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The effects of soluble corn fibre and isomaltooligosacharides on blood glucose, insulin, digestion and fermentation in healthy young males and females

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Dietary fibre refers to nutrients in the diet that gastrointestinal enzymes do not digest. If properly labelled, dietary fibres should not significantly elevate blood glucose or insulin and should ferment in the large intestine. Because of the recent rise in low-carbohydrate products on the market, consumers use these various fibres without adequate knowledge concerning whether or not these ingredients affect any blood parameters and constitute a dietary fibre. The aim of this study was to examine the impact of isomaltooligosaccharides (IMO) as compared to soluble corn fibre (SCF) consumption on blood glucose, insulin and breath hydrogen responses in healthy young men and women. After an overnight fast, nine individuals consumed 25 g of either placebo (PLA), IMO or SCF. Breath hydrogen was significantly higher in the SCF condition than in the IMO and PLA at 90, 120, 150 and 180 min (p < 0.0001). Blood glucose and insulin were higher in the IMO condition (p < 0.0001) at 30 min compared to the SCF or PLA conditions, which were not significantly different from each other. These data suggest that IMO does not constitute a dietary fibre and instead should be explored as a slow-digesting carbohydrate.
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Journal of Insulin Resistance
ISSN: (Online) 2519-7533, (Print) 2412-2785
Page 1 of 6 Original Research
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Authors:
Ryan P. Lowery1,2
Jacob M. Wilson2
Andrew Barninger2
Mahew H. Sharp2
Christopher Irvin2
Mahew Stefan2
William A. Wallace2
Gabriel J. Wilson3
Michael D. Roberts4
Ronald Wagner1
Aliaons:
1Department of Health and
Human Performance,
Concordia University Chicago,
United States
2Applied Science and
Performance Instute,
United States
3Maximum Human
Performance, United States
4Molecular and Applied
Sciences Lab, School of
Kinesiology, Auburn
University, United States
Corresponding author:
Ryan Lowery,
rlowery@theaspi.com
Dates:
Received: 07 Nov. 2017
Accepted: 12 Dec. 2017
Published: 26 Feb. 2018
How to cite this arcle:
Lowery RP, Wilson JM,
Barninger A, et al. The eects
of soluble corn bre and
isomaltooligosacharides on
blood glucose, insulin,
digeson and fermentaon in
healthy young males and
females. J. insul. resist.
2018;3(1), a32. hps://doi.
org/10.4102/jir.v3i1.32
Introducon
Dietary fibres are non-digestible carbohydrates in the diet that, when consumed, pass through the
small intestine into the large intestine where colonic microflora may partially or wholly ferment
them.1,2 While fibre intake is associated with lower body fat and decreased occurrence of diabetes
and heart disease, less than 5% of the United States population meets the standard general
recommendation of 25 g to 30 g daily.2 As a solution to the problem, scientists have attempted to
add novel forms of dietary fibres to various food sources called functional fibres.3 Two popular
sources that have risen in the food and supplement industry are isomaltooligosaccharides (IMO)
and soluble corn fibre (SCF).
Isomaltooligosaccharides primarily derive from exposure of the maltose-rich syrup to the
transglucosidase enzyme4 resulting in an isomaltose-rich syrup, high in digestion-resistant 1,6
alpha bond linkages. In vitro resistance to pancreatic enzyme digestion has led nutrition companies
to list IMO as a fibre.5 However, previous research has demonstrated that isomaltose itself is
almost completely digested (83% or more) by enzymes on the small intestinal border.4,6 Soluble
corn fibre is a newer digestion-resistant substance that still allows for the versatility of IMO in
various food preparations.7 Soluble corn fibre forms first through exposing corn syrup to a suite
of pancreatic and brush border enzymes for 48 h or more, which leaves a stream of sugars and
digestion-resistant carbohydrates.3 This syrup is then filtered repeatedly until the substance is
composed of virtually all non-digestible fibres.8,9
Numerous companies and nutrition products include and list both IMO and SCF as fibre sources.
However, to date, research has not examined the comparison of these two carbohydrates in vivo
in the same setting. Based on the criteria of fibre previously stated, for nutrition products to list
IMO or SCF as a fibre, individuals should experience all of the following criteria succeeding
consumption: (1) a non-significant change in blood glucose, (2) a resultant non-significant change
in blood insulin levels and (3) the demonstration of fermentation via the elevation of the collected
breath hydrogen samples. Given these criteria, the purpose of this study was to investigate the
impact of IMO compared to SCF consumption on blood glucose, insulin and breath hydrogen
responses in healthy young men and women.
