2017
DOI: 10.1111/1751-2980.12561
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Treatment efficacy of a probiotic preparation for non‐alcoholic steatohepatitis: A pilot trial

Abstract: Short-term treatment with the probiotic cocktail caused significant improvement of liver inflammation without adverse events and, thus, may represent a promising candidate therapeutic approach for NASH.

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Cited by 84 publications
(69 citation statements)
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“…We identified 1934 records, from which we selected 986 individual abstracts and 161 potentially relevant articles for full review (figure 1). We identified 105 articles19 25–128 reporting data from 99 different research studies including 111 different randomised comparisons of probiotics versus control (further called randomised clinical trials [RCTs], see online supplementary table 1-2) with the following outcomes: BW (number of RCTs: k=58, n=3422 individuals, median=77.4 kg), BMI (k=68, n=4015, 28.2 kg/m²), WC (k=26, n=1583, 98.8 cm); BFM (k=27, n=1562, 27.8 kg), SAT and VAT (k=5, n=543, 192.4 cm² and 114.7 cm², respectively), FG (k=83, n=5188, 6.1 mmol), HbA 1c (k=28, n=1796, 6.3%), INS (k=63, n=3854, 11.0 mU/L), HOMA-IR (k=52, n=3513, 3.2), CRP (k=41, n=2376, 3.6 mg/L), TG (k=74, n=4461, 145.4 mg/dL), ALAT (k=26, n=1466, 38.6 IU/L), ASAT (k=23, n=1340, 36.1 IU/L) and GGT (k=14, n=816, 41.5 IU/L). The median duration of the follow-up was 8 weeks (range: 2–28 weeks), probiotics dose ranged from 10 7 to 10 12 CFU daily, and 43 trials were conducted in one country (Iran).…”
Section: Resultsmentioning
confidence: 99%
“…We identified 1934 records, from which we selected 986 individual abstracts and 161 potentially relevant articles for full review (figure 1). We identified 105 articles19 25–128 reporting data from 99 different research studies including 111 different randomised comparisons of probiotics versus control (further called randomised clinical trials [RCTs], see online supplementary table 1-2) with the following outcomes: BW (number of RCTs: k=58, n=3422 individuals, median=77.4 kg), BMI (k=68, n=4015, 28.2 kg/m²), WC (k=26, n=1583, 98.8 cm); BFM (k=27, n=1562, 27.8 kg), SAT and VAT (k=5, n=543, 192.4 cm² and 114.7 cm², respectively), FG (k=83, n=5188, 6.1 mmol), HbA 1c (k=28, n=1796, 6.3%), INS (k=63, n=3854, 11.0 mU/L), HOMA-IR (k=52, n=3513, 3.2), CRP (k=41, n=2376, 3.6 mg/L), TG (k=74, n=4461, 145.4 mg/dL), ALAT (k=26, n=1466, 38.6 IU/L), ASAT (k=23, n=1340, 36.1 IU/L) and GGT (k=14, n=816, 41.5 IU/L). The median duration of the follow-up was 8 weeks (range: 2–28 weeks), probiotics dose ranged from 10 7 to 10 12 CFU daily, and 43 trials were conducted in one country (Iran).…”
Section: Resultsmentioning
confidence: 99%
“…In this phase, liver fibrosis is irreversible due to development of collagen crosslinks; as a result, any beneficial effects of probiotics at this stage of fibrosis would be highly improbable. Hence, while recent investigations with numerous strains of probiotics, including Lactobacillus rhamnosus, Lactobacillus plantarum bulgaricus, and Lactobacillus casei showed positive effects in rodent models [134][135][136][137], randomized clinical trial data collected long-term are not presently available.…”
Section: Association Between Probiotics and Clinical Outcomes In Hepamentioning
confidence: 99%
“…The continuous and recurrent course of hepatic and intestinal diseases is accompanied by a progressive structural and functional damage of these organs and is accompanied by a significant decrease in quality of life. This allows considering these diseases in terms of being both important medical and social problems and envisages the search for new directions of improving treatment and prevention of this pathology [1][2][3][4][5].…”
Section: Introductionmentioning
confidence: 99%
“…According to the literature, 37% of all patients with chronic colitis (CC) are diagnosed with fatty infiltration of the liver [6,7]. The course of hepatic and intestinal diseases is often accompanied by the damage to the intestinal microflora that contributes to the development of metabolic disorders and chronic intoxication [3]. Excessive accumulation of free radicals and lipid peroxidation products is one of the leading pathogenetic mechanisms of hepatocellular lesions due to the damage to the lipid layer of cell membranes and to metabolic disorders in the liver with the subsequent development of biliary insufficiency (BI) [8,9].…”
Section: Introductionmentioning
confidence: 99%