Completed Diabetes, Hormones & Metabolism Cancer

Understanding and disrupting the link between obesity and metabolic disease

In plain English

AI plain-English summary

A single DNA letter change in a fat-storage gene can be as powerful a driver of type 2 diabetes and heart disease as carrying extra weight around the belly. This matters because obesity is strongly linked to metabolic diseases, but not everyone with obesity develops them, and some lean people do. The researchers have discovered that subtle, inherited defects in fat storage—partial lipodystrophy—are a major hidden factor in common insulin resistance. They found that genetic variants linked to reduced hip fat are as strongly tied to diabetes and heart disease risk as variants linked to central obesity. The project will deepen understanding of how fat cells form and store energy, test whether a very low energy diet can reverse metabolic disease in people with partial lipodystrophy, and investigate two stress hormones—GDF15 and FGF21—that may be released during overnutrition. Both hormones are promising drug targets. If successful, this work could shift how doctors assess metabolic disease risk—looking beyond body weight to fat distribution and genetic profile—and open new routes for treating insulin resistance by targeting fat storage capacity directly.

View original technical description
Obesity is strongly associated with common metabolic diseases (T2DM, fatty liver and cardiovascular disease) which collectively account for a huge global health burden. Insulin resistance underpins this association and our goal is to understand, and reverse, its molecular pathogenesis. Having worked on rare monogenic lipodystrophies, almost all of which are associated with the metabolic diseases typically seen in obesity, for ~20 years, we have recently convincingly shown that subtle forms of lipodystrophy are a major factor in common insulin resistance/metabolic disease. Specifically we showed that SNPs associated primarily with reduced hip (femorogluteal) fat, are as strongly associated with T2DM and cardiovascular disease risk as variants associated with central adiposity. We will build on this step-change in understanding by: - Deepening understanding of the molecular mechanisms by which adipocytes form and then store surplus energy in unilocular lipid droplets - Performing an experimental medicine intervention study designed to demonstrate the clinical and molecular impact of alleviating energetic overload using a very low energy diet in patients with partial lipodystrophy. - Investigating the source and action of two hormones (GDF15 and FGF21) which we hypothesize to be stress signals released in response to sustained overnutrition. Both of these molecules represent exciting therapeutic opportunities.

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Researchers

David Savage (EPMC Awardee)Stephen O'Rahilly (EPMC Awardee)

Related Research

Grants with similar aims, by meaning.

Fundamental mechanisms controlling human energy homeostasis
Targeting therapy to molecular mechanism of disease in obesity and related metabolic disorders
Coupling novel non-invasive imaging methods and new gene therapies to detect and treat type 2 diabetes
Adipose tissue dysfunction and lipotoxicity
Using genetics to test the disease consequences of higher adiposity uncoupled from its adverse metabolic effects

Original classification

Senior Research Fellowship Renewal

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