EventsThe 4th International Electronic Conference on Metabolomics
Published
This submission belongs to the session S1. Clinical Application of Metabolomics with Special Reference to the Endocrinological Arena of the event The 4th International Electronic Conference on Metabolomics
Published date
10 Oct, 2025
Academic Editor
author-avatarYunping Qiu
Citation
Raúl González-Domínguez, Lucía Jurado-Sumariva, Álvaro González-Domínguez, Otto Savolainen, Rikard Landberg, Adverse neonatal outcomes predispose individuals to exacerbated metabolic disturbances in childhood obesity, in Proceedings of The 4th International Electronic Conference on Metabolomics, 13 October–15 October 2025, MDPI: Basel, Switzerland
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Adverse neonatal outcomes predispose individuals to exacerbated metabolic disturbances in childhood obesity

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Otto Savolainen 2
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1. Instituto de Investigación e Innovación Biomédica de Cádiz (INiBICA), Universidad de Cádiz, Cádiz, 11009, Spain., Spain
2. Division of Food and Nutrition Science, Chalmers University of Technology, Gothenburg, SE-412 96, Sweden., Sweden
Abstract

Introduction: The perinatal period is highly sensitive to obesogenic determinants, and it is consistently reported that adverse birth outcomes are among the most important early risk factors for childhood obesity. Nevertheless, the molecular mechanisms underpinning this greater predisposition remain to be elucidated.

Methods: To obtain deeper insights into the influence of neonatal conditions in obesity-related metabolic disturbances occurring later during childhood, we applied high-throughput metabolomics (UHPLC-HRMS) to plasma and erythrocyte samples from a cohort of children diagnosed with obesity, from whom birth metrics (i.e., gestational age, weight, and length at birth) were available from their medical records.

Results: The findings of this study evidenced that adverse neonatal outcomes (i.e., low gestational age, weight, and length at birth) may predispose individuals to an unhealthier metabolic status, as reflected in negative associations with anthropometric parameters (e.g., waist circumference) and biochemical markers of insulin resistance (e.g., HOMA-IR) and inflammation (e.g., CRP, inflammatory indices). This was accompanied by exacerbations in a multitude of central metabolic pathways that play a crucial role in obesity pathophysiology, such as energy metabolism, the homeostasis of branched chain and aromatic amino acids, the regulation of oxidative stress, and the biosynthesis of steroid hormones and bile acids.

Conclusion: Accordingly, we hypothesize that even minor variations in neonatal conditions may provoke deleterious molecular programming mechanisms with a strong impact on later metabolic risk.

Keywords
Childhood obesity
Insulin resistance
Metabolomics
Neonatal outcomes
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