A human, double-blind, placebo-controlled, crossover trial of prebiotic, probiotic, and synbiotic supplementation: effects on luminal, inflammatory, epigenetic, and epithelial biomarkers of colorectal cancer

被引:110
作者
Worthley, Daniel L. [1 ,2 ,3 ]
Le Leu, Richard K. [3 ,4 ]
Whitehall, Vicki L. [1 ,2 ]
Conlon, Michael [4 ]
Christophersen, Claus [4 ]
Belobrajdic, Damien
Mallitt, Kylie-Ann [5 ]
Hu, Ying [3 ]
Irahara, Natsumi [6 ]
Ogino, Shuji [6 ,7 ,8 ]
Leggett, Barbara A. [1 ,2 ]
Young, Graeme P. [3 ]
机构
[1] Royal Brisbane & Womens Hosp Res Fdn, Clin Res Ctr, Brisbane, Qld, Australia
[2] Queensland Inst Med Res, Conjoint Gastroenterol Lab, Brisbane, Qld 4006, Australia
[3] Flinders Univ S Australia, Flinders Ctr Canc Prevent & Control, Adelaide, SA, Australia
[4] CSIRO, Preventat Hlth Natl Res Flagship, Adelaide, SA, Australia
[5] Queensland Inst Med Res, Stat Unit, Brisbane, Qld 4006, Australia
[6] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[7] Harvard Univ, Sch Med, Boston, MA USA
[8] Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
关键词
CHAIN FATTY-ACIDS; ISLAND METHYLATOR PHENOTYPE; GENOTOXIN-INDUCED APOPTOSIS; RESISTANT STARCH; DIETARY FIBER; COLON-CANCER; MICROSATELLITE INSTABILITY; BIFIDOBACTERIUM-LACTIS; MAIZE STARCH; FERMENTATION;
D O I
10.3945/ajcn.2009.28106
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background: Diet is an important factor in colorectal carcinogenesis; thus, dietary supplements may have a role in colorectal cancer prevention. Objective: The objective was to establish the relative luminal, epithelial, and epigenetic consequences of prebiotic, probiotic, and synbiotic dietary supplementation in humans. Design: 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. Results: 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. Conclusions: 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. Am J Clin Nutr 2009;90:578-86.
引用
收藏
页码:578 / 586
页数:9
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