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. 2022 Mar 25;10:866868. doi: 10.3389/fped.2022.866868

Table 1.

Main features and results of studies investigating active supplementation of pre- and probiotics.

References Study design Population Conclusion
Pre- and probiotics and asthma/wheezing
(9) Randomized,
double-blind
controlled trial
184 high-risk infants
supplemented in the first 6 months of life
Early LGG supplementation does not prevent the development of asthma at 2 years of age
(10) Randomized
double-blind
controlled trial
253 infants at risk for allergy, supplemented in the first 6 months of life At the age of 5 years, in children who had developed asthma, there were no significant differences between the groups supplemented or not
(11) Randomized
double-blind
controlled trial
231 newborns of women with allergy, supplemented for the first 6 months of life The rate of wheezing was significantly higher in the probiotic group in the second 6 months of life
(12) Randomized
double-blind
controlled trial
153 newborns of women with allergy, supplemented in the first 6 months of life No differences in probiotic and control group in the rate of asthma at 2.5 years
(13) Randomized
double-blind
controlled trial
178 infants with atopic mothers, supplemented in the first 6 months of life No differences in probiotic and control group in the rate of asthma at 5 years
(14) Randomized
controlled trial
75 infants with atopic dermatitis, supplemented in the first 6 months of life The prevalence of frequent wheezing and the number of children treated with asthma medication was significantly lower in the synbiotic than in the placebo group
(15) Randomized
double blind
controlled trial
171 children <13 months of life, supplemented from the 4th to the 13th month of life No long-term effect in infants supplemented with probiotics on development of asthma
(16) Randomized
controlled trial
1,223 mother-infant pairs, supplemented from 36gw (mothers) to 6 months of life (infants) The lifetime prevalence of asthma was similar in the probiotic and placebo groups
(17) Randomized
double blind
controlled trial
232 mother-infant pairs, supplemented from 36gw (mothers) to 12 months of life (infants) No differences in probiotic group and control group in the rate of wheeze at 2 years
(18) Randomized
double blind
controlled trial
1,223 mother-infant pairs, supplemented from 36gw (mothers) to 6 months of life (infants) No differences in probiotic and control group in the rate of asthma at 5 years
(19) Randomized
double blind
controlled trial
131 mother-infant pairs, supplemented from 36gw (mothers) to 6 months of life (infants) No differences in probiotic and control group in the rate of asthma at 5 years
(20) Randomized
controlled trial
425 mother-infant pairs, supplemented from 35gw (mothers) to 6 months of life (infants) No differences in probiotic and control group in the rate of asthma at 4 years
(8) Randomized
double blind
controlled trial
1,223 mother-infant pairs, supplemented from 36gw (mothers) to 6 months of life (infants) No differences in probiotic and control group in the rate of asthma at 13 years
(21) Randomized
double blind
controlled trial
171 infants, supplemented in the first 6 months of life No differences in probiotic and control group in the rate of wheezing
(22) Randomized
controlled trial
83 pregnant women with a positive family history of allergic disease, supplemented during pregnancy (mothers) to the first year of life (infants) No differences in probiotic and control group in the rate of asthma
Pre- and probiotics and RTI
(23) Randomized
double blind
controlled trial
203 children, aged 6-36 months, supplemented for 90 days Use of the probiotic strains BB-12 and L3 statistically reduced the risk of URTIs in healthy children
(24) Randomized,
double-blind
controlled trial
188 infants, supplemented from 6 to 16 months of life Administration of a formula with probiotics may be useful for the prevention of community-acquired and upper RTI
(25) Randomized,
double-blind
controlled trial
81 infants, supplemented for the first 12 months of life Probiotics may offer a safe means of reducing the risk of early acute otitis media and antibiotic use and the risk of recurrent RTI during the first year of life
(26) Randomized,
double-blind
controlled trial
109 infants, supplemented for the first year of life The infants receiving BB-12 were reported to have experienced fewer RTI than the control infants
(27) Randomized,
double-blind
controlled trial
109 infants, supplemented for the first 2 years of life The infants receiving BB-12 were reported to have experienced fewer RTI than the control infants
(28) Randomized,
double-blind
controlled trial
224 children, supplemented from 7 to 13 months of life The pro- and prebiotics included in follow-up formula do not reduce the risk of AOM, recurrent AOM, antibiotic use or lower RTI at 1 year
(29) Randomized,
double-blind
controlled trial
43 infants, aged 4-46 months, supplemented for 4 months No significant differences regarding the number of episodes of AOM in the active group and in the placebo group
(30) Randomized,
double-blind
controlled trial
201 infants, aged 4-10 months of life, supplemented for 12 weeks Rate and duration of respiratory illnesses did not differ significantly between groups