AI Article Synopsis

  • The study aimed to examine afamin levels in pregnant women with late fetal growth restriction (FGR) or small for gestational age (SGA) during the third trimester.
  • It involved 126 participants, including 42 with late FGR, 43 with SGA, and 41 healthy controls, measuring and comparing their serum afamin concentrations.
  • Results showed that women with late FGR had significantly higher afamin levels (199 ng/mL) compared to those with SGA (153 ng/mL) and controls (108 ng/mL), suggesting afamin could be useful for predicting late FGR, though further research is needed.

Article Abstract

Objective: To investigate the afamin concentration in the serum of pregnant women diagnosed with late fetal growth restriction (FGR) or small for gestational age (SGA) in the third trimester.

Methods: This prospective case-control study was conducted on 126 pregnant women, 42 of whom were diagnosed with late FGR in the third trimester, 43 were SGA, and 41 were healthy controls. The groups were compared in terms of maternal serum afamin concentrations.

Results: Three groups were similar in terms of demographic characteristics and gestational age at blood sampling for afamin ( < .05). The median afamin concentration was determined as 199 ng/mL in the late FGR group, 153 ng/mL in the SGA group, and 108 ng/mL in the control group ( = .000). In the post-hoc analysis, while maternal serum afamin concentrations were found to be significantly higher in the late FGR group and SGA group compared to the control group but, this significance could not be shown between the FGR group and the SGA group ( = .00001,  = .005,  = .137, respectively). In the ROC analysis, the optimal cutoff value of serum afamin concentration to predict late FGR was determined as 141 ng/mL, with a sensitivity of 66.6% and a specificity of 85.3%.

Conclusions: The serum afamin concentration in the third trimester was found to be higher in pregnant women with late FGR compared to the SGA and control groups. Although afamin is seen as a promising molecule in the clinical prediction of late FGR, this needs to be supported by large series of studies.

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Source
http://dx.doi.org/10.1080/14767058.2023.2240468DOI Listing

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