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Mannheim, 14133p-ASO-food matters-2014-11-18 How quality of carbohydrates support healthy ageing Anke Sentko, Vice President Regulatory Affairs & Nutrition Communication BENEO-Institute, BENEO GmbH, Mannheim, Germany

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Page 1: How quality of carbohydrates support healthy ageingd3hip0cp28w2tg.cloudfront.net › uploads › block_files › 2014...Role of the diet in NCDs & healthy ageing Energy intake Nutrition

Mannheim, 14133p-ASO-food matters-2014-11-18

How quality of carbohydrates support healthy ageing

Anke Sentko, Vice President Regulatory Affairs & Nutrition CommunicationBENEO-Institute, BENEO GmbH, Mannheim, Germany

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© 2014 BENEO

The Environment

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3

The nutrition related challenges

Insufficient energy intake

eating habitsDeficiencies

Overload of energy intake

Non-nutrient influence

Imbalances

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4

Diet related challenges

Overweight & Obesity

Cardiovascular diseases

diet related challenges

Dental health

Impaired glucose tolerance &

Diabetes mellitus

Osteoporosis

Disturbed digestion

processes

Several types of cancer

Inner resistance / Immunity

Microbiotacomposition

Constipation / bowel

movements

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Nutrition & Health are strongly related!

5

Small mistakes in what we eat on a dailybasis may lead to major health problemslater in life!

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infants & smallchildren

schoolchildren & adolescents

young adults& middle age

elderly

very old

6

All population groups are important!

• The older people get, the more obvious nutrition mistakes become• The burden of diet related challenges increases with age

• The scene is often already set in the first years of life• Corrective influences are useful throughout life!

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Increasing overweight & obesity rates…..

Source: OECD Health Data 2012; Eurostat Statistics Database; WHO Global Infobase.http://dx.doi.org/10.1787/888932704095 ;5.11.2014

Increasing obesity rates among adults in European countries, 1990, 2000 and 2010 (or nearest years)

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11.5%

17.1%

24.4%

33.1% 33.1%

30.4%

26.6%

12.3%

20.9%

25.2%

30.2%31.4%

33.7%

28.4%

0%

5%

10%

15%

20%

25%

30%

35%

16‐24 25‐34 35‐44 45‐54 55‐64 65‐74 75+

Prevalen

ce of o

besity

Men Women

11.5%

17.1%

24.4%

33.1% 33.1%

30.4%

26.6%

12.3%

20.9%

25.2%

30.2%31.4%

33.7%

28.4%

0%

5%

10%

15%

20%

25%

30%

35%

16‐24 25‐34 35‐44 45‐54 55‐64 65‐74 75+

Prevalen

ce of o

besity

Men Women

Adult obesity prevalence by ageHealth Survey for England 2010-2012

The published Health Survey for England data used to produce this chart are available from:http://www.hscic.gov.uk/catalogue/PUB13219; http://www.noo.org.uk/slide_sets; 06.11.2014

8

Adult (aged 16+) obesity: BMI ≥ 30kg/m2

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Weight gain…. Small items with big effects….

James Hill estimated basedon U.S. survey data:

• Affecting energy balanceby only 100 kcal/day mayprevent weight gain in most of the populations

• A typical adult gains about1 kg/year over lifetime…

Hill et al, Science 2003; 299; 853-855 9

Stop middle-agedweight gain!

Moderate increase in physical activity

Eat less! - Appetite control- Lower calorie intake

Eat smart! - Drive your metabolism!- Manage your blood sugar and insulin- Increase fat burning

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Avoid weightgain!

This is equallyimportant asweight loss

Weight management

Overweightprevention

10

Weight loss

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Overweight and obesityA risk factor for further diseases

OVERWEIGHT / OBESITY

BLOOD PRESSURE

CHOLESTEROL

TRIGLYCERIDES

INSULIN RESISTANCE

GLUCOSE INTOLERANCE

THROMBOSIS RISK

ENDOTHELIAL DISFUNCTION

HYPERTENSION

CARDIO-VASCULAR

DISEASE(CVD)

TYPE-2 DIABETES MELLITUS

SOME CANCERS

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Increasing diabetes rates…..

12Source: International Diabetes Federation, IDF Diabetes Atlas 6th Edition 2013

In Europe by 2035 one in ten isaffected!

