4.4 Article

Changes of the Intestinal Microbiota, Short Chain Fatty Acids, and Fecal pH in Patients with Colorectal Cancer

Journal

DIGESTIVE DISEASES AND SCIENCES
Volume 58, Issue 6, Pages 1717-1726

Publisher

SPRINGER
DOI: 10.1007/s10620-012-2526-4

Keywords

Colorectal cancer; Adenoma; Microbiota; Short chain fatty acid; Fecal pH

Funding

  1. St. Luke's Life Science Institute

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Background New molecular biology-based methods of bacterial identification are expected to help elucidate the relationship between colorectal cancer (CRC) and intestinal microbiota. Although there is increasing evidence revealing the potential role of microbiota in CRC, it remains unclear whether microbial dysbiosis is the cause or the result of CRC onset. Aim We investigated the changes of intestinal environments in CRC or adenoma. Methods We analyzed 13 groups of microbiota, 8 types of organic acids, and pH in feces obtained from the following 3 groups: individuals with CRC, adenoma, and nonadenoma. Ninety-three patients with CRC and 49 healthy individuals (22 with adenoma and 27 without adenoma) were enrolled. Results The counts of total bacteria (10.3 +/- 0.7 vs. 10.8 +/- 0.3 log(10) cells/g of feces; p < 0.001), 5 groups of obligate anaerobe, and 2 groups of facultative anaerobes were significantly lower in the CRC group than in the healthy individuals. While the concentrations of short chain fatty acids (SCFAs) were significantly decreased in the CRC group, the pH was increased in the CRC group (7.4 +/- 0.8 vs. 6.9 +/- 0.6; p < 0.001). Comparison among the CRC, adenoma, and non-adenoma groups revealed that fecal SCFAs and pH in the adenoma group were intermediate to the CRC group and the non-adenoma group. Within the CRC group, no differences in microbiota or organic acids were observed among Dukes stages. Conclusions CRC patients showed significant differences in the intestinal environment, including alterations of microbiota, decreased SCFAs, and elevated pH. These changes are not a result of CRC progression but are involved in CRC onset.

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