Journal List > Korean J Perinatol > v.24(4) > 1013684

Kim: Intestinal Microbiota in Preterm Infants and Probiotics Use for Disease Prevention

Abstract

Infectious complications such as necrotizing enterocolitis (NEC) or neonatal sepsis are main causes of mortality and disability in very low birth weight infants (VLBWIs). Because preterm infants are exposed to too unfavorable environment to promote appropriate intestinal colonization, pathologic organisms can easily colonize and host defense systems are also down-regulated in preterm gut, causing infectious complications such as NEC. To promote appropriate intestinal microbiota, probiotics have been studied for potential benefits by increasing mucosal barrier function, reducing intestinal pathogens, up-regulating immune system balancing inflammation. Large randomized controlled trials have shown favorable effects of probiotics on preterm NEC and mortality. Meta-analysis of clinical trials showed consistent evidence of probiotics uses in preterm infants. However, adequate type, dose, timing, and duration of probiotics have not been standardized for clinical applications. In addition, other interventions promoting preterm intestinal micobiota and immunity, such as prebiotics or lactoferrin, are on studies in combination with probiotics. More clinical trials should be added for the evidence-based clinical use of probiotics in preterm infants.

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Fig. 1
Factors that influence intestinal microbiota of newborn. Adopted from Bourlioux P, et al.
kjp-24-221f1.tif
Fig. 2
Potentially harmful and potentially beneficial bacteria. P., Pseudomonas; E., Escherichia. Adopted from Bourlioux P, et al.
kjp-24-221f2.tif
Fig. 3
Mechanism of probiotics. Adopted from Claud EC, et al.
kjp-24-221f3.tif
Table 1.
Probiotics Study of Very Low Birth Weight Infants for NEC, Sepsis, or Mortality Reduction
Study Case (n) Control (n) Bwt/GA Probiotics Dose(CFU)/duration
Kitajima28 45 46 <1,500 g B. breve 0.5x109, 28 days
Dani29 295 290 <33 wk or <1,500 g L. GG 6x109, till discharge
Costalos30 51 36 28-32 wk S. boulardii 109/kg, twice daily, 30 days
Bin-Nun31 72 73 <1,500 g Mixture till 36 wk
Lin32 180 187 <1,500 g Mixture twice daily, till discharge
Manzoni34 39 41 <1,500 g L. GG 6x109, till discharge
Stratiki11 38 31 <34 wk & <1,500 g B. lactis 2x107, 30 days
Lin33 217 217 <34 wk & <1,500 g Mixture 2x109, 6 wk
Manzoni35 151 168 <1,500 g L. GG 6x109, till discharge
Rouge12 45 49 <32 wk & <1,500 g Mixture 1x108, till discharge
Samanta36 92 95 <34 wk & <1,500 g MixtureII 2.5x109, till discharge
Mihatsch13 91 89 <30 wk & <1,500 g B. lactis 12x109/kg, 6 wk
Braga14 119 112 <1,500 g Mixture 30 day of life
Sari15 110 111 <33 wk or <1,500 g L. sporogenes 3.5x108, till discharge
Fernandez37 75 75 <1,500 g Mixture∗∗ 1 g/day, till discharge
Jacobs38 548 551 <32 wk & <1,500 g Mixture†† 109/1.5 g, till discharge

Abbreviations: NEC, necrotizing enterocolitis; Bwt, birth weight; GA, gestational age; CFU, colny forming unit; B, Bifidobacterium; L,Lactobacillus; S,SaccharomycesB. infantis (0.35x109)+Streptococcus thermophilus (0.35x109)+B. bifidus (0.35x109);

L. acidophilus (1004356 organisms)+B. infantis (1015697 organisms);

B. bifidus+L. acidophilus;

B. longum+L.GG;

II B. bifidus+B. lactis+B. infantis+L. acidophilus;

B. breve+L. casei (3.5x107-3.5x109);

∗∗ L. acidophilus (109)+L. rhamnosus (4.4x108)+L. casei (109)+L. plantarum (1.76x108)+B. infantis (2.76 x107)+Streptococcus thermophilus (6.6x105);

†† B. infantis (3x108)+Streptococcus thermophilus (3.5x108)+B. lactis (3.5 x108)

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