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Protein, Fiber, and Metabolic Syndrome - The PROFIMET Study (PROFIMET)

Primary Purpose

Overweight, Obesity, Metabolic Syndrome

Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
control diet, supported by dietary supplement twice daily
high cereal fiber diet, supported by dietary supplement twice daily
high protein diet, supported by dietary supplement twice daily
diet moderately high both in cereal fiber and protein, supported by dietary supplement twice daily
Sponsored by
German Institute of Human Nutrition
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Overweight focused on measuring parameters of metabolic syndrome

Eligibility Criteria

24 Years - 70 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Waist > 80 cm (females) or > 94 cm (males)
  • BMI > 25 kg/m²
  • IFG, IGT, or insulin resistance; and/or dyslipidemia; and/or high blood pressure
  • Willingness to comply with one of the randomly assigned diets over the study period

Exclusion Criteria:

  • Diabetes type 1 and type 2
  • Pregnancy
  • Allergies including food allergies
  • Metal implants
  • Chronic disease of heart, kidney, or liver
  • Relevant deviation of body weight during isoenergetic 6-weeks period (+/- 3 kg)
  • Intake of drugs with known impact on whole-body insulin sensitivity during the study (e.g. cortisone, ASS, antibiotics)
  • Missing data about primary outcome measures (Clamp data, data about dietary intake from food diaries or 3-day food protocols)
  • Significant deviation from dietary targets during the monitored 6 weeks isoenergetic period (e.g. significant deviation from 30% target for dietary fat in all groups, intake of a low protein or low fiber diet in the high protein or high fiber groups, respectively)

Sites / Locations

  • Deutsches Diabetes Zentrum; Heinrich Heine University
  • Diagnostic and Interventional Radiology, Klinikum Ernst von Bergmann, Academic Teaching Hospital, Charité University Medicine Berlin
  • Eberhard-Karls University Tübingen, Section on Experimental Radiology, Department of Diagnostic and Interventional Radiology
  • University Hospitals Coventry and Warwickshire NHS Trust

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Placebo Comparator

Experimental

Experimental

Experimental

Arm Label

1

2

3

4

Arm Description

Intervention: 'control diet, supported by dietary supplement twice daily' control diet [carbohydrates 55(50 - 60)% , protein 15(10 - 20)% protein; fat ca. 30% of energy content; dietary fiber < 15 g/1000 kcal and day; intensive dietary advice plus supplement (2 x basic supplement daily)]

Intervention: 'high cereal fiber diet, supported by dietary supplement twice daily'. high cereal fiber diet [carbohydrates 55(50 - 60)% , protein 15(10 - 20)% protein; fat ca. 30% of energy content; dietary fiber > 20 g/1000 kcal and day; intensive dietary advice plus supplement (2 x basic supplement including 2 x 15 g cereal fiber daily)]

Intervention: 'high protein diet, supported by dietary supplement twice daily' high protein diet [carbohydrates 40 - 45% , protein > 25 - 30%; fat ca. 30% of energy content; dietary fiber < 15 g/1000 kcal and day; intensive dietary advice plus supplement (2 x basic supplement including 2 x 25 g whey and plant protein daily)]

Intervention: "diet moderately high both in cereal fiber and protein, supported by dietary supplement twice daily". high cereal fiber/high protein (MIX) moderately high cereal fiber/high protein diet (carbohydrates 45- 50)% , protein 20 - 25%; fat ca. 30% of energy content; dietary fiber 15 - 20 g/1000 kcal and day; intensive dietary advice plus supplement (2 x basic supplement including 2 x 15 g cereal fiber and 2 x 25 g whey and plant protein daily)

Outcomes

Primary Outcome Measures

change in insulin sensitivity
whole-body insulin sensitivity measured with euglycemic hyperinsulinemic clamp; hepatic insulin sensitivity measured with stable isotope techniques (DD-glucose) during the clamps; relation with secondary outcome measures
change in insulin sensitivity
whole-body insulin sensitivity measured with euglycemic hyperinsulinemic clamp; hepatic insulin sensitivity measured with stable isotope techniques (DD-glucose) during the clamps; relation with secondary outcome measures

