Issue: November 2013
October 15, 2013
2 min read
Save

Identical twins study sheds light on metabolically healthy obese

Issue: November 2013
You've successfully added to your alerts. You will receive an email when new content is published.

Click Here to Manage Email Alerts

We were unable to process your request. Please try again later. If you continue to have this issue please contact customerservice@slackinc.com.

Maintaining high mitochondrial transcription and preventing inflammation in adipose tissue are associated with low liver fat and metabolically healthy obesity, according to findings in a recent research paper in Diabetologia.

Perspective from Norbert Stefan, MD

Jussi Naukkarinen, MD, PhD, of the Institute for Molecular Medicine and the University of Helsinki, and colleagues aimed to study various fat depots and transcriptional pathways in subcutaneous adipose tissue (SAT) as it relates to metabolically healthy obesity.

They examined the metabolic characteristics of 16 rare young adult obesity-discordant monozygotic twin pairs (aged 22.8 to 35.8 years) to understand the link between mitochondrial function and inflammation in SAT.

“Genetic and multiple environmental factors, as well as age, sex and age of onset of weight gain, may play a role in an individual’s metabolic response to obesity,” the researchers wrote.

They identified two metabolically different subgroups based on liver fat accumulation, according to data.

Of the 16 pairs of Finnish twins, half of the obese co-twins (weight change: 17.1 kg) displayed significantly higher levels of liver fat, a 78% increase in the area under the curve (AUC) insulin during oral glucose tolerance test and C-reactive protein, significantly more interrupted lipids and a greater tendency for hypertension compared with the lean co-twin, according to data.

However, in the other half of patients (weight change: 17.4 kg) studied, obese twins did not demonstrate differences in liver fat (percent change: 8%), insulin sensitivity, C-reactive protein, lipids, hypertension or SAT transcriptomics, researchers wrote.

“Future studies of the metabolically healthy obesity phenotype may suggest new potentially druggable targets — with the most proximal intervention point perhaps being improving mitochondrial function and prevention of inflammation in adipose tissue,” researchers wrote.

Disclosure: The researchers report no relevant financial disclosures.