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107篇 您的检索式:作者名="Lerin"
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1Saccharomyces cerevisiae CNCM I-3856 in irritable bowel syndrome: An individual subject meta-analysis显示文摘AIM To confirm previous conclusions on Saccharomyces cerevisiae(S. cerevisiae) CNCM I-3856 for irritable bowel syndrome(IBS) management.METHODS An individual patient data meta-analysis was performed on two randomized clinical trials studying the effect of S. cerevisiae CNCM I-3856 supplementation on gastrointestinal(GI) symptoms in IBS subjects. A total of 579 IBS subjects were included. Outcomes were the daily Likert scale scores of abdominal pain/discomfort and bloating [area under the curve(AUC) and weekly means], responder status, and bowel movements(stool frequency and consistency). Statistical analyses were conducted in Intent to Treat(ITT) population, IBS-C subjects and IBS-C subjects with an abdominal pain/discomfort score higher than or equal to 2 at baseline('IBS-C ≥ 2 subpopulation').RESULTS S. cerevisiae CNCM I-3856 significantly improved abdominal pain/discomfort and bloating during the second month of supplementation [AUC(W5-W8)]with improvement up to the minimal clinically relevant threshold of 10%: a 12.3% reduction of abdominal pain/discomfort in the ITT population compared to the Placebo group(P = 0.0134) has been observed. In the IBS-C ≥ 2 subpopulation, there were a 13.1% reduction of abdominal pain/discomfort and a 14.9% reduction of bloating compared to the Placebo group(P = 0.0194 and P = 0.0145, respectively). GI symptoms significantly decreased during supplementation but no statistical differences were reported between groups at the end of the supplementation period. Responder status was defined as a subject who experienced a decrease of 1 arbitrary unit(a.u.) or 50% of the abdominal discomfort score from baseline for at least 2 wk out of the last 4 wk of the study. A significant difference between groups was reported in the ITT population, when considering the first definition: subjects in the Active group had 1.510 higher odds to be a responder(reduction of 1 a.u. of abdominal pain/discomfort) compared with subjects in the Placebo group(P = 0.0240). At the end of supplementation period, stool consistency in the Active group of the ITT population was significantly improved and classified as 'normal' compared to Placebo(respectively 3.13 ± 1.197 a.u. vs 2.58 ± 1.020 a.u., P = 0.0003). Similar results were seen in the IBS-C ≥ 2 subpopulation(Active group: 3.14 ± 1.219 a.u. vs Placebo group: 2.59 ± 1.017 a.u., P = 0.0009).CONCLUSION This meta-analysis supports previous data linking S. cerevisiae I-3856 and improvement of GI symptoms, in IBS overall population and in the IBS-C and IBS-C ≥ 2 subpopulations.Amélie Cayzeele-Decherf Fanny Pélerin Sébastien Leuillet Benoit Douillard Béatrice Housez Murielle Cazaubiel Gunnard K Jacobson Peter Jüsten Pierre Desreumaux 2017World Journal of Gastroenterology2017,23,2:2
2Resveratrol Improves Mitochondrial Function and Protects against Metabolic Disease by Activating SIRT1 and PGC-1α显示文摘Marie Lagouge Carmen Argmann Zachary Gerhart-Hines Hamid Meziane Carles Lerin Frederic Daussin Nadia Messadeq Jill Milne Philip Lambert Peter Elliott Bernard Geny Markku Laakso Pere Puigserver Johan Auwerx 2006Cell2006,,6:2
3Resveratrol Improves Mitochondrial Function and Protects against Metabolic Disease by Activating SIRT1 and PGC-1α显示文摘Marie Lagouge Carmen Argmann Zachary Gerhart-Hines Hamid Meziane Carles Lerin Frederic Daussin Nadia Messadeq Jill Milne Philip Lambert Peter Elliott Bernard Geny Markku Laakso Pere Puigserver Johan Auwerx 2006Cell2006,,6:2
4Metabolic adaptations through the PGC-1α and SIRT1 pathways显示文摘RODGERS J T LERIN C GERHART-HINES Z 2008FEBS Letters2008,582,1:1
5large trials vs meta-analysis of smaller trials显示文摘Klebanoff Ma Lerine RJ Dersimonian R 1997JAMA1997,277,:1
6Resveratrol improves health and survival of mice on a high-calorie diet显示文摘Baur JA Pearson KJ Price NL Jamieson HA Lerin C Kalra A 2006Nature2006,444,:1
7Metabolic adaptations through the PGC - 1 alpha and SIRT1 pathways 显示文摘Rodgers JT Lerin C Gerhart - Hines Z 2008FEBS Lett2008,582,1:1
8Vegetative state after closed-head injury-atrumatic coma date bata bank显示文摘Lerin HS Saydijaric Eisengerg HM 1991Veport Arch Neurol1991,48,:1
9Microorganismsscreening for limonene oxidation显示文摘Lindomar LERIN’Geciane TONIAZZO 2010Food Science andTechnology2010,30,2:1
10GCN5-mediated transcriptional control of the metabolic coactivator PGC-1β through lysine acetylation 显示文摘Kelly T J Lerin C Haas W 2009J Biol Chem2009,284,30:1
11Nutrient control of glucose homeostasis through a complex of PGC-1alpha and SIRT1显示文摘Rodgers JT Lerin C Haas W 2005Nature2005,434,7029:1
12Intranasal endoscopic analysis of dacryocystorhinostomy failure 显示文摘Allen KM Berlin A J Lerine HL 1988Ophthalmic Plast Reconstr Surg1988,4,1:1
13Nutrient control of glucose homeostasis through a complex of PGC-1alpha and SIRT1显示文摘Rodgers JT Lerin C Haas W 2005Nature2005,434,7029:1
14Value of barium studies for predicting primary versus secondary non-Hogkin's gastrointestinal jymphoma显示文摘Foo CC Lerine MS Mclarney JK 2000Abdam Imaging2000,25,4:1
15Relombinant bactericidel premeability-inereasing protein(rBPI21)as adiunctire freatment for children with serere meningcococal sepsis:a randomised tria显示文摘 Quint P A Goldstein B 2000Lancent2000,356,9234:1
16Nutrient control of glucose homeostasis through a complex of PGC-1alpha and SIRT1显示文摘RODGERS J T LERIN C HAAS W 2005Nature2005,434,7029:1
17The P53 tumor suppressor gene显示文摘Lerine AJ Momand J Finlay CA 1991Nature1991,351,:1
18Nutrient control of glucosehomeostasis through a complex of PGC-1 alpha and SIRT1 显示文摘Rodgers JT Lerin C Haas W 2005Nature2005,434,:1
19Eisenberg HM Vegetative state after closed-heodinjury-atrumatie coma date bata bank显示文摘 Saydjari C 1991Veport Arch Neuro1991,48,:1
20Metabolic adaptations through the PGC- 1 alpha and SIRT1 pathways 显示文摘Rodgers JT Lerin C Gerhart-Hines Z 2008FEBS Lett2008,582,1:1
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