Enhancing Differential Diagnosis Related to Oxidative Stress, Nitrous Oxide, and Nutrition by Rapid Plasma Homocysteine Measurement.

IF 6.8 Q1 TOXICOLOGY Journal of Xenobiotics Pub Date : 2024-09-27 DOI:10.3390/jox14040075
Guillaume Grzych, Farid Zerimech, Benjamin Touze, Clarence Descamps, Marie-Adélaïde Bout, Marie Joncquel, Claire Douillard, Isabelle Kim, Céline Tard, Thierry Brousseau
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Abstract

Background: Historically used as a marker for inherited disorders, the current interest in plasma homocysteine measurement lies in its ability to provide valuable information about the metabolic and nutritional status of patients. Specifically, nitrous oxide (N2O) abuse can lead to functional vitamin B12 deficiency by oxidation and increase oxidative stress, resulting in elevated plasma homocysteine levels, which mimic neurological conditions such as Guillain-Barré syndrome. Rapid identification of hyperhomocysteinemia is crucial for timely intervention and avoiding costly, unnecessary treatments.

Objective: This study evaluates the performance of a rapid immunoassay technique (Snibe) compared to mass spectrometry (LC-MS/MS) for measuring plasma homocysteine levels in patients with nitrous oxide abuse and non-inherited caused of elevated homocysteine, aiming to enhance differential diagnosis related to oxidative stress.

Methods: 235 patients from Lille University Hospital were included. EDTA blood samples were collected and analyzed using both rapid immunoassay (Snibe) and LC-MS/MS. Neurological assessment was performed using the peripheral neuropathy disability (PND) score.

Results: Firstly, significant elevations in plasma homocysteine levels were observed in patients abusing nitrous oxide measured by LC-MS/MS. Secondly, the immunoassay provided rapid results, essential for early clinical decision-making, but tended to underestimate high values compared to LC-MS/MS. A good correlation was found between the methods for low and moderate values.

Conclusion: The immunoassay tended to underestimate high-value samples compared to LC-MS/MS, which is a common problem with the competitive methodology. The rapid immunoassay technique is effective for initial screening and early intervention, aiding in the differential diagnosis of conditions related to oxidative stress. Therefore, it is recommended to use the CLIA method for initial screening and confirm with mass spectrometry if there are abnormal samples. Integrating both techniques can enhance diagnostic accuracy and improve patient outcomes.

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通过快速血浆同型半胱氨酸测量加强与氧化应激、氧化亚氮和营养相关的鉴别诊断。
背景:血浆同型半胱氨酸测量历来被用作遗传性疾病的标志物,目前人们对它的兴趣在于它能够提供有关患者代谢和营养状况的宝贵信息。具体来说,一氧化二氮(N2O)滥用可通过氧化导致功能性维生素 B12 缺乏,并增加氧化应激,导致血浆同型半胱氨酸水平升高,从而模拟神经系统疾病,如格林-巴利综合征。快速识别高同型半胱氨酸血症对于及时干预和避免昂贵、不必要的治疗至关重要:本研究评估了快速免疫测定技术(Snibe)与质谱法(LC-MS/MS)在测量一氧化二氮滥用和非遗传性同型半胱氨酸升高患者血浆同型半胱氨酸水平方面的性能比较,旨在加强与氧化应激相关的鉴别诊断。采集 EDTA 血液样本,并使用快速免疫分析法(Snibe)和 LC-MS/MS 进行分析。使用周围神经病变残疾(PND)评分进行神经评估:结果:首先,通过 LC-MS/MS 测定,发现滥用一氧化二氮的患者血浆同型半胱氨酸水平明显升高。其次,免疫测定能快速得出结果,这对早期临床决策至关重要,但与 LC-MS/MS 相比,免疫测定往往会低估高值。结论:免疫测定法倾向于低估高值:结论:与 LC-MS/MS 相比,免疫测定往往会低估高值样本,这是竞争性方法的一个常见问题。快速免疫测定技术对于初步筛查和早期干预非常有效,有助于对氧化应激相关疾病进行鉴别诊断。因此,建议使用 CLIA 方法进行初步筛查,如有异常样本,则使用质谱法进行确认。将这两种技术相结合可提高诊断的准确性,改善患者的预后。
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来源期刊
CiteScore
5.30
自引率
1.70%
发文量
21
审稿时长
10 weeks
期刊介绍: The Journal of Xenobiotics publishes original studies concerning the beneficial (pharmacology) and detrimental effects (toxicology) of xenobiotics in all organisms. A xenobiotic (“stranger to life”) is defined as a chemical that is not usually found at significant concentrations or expected to reside for long periods in organisms. In addition to man-made chemicals, natural products could also be of interest if they have potent biological properties, special medicinal properties or that a given organism is at risk of exposure in the environment. Topics dealing with abiotic- and biotic-based transformations in various media (xenobiochemistry) and environmental toxicology are also of interest. Areas of interests include the identification of key physical and chemical properties of molecules that predict biological effects and persistence in the environment; the molecular mode of action of xenobiotics; biochemical and physiological interactions leading to change in organism health; pathophysiological interactions of natural and synthetic chemicals; development of biochemical indicators including new “-omics” approaches to identify biomarkers of exposure or effects for xenobiotics.
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