Honorary Consultant Diabetologist @NHSBartsHealth
Co-lead @eastlondongenes
#medsky #academicsky
A huge thank you to our 64,848 volunteers and Community Advisory Board, funders and many partners for their incredible contributions to this work.
A huge thank you to our 64,848 volunteers and Community Advisory Board, funders and many partners for their incredible contributions to this work.
We are using genetic tools to study diabetes misclassification (when we confuse type 1 and type 2 diabetes), misdiagnosis (when tests like HbA1c go wrong). Soon we will also start work on monogenic and mitochondrial diabetes. Watch this space!
We are using genetic tools to study diabetes misclassification (when we confuse type 1 and type 2 diabetes), misdiagnosis (when tests like HbA1c go wrong). Soon we will also start work on monogenic and mitochondrial diabetes. Watch this space!
Not necessarily. We can work out who has a genetic signature for low insulin production using a blood test called C-peptide, or unhealthy fat distribution by using a tape measure around the waist and hips.
Not necessarily. We can work out who has a genetic signature for low insulin production using a blood test called C-peptide, or unhealthy fat distribution by using a tape measure around the waist and hips.
People with the highest risk of both low insulin production AND unhealthy fat distribution developed type 2 diabetes 8 years earlier, with a BMI 3mkg2 lower, and were more likely to develop eye complications.
People with the highest risk of both low insulin production AND unhealthy fat distribution developed type 2 diabetes 8 years earlier, with a BMI 3mkg2 lower, and were more likely to develop eye complications.
Good question! This isn’t just about satisfying our curiosity. Partitioned polygenic scores point towards ways to improve T2D treatment. People with a high genetic risk for low insulin production were less likely to respond to SGLT2 inhibitors and more likely to need insulin treatment.
Good question! This isn’t just about satisfying our curiosity. Partitioned polygenic scores point towards ways to improve T2D treatment. People with a high genetic risk for low insulin production were less likely to respond to SGLT2 inhibitors and more likely to need insulin treatment.
Partitioned polygenic scores helped us shine a light on the specific reasons for this:
Partitioned polygenic scores helped us shine a light on the specific reasons for this:
Focus is often put on lifestyle factors. We find that south Asians have a greater genetic risk of T2D than white Europeans. So, lifestyle is important, but south Asians carry a greater predisposition from genetic factors that they cannot change.
Focus is often put on lifestyle factors. We find that south Asians have a greater genetic risk of T2D than white Europeans. So, lifestyle is important, but south Asians carry a greater predisposition from genetic factors that they cannot change.