Worthley Daniel L, Le Leu Richard K, Whitehall Vicki L, Conlon Michael, Christophersen Claus, Belobrajdic Damien, Mallitt Kylie-Ann, Hu Ying, Irahara Natsumi, Ogino Shuji, Leggett Barbara A, Young Graeme P
Royal Brisbane and Women's Hospital Research Foundation, Clinical Research Centre, Brisbane, Australia.
Am J Clin Nutr. 2009 Sep;90(3):578-86. doi: 10.3945/ajcn.2009.28106. Epub 2009 Jul 29.
Diet is an important factor in colorectal carcinogenesis; thus, dietary supplements may have a role in colorectal cancer prevention.
The objective was to establish the relative luminal, epithelial, and epigenetic consequences of prebiotic, probiotic, and synbiotic dietary supplementation in humans.
This was a randomized, double-blind, placebo-controlled, 4-wk crossover trial of resistant starch and Bifidobacterium lactis, either alone or as a combined synbiotic preparation, in 20 human volunteers. Rectal biopsy, feces, and serum samples were collected. The rectal mucosal endpoints were DNA methylation at 16 CpG island loci and LINE-1, epithelial proliferation (Ki67 immunohistochemistry), and crypt cellularity. The fecal endpoints were short-chain fatty acid concentrations, pH, ammonia, and microbiological profiles (by denaturing gradient gel electrophoresis and sequencing). Serum endpoints were a panel of cytokines and high-sensitivity C-reactive protein.
Seventeen subjects completed the entire study. The synbiotic intervention fostered a significantly different fecal stream bacterial community than did either the prebiotic (P = 0.032) or the probiotic (P = 0.001) intervention alone, in part because of a greater proportion of patients harboring fecal Lachnospiraceae spp. These changes developed in the absence of any significant differences in fecal chemistry. There were no differences in epithelial kinetics.
This synbiotic supplementation with B. lactis and resistant starch, in the doses used, induced unique changes in fecal microflora but did not significantly alter any other fecal, serum, or epithelial variables. This trial was registered in the Australian New Zealand Clinical Trials Registry at www.anzctr.org.au as ACTRN012606000115538.
饮食是结直肠癌发生的一个重要因素;因此,膳食补充剂可能在预防结直肠癌方面发挥作用。
目的是确定益生元、益生菌和合生元膳食补充剂对人体管腔、上皮和表观遗传的相对影响。
这是一项随机、双盲、安慰剂对照的4周交叉试验,在20名人类志愿者中,单独或作为联合合生元制剂使用抗性淀粉和乳酸双歧杆菌。收集直肠活检、粪便和血清样本。直肠黏膜终点指标为16个CpG岛位点和LINE-1的DNA甲基化、上皮增殖(Ki67免疫组化)和隐窝细胞密度。粪便终点指标为短链脂肪酸浓度、pH值、氨和微生物谱(通过变性梯度凝胶电泳和测序)。血清终点指标为一组细胞因子和高敏C反应蛋白。
17名受试者完成了整个研究。与单独使用益生元(P = 0.032)或益生菌(P = 0.001)干预相比,合生元干预促进了粪便菌群的显著不同,部分原因是携带粪便毛螺菌科菌属的患者比例更高。这些变化在粪便化学成分无任何显著差异的情况下出现。上皮动力学无差异。
本研究中使用的剂量的乳酸双歧杆菌和抗性淀粉的合生元补充剂可引起粪便微生物群的独特变化,但未显著改变任何其他粪便、血清或上皮变量。该试验在澳大利亚新西兰临床试验注册中心(www.anzctr.org.au)注册,注册号为ACTRN012606000115538。