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Published on: June 29, 2013
Sex- and growth-specific characteristics of small for gestational age infants: a prospective cohort study
Eva R van der Vlugt1,2, Petra E Verburg1,3,4, Shalem Y Leemaqz1
1The Robinson Research Institute and Adelaide Medical School, University of Adelaide, Adelaide, Australia.
Insights
Fetal growth asymmetry and male sex impact small for gestational age (SGA) outcomes differently. Symmetric SGA links to maternal factors, while asymmetric SGA suggests distinct developmental pathways.
Area of Science:
- Neonatalogy
- Perinatal Medicine
- Fetal Development
Background:
- Asymmetric fetal growth and male sex are linked to adverse neonatal outcomes.
- Infants born small for gestational age (SGA) face increased risks.
- Limited understanding exists on how asymmetric growth and sex influence SGA neonates.
Purpose of the Study:
- To investigate risk factors for SGA in a manner specific to fetal sex and growth symmetry.
- To elucidate the distinct pathways and risk profiles within the SGA population.
Main Methods:
- Prospective, multicenter cohort study using data from the Screening for Pregnancy Endpoints (SCOPE) study.
- Analysis of 5628 nulliparous participants, identifying 633 (11.3%) SGA pregnancies.
- Multivariable analyses assessed associations between risk factors, SGA subgroups, and uncomplicated pregnancies.
Main Results:
- Asymmetric growth was prevalent in 45.8% of SGA infants.
- SGA males showed significantly more asymmetric growth than SGA females (51.2% vs 40.4%).
- Maternal diet and BMI were associated with symmetric SGA, not asymmetric SGA. Asymmetric SGA infants had lower birthweight percentiles and fewer stillbirths.
Conclusions:
- Low birthweight percentiles and male sex are associated with asymmetric growth in SGA infants.
- Symmetric SGA is linked to maternal risk factors in early pregnancy.
- Growth symmetry in SGA infants influences risk factors and neonatal outcomes, suggesting different underlying causes.
Background:
Asymmetric fetal growth and male sex are both associated with adverse neonatal outcome. However, less is known about the influence of asymmetric growth and fetal sex within SGA neonates, a group of infants already at increased risk for adverse neonatal outcomes. The aim of the present study was to provide insight into variance in risk factors for SGA in a fetal sex- and growth symmetry-specific way.
Methods:
For this prospective, multicenter cohort study, data from the Screening for Pregnancy Endpoints (SCOPE) study were used with 5628 nulliparous participants, of which 633 (11.3%) pregnancies were complicated with SGA and 3376 (60.0%) women had uncomplicated pregnancies. Association between risk factors for SGA, SGA subgroups, and uncomplicated pregnancies were assessed with multivariable analyses.
Results:
Prevalence of asymmetric growth varied from 45.8% of SGA infants to 5.5% of infants with a customized birthweight > 90th percentile (p < 0.001). Significantly more SGA males had asymmetric growth compared to SGA female infants (51.2% vs 40.4%, p = 0.009). Maternal pre-pregnancy diet and BMI < 20 and ≥ 30 were significantly associated with symmetric SGA but not with asymmetric SGA. Asymmetric SGA infants had not only lower customized birthweight percentile (4.4 (SD 2.8) vs 5.0 (SD 3.0), p < 0.001), but also lower rates of stillbirth (p = 0.041) and less often Apgar scores < 7 (p = 0.060).
Conclusions:
Among SGA infants, low customized birthweight percentiles and male sex are associated with asymmetric growth. Only symmetric SGA is significantly associated with maternal risk factors in early pregnancy. There is a substantial variance in risk factors and neonatal outcomes for SGA based on growth symmetry, implying a different pathogenesis.
Trial Registration:
ACTRN12607000551493.
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