Gastroenterology and Nutrition Sciences 3912 Taubman Center, SPC 5362, Ann Arbor, MI 48109, USA.
Division of Gastroenterology, University of California San Diego, San Diego, CA 92093, USA.
Nutrients. 2020 Apr 10;12(4):1058. doi: 10.3390/nu12041058.
Lactose intolerance (LI) is a global problem affecting more than half of the world's population. An ultra-purified, high-concentration galacto-oligosaccharide, RP-G28, is being developed as a treatment for patients with LI. The efficacy and safety of RP-G28 in reducing symptoms of lactose intolerance were assessed in a blinded, randomized, placebo-controlled trial. In this multiclinical site, double-blinded, placebo-controlled trial, 377 patients with LI were randomized to one of two doses of orally administered RP-G28 or placebo for 30 days. A LI test and symptom assessment were performed at baseline and on day 31. The primary endpoint was a ≥4-point reduction or a score of zero on LI composite score on day 31. Voluntary milk and dairy intake and global outcome measures assessed patients' overall treatment satisfaction and quality of life before therapy and 30 days after therapy. This study received Institutional Review Board (IRB) approval. For the primary endpoint, 40% in the RP-G28 groups reported a ≥4-point reduction or no symptoms on LI symptom composite score compared to 26% with placebo (P = 0.016). Treatment with RP-G28 also led to significantly higher levels of milk and dairy intake and significant improvements in global assessments compared to placebo. RP-G28 but not placebo led to significant increases in five taxa. RP-G28 for 30 days significantly reduced symptoms and altered the fecal microbiome in patients with LI. Treatment with RP-G28 also improved milk/dairy consumption and quality of life and was safe and well tolerated.
乳糖不耐受(LI)是一个全球性问题,影响着全球一半以上的人口。一种超纯、高浓度半乳糖寡糖 RP-G28 正在被开发为 LI 患者的治疗方法。在一项双盲、随机、安慰剂对照试验中,评估了 RP-G28 减少乳糖不耐受症状的疗效和安全性。在这项多临床中心、双盲、安慰剂对照试验中,377 名 LI 患者被随机分配到口服 RP-G28 的两个剂量组或安慰剂组,治疗 30 天。在基线和第 31 天进行 LI 测试和症状评估。主要终点是第 31 天 LI 综合评分至少降低 4 分或得分为 0。自愿摄入牛奶和乳制品以及全球疗效评估指标在治疗前和治疗 30 天后评估了患者的整体治疗满意度和生活质量。这项研究获得了机构审查委员会(IRB)的批准。对于主要终点,40%的 RP-G28 组报告 LI 症状综合评分至少降低 4 分或无症状,而安慰剂组为 26%(P=0.016)。与安慰剂相比,RP-G28 治疗还导致牛奶和乳制品摄入量显著增加,整体评估显著改善。与安慰剂相比,RP-G28 但不是安慰剂导致 5 个菌属的丰度显著增加。30 天的 RP-G28 治疗显著减轻了 LI 患者的症状,并改变了粪便微生物组。RP-G28 治疗还改善了牛奶/乳制品的摄入和生活质量,且安全且耐受良好。