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Published in: Diabetologia 2/2015

01-02-2015 | Article

Low-energy diets differing in fibre, red meat and coffee intake equally improve insulin sensitivity in type 2 diabetes: a randomised feasibility trial

Authors: Bettina Nowotny, Lejla Zahiragic, Alessandra Bierwagen, Stefan Kabisch, Jan B. Groener, Peter J. Nowotny, Ann Kristin Fleitmann, Christian Herder, Giovanni Pacini, Iris Erlund, Rikard Landberg, Hans-Ulrich Haering, Andreas F. H. Pfeiffer, Peter P. Nawroth, Michael Roden

Published in: Diabetologia | Issue 2/2015

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Abstract

Aims/hypothesis

Epidemiological studies have found that a diet high in fibre and coffee, but low in red meat, reduces the risk for type 2 diabetes. We tested the hypothesis that these nutritional modifications differentially improve whole-body insulin sensitivity (primary outcome) and secretion.

Methods

Inclusion criteria were: age 18–69 years, BMI ≥30 kg/m2, type 2 diabetes treated with diet, metformin or acarbose and known disease duration of ≤5 years. Exclusion criteria were: HbA1c >75 mmol/mol (9.0%), type 1 or secondary diabetes types and acute or chronic diseases including cancer. Patients taking any medication affecting the immune system or insulin sensitivity, other than metformin, were also excluded. Of 59 patients (randomised using randomisation blocks [four or six patients] with consecutive numbers), 37 (54% female) obese type 2 diabetic patients completed this controlled parallel-group 8-week low-energy dietary intervention. The participants consumed either a diet high in cereal fibre (whole grain wheat/rye: 30–50 g/day) and coffee (≥5 cups/day), and free of red meat (L-RISK, n = 17) or a diet low in fibre (≤10 g/day), coffee-free and high in red meat (≥150 g/day) diet (H-RISK, n = 20). Insulin sensitivity and secretion were assessed by hyperinsulinaemic–euglycaemic clamp and intravenous glucose tolerance tests with isotope dilution. Whole-body and organ fat contents were measured by magnetic resonance imaging and spectroscopy.

Results

Whole-body insulin sensitivity increased in both groups (mean [95% CI]) (H-RISK vs L-RISK: 0.8 [0.2, 1.4] vs 1.0 [0.4, 1.7] mg kg−1 min−1, p = 0.59), while body weight decreased (−4.8% [−6.1%, −3.5%] vs −4.6% [−6.0%, −3.3%], respectively). Hepatic insulin sensitivity remained unchanged, whereas hepatocellular lipid content fell in both groups (−7.0% [−9.6%, −4.5%] vs −6.7% [−9.5%, −3.9%]). Subcutaneous fat mass (−1,553 [−2,767, −340] cm3 vs −751 [−2,047; 546] cm3, respectively) visceral fat mass (−206 [−783, 371] cm3 vs −241 [−856, 373] cm3, respectively) and muscle fat content (−0.09% [−0.16%, −0.02%] vs −0.02% [−0.10%, 0.05%], respectively) decreased similarly. Insulin secretion remained unchanged, while the proinflammatory marker IL-18 decreased only after the L-RISK diet.

Conclusions/interpretation

No evidence of a difference between both low-energy diets was identified. Thus, energy restriction per se seems to be key for improving insulin action in phases of active weight loss in obese type 2 diabetic patients, with a potential improvement of subclinical inflammation with the L-RISK diet.
Trial Registration: Clinicaltrials.gov NCT01409330
Funding: This study was supported by the Ministry of Science and Research of the State of North Rhine-Westphalia (MIWF NRW), the German Federal Ministry of Health (BMG), the Federal Ministry for Research (BMBF) to the Center for Diabetes Research (DZD e.V.) and the Helmholtz Alliance Imaging and Curing Environmental Metabolic Diseases (ICEMED).
Appendix
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Metadata
Title
Low-energy diets differing in fibre, red meat and coffee intake equally improve insulin sensitivity in type 2 diabetes: a randomised feasibility trial
Authors
Bettina Nowotny
Lejla Zahiragic
Alessandra Bierwagen
Stefan Kabisch
Jan B. Groener
Peter J. Nowotny
Ann Kristin Fleitmann
Christian Herder
Giovanni Pacini
Iris Erlund
Rikard Landberg
Hans-Ulrich Haering
Andreas F. H. Pfeiffer
Peter P. Nawroth
Michael Roden
Publication date
01-02-2015
Publisher
Springer Berlin Heidelberg
Published in
Diabetologia / Issue 2/2015
Print ISSN: 0012-186X
Electronic ISSN: 1432-0428
DOI
https://doi.org/10.1007/s00125-014-3457-8

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