Plasma Proteomic Profiling of a Group of Anxious Dogs by LC-MS/MS: A Case-Control Study.

IF 2.5 4区 生物学 Q3 BIOCHEMICAL RESEARCH METHODS
PROTEOMICS – Clinical Applications Pub Date : 2025-07-01 Epub Date: 2025-07-04 DOI:10.1002/prca.70014
Claudia Gaither, Robert Popp, Christoph H Borchers, Francis Beaudry, Marion Desmarchelier
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引用次数: 0

Abstract

Purpose: Anxiety is the most common underlying cause of behavioral problems in dogs, which remain a top reason for relinquishment and euthanasia. Despite its high prevalence, anxiety is often underdiagnosed, partly due to a limited understanding of biological processes and absence of diagnostic biomarkers. Our study aims to address this knowledge gap.

Experimental design: Plasma from 10 anxious and 10 matched control dogs were analyzed following a label-free quantitation proteomics workflow based on data-dependent acquisition using a Thermo Q Exactive Plus coupled to an EASY-nLC 1200, Vanquish UHPLC, or Evosep One. Data were processed with Proteome Discoverer 2.4 (Thermo), Perseus (Max Planck Institute), Cytoscape and other bioinformatic tools.

Results: Between 279 and 350 proteins were identified, and proteins such as fibrinogen, apolipoproteins, and complement system and coagulation cascade proteins were significantly different between groups. Additionally, we identified two putative subgroups of anxious dogs, suggesting potentially different underlying pathophysiological mechanisms for a single anxiety phenotype.

Conclusions and clinical relevance: To our knowledge, this is the first comprehensive clinical in-depth proteomic profiling of plasma from anxious dogs. Our findings lay the foundation for elucidating the pathophysiology of canine anxiety and for the future validation and establishment of novel candidate biomarkers for disease diagnosis. Novel biomarkers would allow for a more effective and objective diagnosis of anxiety, even when not phenotypically apparent.

Summary: Previous mass spectrometry (MS) studies have found proteomic profile differences in other diseases and other animal species. This is to our knowledge, the first unbiased and comprehensive clinical in-depth proteomic profiling of plasma from dogs suffering from anxiety disorders. These findings have an impact on animal health as they set the foundation to elucidate the pathophysiology of canine anxiety so that in the future novel candidate biomarkers can be established and validated, furthering the potential development of new drugs and guiding patient-specific therapeutic interventions based on biomarker profiles. In the clinic, novel biomarkers could allow for a more effective and objective diagnosis of anxiety disorders, even when not phenotypically apparent. Detection and measurement of early stages of anxiety disorders as well as treatment monitoring in pet dogs would allow patients to be treated quicker, before the potential onset of aggression, and a faster recovery, thus improving the welfare of companion animals.

用LC-MS/MS分析一组焦虑犬的血浆蛋白质组学:一项病例对照研究。
目的:焦虑是狗的行为问题最常见的潜在原因,这仍然是放弃和安乐死的首要原因。尽管它的患病率很高,但焦虑往往被诊断不足,部分原因是对生物过程的理解有限,缺乏诊断性生物标志物。我们的研究旨在解决这一知识差距。实验设计:使用Thermo Q Exactive Plus与EASY-nLC 1200、Vanquish UHPLC或Evosep One进行数据依赖采集,采用无标记定量蛋白质组学工作流程,对10只焦虑犬和10只匹配的对照犬的血浆进行分析。使用Proteome Discoverer 2.4 (Thermo)、Perseus (Max Planck Institute)、Cytoscape等生物信息学工具对数据进行处理。结果:共鉴定出279 ~ 350种蛋白,纤维蛋白原、载脂蛋白、补体系统和凝血级联蛋白等蛋白在两组间差异显著。此外,我们确定了两个假定的焦虑狗亚群,这表明单一焦虑表型的潜在病理生理机制可能不同。结论和临床意义:据我们所知,这是第一次对焦虑犬的血浆进行全面的临床深入蛋白质组学分析。我们的研究结果为阐明犬焦虑的病理生理学以及未来验证和建立新的候选疾病诊断生物标志物奠定了基础。新的生物标志物将允许对焦虑进行更有效和客观的诊断,即使在表现上并不明显。摘要:以前的质谱(MS)研究已经发现了其他疾病和其他动物物种的蛋白质组谱差异。据我们所知,这是第一次对患有焦虑症的狗的血浆进行公正和全面的临床深入蛋白质组学分析。这些发现对动物健康具有重要影响,因为它们为阐明犬类焦虑的病理生理学奠定了基础,从而在未来可以建立和验证新的候选生物标志物,进一步开发新药,并指导基于生物标志物谱的患者特异性治疗干预。在临床上,新的生物标志物可以更有效和客观地诊断焦虑症,即使在表现上不明显。在宠物狗身上检测和测量焦虑症的早期阶段,以及监测治疗情况,可以让病人在潜在的攻击发作之前得到更快的治疗,并更快地恢复,从而改善伴侣动物的福利。
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来源期刊
PROTEOMICS – Clinical Applications
PROTEOMICS – Clinical Applications 医学-生化研究方法
CiteScore
5.20
自引率
5.00%
发文量
50
审稿时长
1 months
期刊介绍: PROTEOMICS - Clinical Applications has developed into a key source of information in the field of applying proteomics to the study of human disease and translation to the clinic. With 12 issues per year, the journal will publish papers in all relevant areas including: -basic proteomic research designed to further understand the molecular mechanisms underlying dysfunction in human disease -the results of proteomic studies dedicated to the discovery and validation of diagnostic and prognostic disease biomarkers -the use of proteomics for the discovery of novel drug targets -the application of proteomics in the drug development pipeline -the use of proteomics as a component of clinical trials.
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