-98%) healthy individuals. Calculated from EAR and is usually 20% higher
Adequate intake (AI): where no RDA has been established.
Tolerable upper limit (UL): Caution agains’t excess

22. DRI’s for infants
Macronutrients based on average intake of breast milk
Protein less than earlier RDA
Energy: EER

23. DRI’s for infants
Macronutrients based on average intake of breast milk
Protein less than earlier RDA
AAP Recommendations
Vitamin D: 200 IU supplement for breastfed infants and infants taking <500 cc infant formula
Iron: Iron fortified formula (4-12 mg/L), Breastfed Infants supplemented 1mg/kg/d by 4-6 months 23

24. Feeding Guidelines and Recommendations
Public health policy
Health promotion
Prevention

25. Recommendations/guidelines
DRI: Dietary Reference Intakes AI UL
EER
AAP
Bright Futures
Start Healthy feeding guidelines

26. DRI: Dietary Reference Intakes AI: Adequate Intake
Comparison of individual intake data to a reference or estimate of nutrient needs
DRI: Dietary Reference Intakes
periodically revised recommendations (or guidelines) of the National Academy of Sciences
quantitative estimates of nutrient intakes for planning and assessing diets for healthy people
AI: Adequate Intake
UL: Tolerable Upper Intake Level
EER: Estimated Energy Requirement 26

27. DRI’s for infants
Macronutrients based on average intake of breast milk
Protein less than earlier RDA
Factors to consider: fetal endowment, individual variability, impact of diet on bioavailability and need

28. The Start Healthy Feeding Guidelines for Infants and Toddlers (JADA, 2004)28

29. Bright Futures AAP/HRSA/MCHB http://www.brightfutures.org
“Bright Futures is a practical development approach to providing health supervision for children of all ages from birth through adolescence.”

30. Examples Transition Supplements to breastmilk Safety
Allergy prevention
Dental health
other

31. Water

32. Water Water requirement is determined by: water loss
evaporation through the skin and respiratory tract (insensible water loss)
perspiration when the environmental temperature is elevated
elimination in urine and feces.
water required for growth
solutes derived from the diet

33. Water
Water lost by evaporation in infancy and early childhood accounts for more than 60% of that needed to maintain homeostasis, as compared to 40% to 50% later in life
NAS recommends 1.5 ml water per kcal in infancy.

34. Renal
Limited ability to concentrate urine in first year due to immaturities of nephron and pituitary
Potential Renal solute load determined by nitrogenous end products of protein metabolism, sodium, potassium, phosphorus, and chloride.

35. Urine Concentrations
Most normal adults are able to achieve urine concentrations of 1300 to 1400 mOsm/l
Healthy newborns may be able to concentrate to mOsm/l, but isotonic urine of mOsm/l is the goal
In most cases this is not a concern, but may become one if infant has fever, high environmental temperatures, or diarrhea

36. Renal solute load Samuel Foman J Pediatrics Jan 1999 134 # 1 (11-14)
RSL is important consideration in maintaining water balance:
In acute febrile illness
Feeding energy dense formulas
Altered renal concentrating ability
Limited fluid intake

37. Water Needs

38. Water Individual needs Renal concentrating ability Solute in diet
Health
environment

39. Concentrating formula decreases free water and increases RSL
Water vs fluid
Concentrating formula decreases free water and increases RSL
What is the % water in 20 kcal/oz infant formula?
90%
To achieve 100 ml/kg/d needs to consume at least 110 cc/kg/d

40. Energy Requirements
Higher than at any other time per unit of body weight
Highest in first month and then declines
High variability - SD in first months is about 15 kcal/kg/d
Breastfed infants many have slighly lower energy needs
RDA represents average for each half of first year

41. Energy Requirements, cont.
RDA represents additional 5% over actual needs and is likely to be above what most infants need.
Energy expended for growth declines from approximately 32.8% of intake during the first 4 months to 7.4% of intake from 4 to 12 months

42. Energy Partition in Infancy (kcal/kg/d)

43. Energy Intakes by Breastfed and Formula Fed Boys (kcal/kg)

44. 2002 Energy DRI

45. EER 0-3 months (89 x wt -100) + 175 4-6 months (89 x wt -100) + 56
Equations for older children factor in weight, height and physical activity level (PAL)