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13

There is no simple solution – multifactorial causesrequire multifactorial answers

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Nutrition & Health are strongly related!

14

Small mistakes in what we eat on a dailybasis may lead to major health problemslater in life!

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Intake recommendations for macronutrients (% of energy intake)

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Carbohydrates – natural energizing ingredients

Carbohydrates in plants• Produced by photosynthesis in plants• Stored as carbohydrates in plants (e.g. as sucrose or starch)

Carbohydrates in plants• Produced by photosynthesis in plants• Stored as carbohydrates in plants (e.g. as sucrose or starch)

Glucose in the body• Burned in human cells to provide energy for metabolism• The fuel of the body• Limited storage capacity as liver and muscle glycogen

Glucose in the body• Burned in human cells to provide energy for metabolism• The fuel of the body• Limited storage capacity as liver and muscle glycogen

Carbohydrates – natural energizing ingredients• Availability for the body is key: full small intestine digestibility• The way and speed of delivery make a difference! • Go for slow release and sustained energy delivery carbohydrates!: Go

for Palatinose™ (isomaltulose)

Carbohydrates – natural energizing ingredients• Availability for the body is key: full small intestine digestibility• The way and speed of delivery make a difference! • Go for slow release and sustained energy delivery carbohydrates!: Go

for Palatinose™ (isomaltulose)

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Focus on NUTRITION

1850 1900 20001950 2050Role of essential nutrients;

Deficiency diseases

Role of the diet in NCDs & healthy ageing

Energy intake Nutrition requirements

Maintenance of health

Reduction of risk

Energy SupplyVit & Mineral Supply

Functional ingredientsBioactive substances

The diversity of carbohydrates is

increasingly important

1919: Protein

1932: Fat1981: Carbohydrates

Role of macronutrients

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Carbohydrates – food chemistry

SaccharidesSaccharidesMono &

Di (DP 1&2)

Mono & Di

(DP 1&2)

Oligo(DP 3-

9)

Oligo(DP 3-

9)

Poly(DP≥10)

Poly(DP≥10)

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SaccharidesSaccharidesMono &

Di (DP 1&2)

Mono & Di

(DP 1&2)

Oligo(DP 3-

9)

Oligo(DP 3-

9)

Poly(DP≥10)

Poly(DP≥10)

Carbohydrates –food chemistry and the consumer

STARCHES and/orDIETARY FIBRESSUGARS

Consumer

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From food chemistry tophysiology What it really meansfor the consumer !

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Digestibility Availability

Speed ofhydrolysis Release

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When the small intestine „barrier“ is bridged….

Blood glucose Insulin

Fatoxidation

Fuel partitioning

Digestibility Availability

Speed ofhydrolysis Release

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When the large intestine is reached…

Microbiota Obesity aspects

Hunger / Satiety

Immune System

Digestibility Availability

Speed ofhydrolysis Release

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Digestibility of carbohydrates influences energy supplyand blood glucose response

24

Quick hydrolysis andcomplete absorption• fast glucose supply• 4kcal/g

Maltodextrins, starches, sucrose

Slow hydrolysis andcomplete absorption• low, slow, prolongedglucose supply• 4 kcal/gPalatinose™ (isomaltulose)

Very low/no hydrolysisand absorption• virtually no glucosesupply• 2.4 kcal/g

Isomalt

No absorption (= non-digestible carbohydrate/ dietary fibre)• no glucose supply at all• 2 kcal/g (from SCFA)

Chicory fibres (Inulin-type fructans)

-0,5

0,0

0,5

1,0

1,5

2,0

2,5

3,0

3,5

0 30 60 90 120

Ris

e in

blo

od g

luco

se (

mm

ol/L

)

Time (min)

Matodextrin

Sucrose

Palatinose™

Isomalt

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Metabolic Effects of Insulin

Postprandial Metabolic Regulation following CHO-rich Meal(physiological)

High GlucoseHigh Insulin

LipolysisLipogenesis

Fat oxidationCHO oxidation

Fat oxidationDe novo lipogenesis

Fat formationFat mobilisation

König 2008 at the 1st European BENEO Scientific Symposium, 11 April, Brussels

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-50

0

50

100

150

200

250

0 30 60 90 120

insu

lin c

hang

e (p

mol

/l)time (min)

Insulin

High glycemic, rapid release CHO

-1

0

1

2

3

4

0 30 60 90 120

bloo

d gl

ucos

e ris

e (m

mol

/l)

time (min)

