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Published on: August 7, 2017
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.
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.
Background And Objective:
Probiotics may reduce the risk of atopy and asthma in children. However, results from clinical trials have been conflicting, and several of them may have been underpowered. We performed a meta-analysis of randomized, placebo-controlled trials to assess the effects of probiotic supplementation on atopic sensitization and asthma/wheeze prevention in children.
Methods:
Random-effects models were used to calculate pooled risk estimates. Meta-regression was conducted to examine the effect of potential factors on probiotics efficacy.
Results:
Probiotics were effective in reducing total immunoglobulin E (IgE) (mean reduction: -7.59 U/mL [95% confidence interval (CI): -14.96 to -0.22]; P = .044). Meta-regression showed that the reduction in IgE was more pronounced with longer follow-up. Probiotics significantly reduced the risk of atopic sensitization when administered prenatally (relative risk: 0.88 [95% CI: 0.78 to 0.99]; P = .035 for positive result on the skin prick test and/or elevated specific IgE to common allergens) and postnatally (relative risk: 0.86 [95% CI: 0.75 to 0.98]; P = .027 for positive result on skin prick test). Administration of Lactobacillus acidophilus, compared with other strains, was associated with an increased risk of atopic sensitization (P = .002). Probiotics did not significantly reduce asthma/wheeze (relative risk: 0.96 [95% CI: 0.85 to 1.07]).
Conclusions:
Prenatal and/or early-life probiotic administration reduces the risk of atopic sensitization and decreases the total IgE level in children but may not reduce the risk of asthma/wheeze. Follow-up duration and strain significantly modified these effects. Future trials for asthma prevention should carefully select probiotic strain and consider longer follow-up.
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