Secondary Outcome Measures

factors that may contribute explaining changes in primary outcome measures
body fat composition (MRI and ADP), liver fat (H1-spectroscopy); hormones, adipokines, inflammatory and metabolic markers; insulin signaling pathways in adipose tissue (gene expression and protein level); changes in gut microbiota; bile acids; metabolite profiles; amino acid composition in diet and circulating blood. Relation of secondary outcome measures with primary outcome measures.
biomarkers indicating dietary adherence
urinary nitrogen/creatine ratio and fecal BCAA as markers for protein intake; fecal SCFA and breath hydrogen levels as markers for fermentable fiber intake; HDL cholesterol as marker for carbohydrate intake
development of indices for the prediction of insulin resistance (liver, whole-body)
development for indices for the prediction of fat mass (liver, abdominal)

Full Information

First Posted
December 21, 2007
Last Updated
March 6, 2016
Sponsor
German Institute of Human Nutrition
Collaborators
German Federal Ministry of Education and Research, Medical University of Vienna, Heinrich-Heine University, Duesseldorf, University Hospital Tuebingen, Charite University, Berlin, Germany, University Hospitals Coventry and Warwickshire NHS Trust, Coventry University
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1. Study Identification

Unique Protocol Identification Number
NCT00579657
Brief Title
Protein, Fiber, and Metabolic Syndrome - The PROFIMET Study
Acronym
PROFIMET
Official Title
Effects of High Protein and High Cereal Fiber Diets on Insulin Sensitivity in Overweight and Obese Subjects With the Metabolic Syndrome - The PROFIMET Study
Study Type
Interventional

2. Study Status

Record Verification Date
March 2016
Overall Recruitment Status
Completed
Study Start Date
August 2007 (undefined)
Primary Completion Date
March 2010 (Actual)
Study Completion Date
July 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
German Institute of Human Nutrition
Collaborators
German Federal Ministry of Education and Research, Medical University of Vienna, Heinrich-Heine University, Duesseldorf, University Hospital Tuebingen, Charite University, Berlin, Germany, University Hospitals Coventry and Warwickshire NHS Trust, Coventry University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Randomized controlled single-blinded intervention study in 111 overweight and obese subjects with risk factors of developing type 2 diabetes, with the aim to investigate effects of isoenergetic high cereal fiber as compared with high protein diets over 6 and 18 weeks. Proof of principle study with analysis according to study protocol, investigating whether isoenergetic high cereal fiber and high protein diets with comparable fat contents, if adhered to and after exclusion of known confounders such as changes in body weight, intake of drugs with known effects on insulin sensitivity, or relevant changes in physical activity, indeed affect insulin sensitivity.
Detailed Description
This is a randomized controlled single-blinded intervention study in 111 overweight and obese subjects with risk factors of developing type 2 diabetes, with the aim to investigate effects of isoenergetic high cereal fiber versus high protein diets over 6 and 18 weeks. We also investigate effects of a combined high-cereal-fiber/high-protein (mix) diet, and effects in a control group. All diets are based on foods from plants and whey products commonly assumed to be healthy. This trial is designed as a proof of principle study focusing on participants that are likely to adhere to the respective isoenergetic diets, in order to show whether high protein versus high cereal fiber diets indeed affect insulin sensitivity, as indicated by epidemiological observations. Study participants will receive intensive and regular nutritional advice in order to achieve the respective dietary targets. Dietary adherence of the participants will be supported by providing tailored dietary supplements in all four groups, twice daily over 18 weeks. Supplements are provided for twice daily consumption for all participants in all four dietary intervention groups, throughout the 18-wk intervention (each of the participants will be instructed to consume a total 252 portions of tailored supplements during the intervention, which will handed to the participants in sealed single portions at weeks 0, 3, 6 and 12, totalling 63 portions at each occasion). The packaging of the sealed portions for the 4 intervention arms do not indicate the type of dietary intervention for the participant, but are coded for identification by the supplier. Energy contents of the supplements are considered when calculating individual energy intake. Supplements have been specifically designed for this intervention study, in order to facilitate achieving dietary targets. A 6 week strictly controlled isoenergetic study period (regular group and individual sessions, daily food diaries/FFQs over the first 6 weeks with adaptation of food intake, if necessary, as indicated by direct analysis of FFQs and food protocols, and by weighing the participants; 3-day food protocols at weeks 0, 6, 12, and 18; various biomarkers of dietary adherence) will be followed by a further 12 week ad libitum period, with ongoing intake of the respective diet including the supplements, but no further dietary advice. The primary outcome measure is the detection of diet-induced changes in insulin sensitivity during weight maintaining isoenergetic conditions. Secondary outcomes are changes in factors that may explain potential diet-induced alterations of insulin sensitivity. During the 12-weeks ad libitum period we will further investigate potential effects of the respective diet on changes in body weight, body composition and biomarkers related to energy intake. Participants will be re-invited for anthropometric measurements and measurement of biomarkers in blood (18 weeks after completion of the study), as well as for taking a second muscle tissue biopsy (subset of participants that agreed to this procedure).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Overweight, Obesity, Metabolic Syndrome
Keywords
parameters of metabolic syndrome

