Hannah Grace Williams1,2, Caroline Hoad1,3, Neele Dellschaft1,3, Christabella Ng3,4, Alan Smyth3,4, Giles Major2,3, and Penny Gowland1,3
1Sir Peter Mansfield Imaging Centre, University of Nottingham, Nottingham, United Kingdom, 2Nottingham Digestive Diseases Centre, University of Nottingham, Nottingham, United Kingdom, 3National Institute for Health Research (NIHR) Nottingham Biomedical Research Centre, Nottingham University Hospitals NHS Trust and the University of Nottingham, Nottingham, United Kingdom, 4Division of Child Health, Obstetrics and Gynaecology, University of Nottingham, Nottingham, United Kingdom
Synopsis
A key colonic function is the formation of faeces and
the growth and proliferation of the microbiota. This process is little described as it is difficult to study in vivo. We aimed to
investigate it using MRI which can non-invasively monitor changes in the colonic
content. In
8 healthy volunteers we observed the initial process of faecal formation
following purgation. The results suggest that MRI can provide new insights into
the important physiological process of faeces formation and establishment of
the microbiome in the colon.
Introduction
Around 60% of faeces is composed of
bacteria and other organisms, arising from the community of microbiota that is
normally resident in the colon. The gut microbiota plays a central role in
physiology but little is known about the
process by which the bacteria build their ecosystem to form faeces.
Before optical colonoscopy, faeces is
purged from the colon using agents such as polyethylene glycol (PEG). Subsequently
faecal microbes recover to their pre-purgation profiles[1], but this process
of recovery is difficult to study. Studies of bowel preparation for colonoscopy
reported low levels of colonic content for up to 6 hours, suggesting a lack of
faecal formation during this time[2,3]. Previous studies of MRI parameters and stool samples have
shown that up to 4 hours after purgation neither MR measures nor bacteria in
stool samples had returned to baseline values, but that 24 hours after
purgation MR measures and stool bacteria had returned to baseline values[1,4].
However these subjects were nil by mouth 4 hours before and after the purgation
which will have altered the short term colonic response. Dysbiosis of the gut microbiota is associated with several
conditions (including irritable bowel syndrome, celiac disease, inflammatory
bowel disease and obesity) and therapeutic strategies have been proposed to
manage the intestinal ecosystem including the use of probiotics and prebiotics.
Faecal material is not found in a normally
functioning small bowel, but small bowel faecalisation has been observed and
adopted as a marker of bowel obstruction on computed tomography (CT)[5,6].
Standard MR enterography protocols for bowel distension involve agents which
may have a purgative effect, limiting detection of small bowel bacterial
overgrowth. Recently have found signs of small bowel faecalisation in people
with cystic fibrosis (CF) on MRI[7], leading us to raise fundamental questions
about the time course and location of faeces formation in health and disease.Aims
To investigate the change in colonic
content (faecalisation) that occurs after bowel purgation using MRI measures of
free water content, colonic volume, T1 and T2.Methods
8 healthy volunteers were asked to fast from 1pm on the day prior
to the study. At 6pm they consumed 1 litre of PEG and a second litre at 6am to ensure
full purgation of the colon[4]. Upon arrival at 10:15am participants consumed
a test meal (rice pudding, jam, cream and a drink of orange juice and water, 520
kcal). They were scanned immediately after this and then at 60, 120, 180, 240
and 300 minutes after the meal. After the 180 minutes scan a second test meal was
given (macaroni cheese, cheesecake, water, 1007 kcal). Each scan session
acquired a high resolution image and data to measure T1, T2, MR visible free water[8] and volume of the colon, details are given in Figure 1. Due to time
constraints T2 was not assessed until T120. Colonic volume was measured by drawing around
the colon on each image slice in MIPAV[9], T1 and T2 were measured at up to 3
locations along the ascending colon using previously published methods[10,11]. Results
Figure 2 shows example high resolution images acquired throughout
the day in two participants. The amount of colonic content remaining after
purgation varied between participants and may account for the variation in
baseline parameters measured. Between T120 and T300 the free water measurements
decreased on average by 70% and the anatomical volume decreased on average by
8% (Figure 3). Colonic T1 and T2 dropped across the study day (Figures 4 and
5). When combining all data points from all participants a significant strong
correlation was found between T1 and T2 (R = 0.60, p = 0.03, Pearson’s
correlation) and a weak correlation between T1 and colonic free water content
(R = 0.32 p = 0.04). Discussion
The large decreases in colonic free water, T1 and T2
suggests that the colonic contents became progressively drier during the day.