Blood Glucose

High glycemic, rapid release CHO

Effects on energy partitioning and metabolic regulation

Rapid increase of CHO Oxidation High suppression of Fat Oxidation

Promote uptake of Glc Inhibit lipolysis Storage of Fat and Glc (excess)

Energy Metabolism/Fuel Partitioning

Promoting Fat utilisation at the expense of CHO oxidation

Supported for Palatinose™ (isomaltulose) by several human intervention studies

-1

0

1

2

3

4

0 30 60 90 120time (min)

Blood Glucose

low glycaemic, slow release CHO

bloo

d gl

ucos

eris

e (m

mol

/l)

-50

0

50

100

150

200

250

0 30 60 90 120

insu

lin c

hang

e (p

mol

/l)

time (min)

Insulin

low glycaemic, slow release CHO

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Does a sugar exist that is slowlydigested, fully available in a sustainedway and does not boost the insulinprofile?

YES! –it is unique!Its name is Isomaltulose (Palatinose™)You find it in honey and sugar canemolasses …. And you can buy it!

27

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Mode of energy release from Palatinose™

Slow & sustained travel through thesmall intestine and release

Sustained but complete (fullydigestible in the small intestine)

After absorption: Low andsustained blood glucose response

Sustained metabolic processing

28

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Mode of energy release from Palatinose™

Rational Proof Points

release

•Speed of hydrolysis 4-5 times slower•Enzyme kinetics (in vitro)

availablility

•Digestibility study (animal, human)•Breath H2 (animal) – no increase -> it is not reaching the colon

BGR

•> 30 human intervention studies•Blood glucose response always low andsustained

Energyproduction

•Carbohydrate oxidation steady and sustained(RQ) (shift to the right)

•Labelled isotope technique - glucose fluxbalanced & sustained

29

Slow & sustainedtravel through thesmall intestine andrelease

Sustained but complete(fully digestible in thesmall intestine)

After absorption: Low and sustained bloodglucose response

Sustained metabolicprocessing

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Digestion and absorption in the small intestine: Palatinose™ (isomaltulose) is slowly released

• Palatinose™ is hydrolysed at an enzyme complex that is involved in the digestion of sucrose and starch*

• It is hydrolysed at the isomaltase site.

• The rate of hydrolysis is thereby much slower for Palatinose™ compared to sucrose, deccelerated by a factor of about 4 to 5.

* The amylopectine derived glucose-glucose 1-6 linkage

Scheme of hydrolysis of sucrose, starch & Palatinose™ in the small intestine

Hydrolysis of Palatinose™ takes 4-5 times longer compared to sucrose

Rate of hydrolysis – sucrose vs. Palatinose™

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-0,5

0

0,5

1

1,5

2

2,5

3

0 30 60 90 120

Blood glucose response to Palatinose™ in comparison to other carbohydrates in healthy adults. The curves are generated from different studies and represent the response to 50g oral carbohydrate in drinks solution (Livesey)

Difference in blood glucose (mmol/L) SucrosePalatinose™

Time (min.)

With Palatinose™: little increase in blood glucose level

With Palatinose™: no substantial drop of blood glucose level below the base line

With Palatinose™: prolonged energy release in the form of glucose

Palatinose™ - Balanced & Sustained Energy Release in form of glucose

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Palatinose™ Ileostomy Study (Scheppach, University Würzburg)

32

Excretion

Digestibility

Excretion

AbsorptionDigestibility Absorption

Holub et al 2010 Br J Nutr 103, 1730-1737.

N = 10 patients with terminal ileostoma, intake 50g Palatinose™ hourly collection of ileostoma content for 8 hours.

• Virtually complete hydrolysis and absorption in the small intestine• No significant effect of food type

Palatinose™ is a slowly but fully digestible carbohydrate!