46. Examples of EER by age and weight46

47. Energy
Correlate individual intake with growth 47

48. 2002 Carbohydrate DRI

49. Protein
Increases in body protein are estimated to average about 3.5 g/day for the first 4 months, and 3.1 g/day for the next 8 months.
The body content of protein increases from about 11.0% to 15.0% over the first year

50. 2002 Protein DRI

51. 2002 Fat DRI

54. Essential Fatty Acids
The American Academy of Pediatrics and the Food and Drug Administration specify that infant formula should contain at least 300 mg of linoleate per 100 kilocalories or 2.7% of total kilocalories as linoleate.

55. LCPUFA
DHA and ARA

56. LCPUFA: Background

57. LCPUFA: Background
Ability to synthesize 20 C FA from 18 C FA is limited.
n-3 and n-6 fatty acids compete for enzymes required for elongation and desaturation
Human milk reflects maternal diet, provides AA, EPA and DHA
n-3 important for neurodevelopment, high levels of DHA in neurological tissues
n-6 associated with growth & skin integrity

58. DHA represents 10% of total FA in brain grey matter, and 35% in rod and cone membranes of retina
Synthetic ability to convert linolenic acid to DHA present when diet sufficient in w-3 FA (alpha linolenic)
Alterations in visual and neurodevelopmental fx associate with insufficient DHA

59. RCT, 274 healthy full term infants Three groups:
Formula supplementation with long-chain polyunsaturated fatty acids: are there developmental benefits? Scott et al. Pediatrics, Nov
RCT, 274 healthy full term infants
Three groups:
standard formula
standard formula with DHA (from fish oil)
formula with DHA and AA (from egg)
Comparison group of BF

60. Outcomes at 12 and 14 months
No significant differences in Bayley, Mental or Psychomotor Development Index
Differences in vocabulary comprehension across all categories and between formula groups for vocabulary production.

61. Conclusion
“We believe that additional research should be undertaken before the introduction of these supplements into standard infant formulas.”

62. PUFA Status and Neurodevelopment: A summary and critical analysis of the literature (Carlson and Neuringer, Lipids, 1999)
In animal studies use deficient diets through generations - effects on newborn development may be through mothering abilities.
Behaviors of n-3 fatty acid deficient monkeys: higher frequency of stereotyped behavior, locomotor activity and behavioral reactivity

63. Efficacy and safety of docosahexaenoic acid and arachidonic acid addition to infant formulas: can one buy better vision and intelligence? (Koo. J Am Coll Nutr Apr;22(2):101-7)
“Functional benefits in particular visual or neural development from IF containing LCPUFA remains controversial.”
“Potential for excessive and/or imbalanced intake of n-6 and n-3 fatty acids exists with increasing fortification of LCPUFA to infant foods other than IF.”

64. Formula Supplemented with DHA & ARA: A Critical Review of the Research (Wright et al, 2006)
10 RCTs from of variable quality
Considered the strength of each study by looking at indices of research quality.

65. Wright et al, cont. Growth (7 studies) FA in blood (7 studies)
no differences in weight, length, OFC
FA in blood (7 studies)
DHA & ARA higher with supplementation
those supplemented with only DHA had lower levels of ARA than those on standard formula
Supplementation with LCPUFA for only 17 weeks lead to higher EFA levels at 1 year of age

66. Wright et al, cont. Vision (6 trials) Neurodevelopment
2 found better visual function with LCPUFA , 4 did not
Neurodevelopment
1 of 4 found positive results on Bayley Scales of Infant Development II
2 of 5 found positive information processing/IQ/cognitive effects

67. Wright et al, cont Conclusions No detrimental effects found
Possibly a small improvement in visual acuity, but significance of this small effect in global development is questionable
“thoughtful consideration is advised before recommending more expensive formula for term infants.”