Dietary fibre refers to nutrients in the diet that gastrointestinal enzymes do not digest. If properly
labelled, dietary fibres should not significantly elevate blood glucose or insulin and should
ferment in the large intestine. Because of the recent rise in low-carbohydrate products on the
market, consumers use these various fibres without adequate knowledge concerning whether or
not these ingredients affect any blood parameters and constitute a dietary fibre. The aim of this
study was to examine the impact of isomaltooligosaccharides (IMO) as compared to soluble corn
fibre (SCF) consumption on blood glucose, insulin and breath hydrogen responses in healthy
young men and women. After an overnight fast, nine individuals consumed 25 g of either placebo
(PLA), IMO or SCF. Breath hydrogen was significantly higher in the SCF condition than in the
IMO and PLA at 90, 120, 150 and 180 min (p < 0.0001). Blood glucose and insulin were higher in
the IMO condition (p < 0.0001) at 30 min compared to the SCF or PLA conditions, which were not
significantly different from each other. These data suggest that IMO does not constitute a dietary
fibre and instead should be explored as a slow-digesting carbohydrate.
The eects of soluble corn bre and
isomaltooligosacharides on blood glucose, insulin,
digeson and fermentaon in healthy young males
and females
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Copyright: © 2018. The Authors. Licensee: AOSIS. This work is licensed under the Creave Commons Aribuon License.
Page 2 of 6 Original Research
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Research methods and design
Study design
A randomised, double-blind, crossover study was performed
to assess the impact of IMO as compared to SCF consumption
on blood glucose, insulin and breath hydrogen responses in
healthy young men and women. Subjects reported to the
laboratory on five separate occasions (two familiarisations
and three experimental days). On occasions one and two,
subjects familiarised themselves with the breath hydrogen
testing protocol. On occasions three to five, subjects were
divided randomly into three conditions consisting of a non-
calorie water-based placebo PLA, a bolus of IMO or SCF.
Study populaon and sampling strategy
Ten men and women (aged 27.1 ± 2.7 years, body mass of
81.2 kg ± 4.4 kg, and an average height of 176.7 cm ± 2.8 cm)
in the Tampa Bay, Florida, area were recruited for this
study. No subject had any physical or medical health
complications according to past health examinations, and
all subjects were non-smokers for inclusion in this study.
Participants were required to abstain from consuming any
fibre supplements for one month prior to and during the
washout period. The subjects completed a 12 h, overnight
fast before the morning of the study and were instructed to
avoid high-fibre items (> 5 g per serving) for 24 h before
the experimental conditions. The IntegReview IRB (Austin,
TX) #8100 approved all procedures for the study, which
was carried out at the Applied Science and Performance
Institute.
Intervenon
Randomly-assigned participants consumed a non-calorie
water-based PLA, 25 g of IMO syrup (Tate & Lyle, PLC,
United Kingdom) or 25 g of SCF syrup (Tate & Lyle, PLC,
United Kingdom). Participants consumed both syrups as a
liquid formulation by mixing 25 g of syrup with eight ounces
of water and stirred until the solution was clear. A one-week
washout period existed between experimental conditions.
The identity of the conditions that were given to the
participants remained unknown to both the participants and
the primary researchers for the entire study. These solutions
were labelled as A, B or C and given to the researchers
working directly with the subjects to maintain a double-
blinded method.
Data collecon
Subjects’ blood and breath hydrogen were taken at baseline
and at 30, 60, 90, 120, 150 and 180 min following consumption
of their respective solutions. Next, venous blood was collected
from the antecubital vein using a 21-gauge needle into a
4 mL EDTA tube (BD Vacutainer®, Becton, Dickinson and
Company, Franklin Lakes, NJ) by a certified phlebotomist.
Then, blood was prepped and assayed following the 180-min
experiment for blood glucose and insulin. Finally, breath
hydrogen was gathered in real time using a Gastro+
Gastrolyzer® (coVita LLC, Santa Barbara, CA) according to
the manufacturer’s instructions.
Stascal analysis
Before carrying out the parametric statistical analysis,
dependent variables were examined for a normal distribution
and outliers through investigation of boxplots and a
normality test (e.g. Shapiro Wilk). No outliers were detected
and data pasted normality testing (Table 1). Repeated
measures analysis of variance (ANOVA) were used to
scrutinise the effects of supplementation on dependent
variables assuming group (SCF, IMO and PLA) and time
(0, 30, 60, 90, 120, 150 and 180 min) as fixed factors (GraphPad
Prism 7®, La Jolla, CA). Whenever a significant F-value was
obtained, a post-hoc test with a Tukey’s adjustment was
performed for multiple comparison purposes. The significance
level was previously set at p < 0.05. Results are expressed as
mean ± standard error mean.
