Hepatic insulin resistance is an early determinant of declining ?-cell function in the first year postpartum after glucose intolerance in pregnancy.

ABSTRACT: OBJECTIVE The increased risk of type 2 diabetes in women with glucose intolerance in pregnancy is mediated by deterioration of their ?-cell function, which occurs as early as the first year postpartum. We thus sought to identify early determinants of their declining ?-cell function. RESEARCH DESIGN AND METHODS Women with recent gestational glucose intolerance (166) underwent oral glucose tolerance test at 3 and 12 months postpartum. They were stratified into those in whom ?-cell function (Insulin Secretion-Sensitivity Index-2 [ISSI-2]) declined over this time (decliners; n = 92) and those in whom it did not (nondecliners; n = 74). RESULTS Between 3 and 12 months, hepatic insulin sensitivity (1/homeostasis model assessment of insulin resistance [HOMA-IR]) decreased in decliners but not in nondecliners. Over this time, the change in 1/HOMA-IR emerged as an independent predictor of the change in ISSI-2 (t = 5.5; P < 0.0001). Increased hepatic insulin sensitivity independently predicted a lower likelihood of declining ?-cell function (odds ratio = 0.13 [95% CI 0.06-0.29]; P < 0.0001). CONCLUSIONS Hepatic insulin resistance is an early determinant of declining ?-cell function after gestational dysglycemia.

SUBMITTER: Retnakaran R 

PROVIDER: S-EPMC3198270 | biostudies-literature | 2011 Nov

REPOSITORIES: biostudies-literature