Background-Low fat and wheat interventions significantly reduced growt
h of small to large adenomas and modestly suppressed rectal epithelial
cell proliferation in the Australian Polyp Prevention Project. Aim-To
study the effect of unprocessed wheat bran, unprocessed oat bran and
processed wheat bran (Kellogg's All Bran) on rectal epithelial cell pr
oliferation. Patients-Twenty subjects with recent adenomas and a high
fat background diet were recruited. Methods-Rectal biopsy specimens we
re taken at entry and at the end of three six-week periods of oat bran
(64 g/day), wheat bran (25 g/day) and All Bran (38 g/day), all in ass
ociation with a diet <25% energy as fat, in a randomised cross-over tr
ial. Each of the bran supplements had a total of 11 g dietary fibre. T
he biopsy specimens were fixed in methacarn and stained immunohistoche
mically for presence of the proliferating cell nuclear antigen (PCNA).
The kinetics used to measure proliferation were labelling index, whol
e distribution of labelled cells, and labelled cells in the top two-fi
fths of crypts using analysis of variance. Results-There were no signi
ficant differences in mean labelling indexes between or in the percent
age of in the top two-fifths (p=0.59), but activity in the top two-fif
ths of crypts was lowest with wheat bran. The mean (SD) labelling inde
xes were 2.23 (0.11)% for control, 2.13 (0.08)% for wheat bran, 2.19 (
0.09)% for oat bran, and 2.12 (0.08)% for All Bran. The proportion in
the top two-fifths of the crypts was 2.6 (0.6)% for control, 2.15 (0.5
)% for wheat bran, 3.3 (0.9)% for oat bran, and 3.1 (0.9)% for All Bra
n. On analysis of whole distribution, there was no significant overall
effect of diets but there was a difference between subjects. Analysis
including total fibre intake also did not identify effects on prolife
ration. Conclusion-In this study of high risk subjects with initial hi
gh fat diets, dietary fibre in association with a low fat diet had no
effect on rectal epithelial cell proliferation, although wheat bran ha
d the greatest effect on percentage of labelled cells in the top two-f
ifths of crypts.