Results
Of the 10 subjects, nine completed the trial, while one
withdrew from the study because of nausea associated
with measures taken during baseline testing. Thus, all
data are reported based on the final subject pool. A group
by time interaction was demonstrated for breath hydrogen
response (p < 0.0001) and post-hoc analysis revealed
that SCF was significantly higher than IMO and PLA at
90, 120, 150 and 180 min (Figure 1a and Table 2). No
significant differences occurred throughout the trial
between PLA and IMO for breath hydrogen. A group by
time interaction was demonstrated for blood glucose
response (p < 0.0001) and post-hoc analysis revealed that
IMO was significantly higher than SCF at 30 min (p <
0.0001; Figure 1b and Table 3). There were no significant
differences between SCF and PLA throughout the trial for
blood glucose. A group by time interaction was noted
for insulin (p < 0.0001), whereby IMO was significantly
higher than SCF and PLA at 30 and 60 min (Figure 1c and
Table 4). No significant differences in blood glucose were
detected between SCF and PLA throughout the trial.
In addition, Figures 2, 3 and 4 represent the individual
responses for breath hydrogen, blood glucose and insulin,
respectively.
Discussion
The purpose of this study was to investigate the impact of
IMO as compared to SCF consumption relative to the PLA on
blood glucose, insulin and breath hydrogen responses in
healthy men and women. The primary findings of this study
TABLE 1: Baseline values of dependent variables.
Variable SCF IMO PLA p
Breath hydrogen (ppm) 4 ± 3 4 ± 3 3 ± 3 0.699
Blood glucose (mg/dL) 82 ± 8 83 ± 9 86 ± 9 0.635
Insulin (IU/mL) 3.8 ± 2.3 4.1 ± 2.4 4.0 ± 2.8 0.908
IMO, isomaltooligosaccharides; PLA, placebo; SCF, soluble corn bre.
Page 3 of 6 Original Research
hp://www.insulinresistance.org Open Access
were that SCF did not raise either blood glucose or insulin as
compared to PLA. However, SCF produced a significant rise
in breath hydrogen, indicating that it arrived in the large
intestine intact and was fermented by bacteria. In contrast,
IMO produced a robust rise in blood glucose and insulin
30 min after meal consumption and did not increase breath
hydrogen. Following is a discussion of each of these variables.
Blood glucose and insulin responses
Regulation of blood glucose is highly sought after in our
society. With the resurgence of low-carbohydrate, high-fat,
ketogenic diets, it is essential to identify ingredients that do
not significantly impact blood glucose or insulin. Our
results demonstrated that IMO consumption led to a rise
of nearly 50 mg/dL in blood glucose, with a concomitant
five-fold rise in insulin at 30 min. However, no change was
seen in SCF in either variable. Consequently, these results
agreed with that of Kohmoto et al.4, who found that
IMO were nearly 85% digested. Moreover, Cervantes-Pahm
et al.8 and Kendall et al.9 found virtually no digestion in
SCF, both in vivo and in vitro.
Fermentaon
This study operationalised fermentation through the breath
hydrogen technique. Resting levels of breath hydrogen are
typically below 10 ppm; however, resting values in our study
were approximately 4 ppm in all conditions. Our results
demonstrated no change in the IMO condition relative to the
PLA. Nevertheless, SCF increased to nearly four-fold to
120 min, and remained as such throughout the experiment.
These results agreed with previous research, which
demonstrated no change in breath hydrogen over 180 min
following IMO consumption.10 It is important to note that
two subjects showed no breath hydrogen response, which
had previously been demonstrated to occur in over 15% of
c
30 60 90 120 150 180
0
Time (min)
0
5
10
15
20
25
30
Insulin (uIU/mL)
^
#,
*
# = IMO significantly higher than PLA (p < 0.01)
* = IMO significantly higher than SCF (p < 0.05)
^ = IMO signifcantly higher than SCF and PLA (p < 0.0001)
SCF
IMO
PLA
b
Time (min)
30 60 90 120 150 180
0
60
70
80
90
100
110
120
130
140
150
Blood glucose (mg/d L)
^
030 60 90 120 150 180
0
5
10
15
20
25
Time (min)
Hydrogen (ppm)
^^
^
#,*
a
SCF
IMO
PLA
# = SCF significantly higher than PLA (
p < 0.01)
* = SCF significantly higher than IMO (p < 0.05)
^ = SCF significantly higher than IMO and PLA (p < 0.0001)
^ = IMO significantly higher than SCF
and PLA(p < 0.0001)
SCF
IMO
PLA
FIGURE 1: (a) Group hydrogen responses, (b) glucose group responses (c) insulin
group responses.
