James-Todd Tamarra, Cohen Allison, Wenger Julia, Brown Florence
a Department of Environmental Health/Department of Epidemiology , Harvard T.H. Chan School of Public Health , Boston , MA , USA.
b Adult Diabetes Section , Joslin Diabetes Center and Harvard Medical School , Boston , MA , USA.
Hypertens Pregnancy. 2016 Aug;35(3):436-46. doi: 10.3109/10641955.2016.1172085. Epub 2016 Jun 23.
Determine the independent association between time-specific placental growth factor (PIGF)-a marker of placental vasculature-and infant birth weight in offspring of mothers with preexisting type 1 and 2 diabetes.
A total of 150 women were recruited from Joslin Diabetes Center's/Beth Israel Deaconess Medical Center's Diabetes in Pregnancy Program. PlGF was measured up to four times during pregnancy. Infant birth weight and covariate data were collected from medical records. Hemoglobin A1c was assessed from drawn blood samples. We used generalized linear and log-binomial models to calculate the change in continuous birth weight, as well as macrosomia for every unit change in time-specific ln-transformed PlGF, respectively. Models were adjusted for potential confounders.
Approximately 75% of women had type 1 diabetes. Third trimester PlGF levels were significantly associated with infant birth weight (r = 0.24, p = 0.02 at 27-34 weeks; r = 0.26, p < 0.009 for 36-40 weeks). After full adjustment, there was a 6.1% and 6.6% increase in birth weight for gestational age percentile for each unit increase in ln-transformed PlGF level at 27-34 weeks and 35-40 weeks, respectively (95% CI for 27-34 weeks gestation: 1.1, 11.0, and 95% CI for 35-40 weeks gestation: 0.7%, 12.5%). We found a statistically significant increased risk of macrosomia among women with higher ln-transformed PlGF levels (RR: 1.72; 95% CI: 1.09, 2.70). Associations were not mediated by hemoglobin A1c.
Third trimester PlGF levels were associated with higher birth weight in women with preexisting diabetes. These findings may provide insight to the pathophysiology of fetal overgrowth in women with diabetes.
确定特定时间的胎盘生长因子(PIGF)——胎盘血管系统的一个标志物——与患有1型和2型糖尿病的母亲所生后代的婴儿出生体重之间的独立关联。
从乔斯林糖尿病中心/贝斯以色列女执事医疗中心的妊娠糖尿病项目中招募了150名女性。在孕期对PIGF进行多达四次的测量。从医疗记录中收集婴儿出生体重和协变量数据。从采集的血样中评估糖化血红蛋白。我们分别使用广义线性模型和对数二项模型来计算特定时间的自然对数转换后的PIGF每单位变化时连续出生体重的变化以及巨大儿的情况。模型针对潜在混杂因素进行了调整。
约75%的女性患有1型糖尿病。孕晚期PIGF水平与婴儿出生体重显著相关(27 - 34周时r = 0.24,p = 0.02;36 - 40周时r = 0.26,p < 0.009)。在完全调整后,27 - 34周和35 - 40周时,自然对数转换后的PIGF水平每增加一个单位,出生体重相对于胎龄百分位数分别增加6.1%和6.6%(27 - 34周妊娠的95%置信区间:1.1%,11.0%;35 - 40周妊娠的95%置信区间:0.7%,12.5%)。我们发现自然对数转换后的PIGF水平较高的女性中巨大儿风险有统计学意义的增加(相对风险:1.72;95%置信区间:1.09,2.70)。关联并非由糖化血红蛋白介导。
孕晚期PIGF水平与患有糖尿病的女性出生体重较高有关。这些发现可能为糖尿病女性胎儿过度生长的病理生理学提供见解。