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Banting Memorial Lecture 2012 Reversing the twin cycles of Type 2 diabetes

Lookup NU author(s): Professor Roy Taylor

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Abstract

It has become widely accepted that Type 2 diabetes is inevitably life-long, with irreversible and progressive beta cell damage. However, the restoration of normal glucose metabolism within days after bariatric surgery in the majority of people with Type 2 diabetes disproves this concept. There is now no doubt that this reversal of diabetes depends upon the sudden and profound decrease in food intake, and does not relate to any direct surgical effect. The Counterpoint study demonstrated that normal glucose levels and normal beta cell function could be restored by a very low calorie diet alone. Novel magnetic resonance methods were applied to measure intra-organ fat. The results showed two different time courses: a) resolution of hepatic insulin sensitivity within days along with a rapid fall in liver fat and normalisation of fasting glucose levels; and b) return of normal beta cell insulin secretion over weeks in step with a fall in pancreas fat. Now that it has been possible to observe the pathophysiological events during reversal of Type 2 diabetes, the reverse time course of events which determine the onset of the condition can be identified. The twin cycle hypothesis postulates that chronic calorie excess leads to accumulation of liver fat with eventual spill over into the pancreas. These self-reinforcing cycles between liver and pancreas eventually cause metabolic inhibition of insulin secretion after meals and onset of hyperglycaemia. It is now clear that Type2 diabetes is a reversible condition of intra-organ fat excess to which some people are more susceptible than others.


Publication metadata

Author(s): Taylor R

Publication type: Review

Publication status: Published

Journal: Diabetic Medicine

Year: 2013

Volume: 30

Issue: 3

Pages: 267-275

Print publication date: 01/03/2013

ISSN (print): 0742-3071

ISSN (electronic): 1464-5491

Publisher: WILEY-BLACKWELL

URL: http://dx.doi.org/10.1111/dme.12039

DOI: 10.1111/dme.12039


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