TABLE 2: Group breath hydrogen response in parts per million (ppm).
Condion 0 min 30 min 60 min 90 min 120 min 150 min 180 min
SCF 4 ± 1 5 ± 1 7 ± 2 9 ± 3a,b 16 ± 4c17 ± 4c16 ± 4c
IMO 4 ± 1 4 ± 1 2 ± 1 2 ± 1 1 ± 1 2 ± 1 1 ± 0
PLA 3 ± 1 4 ± 1 3 ± 1 3 ± 1 2 ± 1 1 ± 1 0 ± 0
IMO, isomaltooligosaccharides; PLA, placebo; SCF, soluble corn bre.
a SCF signicantly higher than PLA (p < 0.01).
b SCF signicantly higher than IMO (p < 0.05).
c SCF signicantly higher than IMO and PLA (p < 0.0001).
TABLE 3: Group blood glucose response in mg/dL.
Condion 0 min 30 min 60 min 90 min 120 min 150 min 180 min
SCF 82 ± 3 89 ± 4 83 ± 4 84 ± 5 81 ± 4 82 ± 4 82 ± 3
IMO 83 ± 3 132 ± 6a91 ± 6 84 ± 4 85 ± 4 85 ± 4 86 ± 3
PLA 86 ± 3 88 ± 4 86 ± 3 87 ± 4 87 ± 4 85 ± 4 85 ± 3
IMO, isomaltooligosaccharides; PLA, placebo; SCF, soluble corn bre.
a IMO signicantly higher than SCF and PLA (p < 0.0001).
TABLE 4: Group insulin response in μIU/mL.
Condion 0 min 30 min 60 min 90 min 120 min 150 min 180 min
SCF 3.8 ± 0.8 5.4 ± 1.2 4.5 ± 0.9 4.5 ± 0.9 3.5 ± 0.9 3.8 ± 0.8 3.3 ± 0.8
IMO 4.1 ± 0.8 22.0 ± 3.7a9.4 ± 1.1b,c 6.0 ± 0.9 4.3 ± 0.8 3.9 ± 0.5 3.9 ± 0.5
PLA 4.0 ± 0.9 4.2 ± 1.0 4.2 ± 1.0 3.7 ± 0.6 3.4 ± 0.7 3.7 ± 0.7 3.0 ± 0.5
IMO, isomaltooligosaccharides; PLA, placebo; SCF, soluble corn bre.
a IMO signicantly higher than SCF and PLA (p < 0.0001).
b IMO signicantly higher than PLA (p < 0.01).
c IMO signicantly higher than SCF (p < 0.05).
Page 4 of 6 Original Research
hp://www.insulinresistance.org Open Access
030 60 90 120 150 180
Hydrogen (ppm)
0
10
20
30
40
Time (min)
030 60 90 120 150 180
Hydrogen (ppm)
0
3
6
9
12
15
0
3
6
9
12
15
Time (min)
030 60 90 120 150 180
Hydrogen (ppm)
Time (min)
a b
c
IMO
PLA
SCF
FIGURE 2: Individual breath hydrogen responses to (a) soluble corn bre, (b) isomaltooligosaccharides and (c) placebo.
030 60 90 120 150 180
Blood glucose (mg/dL)
60
70
80
90
110
110
120
60
70
80
90
110
110
120
Time (min)
030 60 90 120 150 180
Blood glucose (mg/dL)
60
70
80
90
100
110
120
140
150
160
Time (min)
030 60 90 120 150 180
Blood glucose (mg/dL)
Time (min)
a b
c
IMO
PLA
SCF
FIGURE 3: Individual blood glucose responses to (a) soluble corn bre, (b) isomaltooligosaccharides and (c) placebo.
