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Pediatr Res ; 82(5): 768-775, 2017 Nov.
Article in English | MEDLINE | ID: mdl-28604759

ABSTRACT

BackgroundTo test the hypothesis that infants born to obese women with pre-gestational type 2 diabetes mellitus (IBDMs) have ventricular dysfunction at 1 month that is associated with markers of maternal lipid and glucose metabolism.MethodsIn a prospective observational study of IBDMs (OB+DM, n=25), echocardiographic measures of septal, left (LV) and right ventricular (RV) function, and structure were compared at 1 month of age with those in infants born to OB mothers without DM (OB, n=24) and to infants born to non-OB mothers without DM (Lean, n=23). Basal maternal lipid and glucose kinetics and maternal plasma and infant (cord) plasma were collected for hormone and cytokine analyses.ResultsRV, LV, and septal strain measures were lower in the OB+DM infants compared with those in other groups, without evidence of septal hypertrophy. Maternal hepatic insulin sensitivity, maternal plasma free-fatty-acid concentration, and cord plasma insulin and leptin most strongly predicted decreased septal strain in OB+DM infants.ConclusionIBDMs have reduced septal function at 1 month in the absence of septal hypertrophy, which is associated with altered maternal and infant lipid and glucose metabolism. These findings suggest that maternal obesity and DM may have a prolonged impact on the cardiovascular health of their offspring, despite the resolution of cardiac hypertrophy.


Subject(s)
Blood Glucose/metabolism , Diabetes Mellitus, Type 2/complications , Lipids/blood , Obesity/complications , Pregnancy in Diabetics , Prenatal Exposure Delayed Effects , Ventricular Dysfunction, Left/etiology , Ventricular Dysfunction, Right/etiology , Ventricular Function, Left , Ventricular Function, Right , Adult , Biomarkers/blood , Diabetes Mellitus, Type 2/blood , Diabetes Mellitus, Type 2/diagnosis , Echocardiography , Female , Fetal Blood/metabolism , Humans , Infant , Infant, Newborn , Obesity/blood , Obesity/diagnosis , Pregnancy , Prospective Studies , Risk Factors , Time Factors , Ventricular Dysfunction, Left/blood , Ventricular Dysfunction, Left/diagnostic imaging , Ventricular Dysfunction, Left/physiopathology , Ventricular Dysfunction, Right/blood , Ventricular Dysfunction, Right/diagnostic imaging , Ventricular Dysfunction, Right/physiopathology , Young Adult
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