68. Longchain polyunsaturated fatty acid supplementation in infants born at term (Cochrane, 2001).
At present there is little evidence from randomised trials of LCPUFA supplementation to support the hypothesis that LCPUFA supplementation confers a benefit for visual or general development of term infants.
A beneficial effect on information processing is possible but larger studies over longer periods are required to conclude that LCPUFA supplementation provides a benefit when compared with standard formula.
Data from randomised trials do not suggest that LCPUFA supplements influence the growth of term infants

69. Omega-3 FA and Neural Development to 2 years of Age: Do we Know enough for Dietary Recommendations: Innis JPGN 48:S16-24:2009
Estimated requirement and variability among individuals necessary to set DRI
Dietary recommendations affect food supply and supplements and are used in labeling
When scientific information is incomplete, consideration must be given to implications of recommendations

70. Omega-3 FA and Neural Development to 2 years of Age: Do we Know enough for Dietary Recommendations: Innis JPGN 48:S16-24:2009
“ While there is no doubt that DHA is critical for the developing brain, western diets poor in w-3 FA and rich in w-6 FA are becoming increasingly implicated in contributing to risk of poor neurodevelopment and function…..The w-3 FAs are clearly essential nutrients, suggesting that dietary recommendations, such as AI, to minimize risk of poor CNS development can be justified, and are consistent with a philosophy of dietary advice that promotes optimal child development and health. However, because dietary recommendations often promulgate changes in the food supply and supplement use…..premature recommendations based on incomplete science that focus on individual nutrients rather than dietary practices such as breastfeeding and foods such as fish rich in DHA are not necessarily in the best public interest”

71. Vitamin K

72. Vitamin K
2 forms: K1 or phylloquinone (plant form) and K2 (synthesized by bacteria)
Function: cofactor inmetabolic conversion of precursors of Vitamin K dependent proteins to active form ( eg: prothrombins, osteocalcin)

73. Vitamin K
Lack of specific information regarding an infant’s requirement
Vitamin K concentration of breastmilk is low and for the breastfeeding infant a deficiency state has been described
No “gold standard” available

74. Vitamin K DRI for infants 2-2.5 ug/day Formula provides 7-9 ug/kg/d
BM contains < 10 ug/L
Hemorrhagic disease of the Newborn…Vitamin K deficiency
Prophylaxis: 1 mg Vitamin K IM for all newborn infants

75. Vitamin K Controversy Adequacy of BM
Maternal Diet and Vitamin A content of BM
? Significance/prevalence of hemorrhagic disease of newborn
IM injections of all newborns

76. Controversies Concerning Vitamin K and the Newborn: AAP Policy Statement, 2003

77. Vitamin K Deficiency- definitions – AAP, 2003
Term
Age and Incidence
Symptoms
Early vitamin K deficiency bleeding (VKDB)*
First week of life:
Unexpected bleeding in previously healthy-appearing neonates
Late VKDB
2-12 weeks of age
unexpected bleeding attributable to severe vitamin K deficiency
* Formerly known as classic hemorrhagic disease of the newborn

78. Incidence of VKDB Early: 0.25%–1.7% incidence Late:
No vitamin K prophylaxis: 4.4 to 7.2 per 100,000 births
Single oral vitamin K prophylaxis:1.4 to 6.4 per births
IM vitamin K prophylaxis: 0
Oral vitamin K has effect similar to IM in preventing early VKDB, but not in preventing late VKDB

79. Danielson et al Arch Dis Child 2004 89:F546-550
Late onset vitamin K deficient bleeding in infants who did not receive prophylactic vitamin K at birth in Hanoi province
Incidence: 116 per 100,000 births
Higher in rural areas
9% mortality
42% impaired neurodevelopmental status at discharge in survivors

80. Incidence Netherlands 2005: 3.2 per 100,000 births
Canada 2004: 0.45 per 100,000 births
Conclude low incidence associated with current practice of prophylactic Vitamin K at birth

81. Closing the Loophole:Midwives and the Administration of Vitamin K in the Neonate
Adame and Carpenter J Pediatr :
Case Report of a previously healthy, exclusively breastfed 6 week old infant delivered by a midwife on the south Texas border. Did not receive Vitamin K at birth. Admitted with severe intracranial hemorrhage, cooagulopathy, and seizures, unresponsive, pupils fixed and dialated

