Literature DB >> 17576204

Lifestyle intervention in individuals with normal versus impaired glucose tolerance.

S Schäfer1, K Kantartzis, J Machann, C Venter, A Niess, F Schick, F Machicao, H-U Häring, A Fritsche, N Stefan.   

Abstract

BACKGROUND: Lifestyle intervention is effective in the prevention of type 2 diabetes in individuals with impaired glucose tolerance (IGT). It is currently unknown whether it has beneficial effects on metabolism to a similar extent, in individuals with normal glucose tolerance (NGT) compared to individuals with IGT.
MATERIALS AND METHODS: Data from 181 subjects (133 with NGT and at risk for type 2 diabetes and 48 with IGT) who participated in the Tuebingen Lifestyle Intervention Program with increase in physical activity and decrease in caloric intake were included into this study. Body fat distribution was quantified by whole-body magnetic resonance (MR) tomography and liver fat and intramyocellular fat by (1)H-MR spectroscopy. Insulin sensitivity was estimated from an oral glucose tolerance test (OGTT).
RESULTS: After 9 +/- 2 months of follow-up, the diagnosis of IGT was reversed in 24 out of 48 individuals. Only 14 out of 133 participants with NGT developed IGT. Body weight decreased in both groups by 3% (both P < 0.0001). Two-hour glucose concentrations during an OGTT decreased in individuals with IGT (-14%, P < 0.0001) but not with NGT (+2%, P = 0.66). Insulin sensitivity increased both in individuals with IGT (+9%, P = 0.04) and NGT (+17%, P < 0.0001). Visceral fat (-8%, P = 0.006), liver fat (-28%, P < 0.0001) and intramyocellular fat (-15%, P = 0.006) decreased in participants with IGT. In participants with NGT these changes were significant for visceral fat (-16%, P < 0.0001) and liver fat (-35%, P < 0.0001).
CONCLUSIONS: Moderate weight loss under a lifestyle intervention with reduction in total, visceral and ectopic fat and increase in insulin sensitivity improves glucose tolerance in individuals with IGT but not with NGT. In individuals with NGT, the beneficial effects of a lifestyle intervention on fat distribution and insulin sensitivity possibly prevent future deterioration in glucose tolerance.

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Year:  2007        PMID: 17576204     DOI: 10.1111/j.1365-2362.2007.01820.x

Source DB:  PubMed          Journal:  Eur J Clin Invest        ISSN: 0014-2972            Impact factor:   4.686


  36 in total

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Authors:  K Müssig; M Heni; C Thamer; K Kantartzis; F Machicao; N Stefan; A Fritsche; H-U Häring; H Staiger
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Review 2.  Metabolic syndrome and lifestyle modification.

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Review 4.  Effects of physical activity upon the liver.

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Journal:  Eur J Appl Physiol       Date:  2014-11-04       Impact factor: 3.078

5.  Nor-1, a novel incretin-responsive regulator of insulin genes and insulin secretion.

Authors:  Anna-Maria Ordelheide; Felicia Gerst; Oliver Rothfuss; Martin Heni; Carina Haas; Inga Thielker; Silke Herzberg-Schäfer; Anja Böhm; Fausto Machicao; Susanne Ullrich; Norbert Stefan; Andreas Fritsche; Hans-Ulrich Häring; Harald Staiger
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6.  Gene variants of TCF7L2 influence weight loss and body composition during lifestyle intervention in a population at risk for type 2 diabetes.

Authors:  Axel Haupt; Claus Thamer; Martin Heni; Caroline Ketterer; Jürgen Machann; Fritz Schick; Fausto Machicao; Norbert Stefan; Claus D Claussen; Hans-Ulrich Häring; Andreas Fritsche; Harald Staiger
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7.  Metabonomic fingerprints of fasting plasma and spot urine reveal human pre-diabetic metabolic traits.

Authors:  Xinjie Zhao; Jens Fritsche; Jiangshan Wang; Jing Chen; Kilian Rittig; Philippe Schmitt-Kopplin; Andreas Fritsche; Hans-Ulrich Häring; Erwin D Schleicher; Guowang Xu; Rainer Lehmann
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8.  Glycemia determines the effect of type 2 diabetes risk genes on insulin secretion.

Authors:  Martin Heni; Caroline Ketterer; Claus Thamer; Silke A Herzberg-Schäfer; Martina Guthoff; Norbert Stefan; Fausto Machicao; Harald Staiger; Andreas Fritsche; Hans-Ulrich Häring
Journal:  Diabetes       Date:  2010-08-29       Impact factor: 9.461

9.  The D299G/T399I Toll-like receptor 4 variant associates with body and liver fat: results from the TULIP and METSIM Studies.

Authors:  Peter Weyrich; Harald Staiger; Alena Stančáková; Fausto Machicao; Jürgen Machann; Fritz Schick; Norbert Stefan; Johanna Kuusisto; Markku Laakso; Silke Schäfer; Andreas Fritsche; Hans-Ulrich Häring
Journal:  PLoS One       Date:  2010-11-15       Impact factor: 3.240

10.  Common polymorphisms within the NR4A3 locus, encoding the orphan nuclear receptor Nor-1, are associated with enhanced beta-cell function in non-diabetic subjects.

Authors:  Peter Weyrich; Harald Staiger; Alena Stancáková; Silke A Schäfer; Kerstin Kirchhoff; Susanne Ullrich; Felicia Ranta; Baptist Gallwitz; Norbert Stefan; Fausto Machicao; Johanna Kuusisto; Markku Laakso; Andreas Fritsche; Hans-Ulrich Häring
Journal:  BMC Med Genet       Date:  2009-08-14       Impact factor: 2.103

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