It’s Thursday and four days have passed since finishing the
Ironman. I’m feeling good as new, and if it wasn’t for doctor’s advice not to
run on the broken toe, I’d happily get out there and knock out a long run – I’m
actually itching to do it, but I’ve opted for an 8.5km swim tomorrow morning
instead. The water’s cooled off discernably in the past week, so I figure this
is one of my last chances to do an epic swim this year, so I’ve decided to head
up to a lake nearby and do the swim before work tomorrow morning. It’ll take a
couple of hours, so I’ll try to get in the water by 6am. Despite my best
efforts to drag someone else along, this didn’t work out, so I’ll be on my own.
The furthest I’ve ever swum straight before is 5 km, so this’ll be a new
personal record if all goes well.
My working week has been intense, with a bunch of heavy
deadlines, most of which are met or on their way to being so. Most of my team
is also back from their summer vacations, so lots of meetings to discuss
projects. One really nice bit of news arrived today in the form of 3.7m SEK of
funding (about ½ million USD) from the Novo Nordisk Foundation for a study of
the genetic predictors of long-term deteriorations in blood glucose control. The
grant follows two recent scientific reports from my team, where we reported
genetic determinants of 10 year changes in blood glucose levels (Renström et
al, Diabetes, 2011) and blood lipid levels (Varga et al, PLOS Genet., 2014).
Those studies reported seminal findings that illustrate that there are DNA
sequence variants in the human genome that worsen a persons ability to dispose
of glucose and metabolize blood fats, which in turn raise the risk of diabetes
and heart disease respectively. The studies were part of a new direction in
which we’re heading, which is to map the genetic basis to these long-term
metabolic adaptions, an area that is yet to be studied in great depth. The
grant from Novo Nordisk will allow us to extend our research by using genetic
assessment methods that are much more precise and by studying much large
populations, both of which are likely to lead to further exciting discoveries.
We’ve also had other exciting research published recently.
Clinical trials designed to prevent diabetes typically focus on weight loss
using lifestyle interventions and medication. There are quite wide-ranging
responses to these interventions, with some people doing very well and others
not. In a recent paper from a study called the Diabetes Prevention Program,
which includes about 3,000 adults, we showed that although the total amount of
weight lost across two years has the biggest preventive effect on diabetes
risk, rapid weight loss (within 6 months of starting the lifestyle program)
also helps prevent the disease. We also showed that when people weight cycle
(successively gaining and losing weight) they are more likely to develop
diabetes (Delahanty et al, Diabetes Care,
2014). In another study published recently, led by Dr. Louise Bennet, focused
on Iraqi immigrants to Sweden, showing that insulin action in this population
is inhibited compared with native Swedes, which raises the risk of diabetes in
this minority group (Bennet et al. Diab
Res Clin Prac. 2014). We also had a
paper on the genetic basis of stomach fat, which is a particularly dangerous
form of obesity, accepted in the journal Nature.
One of my PhD students, Dmitry Shungin, has led this work and when it’s
published later this year it’ll likely be a big news story – look out for it!
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