82. Cochran Prophylactic Vitamin K for preventing haemorrhagic disease in newborn infants
Vitamin K deficiency can cause bleeding in an infant in the first weeks of life. This is known as Haemorrhagic Disease of the Newborn (HDN) or Vitamin K Deficiency Bleeding (VKDB). 82

83. Cochran
The risk of developing vitamin K deficiency is higher for the breastfed infant because breast milk contains lower amounts of vitamin K than formula milk or cow's milk

84. Cochran
In different parts of the world, different methods of vitamin K prophylaxis are practiced.

85. Cochran
Oral Doses:
The main disadvantages are that the absorption is not certain and can be adversely affected by vomiting or regurgitation. If multiple doses are prescribed the compliance can be a problem

86. Cochran
I.M. prophylaxis is more invasive than oral prophylaxis and can cause a muscular haematoma. Since Golding et al reported an increased risk of developing childhood cancer after parenteral vitamin K prophylaxis (Golding 1990 and 1992) this has been a reason for concern .

87. Cochrane Conclusions, 2000
A single dose (1.0 mg) of intramuscular vitamin K after birth is effective in the prevention of classic HDN.
Either intramuscular or oral (1.0 mg) vitamin K prophylaxis improves biochemical indices of coagulation status at 1-7 days.
Neither intramuscular nor oral vitamin K has been tested in randomized trials with respect to effect on late HDN.
Oral vitamin K, either single or multiple dose, has not been tested in randomized trials for its effect on either classic or late HDN.

88. Brousson and Klien, Controversies surrounding the administration of vitamin K to newborns; a review CMAJ. 154(3): , February 1, 1996.
Study selection: Six controlled trials met the selection criteria: a minimum 4-week follow-up period, a minimum of 60 subjects and a comparison of oral and intramuscular administration or of regimens of single and multiple doses taken orally. All retrospective case reviews were evaluated. Because of its thoroughness, the authors selected a meta-analysis of almost all cases involving patients more than 7 days old published from 1967 to Only five studies that concerned safety were found, and all of these were reviewed

90. Brousson and Klien, Controversies surrounding the administration of vitamin K to newborns; a review CMAJ. 154(3): , February 1, 1996.
Data synthesis: Vitamin K (1 mg, administered intramuscularly) is currently the most effective method of preventing HDNB. The previously reported relation between intramuscular administration of vitamin K and childhood cancer has not been substantiated. An oral regimen (three doses of 1 to 2 mg, the first given at the first feeding, the second at 2 to 4 weeks and the third at 8 weeks) may be an acceptable alternative but needs further testing in largeclinical trials.

91. Brousson and Klien, Controversies surrounding the administration of vitamin K to newborns; a review CMAJ. 154(3): , February 1, 1996
Conclusion: There is no compelling evidence to alter the current practice of administering vitamin K intramuscularly to newborns.

92. AAP Recommendations: Pediatrics:Vol112#1 July 2003
1. Vitamin K1 should be given to all newborns as a single, intramuscular dose of 0.5 to 1 mg.
2. Further research on the efficacy, safety, and bioavailability of oral formulations of vitamin K is warranted.

93. AAP Recommendations
3. Health care professionals should promote awareness among families of the risks of late VKDB associated with inadequate vitamin K prophylaxis from current oral dosage regimens, particularly for newborns who are breastfed exclusively
4. Earlier concern regarding a possible causal association between IM vitamin K and childhood cancer has not been substantiated

94. Note put recent articles on re-emergence of HDNB texas, ? Japan

95. Vitamin D

96. Vitamin D
Role
Source
Dietary
sunlight
Deficiency
Rickets

97. Role Enhances intestinal absorption of Ca
Increase tubular resorption of Ph
Mediation of recycling of Ca and Ph for bone growth and remodeling
Sterol hormone
Deficiency: Rickets

98. Role Extraskeletal effects of Vitamin D
Modulates B and T Lymphocyte fx and deficiency may be associated with autoimmune diseases (diabetes, MS associations)
Regulation of cell growth (assoc with breast, prostrate, and colon cancer)

99. Prevalence Thought to be disease of past (prior to 1960’s)
Disappeared secondary to recognition of role of sunlight, fortification of milk, use of multivitamins, AAPCON recommendation for 400 IU supplementation of infants

