Glucose homeostasis markers in twins are similar to those found in type 2 diabetes

Markers of fetal environment and glucose homeostasis in twins are linked to similar defects found in type 2 diabetes.

“According to the ‘fetal origins hypothesis’, monozygotic (MZ) twins may be more prone to develop various metabolic abnormalities compared with dizygotic (DZ) twins, and twins all together may be more predisposed to metabolic defects compared with singletons. To determine the impact of twin and zygosity status as well as birth size on in vivo measures of glucose metabolism, we examined 123 young (aged 22-31 years) and 103 elderly (aged 57-66 years) MZ and DZ twins and age-matched singleton control subjects,” investigators in Denmark report.

“All participants were born at term with available birth records. Peripheral and hepatic insulin action and intracellular glucose partitioning was determined by a euglycemichyperinsulinemic clamp using tritiated glucose combined with indirect calorimetry,” described P. Poulsen and colleagues, Steno Diabetes Center.

The diabetologists found, “In elderly subjects, zygosity status influenced nonoxidative glucose metabolism, while twin status per se was associated with elevated hepatic glucose production during both steady-state periods. Birth weight was associated with nonoxidative glucose metabolism in a nongenetic manner within twins and with a high glucose and low lipid oxidation in singletons. In younger subjects, twin status influenced glucose and lipid oxidation rates.”

“We demonstrate,” concluded the authors, “a complex age- or time-dependent relationship between independent markers of fetal environment and glucose homeostasis in twins. The documented differential programming effects associated with either low birth weight and twin or zygosity status all represent known defects of glucose homeostasis in type 2 diabetes.”

Poulsen and colleagues published their study in Diabetes (The intrauterine environment as reflected by birth size and twin and zygosity status influences insulin action and intracellular glucose metabolism in an age- or time-dependent manner. Diabetes, 2006;55 (6):1819-1825).

For additional information, contact P. Poulsen, Steno Diabetes Center, Niels Steensens Vej 2, DK-2820 Gentofte, Denmark.

The publisher of the journal Diabetes can be contacted at: American Diabetes Association, 1701 N Beauregard St., Alexandria, VA 22311-1717, USA.

Provided by ArmMed Media
Revision date: July 7, 2011
Last revised: by David A. Scott, M.D.