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Effects of Lactobacillus rhamnosus Strain GG in Pediatric Obesity‐related Liver Disease

医学 内科学 安慰剂 胃肠病学 鼠李糖乳杆菌 非酒精性脂肪肝 丙氨酸转氨酶 脂肪肝 肝病 肝功能 益生菌 疾病 病理 细菌 替代医学 生物 遗传学
作者
Pietro Vajro,Claudia Mandato,Maria Rosaria Licenziati,Adriana Franzese,Dino Franco Vitale,Selvaggia Lenta,M. Caropreso,Gianfranco Vallone,Rosaria Meli
出处
期刊:Journal of Pediatric Gastroenterology and Nutrition [Lippincott Williams & Wilkins]
卷期号:52 (6): 740-743 被引量:299
标识
DOI:10.1097/mpg.0b013e31821f9b85
摘要

ABSTRACT Objective: Various lines of evidence suggest that malfunctioning of the gut–liver axis contributes to hepatic damage of rodents and humans with nonalcoholic fatty liver disease. We evaluated the effects of short‐term probiotic treatment in children with obesity‐related liver disease who were noncompliant with lifestyle interventions. Patients and Methods: Twenty obese children (age 10.7 ± 2.1 years) with persisting hypertransaminasemia and ultrasonographic (US) bright liver were enrolled in this double‐blind, placebo‐controlled pilot study. At baseline, patients underwent clinical and laboratory anthropometric evaluation, measurement of the US hepatorenal ratio, standard liver function tests, oral glucose tolerance test, serum tumor necrosis factor‐alpha, the glucose hydrogen breath test, and evaluation of serum antibodies to antipeptidoglycan‐polysaccharide polymers. After exclusion of causes of liver disease other than obesity, patients received either probiotic Lactobacillus rhamnosus strain GG (12 billion CFU/day) or placebo for 8 weeks. Results: Multivariate analysis after probiotic treatment revealed a significant decrease in alanine aminotransferase (average variation vs placebo P = 0.03) and in antipeptidoglycan‐polysaccharide antibodies (average variation vs placebo P = 0.03) irrespective of changes in BMI z score and visceral fat. Tumor necrosis factor‐alpha, and US bright liver parameters remained fairly stable. Conclusions: Probiotic L rhamnosus strain GG warrants consideration as a therapeutic tool to treat hypertransaminasemia in hepatopathic obese children noncompliant with lifestyle interventions.
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