100. Prevalence Increased incidence and case reports 1970’2
No national data in US
Georgia : 9 per million hospitalized children
National Hospital Discharge Survey: 9 per million
Pediatric Research in Office Setting (AAP):23-32 hospitalized cases reported

101. Prevalence Literature Review 13 articles published between 1996-2001
122 case reports

102. PEDIATRICS Vol. 111 No. 4 April 2003, pp. 908-910
Prevention of Rickets and Vitamin D Deficiency: New Guidelines for Vitamin D Intake
PEDIATRICS Vol. 111 No. 4 April 2003, pp

103. Vitamin D and Sunlight
Vitamin D requirements are dependent on the amount of exposure to sunlight.
Dermatologists recommend caution with sun exposure.
Sunscreens markedly decrease vitamin D production in the skin
Decreased sunlight exposure occurs during the winter and other seasons and when sunlight is attenuated by clouds, air pollution, or the environment
AAP recommends against exposing infants < 6 months to direct sun

104. Breastfeeding and Vitamin D
Breastmilk has < 25 IU/L Recommended adequate intake can not be met with breastmilk alone
Formerly stated that needs could be met with sun exposure, but now, due to cancer concerns recommend against this

105. Vitamin D Recommendations
Before 2003 AAP recommended 10 mg (400 IU) per day for breastfeed infants
2003: American Academy of Pediatrics recommends supplements of 5 mg (200 IU) per day for all infants as recommended in DRIs.
10/14/2008: AAP updates guidelines vor vitamin D intake for infants, children, and teens to be published in Nov 5th ed Pediatrics
400 IU per day intake of vitamin D beginning in first few days of life

106. Formulas
if an infant is ingesting at least 500 mL per day of formula (vitamin D concentration of 400 IU/L), he or she will receive the recommended vitamin D intake of 200 IU per day.
If intake is less than 500 ml recommend additional supplement of vitamin D

107. Summary of AAP Recommendations, 2003
All breastfed infants unless they are weaned to at least 500 mL per day of vitamin D-fortified formula or milk.
All nonbreastfed infants who are ingesting less than 500 mL per day of vitamin D-fortified formula or milk.
Children and adolescents who do not get regular sunlight exposure, do not ingest at least 500 mL per day of vitamin D-fortified milk, or do not take a daily multivitamin supplement containing at least 200 IU of vitamin D.

108. AAP Recommendations for Vitamin D
2008
Intake of 400 IU beginning in first few days of life
Supplement breastfed, partially breastfed, infants and children consuming less than 1 liter formula or vitamin D fortified whole milk
Wagner et al: Prevention of Rickets and Vitamin D Deficiency in Infants, Children, and Adolescents: Pediatrics 2008;122;

109. Vitamin D
DRI: B-6 months 200 IU, 7-12 months 250 IU
UL: 1000 IU

110. Iron

111. Iron Function Source Deficiency Formula, breast milk, other foods
Bioavailability:
Breast milk
Soy formula
Deficiency
Anemia

112. Anemia Anemia (low Hct, Hgb: not specific for iron deficiency) Causes:
Inadequate iron in diet
Loss
GI bleeding, cows milk proteins, infectious agents
Other
Genetics
Lead
Other nutrients

113. Iron Biological function Oxygen transport primarily in hemoglobin
Component of other proteins including cytochrome a, b, c, and cytochrome oxidase essential for electron transport and cellular energetics

114. Iron deficiency (ID and IDA)
Anemia: Hgb <11 g/dl months
Iron deficiency Anemia (IDA): anemia due to iron deficiency
Iron deficiency: Insufficient iron to maintain normal physiologic functions leading to decrease in iron stores as measured by serum ferritin with or without IDA

115. Association between ID an IDA and neurobehavioral development
Lozoff
McCann and Ames
Cochrane review
Carter
Recent sleep studies

116. Iron Deficiency Anemia
Impact on social, neurobehavioral and sleep
Peirano et al: Sleep and Neurofunction Throughout Child development: Lasting Effects of Early Iron Deficiency J Ped Gastroenterology and Nutr :S8-S15
Lozoff et al: Dose-Response Relationships between Iron deficiency with or without anemia and Infant Social-emotional Behavior J Pediatr :

