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A non-targeted LC-MS metabolic profiling of pregnancy: longitudinal evidence from healthy and pre-eclamptic pregnancies

Laivuori Hannele; Heinonen Seppo; Klåvus Anton; Jokkala Jenna; Kärkkäinen Olli; Hanhineva Kati; Lehtonen Marko; Auriola Seppo; Jääskeläinen Tiina; The FINNPEC Core Investigator Group

A non-targeted LC-MS metabolic profiling of pregnancy: longitudinal evidence from healthy and pre-eclamptic pregnancies

Laivuori Hannele
Heinonen Seppo
Klåvus Anton
Jokkala Jenna
Kärkkäinen Olli
Hanhineva Kati
Lehtonen Marko
Auriola Seppo
Jääskeläinen Tiina
The FINNPEC Core Investigator Group
Katso/Avaa
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Springer
doi:10.1007/s11306-020-01752-5
URI
https://doi.org/10.1007/s11306-020-01752-5
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Julkaisun pysyvä osoite on:
https://urn.fi/URN:NBN:fi-fe2022020818024
Tiivistelmä

Introduction
Maternal metabolism changes substantially during pregnancy. However, few studies have used metabolomics technologies to characterize changes across gestation.
Objectives and methods
We applied liquid chromatography–mass spectrometry (LC–MS) based non-targeted metabolomics to determine whether the metabolic profile of serum differs throughout the pregnancy between pre-eclamptic and healthy women in the FINNPEC (Finnish Genetics of Preeclampsia Consortium) Study. Serum samples were available from early and late pregnancy.
Results
Progression of pregnancy had large-scale effects to the serum metabolite profile. Altogether 50 identified metabolites increased and 49 metabolites decreased when samples of early pregnancy were compared to samples of late pregnancy. The metabolic signatures of pregnancy were largely shared in pre-eclamptic and healthy women, only urea, monoacylglyceride 18:1 and glycerophosphocholine were identified to be increased in the pre-eclamptic women when compared to healthy controls.
Conclusions
Our study highlights the need of large-scale longitudinal metabolomic studies in non-complicated pregnancies before more detailed understanding of metabolism in adverse outcomes could be provided. Our findings are one of the first steps for a broader metabolic understanding of the physiological changes caused by pregnancy per se.

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