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
111 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Placebo Comparator
Arm Description
Intervention: 'control diet, supported by dietary supplement twice daily' control diet [carbohydrates 55(50 - 60)% , protein 15(10 - 20)% protein; fat ca. 30% of energy content; dietary fiber < 15 g/1000 kcal and day; intensive dietary advice plus supplement (2 x basic supplement daily)]
Arm Title
2
Arm Type
Experimental
Arm Description
Intervention: 'high cereal fiber diet, supported by dietary supplement twice daily'. high cereal fiber diet [carbohydrates 55(50 - 60)% , protein 15(10 - 20)% protein; fat ca. 30% of energy content; dietary fiber > 20 g/1000 kcal and day; intensive dietary advice plus supplement (2 x basic supplement including 2 x 15 g cereal fiber daily)]
Arm Title
3
Arm Type
Experimental
Arm Description
Intervention: 'high protein diet, supported by dietary supplement twice daily' high protein diet [carbohydrates 40 - 45% , protein > 25 - 30%; fat ca. 30% of energy content; dietary fiber < 15 g/1000 kcal and day; intensive dietary advice plus supplement (2 x basic supplement including 2 x 25 g whey and plant protein daily)]
Arm Title
4
Arm Type
Experimental
Arm Description
Intervention: "diet moderately high both in cereal fiber and protein, supported by dietary supplement twice daily". high cereal fiber/high protein (MIX) moderately high cereal fiber/high protein diet (carbohydrates 45- 50)% , protein 20 - 25%; fat ca. 30% of energy content; dietary fiber 15 - 20 g/1000 kcal and day; intensive dietary advice plus supplement (2 x basic supplement including 2 x 15 g cereal fiber and 2 x 25 g whey and plant protein daily)
Intervention Type
Other
Intervention Name(s)
control diet, supported by dietary supplement twice daily
Intervention Description
control diet, see above
Intervention Type
Other
Intervention Name(s)
high cereal fiber diet, supported by dietary supplement twice daily
Intervention Description
high cereal fiber diet, see above
Intervention Type
Other
Intervention Name(s)
high protein diet, supported by dietary supplement twice daily
Intervention Description
high protein diet, see above
Intervention Type
Other
Intervention Name(s)
diet moderately high both in cereal fiber and protein, supported by dietary supplement twice daily
Intervention Description
MIX diet, see above
Primary Outcome Measure Information:
Title
change in insulin sensitivity
Description
whole-body insulin sensitivity measured with euglycemic hyperinsulinemic clamp; hepatic insulin sensitivity measured with stable isotope techniques (DD-glucose) during the clamps; relation with secondary outcome measures
Time Frame
6 weeks
Title
change in insulin sensitivity
Description
whole-body insulin sensitivity measured with euglycemic hyperinsulinemic clamp; hepatic insulin sensitivity measured with stable isotope techniques (DD-glucose) during the clamps; relation with secondary outcome measures
Time Frame
18 weeks
Secondary Outcome Measure Information:
Title
factors that may contribute explaining changes in primary outcome measures
Description
body fat composition (MRI and ADP), liver fat (H1-spectroscopy); hormones, adipokines, inflammatory and metabolic markers; insulin signaling pathways in adipose tissue (gene expression and protein level); changes in gut microbiota; bile acids; metabolite profiles; amino acid composition in diet and circulating blood. Relation of secondary outcome measures with primary outcome measures.
Time Frame
0, 6, 18 weeks
Title
biomarkers indicating dietary adherence
Description