117. Peirano Slower neurotransmission in auditory and visual systems
Different motor activity patterning sleep-waking and sleep state organization
Alterations in behavioral and cognitive function

118. Lozoff
N=77
“Infant social-emotional behavior appears to be adversely affected by iron deficiency with or without anemia”
Shyness, orientation engagement, soothability

119. Carter et al: Iron Deficiency Anemia and Cognitive Function in Infancy: Pediatrics ;2427-e434
N= 87 (28 IDA, 49 no anemia)
Methods: at 9 and 12 months series of cognitive, intellegent and behavioral tests administered (Fagan test of infant intellegence (FTII), Emotionality, Activity and Sociability Temperment Survey, and Behavior Rating Scale (BRS))

120. Carter et al: Iron Deficiency Anemia and Cognitive Function in Infancy: Pediatrics ;2427-e434
N= 87 (28 IDA, 49 no anemia)
Methods: at 9 and 12 months series of cognitive, intellegent and behavioral tests administered (Fagan test of infant intellegence (FTII), Emotionality, Activity and Sociability Temperment Survey, and Behavior Rating Scale (BRS))

121. Results Sociodemographic background similar between 2 groups
Carter et al: Iron Deficiency Anemia and Cognitive Function in Infancy: Pediatrics ;2427-e434
Results
Sociodemographic background similar between 2 groups
IDA infants less likely to exhibit object permanence, less novelty preference on the FTII, lower BRS scores, and decrease engagement/orientation, described as “shyer”

122. Iron Deficiency
Among children in developing world, iron is the most common single nutrient deficiency
No national statistics for prevalence of ID or IDA < 12 months

123. Iron Fortification of Formula
“The increased use of iron-fortified infant formulas from the early 1970s to the late s has been a major public health policy success. During the early 1970s, formulas were fortified with 10 mg/L to 12 mg/L of iron in contrast with nonfortified formulas that contained less than 2 mg/L of iron. The rate of iron-deficiency anemia dropped dramatically during that time from more than 20% to less than 3%.”

124. ID and IDA 12-35 Months NHANES 2002
Population
ID (%)
IDA (%)
General US
9.2
2.1
Above poverty
8.9
2.2
Below poverty
8.6
2.3
Enrolled in WIC
10.7
3.2
Mexican American
13.9
0.9
Other ethnicity
15.2
4.4

125. Iron Iron absorption from soy formulas is less
Greater bioavailabilty of iron in breastmilk

126. Iron Absorption In Infancy

127. Iron Deficiency in Breastfeeding
At 4 to 5 months prevalence of low iron stores in exclusively breastfed infants is %.
A higher rate (20%-30%) of iron deficiency has been reported in breastfed infants who were not exclusively breastfed
The effect of iron obtained from formula or beikost supplementation on the iron status of the breastfed infant remains largely unknown and needs further study.

128. Foman on Iron
Proposes that breastfed infants should have supplemental iron (7 mg elemental) starting at 2 weeks.
Rational:
some exclusively breastfed infants will have low iron stores or iron deficiency anemia
Iron content of breastmilk falls over time
animal models indicate that deficits due to Fe deficiency in infants may not be recovered when deficiency is corrected.

129. AAP recommendations for Dx and prevention of ID and IDA:2010 Pediatrics 2010 126 #5
Birth-6 months: 0.27 mg/d
Assuming average content Breastmilk 0.35 mg/L and average intake 0.78 L/day
Noted variability of iron content of breastmilk, high risk populations (IUGR, LGA associate with maternal IDM, maternal anemia, Preterm birth)

130. AAP recommendations for Dx and prevention of ID and IDA:2010 Pediatrics 2010 126 #5
7-12 months: 11 mg/d
Factorial approach: iron loss, iron needed for increased blood volume, tissue mass, and stores
Noted that there isn’t a sudden increase in needs from 6 to 7 months.