Drink (500 ml) Drink (500 ml) + Biscuits (140 g)

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Incretin secretion

Maeda et al (2013) 33

GIP (glucose-dependent insulinotropicpeptide)

• releasing K cells are situated in the upper part of the small intestine and are stimulated by monosaccharides

• GIP concentration after Palatinose is significantly lower

• probably because of the slow hydrolysis

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Incretin secretion

Maeda et al (2013) 34

• GLP-1 (glucagon-like peptide-1) is released from L cells in lower GI tract (distal small intestine and colon)

• Higher GLP-1 response with Palatinose

OVERALL CONCLUSION:

More favorable effects with Palatinose™ on glucose metabolism and pancreatic functions

The lower GIP levels and higherGLP-1 levels confirm the sustainedenergy release from Palatinose™

OVERALL CONCLUSION:

More favorable effects with Palatinose™ on glucose metabolism and pancreatic functions

The lower GIP levels and higherGLP-1 levels confirm the sustainedenergy release from Palatinose™

Total GLP-1

Total GLP-1 AUC

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Findings from Ang & Linn 2014: Conclusion

• Confirms low-glycaemic and -insulinaemic properties of isomaltulose in T2DM patients

• Benefits for the incretin response after isomaltulose ingestion by lowering GIP and increasing GLP-1 levels (conform to study by Maeda et al.)

• Provides data on the glucose flux after isomaltulose ingestion in humans based on stable isotope measurements:• Prolonged intestinal absorption of isomaltulose• Suppressed endogenous glucose production• Lower rate of glucose appearance in the circulation

35Ang & Linn. Am J Clin Nutr. 2014 Oct;100(4):1059-68

Slowly available isomaltulose improved overall postprandial glucose flux compared with ingestion of rapidly absorbed sucroseSlowly available isomaltulose improved overall postprandial glucose flux compared with ingestion of rapidly absorbed sucrose

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Blood Glucose and Insulin Responses –Summary from human trials with Palatinose™

Mean

-50 -40 -30 -20 -10 0 10 20 30 40 50

Difference of blood glucose peak [Isomaltulose vs Reference] (in %)

LOWER HIGHER

Mean

-100 -80 -60 -40 -20 0 20 40 60 80 100

Difference of Insulin peak [Isomaltulose vs Reference] (in %)

LOWER HIGHER

Indi

vidu

al S

tudi

esIndividual S

tudiesMaximum rise in

Blood glucose and insulin

Difference in blood glucose

Difference in insulin

Consistent findings-LOWER and SUSTAINED blood glucose response -and lower insulin with PALATINOSE™

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EFSA Opinion on Sugar ReplacersDental Health & Glycaemic Responses

37

“The Panel considers that the reduction of post-prandial glycaemic responses (as long as post-prandial insulinaemic responses are not disproportionally increased) may be a beneficial physiological effect.”

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ResultsBetter memory with Palatinose™

• After 3 hours, those having consumed the Palatinose™ based breakfast had significantly better memories (P<0.01).

• There was a significantly decrease over time in those eating the glucosebased breakfast (P<0.001).

38Young & Benton 2014 , epub ahead of print in the Eur J Nutr

20

21

22

23

24

25

26

27

1 hour 3 hours

Imm

edia

te m

emor

y (n

umbe

rof w

ords

reca

lled

±SE

) Palatinose™ Glucose

*

* P<0.01

0

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ResultsBetter mood with Palatinose™

39

• Children of the Palatinose™ group had a significantly better mood after 3 hours (P<0.03).

Young & Benton 2014 , epub ahead of print in the Eur J Nutr

4

5

6

7

1 hour 3 hours

Moo

d (m

ood

scor

es ±

SE)

Palatinose™ Glucose

*

* P<0.03

0

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Young & Benton 2014

40

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Effect of Palatinose™ on cognition in elderly

Older adults with better glucose tolerance and LBG above baselineresponded to Palatinose™ with:

• better mood ratings:• Significant vs sucr @ 105 min (p<0.01)• Significant vs gluc @ 195 min (p<0.03)

• better episodic memory:• Significant vs gluc @ 105 min (p<0.03) + @195 min (p<0.05)• Significant vs sucr @ 30 min (p<0.029), @ 105 min (p<0.04) + @ 195 min

(p<0.03)

• better working memory:• Significant vs gluc @ 180 min (p<0.05)

41Young, Benton (2014) e-SPEN 9(4):e147–e154

Palatinose™ improved cognitition andmood in older adults with better GT andno cognitive decline, effects mostpronounced in later test blocks

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Metabolic Effects of Insulin

Postprandial Metabolic Regulation following CHO-rich Meal(physiological)

High GlucoseHigh Insulin

LipolysisLipogenesis

Fat oxidationCHO oxidation

Fat oxidationDe novo lipogenesis

Fat formationFat mobilisation

König 2008 at the 1st European BENEO Scientific Symposium, 11 April, Brussels

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Palatinose™ and Fat oxidation

Effects of Palatinose™ (isomaltulose) in comparison to conventional high glycaemic carbohydrates on fat oxidation have been studied

0

20

40

60

80

100

%higher  Fat Ox. 

