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1.
Am J Perinatol ; 33(6): 618-24, 2016 05.
Article in English | MEDLINE | ID: mdl-26788786

ABSTRACT

Objective In nonpregnant populations the waist-to-hip ratio (WHR) is a better predictor of obesity-related outcomes than body mass index (BMI). Our objective was to determine, in pregnancy, the relationship between these measures of obesity, and large-for-gestational age (LGA) and cesarean delivery (CD). Methods This is a secondary analysis of data from the Combined Antioxidant and Preeclampsia Prediction Study. Women with a WHR of ≥ 0.85 and 0.80 to 0.84 at 9 to 16 weeks gestation were compared with those with a WHR < 0.80. Women with early pregnancy BMI ≥ 30.0 kg/m(2) (obese) and 25.0 to 29.9 kg/m(2) (overweight) were compared with those < 25.0 kg/m(2). LGA was defined as > 90% by Alexander nomogram. Univariable analysis, logistic regression, and receiver operating characteristic curves were used. Results Data from 2,276 women were analyzed. After correcting for potential confounders, only BMI ≥ 30 was significantly associated with LGA (adjusted odds ratio [aOR]: 2.07, 1.35-3.16) while BMI 25.0-29.9 (aOR: 1.5, 0.98-2.28), WHR 0.8-0.84 (aOR: 1.33, 0.83-2.13), and WHR ≥ 0.85 (aOR: 1.05, 0.67-1.65) were not. Risk for CD was increased for women with elevated WHR and with higher BMI compared with normal. Conclusion WHR is not associated with LGA. While BMI performed better than WHR, neither was a strong predictor of LGA or need for CD in low-risk nulliparous women.


Subject(s)
Birth Weight , Body Mass Index , Cesarean Section/statistics & numerical data , Obesity/complications , Pregnancy Complications/etiology , Waist-Hip Ratio , Adolescent , Adult , Female , Gestational Age , Humans , Logistic Models , Multivariate Analysis , Pregnancy , Pregnancy Outcome , Prognosis , ROC Curve , United States , Young Adult
2.
Neurotoxicol Teratol ; 32(6): 605-10, 2010.
Article in English | MEDLINE | ID: mdl-20553856

ABSTRACT

Our objective was to assess the effects of repeated antenatal corticosteroid treatments on the neonatal auditory brainstem response (ABR), a sensitive measure of neonatal brain maturity and auditory function. To achieve this, we performed and blindly evaluated neonatal ABRs on a subset of infants delivering within a multicenter randomized placebo-controlled clinical trial comparing single versus repeated courses of antenatal corticosteroid treatments for women at 23-31 weeks gestation who remained at increased risk for preterm birth. The women were randomly assigned to either the single or the repeated antenatal corticosteroid treatment group. Women in the repeated antenatal corticosteroid group received weekly antenatal corticosteroid treatments until 34 weeks gestation or until they reached a study-determined limited number of courses, whereas women in the single antenatal corticosteroid group received an initial course of corticosteroid followed by weekly placebo injections. We performed ABR testing on their infants prior to discharge. The latencies of waves I, III and V and the peak-to-trough amplitudes of waves I and V were compared between those in the single (n=27) and repeated antenatal corticosteroid treatment (n=24) groups. The majority of repeated antenatal corticosteroid infants (20 of 24) were exposed to ≥ 4 antenatal corticosteroid treatments. Even though gestational age was similar between our subset of single and repeated antenatal corticosteroid treatment groups, infant birth weight and length and head circumference were significantly smaller in the repeated antenatal corticosteroid group (p <0.05). Despite these differences in birth sizes, there were no significant group differences in the ABR wave latencies or amplitudes. We concluded that our repeated antenatal corticosteroid treatments, in comparison to a single treatment, did not significantly benefit or harm the neonatal ABR despite significant effects on birth size.


Subject(s)
Betamethasone/adverse effects , Brain/physiopathology , Evoked Potentials, Auditory, Brain Stem/drug effects , Glucocorticoids/adverse effects , Prenatal Exposure Delayed Effects/physiopathology , Acoustic Stimulation , Betamethasone/administration & dosage , Betamethasone/therapeutic use , Brain/drug effects , Brain/growth & development , Dose-Response Relationship, Drug , Evoked Potentials, Auditory, Brain Stem/physiology , Female , Gestational Age , Glucocorticoids/administration & dosage , Glucocorticoids/therapeutic use , Humans , Infant, Newborn , Male , Pregnancy , Prenatal Exposure Delayed Effects/chemically induced , Reproducibility of Results , United States , Young Adult
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