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DOI 10.1016/j.jcf.2024.07.006

Медицинская библиотека · Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society · 2024

Breastfeeding, growth, and lung disease in the first 3 years of life in children with cystic fibrosis.

Lai HuiChuan J, Bach Taiya R, Miller Tami, McDonald Catherine M, Maguiness Karen M, Seffrood Erin E, Leonard Jessica B, Farrell Philip M

СтатьяМногоцентровое исследованиеПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАПоддержка службы здравоохранения СШАПеревод пока не подготовлен

Аннотация

BACKGROUND

The 2009 cystic fibrosis (CF) infant care guidelines recommend breastmilk as the initial feeding but do not address if/when it should be fortified or supplemented with formula to promote optimal growth and pulmonary health.

METHODS

We conducted a prospective multi-center cohort study in breastfed and formula-fed infants that included 172 infants with CF who were born during 2012-17, enrolled after newborn screening at age 1.9 ± 1.0 months, and evaluated growth and lung disease manifestations in the first 3 years of life.

RESULTS

Seventy-two percent of our study cohort was breastfed at birth, but 64 % transitioned to receiving fortified feedings (breastmilk, formula, or a combination) by 6 months of age to reverse the downward trajectory of their growth curves. Fortified feedings accelerated catch-up growth to normal weight-for-age (0.12 ± 0.80 z-score) and near normal height-for-age (-0.13 ± 0.90 z-score) at 3 years of age. Within the fortified group, breastmilk and formula were similarly effective in promoting catch-up growth, but proportionately fewer infants with CF fed predominantly breastmilk (30 %) experienced severe or moderate early-onset lung disease compared to those fed predominantly formula (62 %), p = 0.02.

CONCLUSIONS

Most infants with CF require fortified feedings to recuperate from growth faltering and achieve normal growth at 3 years of age. For these infants, the proactive/preventive strategy of fortified breastmilk feedings starting soon after CF diagnosis, an alternative to the reactive/monitoring approach, can minimize the risk of prolonged postnatal growth faltering, accelerate the potential of attaining catch-up growth, and decrease the likelihood of experiencing more severe early-onset lung disease.

Для цитирования: Lai HuiChuan J, Bach Taiya R, Miller Tami, McDonald Catherine M, Maguiness Karen M, Seffrood Erin E, Leonard Jessica B, Farrell Philip M. Breastfeeding, growth, and lung disease in the first 3 years of life in children with cystic fibrosis.. Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society. 2024. DOI: 10.1016/j.jcf.2024.07.006.

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