Comparative analysis of anticoagulant influence on PMI estimation based on porcine blood metabolomics profile measured using GC-MS.

IF 3.9 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Frontiers in Molecular Biosciences Pub Date : 2025-01-07 eCollection Date: 2024-01-01 DOI:10.3389/fmolb.2024.1400622
Patrycja Mojsak, Paulina Samczuk, Paulina Klimaszewska, Michal Burdukiewicz, Jaroslaw Chilimoniuk, Krystyna Grzesiak, Karolina Pietrowska, Justyna Ciborowska, Anna Niemcunowicz-Janica, Adam Kretowski, Michal Ciborowski, Michal Szeremeta
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Abstract

Introduction: Accurate post-mortem interval (PMI) estimation is essential in forensic investigations. Although various methods for PMI determination have been developed, only an approximate estimation is still achievable, and an accurate PMI indication is still challenging. Therefore, in this study, we employed gas chromatography-mass spectrometry (GC-MS)-based metabolomics to assess post-mortem changes in porcine blood samples collected with and without the addition of anticoagulant (EDTA). Our study aimed to identify metabolites dependent on the EDTA addition and time (taking into account the biodiversity of the studied organism) and those that are time-dependent but resistant to the addition of an anticoagulant.

Methods: The experiment was performed on blood samples collected from 16 animals (domestic pig, breed: Polish Large White), 8 with and 8 without EDTA addition. The moment of death (time 0) and 15 additional time points (from 3 to 168 h after death) were selected to examine changes in metabolites' levels in specific time intervals. We employed linear mixed models to study the relationship between metabolite intensities, time and presence of EDTA while accounting for the effect of individual pigs.

Results and discussion: We confirmed that the intensity of 16 metabolites (mainly amino acids) significantly depends on PMI and the presence of EDTA. However, the intensity of the ideal biomarker(s) for PMI estimation should be determined only by the time after death and not by external factors such as the presence of the anticoagulant agent. Thus, we identified 41 metabolites with time-dependent intensities that were not susceptible to EDTA presence. Finally, we assessed the performance of these metabolites in a PMI predictive model. Citraconic acid yielded one of the lowest errors in general PMI estimation (32.82 h). Moreover, similar errors were observed for samples with and without EDTA (33.32 h and 32.34 h, respectively). Although the small sample size and information leak in predictive modelling prevent drawing definite conclusions, citraconic acid shows potential as a robust PMI estimator.

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采用气相色谱-质谱法测定猪血液代谢组学特征,对比分析抗凝剂对PMI估计的影响。
准确的死后间隔(PMI)估计是法医调查必不可少的。虽然已经开发了各种PMI测定方法,但仍然只能实现近似估计,准确的PMI指示仍然具有挑战性。因此,在本研究中,我们采用气相色谱-质谱(GC-MS)为基础的代谢组学来评估在添加抗凝剂(EDTA)和不添加抗凝剂(EDTA)的情况下收集的猪血液样本的死后变化。我们的研究旨在确定依赖于EDTA添加量和时间的代谢物(考虑到所研究生物的生物多样性),以及那些依赖于时间但对抗凝剂添加具有抗性的代谢物。方法:选取16只家猪(品种:波兰大白猪),8只添加EDTA, 8只未添加EDTA。选择死亡时刻(时间0)和15个额外时间点(死亡后3至168 h)来检测特定时间间隔内代谢物水平的变化。我们采用线性混合模型来研究代谢物强度、时间和EDTA存在之间的关系,同时考虑到个体猪的影响。结果和讨论:我们证实16种代谢物(主要是氨基酸)的强度显著依赖于PMI和EDTA的存在。然而,用于PMI估计的理想生物标志物的强度应该仅由死亡后的时间决定,而不是由抗凝剂的存在等外部因素决定。因此,我们确定了41种具有时间依赖性强度的代谢物,这些代谢物不受EDTA存在的影响。最后,我们在PMI预测模型中评估了这些代谢物的性能。柠檬酸在一般PMI估计中的误差最低(32.82 h)。此外,在含有和不含EDTA的样品中观察到类似的误差(分别为33.32 h和32.34 h)。虽然预测模型中的小样本量和信息泄漏阻止了得出明确的结论,但柠檬酸显示出作为稳健PMI估计器的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Frontiers in Molecular Biosciences
Frontiers in Molecular Biosciences Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
7.20
自引率
4.00%
发文量
1361
审稿时长
14 weeks
期刊介绍: Much of contemporary investigation in the life sciences is devoted to the molecular-scale understanding of the relationships between genes and the environment — in particular, dynamic alterations in the levels, modifications, and interactions of cellular effectors, including proteins. Frontiers in Molecular Biosciences offers an international publication platform for basic as well as applied research; we encourage contributions spanning both established and emerging areas of biology. To this end, the journal draws from empirical disciplines such as structural biology, enzymology, biochemistry, and biophysics, capitalizing as well on the technological advancements that have enabled metabolomics and proteomics measurements in massively parallel throughput, and the development of robust and innovative computational biology strategies. We also recognize influences from medicine and technology, welcoming studies in molecular genetics, molecular diagnostics and therapeutics, and nanotechnology. Our ultimate objective is the comprehensive illustration of the molecular mechanisms regulating proteins, nucleic acids, carbohydrates, lipids, and small metabolites in organisms across all branches of life. In addition to interesting new findings, techniques, and applications, Frontiers in Molecular Biosciences will consider new testable hypotheses to inspire different perspectives and stimulate scientific dialogue. The integration of in silico, in vitro, and in vivo approaches will benefit endeavors across all domains of the life sciences.
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