Literature DB >> 21430114

Growth and pulmonary outcomes during the first 2 y of life of breastfed and formula-fed infants diagnosed with cystic fibrosis through the Wisconsin Routine Newborn Screening Program.

Sarah A Jadin1, Grace S Wu, Zhumin Zhang, Suzanne M Shoff, Benjamin M Tippets, Philip M Farrell, Tami Miller, Michael J Rock, Hara Levy, HuiChuan J Lai.   

Abstract

BACKGROUND: The optimal feeding (breast milk, formula, or a combination) for infants with cystic fibrosis (CF) is unknown. Recommendations from the CF Foundation are based on limited data.
OBJECTIVE: We compared growth and pulmonary outcomes between breastfed and formula-fed infants through the age of 2 y.
DESIGN: A total of 103 CF infants born in 1994-2006 and diagnosed through newborn screening in Wisconsin were studied. Breastfed infants were classified by the duration of exclusive breastfeeding (ExBF). Exclusive formula-feeding (ExFM) was classified by the formula's caloric density (ie, standard [0.67 kcal/mL (20 kcal/oz) (ExFM20)] throughout infancy or high density [≥0.74 kcal/mL (22 kcal/oz) (ExFM22+)] for some duration of infancy).
RESULTS: Fifty-three infants (51% of infants) were breastfed and 50 infants (49% of infants) were ExFM. In breastfed infants, the duration of ExBF was <1 mo (53% of infants), 1-1.9 mo (21% of infants), 2-3 mo (17% of infants), and 4-9 mo (9% of infants). In ExFM infants, 23 infants (46%) received a formula with a high caloric density; approximately half (n = 13) of the ExFM infants received the formula by 6 mo of age. Proportionately more infants with pancreatic sufficiency (n = 9) were ExBF ≥1 mo (44% of infants), and none of the infants were ExFM22+, compared with infants with meconium ileus (n = 24; 13% of infants were ExBF ≥1 mo, and 38% of infants were ExFM22+) or pancreatic insufficiency (n = 70; 25% of infants were ExBF ≥1 mo, and 20% of infants were ExFM22+) (P = 0.02). In infants with pancreatic insufficiency, weight z scores declined from birth to 6 mo (P < 0.0001) in infants who were ExBF ≥2 mo, and the number of Pseudomonas aeruginosa infections through the age of 2 y was fewer in breastfed than in ExFM infants (P = 0.003) but did not differ by the duration of ExBF.
CONCLUSION: For infants with CF, ExBF <2 mo does not compromise growth and is associated with a respiratory benefit.

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Mesh:

Year:  2011        PMID: 21430114      PMCID: PMC3076655          DOI: 10.3945/ajcn.110.004119

Source DB:  PubMed          Journal:  Am J Clin Nutr        ISSN: 0002-9165            Impact factor:   7.045


  56 in total

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Authors:  D S FLEISHER; A M DIGEORGE; L A BARNESS; D CORNFELD
Journal:  J Pediatr       Date:  1964-03       Impact factor: 4.406

2.  The influence of newborn screening for cystic fibrosis on pulmonary outcomes in new South Wales.

Authors:  Karen O McKay; Donna L Waters; Kevin J Gaskin
Journal:  J Pediatr       Date:  2005-09       Impact factor: 4.406

3.  Wisconsin cystic fibrosis chest radiograph scoring system: validation and standardization for application to longitudinal studies.

Authors:  R E Koscik; M R Kosorok; P M Farrell; J Collins; M E Peters; A Laxova; C G Green; L Zeng; L S Rusakow; R C Hardie; P W Campbell; J W Gurney
Journal:  Pediatr Pulmonol       Date:  2000-06

4.  Complications associated with symptomatic diagnosis in infants with cystic fibrosis.

Authors:  Frank J Accurso; Marci K Sontag; Jeffrey S Wagener
Journal:  J Pediatr       Date:  2005-09       Impact factor: 4.406

5.  Evidence on improved outcomes with early diagnosis of cystic fibrosis through neonatal screening: enough is enough!

Authors:  Philip M Farrell; HuiChuan J Lai; Zhanhai Li; Michael R Kosorok; Anita Laxova; Christopher G Green; Jannette Collins; Gary Hoffman; Ronald Laessig; Michael J Rock; Mark L Splaingard
Journal:  J Pediatr       Date:  2005-09       Impact factor: 4.406

6.  Nutritional status of patients with cystic fibrosis with meconium ileus: a comparison with patients without meconium ileus and diagnosed early through neonatal screening.

Authors:  H C Lai; M R Kosorok; A Laxova; L A Davis; S C FitzSimmon; P M Farrell
Journal:  Pediatrics       Date:  2000-01       Impact factor: 7.124

Review 7.  Expression of functional immunomodulatory and anti-inflammatory factors in human milk.

Authors:  R P Garofalo; A S Goldman
Journal:  Clin Perinatol       Date:  1999-06       Impact factor: 3.430

8.  Influence of parental smoking on respiratory symptoms during the first decade of life: the Tucson Children's Respiratory Study.

Authors:  R T Stein; C J Holberg; D Sherrill; A L Wright; W J Morgan; L Taussig; F D Martinez
Journal:  Am J Epidemiol       Date:  1999-06-01       Impact factor: 4.897

9.  Siblings, day-care attendance, and the risk of asthma and wheezing during childhood.

Authors:  T M Ball; J A Castro-Rodriguez; K A Griffith; C J Holberg; F D Martinez; A L Wright
Journal:  N Engl J Med       Date:  2000-08-24       Impact factor: 91.245

10.  Growth failure in cystic fibrosis.

Authors:  S A McNaughton; D A Stormont; R W Shepherd; P W Francis; B Dean
Journal:  J Paediatr Child Health       Date:  1999-02       Impact factor: 1.954

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Authors:  Michael J Coffey; Millie Garg; Nusrat Homaira; Adam Jaffe; Chee Y Ooi
Journal:  Cochrane Database Syst Rev       Date:  2020-01-22

2.  Academy of Nutrition and Dietetics: 2020 Cystic Fibrosis Evidence Analysis Center Evidence-Based Nutrition Practice Guideline.

Authors:  Catherine M McDonald; Jessica A Alvarez; Julianna Bailey; Ellen K Bowser; Kristen Farnham; Mark Mangus; Laura Padula; Kathleen Porco; Mary Rozga
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