Rowan Janet A, Rush Elaine C, Plank Lindsay D, Lu Jun, Obolonkin Victor, Coat Suzette, Hague William M
Department of Obstetrics, National Women's Health at Auckland City Hospital, Auckland, New Zealand.
Faculty of Health and Environmental Sciences, Auckland University of Technology, Auckland, New Zealand.
BMJ Open Diabetes Res Care. 2018 Apr 13;6(1):e000456. doi: 10.1136/bmjdrc-2017-000456. eCollection 2018.
To compare body composition and metabolic outcomes at 7-9 years in offspring of women with gestational diabetes (GDM) randomized to metformin (±insulin) or insulin treatment during pregnancy.
Children were assessed at 7 years in Adelaide (n=109/181) and 9 years in Auckland (n=99/396) by anthropometry, bioimpedance analysis (BIA), dual-energy X-ray absorptiometry (DXA), magnetic resonance imaging (MRI) (n=92/99) and fasting bloods (n=82/99).
In the Adelaide subgroup, mothers were similar at enrollment. Women randomized to metformin versus insulin had higher treatment glycemia (p=0.002) and more infants with birth weight >90th percentile (20.7% vs 5.9%; p=0.029). At 7 years, there were no differences in offspring measures. In Auckland, at enrollment, women randomized to metformin had a higher body mass index (BMI) (p=0.08) but gained less weight during treatment (p=0.07). Offspring birth measures were similar. At 9 years, metformin offspring were larger by measures of weight, arm and waist circumferences, waist:height (p<0.05); BMI, triceps skinfold (p=0.05); DXA fat mass and lean mass (p=0.07); MRI abdominal fat volume (p=0.051). Body fat percent was similar between treatment groups by DXA and BIA. Abdominal fat percentages (visceral adipose tissue, subcutaneous adipose tissue and liver) were similar by MRI. Fasting glucose, triglyceride, insulin, insulin resistance, glycosylated hemoglobin (HbA1c), cholesterol, liver transaminases, leptin and adiponectin were similar.
Metformin or insulin for GDM was associated with similar offspring total and abdominal body fat percent and metabolic measures at 7-9 years. Metformin-exposed children were larger at 9 years. Metformin may interact with fetal environmental factors to influence offspring outcomes.
比较妊娠期糖尿病(GDM)女性在孕期随机接受二甲双胍(±胰岛素)或胰岛素治疗后,其后代在7至9岁时的身体成分和代谢指标。
在阿德莱德对7岁儿童(n = 109/181)以及在奥克兰对9岁儿童(n = 99/396)进行评估,评估内容包括人体测量、生物电阻抗分析(BIA)、双能X线吸收法(DXA)、磁共振成像(MRI)(n = 92/99)以及空腹血液检测(n = 82/99)。
在阿德莱德亚组中,母亲们在入组时情况相似。随机接受二甲双胍治疗与胰岛素治疗的女性相比,治疗期间血糖更高(p = 0.002),出生体重>第90百分位数的婴儿更多(20.7%对5.9%;p = 0.029)。7岁时,后代各项指标无差异。在奥克兰,入组时,随机接受二甲双胍治疗的女性体重指数(BMI)较高(p = 0.08),但治疗期间体重增加较少(p = 0.07)。后代出生时的各项指标相似。9岁时,接受二甲双胍治疗的后代在体重、手臂和腰围、腰臀比(p < 0.05);BMI、三头肌皮褶厚度(p = 0.05);DXA脂肪量和瘦体重(p = 0.07);MRI腹部脂肪体积(p = 0.051)等方面更大。通过DXA和BIA测量,各治疗组间的体脂百分比相似。通过MRI测量,腹部脂肪百分比(内脏脂肪组织、皮下脂肪组织和肝脏)相似。空腹血糖、甘油三酯、胰岛素、胰岛素抵抗、糖化血红蛋白(HbA1c)、胆固醇、肝转氨酶、瘦素和脂联素相似。
GDM使用二甲双胍或胰岛素治疗,在7至9岁时,后代的总体和腹部体脂百分比以及代谢指标相似。暴露于二甲双胍的儿童在9岁时体型更大。二甲双胍可能与胎儿环境因素相互作用以影响后代结局。