Page 5 of 6 Original Research
hp://www.insulinresistance.org Open Access
the population.11,12 Also, prebiotic activity is indicative of
digestibility. Using inulin as a standard, Oku et al.10 found
very little prebiotic activity with IMO. More specifically,
IMOs were 14 times less effective than inulin. In contrast,
SCF was found to be equal to inulin in prebiotic activity and
three to four times more tolerable.7
Conclusions
Previous research combined with this study’s results
collectively indicate that of the two carbohydrate sources
examined, SCF – but not IMO – can be listed on food labels as
a dietary fibre source. Given its versatility in food preparation,
SCF appears to be a viable option for manufacturers to
produce high-fibre, palatable food-based products that
would support a low-carbohydrate, ketogenic diet.
Acknowledgements
The authors would like to thank Daniel Orrego and Ron
Penna for their thoughtful insights into this study design.
Leftover funds from a project supported by Quest Nutrition
were used to pay for the blood analysis for this study. Quest
Nutrition sells nutritional products that use soluble corn fibre.
Compeng interests
The authors declare that they have no financial or personal
relationships which may have inappropriately influenced
them in writing this article.
Authors’ contribuons
R.P.L. was the project leader. J.M.W assisted with experimental
and project design. A.B., M.H.S., C.I., W.A.L., and M.S
assisted with experimental and project design and helped
with data collection. G.J.W, M.D.R. and R.W. helped oversee
the draft and final version of the manuscript.
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IMO
PLA
SCF
0
030 60 90 120 150 180
2
4
6
8
10
12
14
Insulin (uIU/mL)
Time (min)
030 60 90 120 150 180
Insulin (uIU/mL)
0
5
10
15
20
25
30
35
40
45
50
Time (min)
030 60 90 120 150 180
Insulin (uIU/mL)
0
2
4
6
8
10
12
14
Time (min)
a b
c
FIGURE 4: Individual insulin responses to (a) soluble corn bre, (b) isomaltooligosaccharides and (c) placebo.
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 9. Kendall C, Esfahani A, Homan A, et al. Eect of novel maize-based dietary bers
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... Recent studies in humans reported conflicting results regarding the effects of IMO ingestion on glycemia (Gourineni, Stewart, Icoz, & Zimmer, 2018;Grubic et al., 2018;Lowery et al., 2018). Concurrent measurement of circulating insulin was done, however, the studies did not report effects of IMO on incretins that act as co-stimulants of insulin along with glucose. ...
... Another human study examining the partial digestibility of a different IMO preparation demonstrated similar incremental increases at 30 min of 1.3 mmol/l and 25.3 µU/ml (878 pg/ml), for glucose and insulin respectively, following 25 g IMO consumption (Kohmoto et al., 1992). More recently, 25 g IMO raised blood glucose by 2.7 mmol/l and insulin by 17.9 µU/ml (626 pg/ml) at 30 min post-ingestion (Lowery et al., 2018). Furthermore, compared with dextrose, blends of 50-70% IMO with mono-and disaccharides elicited similar plasma glucose and Fig. 3. Effect of IMO on circulating incretin hormones. ...
... A digestibility of about 50% of the VitaFiber™ IMO preparation used in this study was recently confirmed in a trial with ileal cannulated swine (Hu, Heyer, Wang, Zijlstra, & Ganzle, 2019). Another IMO preparation had low fermentability based on H 2 breath expiration (Lowery et al., 2018), indicating that it was largely digested. Regarding generalizability of these results, the composition of IMO that are produced from starch is overall comparable, however, different commercial preparations vary with respect to their content of monosaccharides, the average DP, and the ratio of α(1 → 6) to α(1 → 4) linkages; therefore, their effect on glycemia and hormone secretion may also differ. ...
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The postprandial blood glucose and hormonal responses to isomalto-oligosaccharides (IMO) are unclear. The objective of this study was to compare postprandial glucose, insulin and incretin responses of IMO with dextrose in healthy adults. In trial 1, blood glucose responses to IMO, isomaltose, dextran and maltodextrin were compared with dextrose in n = 12 participants. In trial 2, serial glucose and hormone measurements over 2 h were measured in n = 10 participants. The glycemic effect of IMO was calculated using the Glycemic Glucose Equivalents (GGE) and Relative Glycemic Index (RGI). IMO exhibited a hyperglycemic effect compared to dextrose as indicated by a GGE of 1.35 g and an RGI of 27.0 g. The responses to IMO of both active GLP-1 and GIP were similar to that of dextrose. The paradoxical hyperglycemic response despite robust insulin and incretin secretion requires further investigation.
... The injection volume was 20 μl, and the flow rate 1.2 ml/min. The elution of sugars was carried out with 75% acetronitrile with detection with a differential refractometer (RID-10A, Shimadzu, Japan) (Ryan et al, 2018). Initial moisture content of each substrate was 60%. ...
