Probiotics plus vitamin D in irritable bowel syndrome: a prospective multicentric non-interventional study.

IF 1.9 Q3 GASTROENTEROLOGY & HEPATOLOGY
Minerva gastroenterology Pub Date : 2024-09-01 Epub Date: 2024-03-06 DOI:10.23736/S2724-5985.24.03581-2
Pauline Jouët, Claude Altman, Stanislas Bruley DES Varannes, Christine Juhel, Franck Henri
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Abstract

Background: Patients with irritable bowel syndrome (IBS) experience recurrent symptoms and anxiety disorders that significantly impact their quality of life (QoL). The aim of the study was to assess in daily practice the benefit of the combination of three probiotic strains (Lactobacillus plantarum CETC 7484 and CETC 7485; Pediococcus acidilactici CECT 7483) plus vitamin D in patients with diarrhea-predominant IBS (IBS-D) or IBS with mixed bowel movements (IBS-M).

Methods: This was a prospective, multicenter, non-interventional study in adult patients with IBS-D or IBS-M (Rome IV criteria) followed by private-practice gastroenterologists. Patients received daily one sachet of a combination of probiotics (3×109 CFU) and vitamin D (10 μg) for 42 days. The primary endpoint was the responder rate at D42 (≥50% and/or ≥100-point decrease of IBS-Severity Scoring System; IBS-SSS). Gut-related anxiety was measured with the Visceral Sensitivity Index (VSI).

Results: The full analysis set population included 246 patients (mean age, 51.2±15.4 years; women, 73.2%; IBS-D, 56.1%; IBS-M, 43.9%). At D42, among the 89 patients with evaluable data, the responder rate was 62.9% with a mean decrease of IBS-SSS of 146.6±125.9 (P<0.0001). Changes of IBS-SSS were significantly correlated with changes of IBS-QoL (r=-0.78; P<0.0001), HAD-anxiety (r=0.46; P<0.0001), HAD-depression (r=0.61; P<0.001) and VSI (r=0.74; P<0.0001).

Conclusions: These real-life results are in line with a previous randomized clinical trial demonstrating the benefits of this combination in IBS-D and IBS-M. Symptom relief was associated with improvement of IBS-QoL, anxiety, depression and specifically gut-related anxiety.

益生菌加维生素 D 治疗肠易激综合征:一项前瞻性多中心非干预研究。
背景:肠易激综合征(IBS)患者会反复出现症状和焦虑症,严重影响其生活质量(QoL)。本研究的目的是评估三种益生菌株(植物乳杆菌 CETC 7484 和 CETC 7485;酸性乳球菌 CECT 7483)与维生素 D 的组合在腹泻为主的肠易激综合征(IBS-D)或混合性肠易激综合征(IBS-M)患者日常实践中的益处:这是一项前瞻性、多中心、非干预性研究,研究对象是由私人执业胃肠病专家随访的 IBS-D 或 IBS-M (罗马 IV 标准)成年患者。患者每天接受一袋益生菌(3×109 CFU)和维生素 D(10 μg)的组合治疗,为期 42 天。主要终点是D42时的应答率(≥50%和/或IBS-Severity Scoring System;IBS-SSS)下降≥100分。肠道相关焦虑用内脏敏感指数(VSI)进行测量:完整分析组包括 246 名患者(平均年龄为 51.2±15.4 岁;女性占 73.2%;IBS-D 占 56.1%;IBS-M 占 43.9%)。第 42 天,在 89 名有可评估数据的患者中,应答率为 62.9%,IBS-SSS 平均下降率为 146.6±125.9(PConclusions:这些实际结果与之前的一项随机临床试验结果一致,证明了这种联合疗法对 IBS-D 和 IBS-M 的益处。症状缓解与 IBS-QoL、焦虑、抑郁以及肠道相关焦虑的改善有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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