The relatively smaller decrease in colonic volume suggests that bacteria was
being incorporated into the fluid and/or meal residue was replacing water
during the day. The T1 values (1.04 ± 0.19 s) 9.5 hours after purgation (5 hours
after the first test meal) suggest that the colonic contents had not yet fully
recovered to their initial state (0.69 ± 0.17 s, based on unpublished data). This
is consistent with a previous study which found that at 4 hours post purgation
the colonic content was still recovering but by 24 hours it had recovered completely[4]. Future work will investigate whether more specific information about the
microbiome, including the formation of gas, can be obtained by comparing the
different MRI measures.Conclusion
We have documented the initial process of recovery of colonic
contents following purgation. These measurements will be used to plan future
studies aimed at assessing the status of the colonic contents, which will provide
new insights into the growth and proliferation of the microbiota throughout the
gut, the physiological process of faeces formation and colonic function in
general. Acknowledgements
No acknowledgement found.References
[1] Jalanka et al. Effects of bowel cleansing on the
intestinal microbiota. Gut, 2015. 64(10): p. 1562-8.
[2] Kim et al. Importance of the time interval between bowel
preparation and colonoscopy in determining the quality of bowel preparation for
full-dose polyethylene glycol preparation. Gut Liver, 2014. 8(6): p. 625-31.
[3] Seo et al. Optimal preparation-to-colonoscopy interval
in split-dose PEG bowel preparation determines satisfactory bowel preparation
quality: an observational prospective study. Gastrointest Endosc, 2012. 75(3):
p. 583-90.
[4] Marciani et al. Stimulation of colonic motility by oral
PEG electrolyte bowel preparation assessed by MRI: comparison of split vs
single dose. Neurogastroenterol Motil, 2014. 26(10): p. 1426-36.
[5] Mayo-Smith et al. The CT small bowel faeces sign:
description and clinical significance. Clin Radiol, 1995. 50(11): p. 765-7.
[6] Jacobs et al. Small bowel faeces sign in patients
without small bowel obstruction. Clin Radiol, 2007. 62(4): p. 353-7.
[7] Ng C, Dellschaft NS, Hoad CL, Marciani L, Ban L, Prayle
AP, Barr HL, Jaudszus A, Mainz JG, Spiller RC, Gowland P, Major G, Smyth AR.
Postprandial changes in gastrointestinal function and transit in cystic
fibrosis assessed by Magnetic Resonance Imaging. J Cyst Fibros. 2020 Jun
16:S1569-1993(20)30733-5. doi: 10.1016/j.jcf.2020.06.004. Epub ahead of print.
PMID: 32561324.
[8] Hoad, C. L. et al. Non-invasive quantification of small
bowel water content by MRI: a validation study. Phys. Med. Biol. 52, 6909–6922
(2007).
[9] M
J McAuli_e, F M Lalonde, D McGarry, W Gandler, K Csaky, and B L Trus. Medical
Image Processing, Analysis and Visualization in Clinical Research. In Proceedings
14th IEEE Symposium on Computer-Based Medical Systems. CBMS 2001,
pages 381{386, MIPAV. IEEE Comput. Soc. ISBN 0-7695-1004-3. doi:
10.1109/CBMS.2001.941749.
[10] Hoad
C, Garsed K, Marciani L, et al. Measuring T1 of chyme in the ascending colon in
health and diarrhoea predominant Irritable Bowel Syndrome (Abstract 1275). Proc
Intl Soc Mag Reson Med. 20. 2012
[11]
Hoad CL, Cox EF, Gowland PA. Quantification of T(2) in the abdomen at 3.0 T
using a T(2)-prepared balanced turbo field echo sequence. Magn Reson Med 2010;
63: 356–64.