Abstract
BackgroundGestational diabetes (GDM) and milder gestational impaired glucose tolerance (GIGT) identify women at risk of developing type 2 diabetes and cardiovascular disease later in life. Accordingly, the postpartum years after gestational dysglycemia can provide insight into early events in the natural history of these disorders. We thus sought to prospectively evaluate the relationship between gestational glucose tolerance and emerging cardiometabolic biomarkers [adiponectin, chemerin, retinol-binding protein-4 (RBP-4), C-reactive protein (CRP), plasminogen activator inhibitor-1 (PAI-1)] at both 1- and 3-years postpartum in a cohort reflecting the full spectrum of gestational dysglycemia (from normal to GIGT to GDM).MethodsThree-hundred-and-thirty-nine women completed a glucose challenge test (GCT) and oral glucose tolerance test (OGTT) in pregnancy, which identified 4 gestational glucose tolerance groups: GDM (n = 105); GIGT (n = 59); abnormal GCT with normal OGTT (n = 99); and normal GCT with normal OGTT (n = 76). At 1- and 3-years postpartum, the women underwent repeat OGTT with measurement of biomarkers (adiponectin/chemerin/RBP-4/CRP/PAI-1).ResultsSerum adiponectin was lower in women with GDM and GIGT at both 1-year and 3-years (both P ≤ 0.002), whereas chemerin, RBP-4, CRP and PAI-1 showed no differences across the 4 groups. Importantly, the change in PAI-1 between 1- and 3-years progressively increased from the normal GCT group to the abnormal GCT group to GIGT to GDM (P = 0.03). Indeed, both GDM (t = 2.98, P = 0.003) and GIGT (t = 2.14, P = 0.03) independently predicted an increase in PAI-1 from 1- to 3-years postpartum.ConclusionsHypoadiponectinemia and rising PAI-1 over time are early features of the cardiometabolic biomarker profile of women with recent gestational dysglycemia.
Highlights
Gestational diabetes (GDM) and milder gestational impaired glucose tolerance (GIGT) identify women at risk of developing type 2 diabetes and cardiovascular disease later in life
Hypothesizing that these limitations have contributed to this inconclusive literature, we sought to prospectively evaluate the relationship between gestational glucose tolerance status and emerging cardiometabolic biomarkers at both 1- and 3-years postpartum in a well-characterized cohort of women reflecting the full spectrum of gestational dysglycemia and a broad range of future risk of type 2 diabetes (T2DM) and cardiovascular disease (CVD)
There were no significant differences between the groups in chemerin, retinol-binding protein-4 (RBP-4), C-reactive protein (CRP) and plasminogen activator inhibitor-1 (PAI-1)
Summary
Gestational diabetes (GDM) and milder gestational impaired glucose tolerance (GIGT) identify women at risk of developing type 2 diabetes and cardiovascular disease later in life. Previous studies have not addressed the possibility that women with recent gestational dysglycemia may exhibit differential changes over time in these biomarkers, since they comprise a patient population that is very early in the natural history of cardiometabolic disease in whom this risk potential may be evolving over time Hypothesizing that these limitations have contributed to this inconclusive literature, we sought to prospectively evaluate the relationship between gestational glucose tolerance status and emerging cardiometabolic biomarkers (adiponectin, chemerin, RBP-4, CRP, PAI-1) at both 1- and 3-years postpartum in a well-characterized cohort of women reflecting the full spectrum of gestational dysglycemia and a broad range of future risk of T2DM and CVD
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