Saccharomyces cerevisiae I-3856 in irritable bowel syndrome with predominant constipation

被引:17
作者
Mourey, Florian [1 ,5 ]
Decherf, Amelie [1 ]
Jeanne, Jean-Francois [1 ]
Clement-Ziza, Mathieu [2 ]
Grisoni, Marie-Lise [2 ]
Machuron, Francois [2 ]
Legrain-Raspaud, Sophie [1 ]
Bourreille, Arnaud [3 ]
Desreumaux, Pierre [4 ]
机构
[1] Lesaffre Grp, Res & Applicat Dept, Gnosis Lesaffre, F-59700 Marcq En Baroeul, France
[2] Lesaffre Int, Data Sci & Bioinformat Lab, Res & Dev Dept, Lesaffre Grp, F-59700 Marcq En Baroeul, France
[3] Ctr Hospitalier Univ Nantes, Inst Malad Appareil Digest, F-44093 Nantes, France
[4] Ctr Hospitalier Univ Lille, Inst Translat Res Inflammat, F-59000 Lille, France
[5] Res & Applicat Dept, Lesaffre Grp, Gnosis Lesaffre, 137 Rue Gabriel Peri, F-59700 Marcq En Baroeul, France
关键词
Probiotic; Yeast; Saccharomyces cerevisiae; Irritable bowel syndrome; Abdominal pain; Quality of life; QUALITY-OF-LIFE; FUNCTIONAL GASTROINTESTINAL DISORDERS; CEREVISIAE CNCM I-3856; SACCHAROMYCES-CEREVISIAE; ABDOMINAL-PAIN; ASCOMYCETOUS YEASTS; IMPACT; PLACEBO; IDENTIFICATION; POPULATION;
D O I
10.3748/wjg.v28.i22.2509
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BACKGROUND Probiotics are a promising solution for managing irritable bowel syndrome (IBS). Saccharomyces cerevisiae (S. cerevisiae) I-3856 has already demonstrated beneficial effects in IBS subjects, particularly in IBS with predominant constipation (IBS-C). AIM To confirm the efficacy of S. cerevisiae I-3856 in the management of gastrointestinal symptoms in IBS-C. METHODS A randomized, double-blind, placebo-controlled clinical study was performed in a total of 456 subjects. After a run-in period, subjects were randomly assigned to the group receiving S. cerevisiae I-3856 (8 x 10(9 )CFU daily) or the placebo for 8 wk, and they performed daily self-evaluations of gastrointestinal symptoms. The primary objective was to assess the effect of the probiotic on abdominal pain. The secondary objectives were the evaluation of other gastrointestinal symptoms, bowel movement frequency and consistency, and quality of life (QOL). RESULTS A significantly higher proportion of abdominal pain responders was reported in the Probiotic group (45.1% vs 33.9%, P = 0.017). A nonsignificant difference in the area under the curve for abdominal pain over the second month of supplementation was observed in subjects receiving probiotic vs placebo [P = 0.073, 95%CI: -0.59 (-1.23; 0.05)]. No statistically significant differences were reported in the evolution of bowel movement frequency and stool consistency between the groups. After 8 wk of supplementation, the overall QOL score was significantly higher in the Probiotic group than in the Placebo group [P = 0.047, 95%CI: 3.86 (0.52; 7.20)]. Furthermore, exploratory analyses showed statistically significant and clinically relevant improvements in QOL scores in abdominal pain responders vs nonresponders. CONCLUSION The results of this clinical study confirmed the abdominal pain alleviation properties of S. cerevisiae I-3856 in IBS-C. Abdominal pain relief was associated with improved QOL. ClinicalTrials.gov identifier: NCT03150212.
引用
收藏
页码:2509 / 2522
页数:14
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