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鼠李糖乳杆菌 NCIMB 30351 滴剂对婴幼儿功能性胃肠疾病症状及肠道菌群的影响:一项随机、安慰剂对照临床试验的结果。

Effect of Lactobacillus reuteri NCIMB 30351 drops on symptoms of infantile functional gastrointestinal disorders and gut microbiota in early infants: Results from a randomized, placebo-controlled clinical trial.

机构信息

Novo Natum LLC, Moscow, Russia.

出版信息

Eur J Pediatr. 2024 May;183(5):2311-2324. doi: 10.1007/s00431-024-05473-y. Epub 2024 Mar 1.

Abstract

Infantile functional gastrointestinal disorders, such as colic, constipation, diarrhea, and gastroesophageal reflux (regurgitation), often occur in early infancy and, representing one of the causes of significant parental anxiety, lead to a significant strain on the healthcare resources. In this study, we aimed to evaluate the effects of Lactobacillus reuteri drops (L. reuteri NCIMB 30351) on the symptoms of infantile colic, constipation, diarrhea, and gastroesophageal reflux, as well as on the levels of intestinal microbiota in full-term newborns during the first months of life. A randomized, placebo-controlled, single-masked (blinded), post-marketing clinical study was conducted in two clinical units-Children's City Clinical Hospital of Moscow and Medical Center "St. Andrew's Hospitals-NEBOLIT" from March 2020 to May 2022 in 90 infants aged from 1 to 4 months (mean age (± SD) 12.3 ± 5.09 weeks; 53.3% females, 46.7% males). Patients with colic, regurgitation (single symptom or combination of several symptoms), and constipation or diarrhea were randomly allocated in two parallel arms to receive either 5 drops (2 × 10 colony forming unit) of L. reuteri NCIMB 30351 (n = 60) or masked placebo (n = 30) for 25 consecutive days. Two treatment arms had equal numbers of patients with constipation and diarrhea (n = 30 each). Daily crying times and their duration, evacuations, and regurgitations were recorded in a structured diary. The levels of gut microbiota were analyzed by deep sequencing of bacterial 16S rRNA gene. Infants with colic receiving supplementary L. reuteri NCIMB 30351 for 25 days had significant reduction in the numbers of colic (change from baseline - 6.3 (7.34) vs - 3.0 (7.29) in placebo, P < 0.05) and numbers of crying cases and mean duration of crying (decrease from baseline - 144 (70.7) minutes, lower in the diarrhea subgroup than in constipation infants, compared with - 80 (58.9) in placebo, P < 0.0001), as well as regurgitation numbers (decreased by - 4.8 (2.49) with L. reuteri vs - 3 (7.74) with placebo). We also observed increased numbers of evacuations in infants with constipation (L. reuteri 2.2 (2.4) vs 0.9 (1.06) in placebo, P < 0.05). There was a remarkable reduction of evacuations in infants with diarrhea, while not statistically significant. The analysis of bacterial 16S rRNA gene in the collected samples showed that L. reuteri positively influences the proportions of prevalent species, while it negatively affects both conditionally pathogenic and commensal microbes. Additional in vitro test for formation of Clostridium colonies in the presence of the probiotic demonstrated that L. reuteri effectively inhibits the growth of pathogenic Clostridium species. No adverse events were reported in this study.   Conclusion: The uptake of L. reuteri NCIMB 30351 leads to a significant reduction in the number of regurgitations, feeding-induced constipations, and diarrhea as well as mean daily numbers of crying and crying duration in infants during the first months of life. Our results suggest that L. reuteri NCIMB 30351 represents a safe and effective treatment for colic in newborns.  Trial registration: ClinicalTrials.gov : NCT04262648. What is Known: • Infantile functional gastrointestinal disorders, such as colic, constipation, diarrhea, and gastroesophageal reflux (regurgitation), often occur in early infancy and, represent one of the causes of significant parental anxiety. • A number of studies have shown that both the composition and diversity of the intestinal microbiota play important roles in the development and function of the gastrointestinal tract. What is New: • The uptake of L. reuteri NCIMB 30351 leads to a significant reduction in the number of regurgitations, feeding-induced constipations, and diarrhea as well as mean daily numbers of crying and crying duration in infants during the first months of life. • L. reuteri positively influences the proportions of prevalent species, while it negatively affects both conditionally pathogenic and commensal microbes in gut microbiota.

