Metabolomic patterns in fatal carbon monoxide poisoning: A forensic toxicology perspective.

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Title: Metabolomic patterns in fatal carbon monoxide poisoning: A forensic toxicology perspective.
Authors: Ariza-Garcia, Wilmar Alexander1,2 (AUTHOR), Pardo-Rodriguez, Daniel3 (AUTHOR), Taborda-Ocampo, Gonzalo4 (AUTHOR), Rosero-Moreano, Milton4 (AUTHOR), Cala, Mónica P.1,3 (AUTHOR)
Source: Forensic Science International. Dec2025, Vol. 377, pN.PAG-N.PAG. 1p.
Subjects: Carbon monoxide poisoning, Forensic toxicology, Biomarkers, Lipidomics, Metabolomics, Lipid metabolism, Poisons
Abstract: Carbon monoxide (CO) poisoning remains a major forensic and public health concern due to its high lethality and diagnostic challenges. Its colorless, odorless nature and the limited reliability of carboxyhemoglobin (COHb) levels—compounded by postmortem changes—complicate toxicological interpretation. This study employed untargeted metabolomics and lipidomics to characterize systemic biochemical alterations in fatal CO poisoning cases. Integrated metabolomic and lipidomic analyses revealed significant dysregulation in lipid-related pathways, including steroid biosynthesis, mitochondrial β-oxidation, fatty acid and sphingolipid metabolism, and lysophospholipid-mediated membrane destabilization. Impaired biosynthesis of highly unsaturated fatty acids (HUFA) was also observed, potentially compromising membrane structure and signaling. These findings highlight widespread metabolic disruption affecting energy homeostasis and lipid signaling. Among the altered metabolites, carnitine 18:2 (CAR 18:2) demonstrated strong discriminative power (AUC = 0.846) between CO-poisoned and control cases, suggesting its value as a forensic biomarker. Additionally, lysophosphatidylcholine 18:2 (LPC 18:2) and sphingomyelin 44:1;O₂ (SM 44:1;O₂) emerged as promising candidates. These results underscore the systemic metabolic impact of CO toxicity and support the continued exploration and implementation of targeted lipidomics as alternative forensic biomarkers in fatal poisonings. • Untargeted metabolomics and lipidomics revealed systemic biochemical disruptions in fatal CO poisoning. • Lipid pathway dysregulation involved β-oxidation, steroid biosynthesis, and sphingolipid metabolism. • Oxidative stress and impaired lipid homeostasis emerged as central toxicodynamic mechanisms. • CAR 18:2, LPC 18:2, and SM 44:1;O₂ demonstrated strong potential as forensic biomarkers. [ABSTRACT FROM AUTHOR]
Copyright of Forensic Science International is the property of Elsevier B.V. and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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  Data: Metabolomic patterns in fatal carbon monoxide poisoning: A forensic toxicology perspective.
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  Data: Carbon monoxide (CO) poisoning remains a major forensic and public health concern due to its high lethality and diagnostic challenges. Its colorless, odorless nature and the limited reliability of carboxyhemoglobin (COHb) levels—compounded by postmortem changes—complicate toxicological interpretation. This study employed untargeted metabolomics and lipidomics to characterize systemic biochemical alterations in fatal CO poisoning cases. Integrated metabolomic and lipidomic analyses revealed significant dysregulation in lipid-related pathways, including steroid biosynthesis, mitochondrial β-oxidation, fatty acid and sphingolipid metabolism, and lysophospholipid-mediated membrane destabilization. Impaired biosynthesis of highly unsaturated fatty acids (HUFA) was also observed, potentially compromising membrane structure and signaling. These findings highlight widespread metabolic disruption affecting energy homeostasis and lipid signaling. Among the altered metabolites, carnitine 18:2 (CAR 18:2) demonstrated strong discriminative power (AUC = 0.846) between CO-poisoned and control cases, suggesting its value as a forensic biomarker. Additionally, lysophosphatidylcholine 18:2 (LPC 18:2) and sphingomyelin 44:1;O₂ (SM 44:1;O₂) emerged as promising candidates. These results underscore the systemic metabolic impact of CO toxicity and support the continued exploration and implementation of targeted lipidomics as alternative forensic biomarkers in fatal poisonings. • Untargeted metabolomics and lipidomics revealed systemic biochemical disruptions in fatal CO poisoning. • Lipid pathway dysregulation involved β-oxidation, steroid biosynthesis, and sphingolipid metabolism. • Oxidative stress and impaired lipid homeostasis emerged as central toxicodynamic mechanisms. • CAR 18:2, LPC 18:2, and SM 44:1;O₂ demonstrated strong potential as forensic biomarkers. [ABSTRACT FROM AUTHOR]
– Name: AbstractSuppliedCopyright
  Label:
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  Data: <i>Copyright of Forensic Science International is the property of Elsevier B.V. and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.)
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RecordInfo BibRecord:
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      – Type: doi
        Value: 10.1016/j.forsciint.2025.112643
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      – Code: eng
        Text: English
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    Subjects:
      – SubjectFull: Carbon monoxide poisoning
        Type: general
      – SubjectFull: Forensic toxicology
        Type: general
      – SubjectFull: Biomarkers
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      – SubjectFull: Lipidomics
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      – SubjectFull: Metabolomics
        Type: general
      – SubjectFull: Lipid metabolism
        Type: general
      – SubjectFull: Poisons
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    Titles:
      – TitleFull: Metabolomic patterns in fatal carbon monoxide poisoning: A forensic toxicology perspective.
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            NameFull: Ariza-Garcia, Wilmar Alexander
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            NameFull: Pardo-Rodriguez, Daniel
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            NameFull: Rosero-Moreano, Milton
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            – D: 01
              M: 12
              Text: Dec2025
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              Y: 2025
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              Value: 377
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