Evidence map›Paper›PMID 40196912›Full record

ArticleJournal of pediatric endocrinology & metabolism : JPEM2025

Cord blood metabolomic profiling in high risk newborns born to diabetic, obese, and overweight mothers: preliminary report.

Özlem Ünal Uzun, Duygu Eneş, Müge Çınar, Ayla Günlemez Adugit, Büşra Uçar, Ali Duranoğlu, Ufuk Bozkurt Obuz, Mustafa Çelebier, İncilay Lay

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Article in Journal of pediatric endocrinology & metabolism : JPEM, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Özlem Ünal UzunDepartment of Pediatrics, Division of Metabolism, Faculty of Medicine, Kocaeli University, Kocaeli, Türkiye.ORCID https://orcid.org/0000-0001-7937-7721
Duygu EneşDepartment of Analytical Chemistry, Faculty of Pharmacy, Başkent University, Ankara, Türkiye.ORCID https://orcid.org/0000-0002-8908-3177
Müge ÇınarDepartment of Pediatrics, Division of Metabolism, Faculty of Medicine, Kocaeli University, Kocaeli, Türkiye.ORCID https://orcid.org/0000-0003-4309-2331
Ayla Günlemez AdugitDepartment of Pediatrics, Division of Neonatology, Faculty of Medicine, Kocaeli University, Kocaeli, Türkiye.ORCID https://orcid.org/0000-0003-1492-3861
Büşra UçarDepartment of Analytical Chemistry, Faculty of Pharmacy, Hacettepe University, Ankara, Türkiye.ORCID https://orcid.org/0009-0007-0416-1185
Ali DuranoğluDepartment of Pediatrics, Faculty of Medicine, Kocaeli University, Kocaeli, Türkiye.ORCID https://orcid.org/0000-0002-4299-6569
Ufuk Bozkurt ObuzScientific and Technological Research Center, Sinop University, Sinop, Türkiye.ORCID https://orcid.org/0000-0003-4544-9285
Mustafa ÇelebierDepartment of Analytical Chemistry, Faculty of Pharmacy, Hacettepe University, Ankara, Türkiye.ORCID https://orcid.org/0000-0001-7712-5512
İncilay LayDepartment of Medical Biochemistry, Hacettepe University, Ankara, Türkiye.ORCID https://orcid.org/0000-0002-1466-5746

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesNewborns of diabetic and obese/overweight mothers face long-term metabolic risks. Untargeted cord blood metabolomic analysis using quadrupole time-of-flight liquid chromatography/mass spectrometry (Q-TOF LC/MS) was performed to explore metabolic alterations and pathways in these high-risk infants.

methodsCord blood samples were collected from 46 newborns born to mothers with gestational diabetes (10), obesity (14), overweight (18), type 2 diabetes mellitus (3), type 1 diabetes mellitus (1), and 20 newborns born to healthy mothers. Q-TOF LC/MS was used to investigate the alterations in cord blood metabolomic profiles. Data processing was conducted using MZmine 2.53. Putative metabolites were idendtified using MetaboAnalyst 6.0.

resultsDistinct metabolite profiles were observed between diabetes and control groups. Significant identical trend in 19 metabolites were determined in both diabetes and obesity + overweight group vs. control group. Key pathways included steroid and bile acid biosynthesis. Upregulated oxidative stress, clues to sphingophospholipid metabolism, high levels of dihomo-gamma-linolenic acid (DGLA), pantothenic acid, and TRH were detected. The kynurenine pathway was prominent in the diabetes group.

conclusionsEstrogen metabolites from the 16- and 2-pathways may indicate metabolic risk, with increased downstream flux under diabetic conditions. Accelerated bile acid synthesis may alter fetal metabolic programming, since bile acids play crucial roles in cellular energy regulation and signaling. Elevated pantothenic acid, essential for the production of coenzyme-A, suggests significant alterations in carbohydrate, protein, and fat metabolism. High serum DGLA levels emerge as a potential biomarker for metabolic abnormalities. Increased plasma kynurenines could predict cardiovascular risks. Larger targeted studies are required to validate these metabolic profiles and pathways.

Indexed as

BiomarkersDiabetes, GestationalDiabetes Mellitus, Type 1Diabetes Mellitus, Type 2Fetal BloodMetabolomeMetabolomicsObesityOverweightAdultCase-Control StudiesFemaleFollow-Up StudiesHumansInfant, NewbornMaleBiomarkershigh-risk newbornmaternal diabetesmaternal obesitymetabolomicsquadrupole flight time mass spectrometer

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.