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The demand for ultra-processed food products is directly related to people's rapidly changing habits and diet. This transition and the associated detrimental health issues have triggered global health authorities to raise the concern of increasing more fibre, physiologically functional foods, and ingredients into western diets. Human endogenous enzymes can readily digest ultra-processed starch-containing foods; hence, they are highly glycemic and associated with chronic diseases such as diabetes, obesity, and cardiovascular diseases. Therefore, the development of starch-based food ingredients with a low glycemic response is deemed necessary. Starch-derived ingredients, including: polydextrose(PD), resistant dextrins and maltodextrins (RMD), cyclodextrins (CD), Isomaltooligosaccharides (IMO) and resistant starch (RS), have been heavily investigated for their health benefits and various health claims were approved promoting their use in many food applications. These ingredients are either chemically (PD and RS-IV) or enzymatically produced (CD, RMD, and IMO). This review focuses on the various production processes of these novel ingredients, food applications, glycemic response roles, and a commercial overview of available brands. Enzymatically produced starch-ingredients proved functional, promoting their extensive future application since consumers prefer safely produced ingredients to be incorporated into their diet.
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Dietary management of the human gut microbiota towards a more beneficial composition is one approach that may improve host health. To date, a large number of human intervention studies have demonstrated that dietary consumption of certain food products can result in significant changes in the composition of the gut microbiota i.e. the prebiotic concept. Thus the prebiotic effect is now established as a dietary approach to increase beneficial gut bacteria and it has been associated with modulation of health biomarkers and modulation of the immune system. Promitor™ Soluble Corn Fibre (SCF) is a well-known maize-derived source of dietary fibre with potential selective fermentation properties. Our aim was to determine the optimum prebiotic dose of tolerance, desired changes to microbiota and fermentation of SCF in healthy adult subjects. A double-blind, randomised, parallel study was completed where volunteers (n = 8/treatment group) consumed 8, 14 or 21 g from SCF (6, 12 and 18 g/fibre delivered respectively) over 14-d. Over the range of doses studied, SCF was well tolerated Numbers of bifidobacteria were significantly higher for the 6 g/fibre/day compared to 12g and 18g/fibre delivered/day (mean 9.25 and 9.73 Log10 cells/g fresh faeces in the pre-treatment and treatment periods respectively). Such a numerical change of 0.5 Log10 bifidobacteria/g fresh faeces is consistent with those changes observed for inulin-type fructans, which are recognised prebiotics. A possible prebiotic effect of SCF was therefore demonstrated by its stimulation of bifidobacteria numbers in the overall gut microbiota during a short-term intervention.
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The health benefits of dietary fiber have long been appreciated. Higher intakes of dietary fiber are linked to less cardiovascular disease and fiber plays a role in gut health, with many effective laxatives actually isolated fiber sources. Higher intakes of fiber are linked to lower body weights. Only polysaccharides were included in dietary fiber originally, but more recent definitions have included oligosaccharides as dietary fiber, not based on their chemical measurement as dietary fiber by the accepted total dietary fiber (TDF) method, but on their physiological effects. Inulin, fructo-oligosaccharides, and other oligosaccharides are included as fiber in food labels in the US. Additionally, oligosaccharides are the best known "prebiotics", "a selectively fermented ingredient that allows specific changes, both in the composition and/or activity in the gastrointestinal microflora that confers benefits upon host well-bring and health." To date, all known and suspected prebiotics are carbohydrate compounds, primarily oligosaccharides, known to resist digestion in the human small intestine and reach the colon where they are fermented by the gut microflora. Studies have provided evidence that inulin and oligofructose (OF), lactulose, and resistant starch (RS) meet all aspects of the definition, including the stimulation of Bifidobacterium, a beneficial bacterial genus. Other isolated carbohydrates and carbohydrate-containing foods, including galactooligosaccharides (GOS), transgalactooligosaccharides (TOS), polydextrose, wheat dextrin, acacia gum, psyllium, banana, whole grain wheat, and whole grain corn also have prebiotic effects.
