AB-Biotics, S.A., ESADE Creapolis, Av. Torre Blanca, 57, Sant Cugat del Vallès, E-08172 Barcelona, Spain.
Department of Nutrition, Food Science, and Gastronomy, XaRTA ⁻ INSA, Faculty of Pharmacy, University of Barcelona, Campus de l'Alimentació de Torribera, Av. Prat de la Riba, 171, Santa Coloma de Gramenet, E-08921 Barcelona, Spain.
Nutrients. 2019 Jan 30;11(2):293. doi: 10.3390/nu11020293.
Studies of probiotics, fructan-type prebiotics, and synbiotics in patients with ulcerative colitis (UC) show significant heterogeneity in methodology and results. Here, we study the efficacy of such interventions and the reasons for the heterogeneity of their results. Eligible random controlled trials were collected from the PUBMED and SCOPUS databases. A total of 18 placebo-controlled and active treatment-controlled (i.e., mesalazine) studies were selected with a Jadad score ≥ 3, including 1491 patients with UC. Data for prebiotics and synbiotics were sparse and consequently these studies were excluded from the meta-analysis. The UC remission efficacy of probiotics was measured in terms of relative risk (RR) and odds ratio (OR). Significant effects were observed in patients with active UC whenever probiotics containing bifidobacteria were used, or when adopting the US Food and Drug Administration (FDA)-recommended scales (UC Disease Activity Index and Disease Activity Index). By the FDA recommended scales, the RR was 1.55 (CI95%: 1.13⁻2.15, -value = 0.007, ² = 29%); for bifidobacteria-containing probiotics, the RR was 1.73 (CI95%: 1.23⁻2.43, -value = 0.002, ² = 35%). No significant effects were observed on the maintenance of remission for placebo-controlled or mesalazine-controlled studies. We conclude that a validated scale is necessary to determine the state of patients with UC. However, probiotics containing bifidobacteria are promising for the treatment of active UC.
在溃疡性结肠炎(UC)患者中进行的益生菌、果聚糖型益生元和合生元研究在方法和结果上存在显著异质性。在这里,我们研究了这些干预措施的疗效以及其结果异质性的原因。从 PUBMED 和 SCOPUS 数据库中收集了合格的随机对照试验。共选择了 18 项安慰剂对照和活性治疗对照(即美沙拉嗪)研究,Jadad 评分≥3,包括 1491 例 UC 患者。由于益生元和合生元的数据稀疏,因此这些研究被排除在荟萃分析之外。益生菌对 UC 缓解的疗效通过相对风险(RR)和比值比(OR)来衡量。当使用含有双歧杆菌的益生菌或采用美国食品和药物管理局(FDA)推荐的量表(UC 疾病活动指数和疾病活动指数)时,在活动期 UC 患者中观察到显著效果。根据 FDA 推荐的量表,RR 为 1.55(95%CI:1.13⁻2.15,-值=0.007,²=29%);对于含有双歧杆菌的益生菌,RR 为 1.73(95%CI:1.23⁻2.43,-值=0.002,²=35%)。对于安慰剂对照或美沙拉嗪对照研究,在缓解的维持方面没有观察到显著效果。我们的结论是,需要一个经过验证的量表来确定 UC 患者的状态。然而,含有双歧杆菌的益生菌有望成为治疗活动期 UC 的一种方法。