Department of Pediatrics, Wilhelmina Children's' Hospital, University Medical Center, Utrecht, the Netherlands.
Allergy. 2009 Sep;64(9):1349-58. doi: 10.1111/j.1398-9995.2009.02021.x. Epub 2009 Apr 9.
Modification of the intestinal microbiota by administration of probiotic bacteria may be a potential approach to prevent allergic disease. We aimed to study primary prevention of allergic disease in high-risk children by pre- and postnatal supplementation of selected probiotic bacteria.
In a double-blind, randomized, placebo-controlled trial, a mixture of probiotic bacteria selected by in-vitro experiments (Bifidobacterium bifidum, Bifidobacterium lactis, and Lactococcus lactis; Ecologic Panda) was prenatally administered to mothers of high-risk children (i.e. positive family history of allergic disease) and to their offspring for the first 12 months of life.
Parental-reported eczema during the first 3 months of life was significantly lower in the intervention group compared with placebo, 6/50 vs 15/52 (P = 0.035). After 3 months, the incidence of eczema was similar in both groups. Cumulative incidence of parental-reported eczema at 1 and 2 years was 23/50 (intervention) vs 31/48 (placebo) and 27 (intervention) vs 34 (placebo), respectively. The number needed to treat was 5.9 at age 3 and 12 months and 6.7 at age 2 years. The intervention group was significantly more frequently colonized with higher numbers of Lc. lactis. Furthermore, at age 3 months, in vitro production of IL-5 (146 pg/ml vs 72 pg/ml; P = 0.04) was decreased in the probiotic-group compared with the placebo-group.
This particular combination of probiotic bacteria shows a preventive effect on the incidence of eczema in high-risk children, which seems to be sustained during the first 2 years of life. In addition to previous studies, the preventive effect appears to be established within the first 3 months of life.
通过给予益生菌来改变肠道菌群可能是预防过敏性疾病的一种潜在方法。我们旨在通过对高危儿童进行产前和产后补充特定益生菌来研究过敏性疾病的一级预防。
在一项双盲、随机、安慰剂对照试验中,通过体外实验选择的益生菌混合物(双歧杆菌、乳双歧杆菌和乳酸乳球菌;Ecologic Panda)被用于高危儿童(即有过敏病史的家族史)的母亲及其后代,在生命的前 12 个月内进行产前和产后补充。
与安慰剂组相比,干预组在生命的前 3 个月内报告的湿疹发生率显著降低,分别为 6/50 与 15/52(P=0.035)。3 个月后,两组的湿疹发生率相似。1 岁和 2 岁时父母报告的湿疹累积发生率分别为 23/50(干预组)与 31/48(安慰剂组)和 27(干预组)与 34(安慰剂组)。需要治疗的人数分别为 3 个月和 12 个月时为 5.9,2 岁时为 6.7。干预组以更高数量的乳杆菌属(Lactobacillus)定植的频率更高。此外,在 3 个月大时,与安慰剂组相比,干预组的 IL-5 体外产生量(146pg/ml 比 72pg/ml;P=0.04)降低。
这种特定的益生菌组合对高危儿童湿疹的发病率具有预防作用,这种作用似乎在生命的前 2 年持续存在。与之前的研究相比,预防作用似乎在生命的前 3 个月内建立。