Early prediction of macrosomia based on an analysis of second trimester amniotic fluid by capillary electrophoresis

Author:

Boisvert Michel R1,Koski Kristine G2,Burns David H3,Skinner Cameron D4

Affiliation:

1. Department of Chemistry & Biochemistry, Concordia University, Montreal, QC, H4B 1R6, Canada

2. School of Dietetics & Human Nutrition, McGill University (Macdonald Campus), Montreal, QC, H9X 3V9, Canada

3. Department of Chemistry, McGill University, Montreal, QC, H3A 2K6, Canada

4. Department of Chemistry & Biochemistry, Concordia University, Montreal, QC, H4B 1R6, Canada.

Abstract

Aim: To identify, using capillary electrophoresis and chemometrics, early biomarkers in human amniotic fluid of large-for-gestational-age (LGA) infants. Materials & methods: Second trimester amniotic fluid samples, obtained from mothers undergoing age-related amniocentesis, were analyzed by capillary electrophoresis. Electropherogram data were aligned using correlation-optimized warping. A genetic algorithm using a Bayesian evaluation function and a leave-one-out cross-validation strategy for two birth outcomes: appropriate-for-gestational-age (AGA) versus LGA infants. Results: LGA (n = 23) was differentiated from AGA (n = 86) with a sensitivity of 100% and a specificity of 98% using only two wavelets. The first wavelet is associated with albumin and the second wavelet with an unknown small molecule. Conclusion: The approach developed herein allows LGA fetuses to be metabolically distinguished from AGA fetuses early in pregnancy and indicates that the birth of a LGA infant is already associated with an altered biochemical profile by the second trimester.

Publisher

Future Medicine Ltd

Subject

Biochemistry, medical,Clinical Biochemistry,Drug Discovery

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