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组织和血浆蛋白质组学分析表明 AHSG 是升主动脉瘤的潜在生物标志物。

Tissue and plasma proteomic profiling indicates AHSG as a potential biomarker for ascending thoracic aortic aneurysms.

机构信息

Department of Cardiovascular Genetics and The Laboratory of Forensic Genetics, The Cyprus Institute of Neurology and Genetics, Iroon Avenue 6, Agios Dometios, 2371, Nicosia, Cyprus.

OMass Therapeutics, The Schrödinger Building, Heatley Road, The Oxford Science Park, Oxford, OX4 4GE, UK.

出版信息

BMC Cardiovasc Disord. 2023 Mar 16;23(1):138. doi: 10.1186/s12872-023-03154-6.

Abstract

BACKGROUND

Thoracic Aortic Aneurysms (TAAs) develop asymptomatically and are characterized by dilatation of the aorta. This is considered a life-threatening vascular disorder due to the risk of aortic dissection and rupture. There is an urgent need to identify blood-borne biomarkers for the early detection of TAA. The goal of the present study was to identify potential protein biomarkers associated with TAAs, using proteomic analysis of aortic tissue and plasma samples.

METHODS

Extracted proteins from 14 aneurysmal and 12 non-aneurysmal thoracic aortic tissue specimens as well as plasma samples from six TAA patients collected pre-and postoperatively and six healthy controls (HC), were analyzed by liquid chromatography-tandem mass spectrometry. Proteomic data were further processed and following filtering criteria, one protein was selected for verification and validation in a larger cohort of patients and controls using a targeted quantitative proteomic approach and enzyme-linked immunosorbent assay, respectively.

RESULTS

A total of 1593 and 363 differentially expressed proteins were identified in tissue and plasma samples, respectively. Pathway enrichment analysis on the differentially expressed proteins revealed a number of dysregulated molecular pathways that might be implicated in aneurysm pathology including complement and coagulation cascades, focal adhesion, and extracellular matrix receptor interaction pathways. Alpha-2-HS glycoprotein (AHSG) was selected for further verification in 36 TAA and 21 HC plasma samples using targeted quantitative proteomic approach. The results showed a significantly decreased concentration of AHSG (p = 0.0002) in the preoperative plasma samples compared with HC samples. Further analyses using a larger validation dataset revealed that AHSG protein levels were significantly lower (p = 0.03) compared with HC. Logistic regression analysis on the validation dataset revealed males, advanced age, hypertension and hyperlipidaemia as significant risk factors for TAA.

CONCLUSION

AHSG concentrations distinguish plasma samples derived from TAA patients and controls. The findings of this study suggest that AHSG may be a potential biomarker for TAA that could lead to better diagnostic capabilities.

摘要

背景

胸主动脉瘤(TAAs)无症状地发展,其特征是主动脉扩张。由于主动脉夹层和破裂的风险,这被认为是一种危及生命的血管疾病。迫切需要确定血液传播的生物标志物,以早期发现 TAA。本研究的目的是使用主动脉组织和血浆样本的蛋白质组学分析来鉴定与 TAA 相关的潜在蛋白质生物标志物。

方法

从 14 个动脉瘤和 12 个非动脉瘤胸主动脉组织标本以及 6 例 TAA 患者术前和术后的血浆样本中提取蛋白质,通过液相色谱-串联质谱法进行分析。对蛋白质组学数据进行进一步处理,根据过滤标准,使用靶向定量蛋白质组学方法和酶联免疫吸附试验分别在更大的患者和对照组队列中选择一种蛋白质进行验证和验证。

结果

在组织和血浆样本中分别鉴定出 1593 种和 363 种差异表达蛋白。对差异表达蛋白进行途径富集分析显示,许多失调的分子途径可能与动脉瘤病理有关,包括补体和凝血级联、焦点粘附和细胞外基质受体相互作用途径。使用靶向定量蛋白质组学方法,在 36 例 TAA 和 21 例 HC 血浆样本中选择α-2-HS 糖蛋白(AHSG)进行进一步验证。结果表明,与 HC 样本相比,术前血浆样本中 AHSG 的浓度显著降低(p=0.0002)。使用更大的验证数据集进行进一步分析表明,AHSG 蛋白水平明显低于 HC(p=0.03)。对验证数据集的逻辑回归分析显示,男性、年龄较大、高血压和高脂血症是 TAA 的显著危险因素。

结论

AHSG 浓度可区分 TAA 患者和对照者的血浆样本。本研究结果表明,AHSG 可能是 TAA 的潜在生物标志物,可提高诊断能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2826/10018995/d99f2f4a69fa/12872_2023_3154_Fig1_HTML.jpg

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