AI Article Synopsis

  • * Participants, divided into study and control groups based on the Edinburgh Postnatal Depression Scale, underwent metabolic profiling which revealed 22 significant metabolites influencing various metabolic pathways.
  • * LysoPC (24:0) emerged as a promising lipid biomarker for antenatal depression, with a strong predictive ability indicated by an area under the ROC curve (AUC) of 0.858.

Article Abstract

Objective: The study aimed to perform metabolic profiling of serum samples using liquid chromatography with mass spectroscopy (LC-MS) and to explore potential biomarkers of early trimester depression.

Method: Using the Edinburgh Postnatal Depression Scale (EPDS), participants were randomly divided into study and control groups. Serum metabolic profiles of the two groups were analysed by using LC-MS. Differential metabolite and pathway analysis were identified by using orthogonal projections to latent structure-discriminant analysis (OPLS-DA) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis. Additionally, least absolute shrinkage and selection operator (LASSO) logistic and receiver operating characteristic (ROC) curve analyses were also conducted to explore potential biomarkers of antenatal depression (AD).

Results: The study included 41 participants, consisting of 16 subjects with AD and 25 controls. A total of 22 different metabolites were identified ( < .005), mainly affecting glycerophospholipid metabolism, linoleic acid metabolism, synthesis and degradation of ketone bodies, phenylalanine metabolism, and butanoate metabolism. The area under the ROC curve (AUC) for the LysoPC (24:0) was 0.858. This suggests that LysoPC (24:0) may be a potentially effective predictor of risk factors for AD.

Conclusions: The study suggests that LysoPC (24:0) may be an effective and specific lipid biomarker for early trimester depression.

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Source
http://dx.doi.org/10.1177/10398562241286679DOI Listing

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