Consequences of low birthweight on urinary excretion of DNA markers of oxidative stress in young men

Abstract

Objective. Low birthweight (LBW) has been associated with an increased risk of development of type 2 diabetes in adult life. Both type 1 and type 2 diabetes mellitus are characterized by increased oxidative stress. The purpose of this study was to investigate whether young healthy adults born with LBW showed differences in oxidative stress under normal conditions and during the added challenge of a physiological Intralipid infusion. Material and methods. Urinary excretion of DNA markers of oxidative stress were analyzed by LC‐MS/MS in 19 men (aged 19 years) with LBW and in 19 age matched, normal birthweight (NBW) controls pre‐ and post a 3‐fold increase of plasma free fatty acids. Results. Mean excretion rates of 8‐oxo‐guanine (8oxoGua), 8‐oxo‐guanosine (8oxoGuo), 8‐oxo‐2′deoxyguanosine (8oxodG), and 1,N⁶‐ethenodeoxyadenosine (εdA) did not statistically differ between subjects with LBW and NBW (66.9 versus 73.9 nmol/15 h, 17.8 versus 18.5 nmol/15 h, 11.9 versus 14.4 nmol/15 h and 44.0 versus 43.2 pmol/15 h, respectively). Furthermore, Intralipid infusion did not affect excretion of DNA adducts in LBW or NBW subjects. Statistically significant correlations were found between body mass index and urinary excretion of 8oxoGua (r = 0.64, p = 0.003) and 8oxoGuo (r = 0.64, p = 0.003) in the LBW group only. Conclusions. These findings suggest that oxidative stress may be a consequence of diabetes and is not, or at least only partly, involved in the early pathogenesis of type 2 diabetes.

• 8oxoGua
• 8oxoGuo
• 8oxoG
• εdA
• fatty acids
• type 2 diabetes
• urinary excretion