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|Title:||Incident type 2 diabetes in a population with impaired glucose regulation and the effect of early regression to normoglycaemia|
Srinivasan, B. T.
Gray, L. J.
Davies, Melanie J.
Webb, David R.
|Citation:||Diabetic Medicine, 2016 (EarlyView)|
|Abstract:||Aims To report contemporary regression rates from impaired glucose regulation to normal glucose tolerance, identify modifiable factors associated with early regression, and establish whether it affects subsequent diabetes risk in a population-based cohort. Methods Participants with impaired glucose regulation (impaired fasting glucose and/or impaired glucose tolerance on a 75-g oral glucose tolerance test) at baseline in the UK-based ADDITION-Leicester study had annual Type 2 diabetes re-screens for 5 years or until diabetes diagnosis. Logistic regression models investigated modifiable risk factors for regression to normal glucose tolerance at 1 year (n = 817). Cox regression models estimated subsequent diabetes risk (n = 630). Results At 1 year, 54% of participants had regressed to normal glucose tolerance, and 6% had progressed to diabetes. Regression to normal glucose tolerance was associated with weight loss of 0.1–3% [adjusted odds ratio 1.81 (95% CI 1.08, 3.03) compared with maintaining or gaining weight] and a waist circumference reduction of > 3 cm [adjusted odds ratio 1.78 (95% CI 1.03, 3.06) compared with maintaining or increasing waist circumference]. Those with normal glucose tolerance at 1 year subsequently had lower diabetes risk than those who remained with impaired glucose regulation [adjusted hazard ratio 0.19 (95% CI 0.10, 0.37)]. Conclusions Early regression to normal glucose tolerance was associated with reduced diabetes incidence, and might be induced by small reductions in weight or waist circumference. If confirmed in experimental research, this could be a clear and achievable target for individuals diagnosed with impaired glucose regulation.|
|Embargo on file until:||3-Mar-2017|
|Rights:||Copyright © 2016 Diabetes UK. All rights reserved. This is the peer reviewed version of the following article: Diabetic Medicine (2016), which has been published in final form at dx.doi.org/10.1111/dme.13091. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving.|
|Description:||The file associated with this record is under a 12-month embargo from publication in accordance with the publisher's self-archiving policy. The full text may be available through the publisher links provided above.|
|Appears in Collections:||Published Articles, Dept. of Cardiovascular Sciences|
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|FINAL Progression from preDM to T2DM.docx||Post-review (final submitted)||128.89 kB||Unknown||View/Open|
|FINAL Progression from preDM to T2DM.pdf||Post-review (final submitted)||335.23 kB||Adobe PDF||View/Open|
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