urinary nitrogen/creatine ratio and fecal BCAA as markers for protein intake; fecal SCFA and breath hydrogen levels as markers for fermentable fiber intake; HDL cholesterol as marker for carbohydrate intake
Time Frame
0, 6, 18 weeks
Title
development of indices for the prediction of insulin resistance (liver, whole-body)
Time Frame
baseline, validation after 6 -18 weeks
Title
development for indices for the prediction of fat mass (liver, abdominal)
Time Frame
baseline, validation after 6 -18 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
24 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Waist > 80 cm (females) or > 94 cm (males) BMI > 25 kg/m² IFG, IGT, or insulin resistance; and/or dyslipidemia; and/or high blood pressure Willingness to comply with one of the randomly assigned diets over the study period Exclusion Criteria: Diabetes type 1 and type 2 Pregnancy Allergies including food allergies Metal implants Chronic disease of heart, kidney, or liver Relevant deviation of body weight during isoenergetic 6-weeks period (+/- 3 kg) Intake of drugs with known impact on whole-body insulin sensitivity during the study (e.g. cortisone, ASS, antibiotics) Missing data about primary outcome measures (Clamp data, data about dietary intake from food diaries or 3-day food protocols) Significant deviation from dietary targets during the monitored 6 weeks isoenergetic period (e.g. significant deviation from 30% target for dietary fat in all groups, intake of a low protein or low fiber diet in the high protein or high fiber groups, respectively)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Martin O Weickert, MD
Organizational Affiliation
University Hospitals Coventry & Warwickshire; and University of Warwick, UK
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Andreas FH Pfeiffer, Prof
Organizational Affiliation
German Institute of Human Nutrition Potsdam-Rehbrücke; Charité-University-Medicine Berlin
Official's Role
Study Director
Facility Information:
Facility Name
Deutsches Diabetes Zentrum; Heinrich Heine University
City
Düsseldorf
Country
Germany
Facility Name
Diagnostic and Interventional Radiology, Klinikum Ernst von Bergmann, Academic Teaching Hospital, Charité University Medicine Berlin
City
Potsdam
Country
Germany
Facility Name
Eberhard-Karls University Tübingen, Section on Experimental Radiology, Department of Diagnostic and Interventional Radiology
City
Tübingen
Country
Germany
Facility Name
University Hospitals Coventry and Warwickshire NHS Trust
City
Coventry
State/Province
Warwickshire
ZIP/Postal Code
CV2 2DX
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
22104550
Citation
Gogebakan O, Kohl A, Osterhoff MA, van Baak MA, Jebb SA, Papadaki A, Martinez JA, Handjieva-Darlenska T, Hlavaty P, Weickert MO, Holst C, Saris WH, Astrup A, Pfeiffer AF; DiOGenes. Effects of weight loss and long-term weight maintenance with diets varying in protein and glycemic index on cardiovascular risk factors: the diet, obesity, and genes (DiOGenes) study: a randomized, controlled trial. Circulation. 2011 Dec 20;124(25):2829-38. doi: 10.1161/CIRCULATIONAHA.111.033274. Epub 2011 Nov 21.
Results Reference
background
PubMed Identifier
19369060
Citation
Isken F, Klaus S, Osterhoff M, Pfeiffer AF, Weickert MO. Effects of long-term soluble vs. insoluble dietary fiber intake on high-fat diet-induced obesity in C57BL/6J mice. J Nutr Biochem. 2010 Apr;21(4):278-84. doi: 10.1016/j.jnutbio.2008.12.012. Epub 2009 Apr 14.
Results Reference
background
PubMed Identifier
19366767
Citation
Weickert MO, Pfeiffer AF. Low-glycemic index vs high-cereal fiber diet in type 2 diabetes. JAMA. 2009 Apr 15;301(15):1538; author reply 1538-9. doi: 10.1001/jama.2009.483. No abstract available.
Results Reference
background
