Resistant starch supplementation increases crypt cell proliferative state in the rectal mucosa of older healthy participants. Issue 4 (13th April 2020)

• Record Type: Journal Article
• Authors: Malcomson, Fiona C.; Willis, Naomi D.; McCallum, Iain; Xie, Long; Ouwehand, Arthur C.; Stowell, Julian D.; Kelly, Seamus; Bradburn, D. Michael; Belshaw, Nigel J.; Johnson, Ian T.; Mathers, John C.
• Is Part Of: British journal of nutrition. Volume 124:Issue 4(2020)
• Page Start: 374
• Page End: 385
• Publication Date: 2020-04-13
• Subjects: Dietary fibre, -- Resistant starch, -- Polydextrose, -- Crypt cell proliferation, -- Apoptosis, -- Colorectal cancer risk; Nutrition -- Periodicals; 572.4
• DOI: 10.1017/S0007114520001312
• Languages: English
• ISSNs: 0007-1145

Abstract

Abstract: There is strong evidence that foods containing dietary fibre protect against colorectal cancer, resulting at least in part from its anti-proliferative properties. This study aimed to investigate the effects of supplementation with two non-digestible carbohydrates, resistant starch (RS) and polydextrose (PD), on crypt cell proliferative state (CCPS) in the macroscopically normal rectal mucosa of healthy individuals. We also investigated relationships between expression of regulators of apoptosis and of the cell cycle on markers of CCPS. Seventy-five healthy participants were supplemented with RS and/or PD or placebo for 50 d in a 2 × 2 factorial design in a randomised, double-blind, placebo-controlled trial (the Dietary Intervention, Stem cells and Colorectal Cancer (DISC) Study). CCPS was assessed, and the expression of regulators of the cell cycle and of apoptosis was measured by quantitative PCR in rectal mucosal biopsies. SCFA concentrations were quantified in faecal samples collected pre- and post-intervention. Supplementation with RS increased the total number of mitotic cells within the crypt by 60 % ( P = 0·001) compared with placebo. This effect was limited to older participants (aged ≥50 years). No other differences were observed for the treatments with PD or RS as compared with their respective controls. PD did not influence any of the measured variables. RS, however, increased cell proliferation in the crypts of the macroscopically-normal rectum of older adults. Our findings suggest that the effects of RS on CCPS are not only dose, type of RS and health status-specific but are also influenced by age. Abstract :