Individual Studies

• at rest and during physical activity

• trained endurance athletes and moderately active people

• normal weight and overweight people

• normal and impaired glucose tolerance

Lower postprandial glucose and insulin response results in higher fat oxidation in energy metabolism

Studies with Palatinose™ from BENEO

Further published studies

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Published studies on Palatinose™ and body weight / body composition

3 Human studies

• less visceral fat accumulation (obese subjects and IGT subjects) • 12 and 16 week interventions, ~18 g to 45 g/d Isomaltulose vs. conventional

sugar/breakfast • Yamori et al 2007, Oizumi et al 2007, Okuno et al 2010

5 Animal experiments

• 4-8 wk feeding studies with rats or mice• lower visceral fat at equal caloric intakes• Preliminary indications on mechanism from gene expression analysis• Arai et al 2004; Matsuo et al 2007; Sato et al 2007; Kashimura et al 2007; Fujiwara

et al 2007

Lower body fat accumulation in animals Indications for consequences for body fat composition in humans

44

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Options to reduce the blood glucose responseof foods

45

Carbohydrate QUANTITY

consumed with the food

Carbohydrate QUALITY

i.e. carbohydrate type and physiol. properties

“Food matrix” influencing the BGR

of carbohydrate-based foods

Reducing the blood glucose response of available

carbohydrates

Modification of glucose supply

Replacing available carbohydrates by partially or non-

available carbohydrates

Reduction of glucose supplyOptions:

• Smart choice of low glycaemic alternatives: Palatinose™

Options:

• Sugars replacement by polyols: Isomalt

• Sugars/starches replacement by dietary fibre: Inulin & Oligofructose

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Inulin-type fructans = plant extracts and not chemically synthezised !

OligofructosePartial hydrolysis

Chicory roots(15-17% inulin)

InulinExtraction(hot water)

Oligofructose-enriched inulin

Combination(selected chain

length)

Orafti®Synergy1

e.g. Orafti®P95

DP=2-9

GFn and FnGFn

DP=2-60+ ß(2-1)ß(2-1)

Glucose Fructose Reducing fructose

DP= Degree of Polymerisation

(enzymatic)

Terminology used in the market for this dietary fibre:

Chicory fibre, chicory root extract

Inulin, oligofructose, fructo-oligosaccharide, FOS, lcFOS, lc Inulinumbrella terms: chicory fibre, ITF (inulin-type fructans)

Note: scFOS is synthesized from sucrose and not a natural plant extract

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Mechanismby which oligofructose / inulin exert the effect

47

Blo

od g

luco

seco

ncen

trat

ion

Time

100% glycaemic sugars

glycaemic sugars OF/IN

Replacing the content of digestible andglycaemic sugars in a product partly bythe non-digestible fibres oligofructoseand/or inulin reduces the amount ofglucose that enters the body and thus

• lowers the postprandial bloodglucose response

• without disproportionallyincreased insulin levels

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Positive EFSA opinion

48EFSA opinion: http://www.efsa.europa.eu/en/efsajournal/doc/3513.pdf

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Series of human intervention studies by Dehghanand Gargari in 2013…

49

…on the effects of Inulin-type fructans on energy homeostasis, glycaemic control, inflammation, blood lipids

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Publications Dehghan & Gargari et al. 2013

50

HP-Inulin Oligofructose-enriched Inulin

Ener

gy

hom

eost

asi

s

↓* BMI (vs. baseline) ↓* BMI (vs. baseline)

↓* Body weight (vs. baseline) ↓* Body weight (vs. baseline)

↓* Energy intake & fat intake (vs. control / vs. baseline) ↓* Energy intake & fat intake (vs. baseline)

Gly

caem

icco

ntro

l

↓* Fasting blood glucose (vs. control / vs. baseline) ↓* Fasting blood glucose (vs. control / vs. baseline)

↓* HbA1 (vs. control / vs. baseline) ↓* HbA1 (vs. control / vs. baseline)

↓* Fasting insulin (vs. control / vs. baseline) -

↓* HOMA-IR (vs. control) -

Infla

mm

atio

n /

endo

toxe

mia

↓* hs-CRP (vs. control / vs. baseline) ↓* hs-CRP (vs. baseline)

