AI Article Synopsis

  • The study examined the relationship between sFlt-1/PlGF ratios in small for gestational age (SGA) patients and their neonatal birth weights.
  • In a sample of 110 patients, a significant negative correlation was found between the sFlt-1/PlGF ratio and neonatal birth weight, especially in late-onset SGA cases.
  • The findings suggest that lower sFlt-1/PlGF ratios indicate better placental function and could be useful for predicting growth disorders in late-onset SGA cases.

Article Abstract

Unlabelled: We explored whether there was a relationship between the sFlt-1/PlGF ratio in early-late and late-onset SGA patients and whether it is associated with neonatal birth weight.

Material/methods: 110 patients who were diagnosed with a fetal weight below the 10th percentile for gestational age and who at the same time delivered neonates with a birth weight below the 10th percentile for gestational age. For each of the patients sFlt-1, PlGF and the sFlt-1/PlGF ratio were studied and uterine artery (UtA) and umbilical artery (UA) Doppler were performed.

Results: sFlt-1/PlGF ratios and neonatal birth weight which showed significant negative correlation across the entire population studied (R = -0.46, p < 0.001). In late-onset SGA patients this negative correlation was observed, as well (R = -0.54, p < 0.001) In the group of patients with pregnancies older than 34 weeks and an sFlt-1/PlGF ratio ≥38, we observed a significantly lower neonatal birth weight when compared to the same gestational age group with an sFlt-1/PlGF ratio <38 (2045 g vs 2405 g, p < 0.001).

Conclusion: Late-onset SGA syndromes are characterized by lower sFlt-1/PlGF ratios, which indicates a lower degree of placental function impairment. The sFlt-1/PlGF ratio can be a predictor of more significant growth disorders and a lower neonatal birth weight. The sFlt-1/PlGF ratio can be helpful in distinguishing between disordered angiogenesis-dependent and other causes of late-onset SGA cases.

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Source
http://dx.doi.org/10.1016/j.preghy.2018.08.448DOI Listing

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