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Dietary fiber has well-established beneficial effects on laxation. Many fibers have been developed with positive sensory properties and 2 such fibers are polydextrose (PDX) and soluble corn fiber (SCF), which can be added to many commercially produced products. We conducted a randomized, double-blind, placebo-controlled, crossover study comparing the laxative effects of PDX and SCF at a dose of 20 g/d with a low fiber control (LFC) eaten daily as a muffin and cereal in 36 healthy men and women. Each treatment period was 10 d with a 2-wk washout period between. Participants collected fecal samples during the last 5 d of each treatment and completed food diaries and gastrointestinal tolerance questionnaires on d 1, 2, and 10 of each treatment period. Five-day fecal wet weight was higher after the PDX and SCF treatments than the LFC treatment (P ≤ 0.0007). The number of stools per day and daily fecal output also were significantly greater during the PDX treatment compared with the LFC treatment. The whole gut transit time did not differ among treatments. The PDX treatment resulted in a softer stool (P = 0.002) than the SCF and LFC treatments. Fecal pH was lowered by the PDX treatment (P = 0.02), whereas SCF tended to lower it compared with the LFC treatment (P = 0.07). When the participants consumed PDX and SCF, they reported significantly more flatulence and borborygmi compared with when they consumed the LFC. Consumption of PDX and SCF at a dose of 20 g/d results in a mild laxative effect with nominal gastrointestinal tolerance issues.
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The effect of isomalto-oligosaccharides on human fecal flora was studied. Bifidobacteria and the Bacteroides fragilis group from human intestine could utilize isomalto-oligosaccharides but Escherichia coli and other bacteria could not. After the administration of isomaltooligosaccharides (13.5 g daily for 2 weeks) to healthy adult men and senile persons, the numbers of bifidobacteria in the feces increased. The consistency of feces was improved. These studies may support the usefulness of isomalto-oligosaccharides as components of new healthy foodstuffs for the improvement of the intestinal flora.
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We sought to determine whether a low fermentable substrate diet (LFSD) decreases abdominal pain frequency in children with irritable bowel syndrome (IBS) and to identify potential microbial factors related to diet efficacy. Pain symptoms, stooling characteristics, breath hydrogen and methane, whole intestinal transit time, stool microbiome, and metabolite composition were collected and/or documented in eight children with IBS at baseline and during one week of an LFSD intervention. Pain frequency (P<0.05), pain severity (P<0.05), and pain-related interference with activities (P<0.05) decreased in the subjects while on the LFSD. Responders vs. non-responders: four children (50%) were identified as responders (> 50% decrease in abdominal pain frequency while on the LFSD). There were no differences between responders and non-responders with respect to hydrogen production, methane production, stooling characteristics, or gut transit time. Responders were characterized by increased pre-LFSD abundance of bacterial taxa belonging to the genera Sporobacter (P<0.05) and Subdoligranulum (P<0.02) and decreased abundance of taxa belonging to Bacteroides (P<0.05) relative to non-responders. In parallel, stool metabolites differed between responders and non-responders and were associated with differences in microbiome composition. These pilot study results suggest that an LFSD may be effective in decreasing GI symptoms in children with IBS. Microbial factors such as gut microbiome composition and stool metabolites while on the diet may relate to LFSD efficacy.
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IMO, a commercially available mixture of isomaltooligosaccharides, was fractionated by preparative HPLC, and two fractions (IM02 and IM03) were obtained. IM02 contained mainly disaccharides (86.4%), which IM03 contained tri- and higher oligosaccharides (89.9%). The administration of IM02 or IM03, ranging in amount from 5 to 20g/day, increased human intestinal bifidobacteria in dose-dependent manner. An IM02 intake of 10 g/day and IM03 of 5 g/day each produced a significant increase of bifidobacterial number in feces and the ratio in fecal microflora within 12 days.
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Isomaltooligosaccharides (IMO), sweeteners derived from corn-starch, selectively promote the growth of bifidobacteria in the human intestine. The metabolic fate of IMO in healthy men was investigated. The expiration rates of excess 13CO2 and hydrogen of six men were measured while sedentary and while taking physical exercise after the 13C-labeled IMO intakes. The breath H2 excretion kept at a constant state after IMO ingestion in the sedentary test and increased in the exercise test. The serum glucose and serum insulin increased 30 min after IMO ingestion. The 13CO2 recoveries were 28.7% in the sedentary test and 60.9% in the exercise test. These recoveries were 70–80% compared those of maltose. These results indicated that a part of IMO was digested and the residual IMO was fermented by intestinal flora. The energy value of IMO might be about 75% of that of maltose.
