Probiotic administration in early life, atopy, and asthma: a meta-analysis of clinical trials

Nancy Elazab1, Angelico Mendy, Janvier Gasana

  • 1Division of Pediatric Pulmonology, Department of Pediatrics, University of Miami, Miami, FL, USA.

Pediatrics
|August 21, 2013
PubMed

Insights

Probiotic supplementation in early life can lower the risk of atopic sensitization and total immunoglobulin E (IgE) levels in children. However, probiotics do not appear to prevent asthma or wheeze, with strain and follow-up duration influencing outcomes.

Area of Science:

  • Pediatric Allergy and Immunology
  • Microbiome Research
  • Preventive Medicine

Background:

  • Conflicting results exist regarding probiotic efficacy in preventing childhood atopy and asthma.
  • Previous trials may have been underpowered, necessitating a comprehensive meta-analysis.

Purpose of the Study:

  • To assess the impact of probiotic supplementation on atopic sensitization and the prevention of asthma/wheeze in children.
  • To analyze factors influencing probiotic efficacy through meta-regression.

Main Methods:

  • Conducted a meta-analysis of randomized, placebo-controlled trials.
  • Employed random-effects models to calculate pooled risk estimates.
  • Utilized meta-regression to explore the influence of covariates on probiotic effectiveness.

Main Results:

  • Probiotics significantly reduced total immunoglobulin E (IgE) levels (mean reduction: -7.59 U/mL).
  • Prenatal and/or early-life probiotic administration lowered the risk of atopic sensitization (prenatal RR: 0.88, postnatal RR: 0.86).
  • Lactobacillus acidophilus was associated with an increased risk of atopic sensitization; probiotics did not significantly reduce asthma/wheeze risk (RR: 0.96).

Conclusions:

  • Early-life probiotic use effectively reduces atopic sensitization and total IgE levels in children.
  • Probiotic efficacy is influenced by strain type and duration of follow-up.
  • Future asthma prevention trials should prioritize specific probiotic strains and extended follow-up periods.
Abstract

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