摘要

婴儿功能性胃肠疾病,如肠绞痛、便秘、腹泻和胃食管反流(反流),常在婴儿早期发生,是导致父母显著焦虑的原因之一,也对医疗保健资源造成了重大压力。在这项研究中,我们旨在评估罗特氏乳杆菌滴剂(L. reuteri NCIMB 30351)对婴儿绞痛、便秘、腹泻和胃食管反流症状以及足月新生儿生命头几个月肠道微生物群水平的影响。这项随机、安慰剂对照、单盲(盲法)、上市后临床研究于 2020 年 3 月至 2022 年 5 月在莫斯科儿童医院和圣安德鲁医院医疗中心的两个临床单位进行,共纳入 90 名年龄在 1 至 4 个月的婴儿(平均年龄(±标准差)12.3±5.09 周;女性占 53.3%,男性占 46.7%)。患有绞痛、反流(单一症状或多种症状组合)、便秘或腹泻的患者被随机分配到两个平行组,分别接受 5 滴(2×10 菌落形成单位)的罗特氏乳杆菌 NCIMB 30351(n=60)或安慰剂(n=30),连续 25 天。便秘和腹泻的治疗组各有 30 名患者。在结构化日记中记录每日哭泣次数及其持续时间、排便和反流。通过细菌 16S rRNA 基因的深度测序分析肠道微生物群的水平。接受补充罗特氏乳杆菌 NCIMB 30351 治疗 25 天的绞痛婴儿的绞痛(从基线减少 6.3(7.34)vs 安慰剂减少 3.0(7.29),P<0.05)和哭泣次数以及哭泣持续时间的平均减少(从基线减少 144(70.7)分钟,腹泻亚组比便秘婴儿减少,与安慰剂相比,减少 80(58.9)分钟,P<0.0001),以及反流次数减少(罗特氏乳杆菌减少 4.8(2.49),安慰剂减少 3(7.74))。我们还观察到便秘婴儿的排便次数增加(罗特氏乳杆菌 2.2(2.4)vs 安慰剂 0.9(1.06),P<0.05)。腹泻婴儿的排便次数显著减少,但无统计学意义。收集样本的细菌 16S rRNA 基因分析表明,罗特氏乳杆菌积极影响优势种的比例,而消极影响条件致病菌和共生菌。在存在益生菌的情况下进行体外试验以形成梭状芽胞杆菌菌落表明,罗特氏乳杆菌能有效抑制致病性梭状芽胞杆菌的生长。本研究未报告不良事件。结论:摄入罗特氏乳杆菌 NCIMB 30351 可显著减少婴儿生命头几个月的反流、喂养诱导性便秘和腹泻以及每日哭泣次数和哭泣时间。我们的结果表明,罗特氏乳杆菌 NCIMB 30351 是一种安全有效的新生儿绞痛治疗方法。临床试验注册:ClinicalTrials.gov:NCT04262648。已知:•婴儿功能性胃肠疾病,如绞痛、便秘、腹泻和胃食管反流(反流),常在婴儿早期发生,是导致父母显著焦虑的原因之一。•大量研究表明,肠道微生物群的组成和多样性在胃肠道的发育和功能中起着重要作用。新内容:•摄入罗特氏乳杆菌 NCIMB 30351 可显著减少婴儿生命头几个月的反流、喂养诱导性便秘和腹泻以及每日哭泣次数和哭泣时间。•罗特氏乳杆菌积极影响优势种的比例,而消极影响条件致病菌和共生菌在肠道微生物群中的比例。

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