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Background and aim: Current treatment for irritable bowel syndrome (IBS) is suboptimal. Fermentable oligo-, di-, mono-saccharides and polyols (FODMAPs) may trigger gastrointestinal symptoms in IBS patients. Our aim was to determine whether a low FODMAP diet improves symptoms in IBS patients. Methods: Irritable bowel syndrome patients, who had performed hydrogen/methane breath testing for fructose and lactose malabsorption and had received dietary advice regarding the low FODMAP diet, were included. The effect of low FODMAP diet was prospectively evaluated using a symptom questionnaire. Furthermore, questions about adherence and satisfaction with symptom improvement, dietary advice and diet were assessed. Results: Ninety patients with a mean follow up of 15.7 months were studied. Most symptoms including abdominal pain, bloating, flatulence and diarrhoea significantly improved (p < 0.001 for all). 75.6%, 37.8% and 13.3% of patients had fructose, lactose malabsorption or small intestinal bacterial overgrowth respectively. Fructose malabsorption was significantly associated with symptom improvement (abdominal pain odds ratio (OR) 7.09 [95% confidence interval (CI) 2.01-25.0], bloating OR 8.71 (95% CI 2.76-27.5), flatulence OR 7.64 (95% CI 2.53-23.0) and diarrhoea OR 3.39 (95% CI 1.17-9.78), p < 0.029 for all). Most patients (75.6%) were adherent to the diet, which was associated with symptom improvement (abdominal pain, bloating, flatulence and diarrhoea all significantly associated with adherence, r > 0.27, p < 0.011). Most patients (72.1%) were satisfied with their symptoms. Conclusions: The low FODMAP diet shows efficacy for IBS patients. The current strategy of breath testing and dietary advice provides a good basis to understand and adhere to the diet.
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Postprandial hyperglycemia has been associated with increased oxidative stress and the development of diabetes, heart disease and all-cause mortality. To assess the effect of novel maize-based dietary fibers on postprandial glycemia and to assess the correlation between a rapid in vitro digestibility system and the blood glucose response. In a clinical study, 12 healthy volunteers were fed seven test beverages containing maize-based fiber ingredients (25g total carbohydrate) along with 2 control meals on separate occasions in random order. Capillary blood samples were obtained and the relative glycemic and insulinemic responses were assessed by calculating the incremental area under the 2 h blood response curves. In vitro digestibility studies of the test fibers and control were also undertaken to determine if these correlated with the clinical findings. All test fibers resulted in significantly lower glycemic and insulinemic responses for the incremental area under the curve (iAUC) and at all time points compared with the control (P < 0.05). The in vitro digestibility curves were comparable to the cumulative in vivo iAUCs. In vitro data expressed as percent digestion correlated significantly with the in vivo iAUC for the first 30min of the test meal (P < 0.05). These novel maize-based dietary fibers all produce lower postprandial glycemic and insulinemic responses than the control. While further assessment is necessary in beverage and foods containing these fibers, they may be effective in applications for dietary strategies to control diabetes and other chronic diseases. In addition, the in vitro digestibility assay correlated well with in vivo data and may be useful in guiding product development.
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To clarify the difference of digestibility in the small intestine among fructo-oligosaccharide (FOS), galactosyl-sucrose (GS), and isomalto-oligosaccharide (IMO) using breath hydrogen test. The first step: screening test of breath hydrogen excretion and FOS tolerance test to select the subjects. The second step: breath hydrogen test of three kinds of oligosaccharides, carried out using precautionary regulations. The ingestion order was 10 g of FOS, GS, and IMO, with increases, at 1-week interval, up to 20 g, respectively. Breath gas was collected before, at 20 min intervals from 40 to 120 min after, and at 30 min intervals from 120 min to 7 h after ingestion of test substance. Laboratory of Public Health Nutrition, Department of Nutrition and Health Sciences, Siebold University of Nagasaki, Nagasaki, Japan. A total of nine males (average: age 25.7+/-3.5 y, weight 61.9+/-8.8 kg, height 170.0+/-6.0 cm) and 29 females (average: 23.1+/-7.2 y, 52.9+/-5.3 kg, 157.5+/-5.1 cm) from the University of Tokyo and Siebold University of Nagasaki. Breath hydrogen excretion from end-expiratory gas. : Breath hydrogen of FOS was more remarkably excreted than that of GS; that of IMO was slight; and that of AUC (10 g) was significantly different. FOS was 9768+/-3253 ppm, GS was 3662+/-2632 ppm, and IMO was 831+/-1154 ppm. A dose dependence was observed at doses between 10 and 20 g of FOS and GS, and the initial time of 20 g was earlier than that of 10 g. FOS was not hydrolyzed, GS was slightly hydrolyzed, and IMO was readily hydrolyzed by small intestinal enzymes. H(2) gas reflected fermentability in the large intestine. Siebold University of Nagasaki.