Savino Francesco, Garro Maria, Montanari Paola, Galliano Ilaria, Bergallo Massimiliano
Department of Pediatrics, Universitary Hospital Città della Salute e della Scienza di Torino, Turin, Italy.
Department of Pediatrics, Universitary Hospital Città della Salute e della Scienza di Torino, Turin, Italy.
J Pediatr. 2018 Jan;192:171-177.e1. doi: 10.1016/j.jpeds.2017.08.062. Epub 2017 Sep 29.
To evaluate crying time, retinoid-related orphan receptor-γ (RORγ) and forkhead box P3 (FOXP3) messenger RNA levels (transcription factors that can modulate T cell responses to gut microbes), and to investigate gut microbiota and fecal calprotectin in infants treated with Lactobacillus reuteri for infantile colic.
A double-blind, placebo-controlled randomized trial was conducted in primary care in Torino from August 1, 2015 to September 30, 2016. Patients suffering from infantile colic were randomly assigned to receive daily oral L reuteri (1 × 10 colony forming unit) or placebo for 1 month. Daily crying times were recorded in a structured diary. FOXP3 and RORγ messenger RNA in the peripheral blood was assessed with real-time TaqMan reverse transcription polymerase chain reaction. Gut microbiota and fecal calprotectin were evaluated.
After infants with colic were supplemented with L reuteri DSM 17938 for 30 days, crying times were significantly shorter among infants with colic in the probiotic group compared with infants in the placebo group (74.67 ± 25.04 [IQR = 79] minutes /day vs 147.85 [IQR = 135] minutes /day [P = .001]). The FOXP3 concentration increased significantly (P = .009), resulting in decreased RORγ/FOXP3 ratios: 0.61 (IQR = 0.60) at day 0 and 0.48 (IQR = 0.28) at day 30 (P = .028). Furthermore, the probiotic increased the percentage of Lactobacillus (P = .049) and decreased fecal calprotectin (P = .0001).
Infants with colic treated with L reuteri for 30 days had a significantly decreased crying time and an increased FOXP3 concentration, resulting in a decreased RORγ/FOXP3 ratio. The treatment reduced fecal calprotectin.
ClinicalTrials.gov: NCT00893711.
评估哭闹时间、视黄酸相关孤儿受体γ(RORγ)和叉头框蛋白P3(FOXP3)信使核糖核酸水平(可调节T细胞对肠道微生物反应的转录因子),并研究接受罗伊氏乳杆菌治疗婴儿腹绞痛的婴儿的肠道微生物群和粪便钙卫蛋白。
2015年8月1日至2016年9月30日在都灵的初级保健机构进行了一项双盲、安慰剂对照的随机试验。患有婴儿腹绞痛的患者被随机分配接受每日口服罗伊氏乳杆菌(1×10菌落形成单位)或安慰剂,为期1个月。每日哭闹时间记录在结构化日记中。采用实时TaqMan逆转录聚合酶链反应评估外周血中的FOXP3和RORγ信使核糖核酸。评估肠道微生物群和粪便钙卫蛋白。
腹绞痛婴儿补充罗伊氏乳杆菌DSM 17938 30天后,益生菌组腹绞痛婴儿的哭闹时间明显短于安慰剂组婴儿(74.67±25.04[四分位间距=79]分钟/天对147.85[四分位间距=135]分钟/天[P=0.001])。FOXP3浓度显著增加(P=0.009),导致RORγ/FOXP3比值降低:第0天为0.61(四分位间距=0.60),第30天为0.48(四分位间距=0.28)(P=0.028)。此外,益生菌增加了乳酸杆菌的百分比(P=0.049),并降低了粪便钙卫蛋白(P=0.0001)。
接受罗伊氏乳杆菌治疗30天的腹绞痛婴儿哭闹时间显著减少,FOXP3浓度增加,导致RORγ/FOXP3比值降低。该治疗降低了粪便钙卫蛋白。
ClinicalTrials.gov:NCT00893711。