Department of Pediatric Respiratory Medicine and Allergy, Emma Children's Hospital, Amsterdam, The Netherlands.
Clin Exp Allergy. 2010 May;40(5):795-804. doi: 10.1111/j.1365-2222.2010.03465.x. Epub 2010 Feb 22.
Clinical trials investigating the therapeutic effect of probiotics on atopic dermatitis (AD) show inconsistent results. Better results can possibly be achieved by combining probiotics with prebiotics, i.e. synbiotics.
To investigate the therapeutic effect of a synbiotic mixture on the severity of AD in infants.
In a double-blind, placebo-controlled multi-centre trial, 90 infants with AD [SCORing Atopic Dermatitis (SCORAD) score > or =15], aged < 7 months and exclusively formula fed, were randomly assigned to receive either an extensively hydrolysed formula with Bifidobacterium breve M-16V and a galacto-/fructooligosaccharide mixture (Immunofortis), or the same formula without synbiotics for 12 weeks. The primary outcome was severity of AD, assessed using the SCORAD index. A secondary outcome measure was intestinal microbiota composition.
There was no difference in SCORAD score improvement between the synbiotic and the placebo group. The synbiotic group did have a significantly higher percentage of bifidobacteria (54.7% vs. 30.1%, P<0.001) and significantly lower percentages of Clostridium lituseburense/Clostridium histolyticum (0.5 vs. 1.8, P=0.02) and Eubacterium rectale/Clostridium coccoides (7.5 vs. 38.1, P<0.001) after intervention than the placebo group. In the subgroup of infants with IgE-associated AD (n=48), SCORAD score improvement was significantly greater in the synbiotic than in the placebo group at week 12 (-18.1 vs. -13.5 points, P=0.04).
This synbiotic mixture does not have a beneficial effect on AD severity in infants, although it does successfully modulate their intestinal microbiota. Further randomized-controlled trials should explore a possible beneficial effect in IgE-associated AD.
临床试验表明,益生菌对特应性皮炎(AD)的治疗效果不一致。通过将益生菌与益生元结合使用(即合生元),可能会取得更好的效果。
研究合生元混合物对婴儿 AD 严重程度的治疗效果。
在一项双盲、安慰剂对照的多中心试验中,90 名患有 AD(SCORing Atopic Dermatitis [SCORAD]评分>或=15)的婴儿[年龄<7 个月,且仅接受配方奶喂养],随机分为两组,分别接受含有短双歧杆菌 M-16V 和半乳糖/果糖低聚糖混合物的深度水解配方(Immunofortis)或不含合生元的相同配方 12 周。主要结局指标为 AD 的严重程度,采用 SCORAD 指数评估。次要结局指标为肠道微生物群组成。
合生元组和安慰剂组在 SCORAD 评分改善方面无差异。干预后,合生元组双歧杆菌的比例显著升高(54.7%比 30.1%,P<0.001),而梭状芽胞杆菌/溶组织梭菌(0.5%比 1.8%,P=0.02)和真杆菌/梭菌(7.5%比 38.1%,P<0.001)的比例显著降低。在 IgE 相关 AD 的婴儿亚组(n=48)中,合生元组在第 12 周时 SCORAD 评分改善明显大于安慰剂组(-18.1 比-13.5 分,P=0.04)。
该合生元混合物对婴儿 AD 严重程度无有益作用,但可成功调节其肠道微生物群。进一步的随机对照试验应探索其在 IgE 相关 AD 中的可能有益作用。