PubMed Identifier
18287346
Citation
Weickert MO, Pfeiffer AF. Metabolic effects of dietary fiber consumption and prevention of diabetes. J Nutr. 2008 Mar;138(3):439-42. doi: 10.1093/jn/138.3.439.
Results Reference
background
PubMed Identifier
16567814
Citation
Weickert MO, Mohlig M, Schofl C, Arafat AM, Otto B, Viehoff H, Koebnick C, Kohl A, Spranger J, Pfeiffer AF. Cereal fiber improves whole-body insulin sensitivity in overweight and obese women. Diabetes Care. 2006 Apr;29(4):775-80. doi: 10.2337/diacare.29.04.06.dc05-2374.
Results Reference
background
PubMed Identifier
16172868
Citation
Weickert MO, Mohlig M, Koebnick C, Holst JJ, Namsolleck P, Ristow M, Osterhoff M, Rochlitz H, Rudovich N, Spranger J, Pfeiffer AF. Impact of cereal fibre on glucose-regulating factors. Diabetologia. 2005 Nov;48(11):2343-53. doi: 10.1007/s00125-005-1941-x. Epub 2005 Sep 20.
Results Reference
background
PubMed Identifier
21633074
Citation
Weickert MO, Roden M, Isken F, Hoffmann D, Nowotny P, Osterhoff M, Blaut M, Alpert C, Gogebakan O, Bumke-Vogt C, Mueller F, Machann J, Barber TM, Petzke KJ, Hierholzer J, Hornemann S, Kruse M, Illner AK, Kohl A, Loeffelholz CV, Arafat AM, Mohlig M, Pfeiffer AF. Effects of supplemented isoenergetic diets differing in cereal fiber and protein content on insulin sensitivity in overweight humans. Am J Clin Nutr. 2011 Aug;94(2):459-71. doi: 10.3945/ajcn.110.004374. Epub 2011 Jun 1.
Results Reference
result
PubMed Identifier
22177085
Citation
Weickert MO, Arafat AM, Blaut M, Alpert C, Becker N, Leupelt V, Rudovich N, Mohlig M, Pfeiffer AF. Changes in dominant groups of the gut microbiota do not explain cereal-fiber induced improvement of whole-body insulin sensitivity. Nutr Metab (Lond). 2011 Dec 17;8:90. doi: 10.1186/1743-7075-8-90.
Results Reference
result
PubMed Identifier
22761721
Citation
Hattersley JG, Mohlig M, Roden M, Arafat AM, Loeffelholz CV, Nowotny P, Machann J, Hierholzer J, Osterhoff M, Khan M, Pfeiffer AF, Weickert MO. Quantifying the improvement of surrogate indices of hepatic insulin resistance using complex measurement techniques. PLoS One. 2012;7(6):e39029. doi: 10.1371/journal.pone.0039029. Epub 2012 Jun 22.
Results Reference
result
PubMed Identifier
22640465
Citation
Weickert MO. What dietary modification best improves insulin sensitivity and why? Clin Endocrinol (Oxf). 2012 Oct;77(4):508-12. doi: 10.1111/j.1365-2265.2012.04450.x.
Results Reference
result
PubMed Identifier
25157543
Citation
Hattersley JG, Pfeiffer AF, Roden M, Petzke KJ, Hoffmann D, Rudovich NN, Randeva HS, Vatish M, Osterhoff M, Goegebakan O, Hornemann S, Nowotny P, Machann J, Hierholzer J, von Loeffelholz C, Mohlig M, Arafat AM, Weickert MO. Modulation of amino acid metabolic signatures by supplemented isoenergetic diets differing in protein and cereal fiber content. J Clin Endocrinol Metab. 2014 Dec;99(12):E2599-609. doi: 10.1210/jc.2014-2302.
Results Reference
result
PubMed Identifier
25298375
Citation
Cuthbertson DJ, Weickert MO, Lythgoe D, Sprung VS, Dobson R, Shoajee-Moradie F, Umpleby M, Pfeiffer AF, Thomas EL, Bell JD, Jones H, Kemp GJ. External validation of the fatty liver index and lipid accumulation product indices, using 1H-magnetic resonance spectroscopy, to identify hepatic steatosis in healthy controls and obese, insulin-resistant individuals. Eur J Endocrinol. 2014 Nov;171(5):561-9. doi: 10.1530/EJE-14-0112.
Results Reference
result
Links:
URL
http://www.dife.de/en/index.php?request=/en/publikationen/publikationen.php
Description
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Protein, Fiber, and Metabolic Syndrome - The PROFIMET Study

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