131. AAP recommendations for Dx and prevention of ID and IDA:2010 Pediatrics 2010 126 #5
Diagnosis:
Iron status is a continuum with IDA at one end of the spectrum
No single measurement is currently available to characterize iron status
HgB limitations include specificity and sensitivity. Identifies anemia but not necessarily ID or IDA

132. AAP recommendations for Dx and prevention of ID and IDA:2010 Pediatrics 2010 126 #5
Term, healthy infants have sufficient Fe to 4 months.
Formula fed: Fe needs met by standard infant formula with 12 mg/dl and introduction of complementary foods after 4-6 months. Whole milk shouldn’t be used < 12 months
Breastfed: Exclusively breastfed infants are a increasing risk of ID >4 months and should be supplemented with 1 mg/kg/d oral Fe until appropriate complimentary food are introduced

133. AAP recommendations for Dx and prevention of ID and IDA:2010 Pediatrics 2010 126 #5
6-12 months
11 mg/d
Use complimentary foods with higher iron content. Liquid supplement may be needed to augment complimentary foods

134. AAP recommendations for Dx and prevention of ID and IDA:2010 Pediatrics 2010 126 #5
Univeral screening should be done at 12 months with Hgb and risk determination
Additional screening can be preformed at any time if there is a risk of ID/IDA including inadequate intake

135. Lead and Anemia

136. Fluoride Fluoride and dental caries
At beginning of 20th century dental caries was common with extraction only treatment available
Failure to meet minimum standards of 6 opposing teeth was common cause of rejection from military service in WWI and WWII

137. Fluoride
1901 Dr. Frederick S Mckay noted mottled teeth (fluorosis) in practice in Colo Springs Colo that were resistent to decay
1909 Dr. FC Robertson noted same mottling in his area of practice after a new well dug
Believed was due to something in the water

138. Fluoride
1945 study was conducted in 4 city pairs (Michigan, NY, Illinois, Ontario)
Followed years
50-60% reduction in dental caries

139. Fluoride Proposed mode of action
Promotes remineralization of areas of cariogenic lesions
Increases resistance to acid demineralization
Interferes with formation and function of plaque forming microorganisms
Improves tooth morphology

140. Fluoride
Concerns
Excess
Fluorosis
Cancer
other

141. Fluoride
Fluoride Recommendations were changed in 1994 due to concern about fluorosis.
Breast milk has a very low fluoride content.
Fluoride content of commercial formulas has been reduced to about 0.2 to 0.3 mg per liter to reflect concern about fluorosis.
Formulas mixed with water will reflect the fluoride content of the water supply. Fluorosis is likely to develop with intakes of 0.1 mg/kg or more.

142. Fluoride, cont.
Fluoride adequacy should be assessed when infants are 6 months old.
Dietary fluoride supplements are recommended for those infants who have low fluoride intakes.

144. Early Childhood Caries
AKA Baby Bottle Tooth Decay
Rampant infant caries that develop between one and three years of age

145. Early Childhood Caries: Etiology
Bacterial fermentation of cho in the mouth produces acids that demineralize tooth structure
Infectious and transmissible disease that usually involves mutans streptococci
MS is 50% of total flora in dental plaque of infants with caries, 1% in caries free infants

146. Early Childhood Caries: Etiology
Sleeping with a bottle enhances colonization and proliferation of MS
Mothers are primary source of infection
Mothers with high MS usually need extensive dental treatment

147. Early Childhood Caries: Pathogenesis
Rapid progression
Primary maxillary incisors develop white spot lesions
Decalcified lesions advance to frank caries within months because enamel layer on new teeth is thin
May progress to upper primary molars

148. Early Childhood Caries: Prevalence
US overall - 5%
53% American Indian/Alaska Native children
30% of Mexican American farmworkers children in Washington State
Water fluoridation is protective
Associated with sleep problems & later weaning

149. Early Childhood Caries: Cost
$1,000 - $3,000 for repair
Increased risk of developing new lesions in primary and permanent teeth

150. Early Childhood Caries: Prevention
Anticipatory Guidance:
importance of primary teeth
early use of cup
bottles in bed
use of pacifiers and soft toys as sleep aides

151. Early Childhood Caries: Prevention
Chemotheraputic agents: fluoride varnishes and supplements, chlorhexidene mouthwashes for mothers with high MS counts
Community education: training health providers and the public for early detection

152. Infant Feeding
Implications
Translation into practice
Recommendations