↓* TNF-α (vs. control / vs. baseline) ↓* TNF-α (vs. control / vs. baseline)

- ↓* IL-6 (vs. control)

- ↓* IFN-γ (vs. control / vs. baseline)

↑* IL-10 (vs. baseline) ↔ IL-10

↓* LPS (vs. control / vs. baseline) ↓* LPS (vs. control / vs. baseline)

Blo

od li

pids ↓* Total cholesterol (vs. control / vs. baseline) ↓* Total cholesterol (vs. baseline)

↓* Triglycerides (vs. control / vs. baseline) ↓* Triglycerides (vs. control / vs. baseline)

↓* LDL (vs. control / vs. baseline) ↓* LDL (vs. control / vs. baseline)

↑* HDL (vs. control / vs. baseline) ↑* HDL (vs. baseline)

Overall, study findings support metabolic benefits

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Systematic Review and Meta-Analysis on Metabolic benefits of prebiotics in human subjects

51Kellow NJ, Coughlan MT, Reid CM. Br J Nutr. 2014 Apr 14;111(7):1147-61

RESULT: Significantly (p<0.05) reduced postprandial glucose and insulin concentrations

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SubjectiveAppetite Ratings

SatietyRegulation (Hormones)

Energy Intake

Body Weight / Body Composition

I canmeasure it

Satiety, Energy Intake & Body Weight

I cansense it

It works:It makes me eat

less!

It has an effect on me and my body!

Chicory fibres help you toeat less!

Decrease in EI demonstratedin several long-term human

intervention studies

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Positioning of consumer products

sugar out

fibre in

Lower blood glucose

53

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Physiological Properties of chicory fibres

Type of key studies Demonstrated Physiological Properties

Mouth Not fermented

Small Intestine Not digested/absorbed

glycaemic responseInsulin response

When replacing sugars/available carbohydrates reduced glycaemic response. Reduced insulin response

Large Intestine Prebiotic Selective growth of in particular bifidobacteria

Fully fermentable Saccharolytic fermentation leads to 100% benefit -> Short chain fatty acid , pH

Bowel function Improved bowel motor function, frequency

Mineral calcium absorption & bone mineral density

Gastrointestinal Tolerance subjective perception of the increased gut activity might be noticeable at high intakes, but generally not disturbing

Metabolism Weight management energy intake Weight loss, influence on satiety, fat mass

Inner resistance Incidence of illnesses

Attenuation of glycaemia / insulinaemia – long term

Glycosylated haemoglobin and fructosamin, insulin resistance (HOMA)etc

Calorie Reduction /Fibre enrichment/sugar replacement

When replacing starch, sugar or fat calories (caloric value 1-2 kcal/g depending on national legislation) 54

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55

Physiological Properties of Palatinose™

Type of key studies Demonstrated Physiological Properties

Mouth pH-Telemetry Does not promote dental caries

Small Intestine

- Hydrolysis Enzyme kinetics (in vitro) Slow hydrolysis into glucose + fructose (4-5 times slower than sucrose)

- Absorption Ileostomy-study Virtually complete hydrolysis and absorption within the small intestine

Blood glucose response Slow increase, low glycaemic responseGlucose (energy) delivery over a prolonged period of time

Insulin response Low insulin response

glycaemic Index (GI) GI= 32

Incretins (gastrointestinal hormones)

GIP ↓; GLP-1 ↑

Large Intestine

Gastrointestinal Tolerance No distress even at high levels (e.g.120g in a sports study).

Metabolism Respiratory Quotient Promotes fat burning

Body Composition Loss of body fat and body weight/Prevention of weight gain

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The quality of carbohydrates is key: BENEO ingredientscontribute to a better and healthy nutrition

56

Low energy value

Proven prebiotics

Regularity & fermentation

benefitsReduced blood sugar response

Does not promote dental

caries

Slow & complete

hydrolysis and absorption

Prolonged energy supply

Low glycaemicresponse and

low insulin response

Supports fat burning

Helps you to eat less on a

long term

Increased Calcium

absorption & stronger bones

GI tolerance as good as sugar

for Palatinose™!

Palatinose™ (isomaltulose)

Chicory fibre(Orafti® Inulin & oligorfructose

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Thank you for your attention.